US20190169084A1 - Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging - Google Patents

Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging Download PDF

Info

Publication number
US20190169084A1
US20190169084A1 US16/025,826 US201816025826A US2019169084A1 US 20190169084 A1 US20190169084 A1 US 20190169084A1 US 201816025826 A US201816025826 A US 201816025826A US 2019169084 A1 US2019169084 A1 US 2019169084A1
Authority
US
United States
Prior art keywords
alkyl
group
nsaid
cycloalkyl
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/025,826
Inventor
Mark A. Reiley
B. Michael SILBER
Julio Medina
Frank Kayser
William D. Shrader
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Reiley Pharmaceuticals Inc
Original Assignee
Reiley Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Reiley Pharmaceuticals Inc filed Critical Reiley Pharmaceuticals Inc
Priority to US16/025,826 priority Critical patent/US20190169084A1/en
Publication of US20190169084A1 publication Critical patent/US20190169084A1/en
Assigned to Reiley Pharmaceuticals, Inc. reassignment Reiley Pharmaceuticals, Inc. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MEDINA, JULIO, SILBER, B. MICHAEL, SHRADER, WILLIAM D., KAYSER, FRANK, REILEY, MARK A.
Priority to US17/158,967 priority patent/US20220017432A1/en
Priority to US18/207,628 priority patent/US20240190790A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/004Acyclic, carbocyclic or heterocyclic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium or tellurium
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04Organic compounds
    • A61K51/0402Organic compounds carboxylic acid carriers, fatty acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04Organic compounds
    • A61K51/0474Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group
    • A61K51/0478Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group complexes from non-cyclic ligands, e.g. EDTA, MAG3
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04Organic compounds
    • A61K51/0474Organic compounds complexes or complex-forming compounds, i.e. wherein a radioactive metal (e.g. 111In3+) is complexed or chelated by, e.g. a N2S2, N3S, NS3, N4 chelating group
    • A61K51/0487Metallocenes, i.e. complexes based on a radioactive metal complexed by two cyclopentadienyl anions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04Organic compounds
    • A61K51/0497Organic compounds conjugates with a carrier being an organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F13/00Compounds containing elements of Groups 7 or 17 of the Periodic Table
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F13/00Compounds containing elements of Groups 7 or 17 of the Periodic Table
    • C07F13/005Compounds without a metal-carbon linkage

Definitions

  • Conjugates derived from non-steroidal anti-inflammatory drugs (NSAIDs) and methods of use thereof are disclosed, useful for, inter alia, identifying and localizing the site of pathology and/or inflammation responsible for the sensation of pain in a patient, sites of infection, and identifying and localizing the sites of tumor pathology, including benign, malignant, primary, and secondary tumors.
  • NSAIDs non-steroidal anti-inflammatory drugs
  • Tumor screening for the presence of tumors is very common. Some of the difficulties with tumor screening are expense, patient's time, physician's time, and accuracy. Also, many of the screening tests are not particularly accurate. For example, testing for prostate cancer using serum acid phosphatase or prostate specific antigen (PSA) is non-specific, and elevation of the marker in healthy individuals can be cause for an unnecessary surgery, a prostate biopsy.
  • PSA prostate specific antigen
  • An additional example is MRI screening for breast tumors, whose value has recently been questioned for both insensitivity and occasional misinterpretation.
  • Localization of pain is another area where identifying the site of pathology is important for treatment; however, such localization is often not straightforward.
  • the unpleasant sensation of pain serves as an indicator of a disease or pathological state. Pain often occurs at the site of pathology, and can be a helpful guide in determining diagnosis and appropriate treatment. However, in many cases, the area where a patient experiences pain may not be coincident with the area where the actual pathology has occurred.
  • a classic example is sciatica, where pressure on the sciatic nerve due to a herniated disc in the lower spine can result in a sensation of pain in the leg, at a significant distance from the site of pathology.
  • Another example is the difficulty in diagnosing pain in the chest or thorax, which can arise from multiple causes, such as cardiac ischemia, gastroesophageal reflux, or pulmonary embolism.
  • differential diagnosis requires a systematic process of elimination through tests and procedures until the cause and/or location of pathology is identified.
  • pathology is often accompanied by inflammation at the site of the pathology (which is not necessarily the site where pain is experienced), rapid and non-invasive methods of localizing inflammation in a patient experiencing pain would aid enormous in diagnosing and treating the underlying cause of the pain.
  • the current invention provides compounds and methods useful for identification of areas of pathology, including tumors and inflammation, and screening for infections and sites of infections, via non-invasive imaging.
  • the compounds and methods can be used in both human and veterinary medicine.
  • the invention embraces conjugate comprising a non-steroidal anti-inflammatory drug (NSAID), a residue of a NSAID, or a derivative of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter, an X-ray emitter, and a beta emitter; or a pharmaceutically acceptable salt thereof.
  • the imaging moiety can be optionally bonded to the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID via a linker.
  • the radioactive agent in the first embodiment can be 99m Tc, 52 Mn, 186 Re or 188 Re.
  • the imaging moiety of the first or second embodiment can further comprise a chelating group which bonds or complexes to the radioactive agent; and the imaging moiety can be optionally bonded to the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID via a linker.
  • NSAID non-steroidal anti-inflammatory drug
  • the imaging moiety comprising a chelating group bonded or complexed to the radioactive agent of the third embodiment is of the form:
  • M is selected from the group consisting of 99m Tc, 52 Mn, 186 Re or 188 Re, wherein each J is independently selected from the group consisting of NH and S,
  • R 101 , R 102 , and R 103 are independently selected from the group consisting of optionally substituted C 2 -C 4 alkyl, and the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group, either through a linker or directly, at
  • R( ri ) is —CH 3 or —CH 2 CH 3 and p is an integer between 0 and 4 inclusive and the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group either through a linker or directly if no linker is present, at any location on the cyclopentane ring which does not have a (R ri ) group.
  • the NSAID, residue of an NSAID, or derivative of a NSAID and the imaging moiety are bonded or complexed via a linker, where the linker is selected from the group consisting of an optionally substituted C 1 -C 10 hydrocarbylene group; an optionally substituted C 2 -C 10 heterohydrocarbylene group; and a linker of the form -L E -R 4 -L F -, where the linker -L E -R 4 -L F - can be in either orientation with respect to the NSAID, residue of an NSAID, or derivative of a NSAID and the imaging moiety (that is, either L E or L F can be attached to the NSAID, residue of an NSAID, or derivative of a NSAID, and the other of L E or L F is attached to the imaging moiety).
  • the linker is selected from the group consisting of an optionally substituted C 1 -C 10 hydrocarbylene group; an optionally substituted C 2 -C 10 hetero
  • L E is absent or is selected from the group consisting of —NH—, —N(R 8 )—, and —C( ⁇ O)—
  • R 8 is optionally substituted C 1 -C 4 alkyl
  • R 4 is selected from the group consisting of optionally substituted C 1 -C 10 hydrocarbylene, optionally substituted C 2 -C 10 heterohydrocarbylene, C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • R 9 is selected from the group consisting of H and optionally substituted C 1 -C 4 alkyl.
  • the linker is selected from the group consisting of: —(NH)—(CH 2 ) n —, —(NR a )—(CH 2 ) n —, —(NH)—(CH 2 ) n —(NH)—, —(NR a )—(CH 2 ) n —(NR a )—, —(NH)—(CH 2 CH 2 )—(OCH 2 CH 2 ) m —(NH)—, —(NR a )—(CH 2 CH 2 )—(OCH 2 CH 2 ) m —(NR a )—, —(NH)—(CH 2 CH 2 )—((NH)CH 2 CH 2 ) m —(NH)—, —(NR a )—(CH 2 CH 2 )—((NH)CH 2 CH 2 ) m —(NH)—, —(NR a )—(CH 2 CH 2 )—((NH)CH 2 CH
  • the conjugate in any of the first, second, third, fourth, fifth, or sixth embodiments, is of the formula:
  • L E is absent or is selected from the group consisting of —NH—, —N(R 8 )—, and —C( ⁇ O)—
  • R 8 is optionally substituted C 1 -C 4 alkyl
  • R 4 is selected from the group consisting of optionally substituted C 1 -C 10 hydrocarbylene, optionally substituted C 2 -C 10 heterohydrocarbylene, C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 aryl
  • conjugates of the seventh embodiment are of the form:
  • R 38 is —O—(C 1 -C 4 ) alkyl
  • R 39 is selected from the group consisting of H, F, Cl, Br, I, CH 3 , and CF 3
  • R 40 is selected from the group consisting of H, CH 3 , and CF 3
  • R 41 and R 42 are both H, or R 41 is H and R 42 is OH, or R 41 and R 42 together form an oxo group
  • R 43 is selected from the group consisting of (C 1 -C 10 ) hydrocarbylene and (C 2 -C 10 ) heterohydrocarbylene containing one O atom, two O atoms, one (—S( ⁇ O 2 ))— group, two (—S( ⁇ O 2 ))— groups, or one O atom and one (—S( ⁇ O 2 ))— group, where the O atom or atoms of the heteroalkylene are not bonded directly to a nitrogen atom, and where when more than one heteroatom is present, at least one carbon atom
  • conjugates of the eighth embodiment are of the formula:
  • Re is 186 Re or 188 Re; or pharmaceutically acceptable salts thereof.
  • the conjugates of the eighth embodiment are of the formula:
  • Tc is 99m Tc; or pharmaceutically acceptable salts thereof.
  • the conjugates of the eighth embodiment can be selected from the group consisting of the compounds:
  • Re is 186 Re or 188 Re; where Tc is 99m Tc; and pharmaceutically acceptable salts thereof.
  • the conjugates of the first or second embodiment can be of the formula
  • z1 is an integer between 0 and 4 inclusive; z2 is an integer between 0 and 5 inclusive; and -(linker)-(chelator)-M-(terminal ligand) z1 or -(linker)-M-(terminal ligand) z2 is selected from the group consisting of:
  • L E is absent or is selected from the group consisting of —NH—, —N(R 8 )—, and —(C ⁇ O)—
  • R 8 is optionally substituted C 1 -C 4 alkyl , with the proviso that if the L E moiety of the group -L F -R 4 -L E - would be attached to a nitrogen atom, then L E is absent
  • L G is absent or is selected from the group consisting of —NH—, —N(R 8 )—, and —(C ⁇ O)—
  • R 8 is optionally substituted C 1 -C 4 alkyl
  • R 4 is selected from the group consisting of optionally substituted C 10 hydrocarbylene, optionally substituted C 2 -C 10 heterohydrocarbylene, C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • the -(linker)-(chelator)-M-(terminal ligand) z1 or -(linker)-M-(terminal ligand) z2 group of the conjugates of the twelfth embodiment can be selected from the group consisting of:
  • the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID in any of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, or thirteenth embodiments can be selected from the group consisting of:
  • the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID in any of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, or thirteenth embodiment can be selected from the group consisting of:
  • carbon atom or oxygen atom marked with an asterisk * indicates an open valence at that atom at which the NSAID, residue of a NSAID, or derivative of a NSAID is attached to the remainder of the conjugate.
  • the conjugate of the first, second, third, or fourth embodiments can be selected from the group consisting of:
  • Tc is 99m Tc
  • Re is 186 Re or 188 Re; and pharmaceutically acceptable salts thereof.
  • the conjugate of any one of the first, second, or third embodiments can be selected from the group consisting of:
  • Tc is 99m Tc; and pharmaceutically acceptable salts thereof.
  • the conjugate of any one of the first, second, or third embodiments can be selected from the group consisting of:
  • Tc is 99m Tc; and pharmaceutically acceptable salts thereof.
  • the invention embraces a pharmaceutical composition comprising one or more conjugates of any one of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, thirteenth, fourteenth, fifteenth, sixteenth, seventeenth, or eighteenth embodiments, and a pharmaceutically acceptable excipient.
  • the invention embraces a method of imaging a site of pathology or suspected pathology in a subject, comprising:
  • the radioactive agent of the conjugate comprises 99m Tc, 52 Mn, 186 Re or 188 Re;
  • the pathology or suspected pathology of the twentieth embodiment is a tumor or a suspected tumor.
  • the pathology or suspected pathology of the twentieth embodiment is pain (that is, the subject is suffering from pain).
  • the pathology or suspected pathology of the twentieth h embodiment is an infection or a suspected infection.
  • the invention embraces a conjugate disclosed herein which has an IC 50 for inhibition of a cyclooxygenase of less than about 2 micromolar, less than about 1 micromolar, preferably less than about 0.5 micromolar, more preferably less than about 0.3 micromolar, still more preferably less than about 0.1 micromolar, yet more preferably less than about 50 nanomolar; in a twenty-fifth embodiment, the cyclooxygenase is COX-2.
  • the invention embraces a conjugate of any one of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, thirteenth, fourteenth, fifteenth, sixteenth, seventeenth, or eighteenth embodiments which has an IC 50 for inhibition of a cyclooxygenase of less than about 2 micromolar, less than about 1 micromolar, preferably less than about 0.5 micromolar, more preferably less than about 0.3 micromolar, still more preferably less than about 0.1 micromolar, yet more preferably less than about 50 nanomolar; in a twenty-seventh embodiment, the cyclooxygenase is COX-2.
  • the conjugates of the invention can be selected from the group consisting of a conjugate illustrated in FIG. 1 , FIG. 2 , or FIG. 3 ; a rhenium-containing conjugate illustrated in FIG. 1 , FIG. 2 , or FIG. 3 ; a technetium-containing conjugate illustrated in FIG. 1 , FIG. 2 , or FIG. 3 ; a technetium-99m-containing conjugate illustrated in FIG. 1 , FIG. 2 , or FIG. 3 ; or a pharmaceutically acceptable salt thereof
  • the invention embraces a pharmaceutical composition comprising one or more of the foregoing conjugates and a pharmaceutically acceptable excipient.
  • the invention embraces any of the conjugates disclosed herein, with the substitution of a non-radioactive agent for the radioactive agent.
  • a non-radioactive agent for any of the generic structures or specific conjugates disclosed herein containing 99m Tc, 52 Mn, 186 Re, or 188 Re, the invention also embraces those generic structures or specific conjugates with a non-radioactive metal, such as non-radioactive Re, such as 185 Re.
  • the invention embraces any of the conjugates disclosed herein, with the removal of the radioactive agent.
  • the invention also embraces those generic structures or specific conjugates without the metal, that is, with the uncomplexed or free chelator.
  • the invention embraces the synthesis of any of the conjugates described herein, according to the protocols disclosed herein.
  • the invention also embraces methods of imaging a patient or subject.
  • the invention embraces a method of imaging a site of pathology or suspected pathology in a subject, comprising administering one or more conjugates or compositions described herein, including any of the foregoing embodiments, to the subject, wherein the radioactive agent of the conjugate comprises 99m Tc, 52 Mn, 186 Re, or 188 Re; and generating an image of the subject or an image of a portion of the subject.
  • the pathology or suspected pathology in the subject can be a tumor or a suspected tumor.
  • the pathology or suspected pathology in the subject can be an infection or a suspected infection.
  • the subject can be a subject suffering from pain.
  • the invention embraces any of the conjugates and compositions as disclosed herein for use in imaging a subject or for diagnosing a subject. In further embodiments, the invention embraces the use in imaging or in diagnosis of any of the conjugates and compositions as disclosed herein. In further embodiments, the invention embraces the use of any of the conjugates and compositions as disclosed herein for the manufacture of a medicament for use in imaging a subject, or for use in diagnostic purposes.
  • the invention includes conjugates where the ratio of (NSAID, NSAID residue, or NSAID derivative) to (chelating moiety) is 1:1.
  • compositions or methods are recited as “comprising” or “comprises” with respect to their various elements.
  • those elements can be recited with the transitional phrase “consisting essentially of” or “consists essentially of” as applied to those elements.
  • those elements can be recited with the transitional phrase “consisting of” or “consists of” as applied to those elements.
  • a composition or method is disclosed herein as comprising A and B, the alternative embodiment for that composition or method of “consisting essentially of A and B” and the alternative embodiment for that composition or method of “consisting of A and B” are also considered to have been disclosed herein.
  • embodiments recited as “consisting essentially of” or “consisting of” with respect to their various elements can also be recited as “comprising” as applied to those elements.
  • embodiments recited as “consisting essentially of” with respect to their various elements can also be recited as “consisting of” as applied to those elements, and embodiments recited as “consisting of” with respect to their various elements can also be recited as “consisting essentially of” as applied to those elements.
  • composition When a composition is described as “consisting essentially of” the listed components, the composition contains the components expressly listed, and may contain other components which do not substantially affect the condition being treated. That is, the composition either does not contain any other components which do substantially affect the condition being treated other than those components expressly listed; or, if the composition does contain extra components other than those listed which substantially affect the condition being treated, the composition does not contain a sufficient concentration or amount of those extra components to substantially affect the condition being treated.
  • a method is described as “consisting essentially of” the listed steps, the method contains the steps listed, and may contain other steps that do not substantially affect the condition being treated, but the method does not contain any other steps which substantially affect the condition being treated other than those steps expressly listed.
  • FIG. 1 illustrates various 99m Tc-containing conjugates useful in the invention.
  • FIG. 2 illustrates various rhenium-containing conjugates.
  • FIG. 3 ( 3 A- 3 S) illustrates various rhenium-containing and 99m Tc-containing conjugates.
  • Identifying sites of pathology is important for proper diagnosis and treatment of a patient. However, it can often be difficult to pinpoint the precise location of pathology. Extensive imaging and testing may be required to accurately identify the source of pathology.
  • Tumor localization is an example of a condition where it can be difficult to precisely identify the area of pathology, e.g., in a patient with metastatic adenocarcinoma who presents with clear metastasis, but where the primary site of the malignancy is not known.
  • the secondary sites of the tumor (metastases) are difficult to find in many cancer cases.
  • This problem also occurs with “benign tumors” such as giant cell tumors, which rarely metastasize, and “quasi-malignant tumors” such as adamantinomas, which rarely metastasize early, but are known to metastasize late in their course. Because the tumor location can be extremely difficult to find, a new test which could reveal all types of tumor cells would facilitate tumor searches, whether primary tumor sites or metastatic tumor sites, and help determine the appropriate treatment.
  • Prostaglandins are over-expressed in tumor cells.
  • Prostaglandins (such as the PG 2 group of prostaglandins) are also strongly associated with the experience of pain. Because prostaglandins are produced at the site of tumor location, actual injury, or pathology, identifying the site where prostaglandin synthesis occurs will assist in locating the precise area of pathology. Biosynthesis of the PG 2 prostaglandins requires the cyclooxygenase (COX) enzyme.
  • COX cyclooxygenase
  • the cyclooxygenase enzyme exists in (at least) two isoforms, COX-1, which is expressed constitutively, but which may be upregulated at sites of pain and inflammation, and COX-2, which is inducible by inflammatory stimuli. Both COX-1 and COX-2 are upregulated at tumor sites. Areas of high expression of cyclooxygenase will be associated with areas of high expression of prostaglandins, which in turn are associated with the area of pathology. Thus, pinpointing areas of high cyclooxygenase expression will enable identification of the pathological area.
  • NSAIDs non-steroidal anti-inflammatory drugs
  • These non-steroidal anti-inflammatory medicines include several pharmaceutical classes; each class has a number of specific drugs. If a NSAID drug is bonded or complexed to an imaging moiety, partial or total imaging of the patient provides a method of identifying sites of cyclooxygenase overexpression, prostaglandin synthesis, and inflammation, which determines the site of pathology or injury.
  • the invention encompasses conjugates of a NSAID with an imaging moiety, where said conjugate is suitable for imaging with an appropriate imaging modality.
  • conjugates suitable for imaging also encompasses conjugates which are not used for imaging, but which are useful surrogates for studying the chemical, biological, and pharmacokinetic properties of the conjugates suitable for imaging.
  • conjugates suitable for imaging substitution of non-radioactive isotopes of rhenium (Re) for 99m Tc results in a conjugate which can be handled without the need for radiation protection (the most abundant rhenium isotope, 187 Re, has a half-life of on the order of 10 10 years, and the second most abundant rhenium isotope, 185 Re, is stable).
  • conjugates which have non-radioactive rhenium isotopes in place of radioactive technetium isotopes can be useful for chemical, physical, in vitro, and in vivo studies of compound properties in which the imaging properties of the conjugate are not under study, such as studies of toxicity and biological half-life, and the invention embraces both the conjugates suitable for imaging and their analogs which can be handled without radiation precautions.
  • the conjugates are also useful for diagnosis of infections. Infections cause cells to overexpress the COX-1 and COX-2 enzymes. The pattern distribution of the cellular influence for the three major types of infections, bacterial, tuberculosis (TB), or viral, differ in major ways. Bacterial infections (not including TB) affect COX production in the cells of most of the body's organs.
  • the conjugates of the invention can be used for diagnosis of any bacterial infection, and are particularly useful in abscess forming bacteria, in subjects or patients with an organ-specific infection, and in aiding in diagnosis and determination of the cause of a fever of unknown origin (FUO). The organ most involved would produce more COX enzyme than the rest of the body's tissues, even though all tissues may show some increased activity.
  • TB infections can infect almost any organ, such as the lungs, the testes, the spinal column (such as psoas abscess), etc. Scans conducted with conjugates disclosed herein can help pinpoint the major locus of TB infection, which is especially helpful in a subject or patient with a positive skin reaction to TB (such as a positive PPD test).
  • the primary locus for a TB infection would likely be at the site of the highest gamma count on a gamma camera when a gamma-emitting radioactive moiety is used in the conjugate.
  • Viral infections tend to first cause elevated COX production in the spleen to a great extent and in the stomach to a slightly lesser extent.
  • the conjugates disclosed herein can thus be used for the screening of asymptomatic patients infected with a virus. Patients are frequently infectious even before they exhibit symptoms, such as patients with Ebola virus and other viruses. An asymptomatic patient or subject who has been exposed to such viruses, such Ebola virus, influenza viruses, or other viruses deemed sufficiently important for screening, or who has traveled in areas where outbreaks of such viruses have occurred, can be screened by administration of conjugates of the invention, followed by imaging. When a gamma-emitting radioactive moiety is used in the conjugate, a gamma scanner could detect signals above background (and thus increased COX expression) from at least the spleen and probably the stomach, indicating the presence of an infection.
  • a “residue” of a non-steroidal anti-inflammatory drug (NSAID), referred to as an “NSAID residue” or “residue of a NSAID,” is a portion of the NSAID, where the portion of the NSAID retains its ability to bind to cyclooxygenase.
  • a residue of a NSAID refers to the portion of the molecule left after removal of a hydrogen, a hydroxyl, a methyl, or a methoxy group from the NSAID. The residue is then bonded or complexed together with an imaging moiety.
  • NSAID residues also include portions of an NSAID that retains its ability to bind to cyclooxygenase, where the portion is further modified by the replacement of a hydrogen with a halogen or a trifluoromethyl group, or by the replacement of a methyl group with a trifluoromethyl group, or by the replacement of a hydroxyl group with a methoxy group.
  • the residue can be connected to a linker, which linker in turn is attached to a imaging moiety, in order to bond or complex the NSAID residue with the imaging moiety.
  • An NSAID derivative is an NSAID or NSAID residue which has been modified in one or more of the following manners:
  • a hydroxyl group has been replaced with a —O-(C 1 -C 4 alkyl) group, preferably a methoxy group; a halogen; a C 1 -C 4 alkyl group, preferably a methyl group; or a trifluoromethyl group;
  • a methyl group has been replaced with a trifluoromethyl group; a C 2 -C 4 alkyl group; a —O—(C 1 -C 4 alkyl) group, preferably a methoxy group; a halogen; or hydrogen;
  • a methoxy group has been replaced with a hydroxyl group, a —O—(C 2 -C 4 alkyl) group, a C 1 -C 4 alkyl group, preferably a methyl group; a halogen, or a trifluoromethyl group;
  • a halogen has been replaced with a different halogen, a trifluoromethyl group, a —O—(C 1 -C 4 alkyl) group, preferably a methoxy group; a C 1 -C 4 alkyl group, preferably a methyl group; or hydrogen;
  • a hydrogen has been replaced with a halogen, a methyl group, or a trifluoromethyl group
  • a —COOH group has been replaced with a —NH 2 group, or a —C( ⁇ O)—O— group has been replaced by a —NH— group;
  • a —COOH group has been replaced with a —CH 2 NH 2 group, or a —C( ⁇ O)—O— group has been replaced by an —CH 2 NH— group;
  • a trifluoromethyl group has been replaced with a —CH 2 NH 2 group or a —CH 2 NH— group.
  • “Bonded or complexed” indicates that the NSAID, NSAID residue, or NSAID derivative is associated with the imaging moiety in a manner such that the imaging moiety can be localized along with the NSAID, NSAID residue, or NSAID derivative to the intended site, such that the imaging moiety can indicate where the NSAID, NSAID residue, or NSAID derivative bonded or complexed to the imaging moiety has concentrated.
  • “Bonded or complexed” embraces any manner of association sufficiently stable for the foregoing purpose, whether such association is via a covalent bond, an ionic bond, a coordination bond (coordinate covalent bond or dative bond), a donor-acceptor complex, or any other association of NSAID, NSAID residue, or NSAID derivative and imaging moiety which has suitable stability.
  • “bonded or complexed” can indicate a covalent bond.
  • bonded or complexed can indicate a coordination bond.
  • “bonded or complexed” can indicate an ionic bond.
  • “bonded or complexed” can indicate a donor-acceptor complex.
  • Alkyl is intended to embrace a univalent saturated linear or branched hydrocarbon chain having the number of carbon atoms specified, or if no number is specified, having 1 to 8 carbon atoms.
  • Alkylene refers to a similar group, which is divalent.
  • Optionally substituted alkyl refers to either an unsubstituted alkyl group, or an alkyl group substituted with one or more substituents (such as one, two, three, four, or five substituents) selected from the group consisting of —OH, —(C 1 -C 4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C 1 -C 4 alkyl), —(C 1 -C 4 ) haloalkyl, —(C 1 -C 4 ) perhaloalkyl, —O—(C 1 -C 4 alkyl), —O—(C 1 -C 4 haloalkyl), —O—(C 1 -C 4 perhaloalkyl), —(C 1 -C 4 ) perfluoroalkyl, —(C ⁇ O)—(C 1 -C 4 ) alkyl, —(C ⁇ O)—(
  • substituents are —CH 3 , —CH 2 CH 3 , —CF 3 , —CH 2 CF 3 , —CF 2 CF 3 , —OCH 3 , —NH(CH 3 ), —N(CH 3 ) 2 , —SCH 3 , and SO 2 CH 3 .
  • Optionally substituted alkylene” groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups.
  • Cycloalkyl is intended to embrace a univalent saturated cyclic hydrocarbon chain having the number of carbon atoms specified, or if no number is specified, having 3 to 10 carbon atoms, or 3 to 8 carbon atoms, preferably 3 to 6 carbon atoms. “Cycloalkylene” refers to a similar group, which is divalent. Cycloalkyl and cycloalkylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups.
  • Alkenyl is intended to embrace a univalent linear or branched hydrocarbon chain having at least one carbon-carbon double bond, and having the number of carbon atoms specified, or if no number is specified, having 2 to 8 carbon atoms.
  • Alkenylene refers to a similar group, which is divalent. Alkenyl and alkenylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • Cycloalkenyl is intended to embrace a univalent cyclic hydrocarbon chain having at least one carbon-carbon double bond and having the number of carbon atoms specified, or if no number is specified, having 4 to 10 carbon atoms, or 4 to 8 carbon atoms, or 4 to 6 carbon atoms.
  • Cycloalkenylene refers to a similar group, which is divalent. Cycloalkenyl and cycloalkenylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • Alkynyl is intended to embrace a univalent linear or branched hydrocarbon chain having at least one carbon-carbon triple bond, and having the number of carbon atoms specified, or if no number is specified, having 2 to 8 carbon atoms.
  • Alkynylene refers to a similar group, which is divalent. Alkynyl and alkynylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • Aryl is defined as a univalent aromatic ring system.
  • Aryl groups include monocyclic aromatic rings and polycyclic aromatic ring systems containing the number of carbon atoms specified, or if no number is specified, containing six to twenty carbon atoms. In other embodiments, aryl groups may contain six to ten carbon atoms. In some embodiments, aryl groups can be unsubstituted.
  • aryl groups can be substituted with, for example, one, two, or three substituents independently selected from the group consisting of —OH, —(C 1 -C 4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C 1 -C 4 alkyl), —(C 1 -C 4 ) haloalkyl, —(C 1 -C 4 ) perhaloalkyl, —O—(C 1 -C 4 alkyl), —O—(C 1 -C 4 haloalkyl), —O—(C 1 -C 4 perhaloalkyl), —(C 1 -C 4 ) perfluoroalkyl, —(C ⁇ O)—(C 1 -C 4 ) alkyl, —(C ⁇ O)—(C 1 -C 4 ) haloalkyl, —(C ⁇ O)—(C 1 -C 4 ) hal
  • Hydrocarbyl is defined as a univalent hydrocarbon group, that is, a group comprised of hydrogen and carbon, whether aliphatic or aromatic, acyclic or cyclic, or any combination of, or all of, aliphatic, aromatic, acyclic and cyclic. Hydrocarbyl groups have the number of carbon atoms specified, or if no number is specified, having 1 to 10 carbon atoms. “Hydrocarbylene” refers to a similar group, which is divalent. Hydrocarbyl and hydrocarbylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • Heterocycle or a “heterocyclic group” is defined as a ring system which contains the number of carbon atoms specified, and one or more heteroatoms (such as one to six heteroatoms, or one to three heteroatoms, or one heteroatom), where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus.
  • Heteroaryl is defined as an aromatic ring system which contains the number of carbon atoms specified, and one or more heteroatoms (such as one to six heteroatoms, or one to three heteroatoms, or one heteroatom), where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus; heteroaryl groups are a subset of heterocyclic groups.
  • heteroatoms for heterocyclyl and heteroaryl groups are selected from the group consisting of oxygen and nitrogen.
  • heterocyclic groups may contain two to twenty carbon atoms and one to six heteroatoms, two to twelve carbon atoms and one to four heteroatoms, two to twelve carbon atoms and one to three heteroatoms, two to ten carbon atoms and one to three heteroatoms, two to six carbon atoms and one to three heteroatoms, or two to six carbon atoms and two to four heteroatoms.
  • heterocyclic groups can be unsubstituted.
  • heterocyclic groups can be substituted on any chemically possible valence with for example, one, two, or three substituents independently selected from the group consisting of —OH, —(C 1 -C 4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C 1 -C 4 alkyl), —(C 1 -C 4 ) haloalkyl, —(C 1 -C 4 ) perhaloalkyl, —O—(C 1 -C 4 alkyl), —O—(C 1 -C 4 haloalkyl), —O—(C 1 -C 4 perhaloalkyl), —(C 1 -C 4 ) perfluoroalkyl, —(C ⁇ O)—(C 1 -C 4 ) alkyl, —(C ⁇ O)—(C 1 -C 4 ) haloalkyl, —(C ⁇ O)——(C 1
  • heterocycles include aziridine, oxirane, oxetane, azetidine, pyrrolidine, pyrrole, tetrahydrofuran, furan, thiolane, thiophene, imidazolidine, imidazole, pyrazolidine, pyrazole, 1,2,3-triazole, 1,2,4-triazole, piperidine, pyridine, pyran, piperazine, and morpholine.
  • heterohydrocarbyl is defined as a univalent hydrocarbyl group, where one or more of the carbon atoms have been independently replaced by a heteroatom at any chemically possible location, where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus.
  • Heterohydrocarbyl groups have the number of carbon atoms specified, or if no number is specified, having 1 to 10 carbon atoms, and also at least one heteroatom, such as 1 to 5 heteroatoms, 1 to 4 heteroatoms, 1 to 3 heteroatoms, 1 to 2 heteroatoms, or one heteroatom.
  • Heterohydrocarbylene refers to a similar group, which is divalent.
  • heterohydrocarbyl and heterohydrocarbylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • heterohydrocarbyl and heterohydrocarbylene groups include, but are not limited to, ethylene glycol and polyethylene glycol moieties, such as (—CH 2 CH 2 —O n )—H (a monovalent heterohydrocarbyl group) and (—CH 2 CH 2 —O—) n (a divalent heterohydrocarbylene group) where n is an integer from 1 to 12 inclusive, and propylene glycol and polypropylene glycol moieties, such as (—CH 2 CH(CH 3 )—O—) n —H (a monovalent heterohydrocarbyl group) and (—CH 2 CH(CH 3 )—O) n — (a divalent heterohydrocarbylene group) where n is an integer from 1 to 12 inclusive.
  • ethylene glycol and polyethylene glycol moieties such as
  • groups described above can be attached to the remainder of the molecule at any chemically possible location on the fragment, including attachment via a substituent when the group is substituted.
  • groups are typically attached by replacement of a hydrogen, hydroxyl, methyl, or methoxy group on a “complete” molecule to generate the appropriate fragment, and a bond is drawn from the open valence on the fragment to the remainder of the molecule.
  • attachment of the heteroalkyl group —CH 2 —O—CH 3 proceeds by removal of a hydrogen from one of the methyl groups of CH 3 —O—CH 3 , to generate the heteroalkyl fragment —CH 2 —O—CH 3 , from which a bond is drawn from the open valence to the remainder of the molecule.
  • references to “about” a value or parameter herein includes (and describes) variations that are directed to that value or parameter per se. For example, description referring to “about X” includes description of “X”.
  • subject By “subject,” “individual,” or “patient” is meant an individual organism, preferably a vertebrate, more preferably a mammal, most preferably a human.
  • the salts of the compounds comprise pharmaceutically acceptable salts.
  • Pharmaceutically acceptable salts are those salts which can be administered as drugs or pharmaceuticals to humans and/or animals and which, upon administration, retain at least some of the biological activity of the free compound (neutral compound or non-salt compound).
  • the desired salt of a basic compound may be prepared by methods known to those of skill in the art by treating the compound with an acid. Examples of inorganic acids include, but are not limited to, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and phosphoric acid.
  • organic acids include, but are not limited to, formic acid, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, sulfonic acids, and salicylic acid.
  • Salts of basic compounds with amino acids, such as aspartate salts and glutamate salts can also be prepared.
  • the desired salt of an acidic compound can be prepared by methods known to those of skill in the art by treating the compound with a base.
  • Examples of inorganic salts of acid compounds include, but are not limited to, alkali metal and alkaline earth salts, such as sodium salts, potassium salts, magnesium salts, and calcium salts; ammonium salts; and aluminum salts.
  • Examples of organic salts of acid compounds include, but are not limited to, procaine, dibenzylamine, N-ethylpiperidine, N,N′-dibenzylethylenediamine, and triethylamine salts. Salts of acidic compounds with amino acids, such as lysine salts, can also be prepared.
  • salts of acidic compounds with amino acids such as lysine salts, can also be prepared.
  • the invention also includes, where chemically possible, all stereoisomers and geometric isomers of the compounds, including diastereomers, enantiomers, and cis/trans (E/Z) isomers.
  • the invention also includes mixtures of stereoisomers and/or geometric isomers in any ratio, including, but not limited to, racemic mixtures. Unless stereochemistry is explicitly indicated in a structure, the structure is intended to embrace all possible stereoisomers of the compound depicted. If stereochemistry is explicitly indicated for one portion or portions of a molecule, but not for another portion or portions of a molecule, the structure is intended to embrace all possible stereoisomers for the portion or portions where stereochemistry is not explicitly indicated.
  • the invention includes all isotopologues of the compounds disclosed herein, such as, for example, deuterated derivatives of the compounds (where H can be 2 H, i.e., D).
  • NSAIDs Non-Steroidal Anti-Inflammatory Drugs
  • Non-steroidal anti-inflammatory drugs are commonly used to treat pain and inflammation, which occur due to many diseases, such as those involving tumors.
  • NSAIDs which can be used in the invention include:
  • salicylates such as aspirin (acetylsalicylic acid), diflunisal, salsalate, and choline magnesium trisalicylate;
  • propionic acid derivatives such as ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, and loxoprofen;
  • acetic acid derivatives such as indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, and nabumetone;
  • enolic acid (oxicam) derivatives such as piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, and isoxicam;
  • anthranilic acid derivatives such as mefenamic acid, meclofenamic acid, flufenamic acid, and tolfenamic acid;
  • COX-2 inhibitors selective COX-2 inhibitors (coxibs, several of which are not approved, or have been withdrawn, in various countries), such as celecoxib, rofecoxib, valdecoxib, parecoxib, lumiracoxib, etoricoxib, and firocoxib (firocoxib approved for equine and canine use only);
  • sulfonanilides such as nimesulide (which should be used cautiously due to the risk of liver damage);
  • licofelone which is both a cyclooxygenase and lipoxygenase inhibitor.
  • a bond to an atom or atoms on the NSAID compound is replaced with a bond to a linking group in order to facilitate bonding or complexing the NSAID, NSAID residue, or NSAID derivative to the imaging moiety.
  • linking an amine-containing linker to a carboxylic acid-containing NSAID compound can be accomplished by condensing the amine and carboxylic acid to form an amide group.
  • the bond to the —OH portion of the —COOH group has been replaced with a bond to the nitrogen atom of the amine-containing linker.
  • NSAID residue refers to the portion of the NSAID molecule that remains and which is attached to the linker, and, as defined previously, retains its ability to bind to cyclooxygenase.
  • the NSAID residue need not bind to COX with the same affinity or specificity as the NSAID from which the residue is derived, as long as sufficient binding affinity remains for the purposes of the invention.
  • a derivative of a NSAID includes an NSAID or NSAID residue that has been modified as defined herein, and the NSAID derivative portion of the conjugate need not bind to COX with the same affinity or specificity as the NSAID which was modified to form the derivative, as long as sufficient binding affinity remains for the purposes of the invention.
  • An imaging moiety can be bonded or complexed to a NSAID compound by using an appropriate linker (also referred to as a linking group).
  • the linker must be capable of being bonded or complexed to both the NSAID compound, or to a residue or derivative of the NSAID compound, and bonded or complexed to the imaging moiety, for the purpose of localizing the imaging moiety to the site where the NSAID compound or residue or derivative of the NSAID compound concentrates when administered to a patient.
  • a linker group covalently bound to both the NSAID and the imaging moiety or a linker group covalently bound to the NSAID and bonded or complexed via a coordination bond to the imaging moiety, or a linker group covalently bound to the NSAID and bonded or complexed via an ionic bond to the imaging moiety, can be used.
  • the linker should preferably be bonded or complexed to the NSAID molecule or residue or derivative of the NSAID at a site as distant as possible from the region of the NSAID or residue or derivative of the NSAID that binds to cyclooxygenase, in order to preserve the ability of the NSAID or residue or derivative of the NSAID to bind to cyclooxygenase.
  • any attachment to the NSAID molecule or residue or derivative of the NSAID which attachment does not render the conjugate unsuitable for its purpose, can be used.
  • the linker also needs to bind or complex with the imaging moiety.
  • One particularly useful imaging moiety is the metastable isotope of technetium-99, referred to as 99m Tc, Tc99m, or Tc-99m.
  • 99m Tc decays to 99 Tc with a half-life of about 6 hours, via gamma emission at an energy of about 140 keV.
  • 99m Tc is often used in a complex with six methoxyisobutylisonitrile (MIBI) ligands, which is often referred to as 99m Tc-MIBI, technetium Tc99m Sestamibi, or 99m Tc sestamibi (sold as CARDIOLITE, a registered trademark of Lantheus Medical Imaging, Inc., North Billerica, Mass.).
  • MIBI methoxyisobutylisonitrile
  • the linker enables the linker to bind to a radioactive tracer moiety, such as 99m Tc, via the isocyano group, while the remaining open valence on the linker will allow attachment of a NSAID or a residue or derivative of a NSAID.
  • a radioactive tracer moiety such as 99m Tc
  • the structure below can be attached to a radioactive tracer moiety, such as 99m Tc:
  • R 1 , R 2 , and R 3 can be independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with hydroxy, fluoro, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl, or R 1 and R 2 together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, while n is an integer selected from 0 to 4, inclusive.
  • the linker itself may be capable of bonding to or complexing the radioactive agent, as with the methoxyisobutylisonitrile ligands above which directly bond to 99m Tc.
  • the imaging moiety comprises a chelating group and the radioactive agent, and may further comprise additional groups, such as ligands, bound or complexed to the radioactive agent.
  • Chelating groups can comprise a number of ligand systems known to the skilled artisan, such as those described in e.g. Jürgens, S. et al., J. Organomet. Chem. (2014), 751, 83-89 and Liu, G. et al. Anticancer Agents Med. Chem. (2007), 7(3): 367-377.
  • the linker when a linker is used to link a NSAID, NSAID residue, or NSAID derivative to an imaging moiety, can be selected from the group consisting of an optionally substituted C 1 -C 40 hydrocarbylene group; an optionally substituted C 2 -C 40 heterohydrocarbylene group; and a linker of the form -L E -R 4 -L F -, where L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 40 hydrocarbylene and optionally substituted C 2 -C 40 heterohydrocarbylene, C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl,
  • the linker when a linker is used to link a NSAID, NSAID residue, or NSAID derivative to an imaging moiety, can be selected from the group consisting of an optionally substituted C 1 -C 10 hydrocarbylene group; an optionally substituted C 2 -C 10 heterohydrocarbylene group; and a linker of the form -L E -R 4 -L F - ; where L E is absent or is selected from the group consisting of —NH—, —N(R 8 )—, and —C( ⁇ O)—, and R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 10 hydrocarbylene, optionally substituted C 2 -C 10 heterohydrocarbylene, C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalky
  • a useful chelating group for preparation of conjugates is the tetradentate mertiatide group (N-[N-[N-[(acetylthio)acetyl]glycyl]glycyl]-glycine; Fritzberg et al., J. Nuclear Medicine (1986) 27(1):111-116), having the structure:
  • the following structure shows metal complexed with a group derived from mertiatide to form an imaging moiety:
  • the carboxylic acid functionality of the complex allows for a wide range of coupling reactions in order to attach the imaging moiety to the remainder of the molecule.
  • the mertiatide peptide is coupled via its carboxylate group prior to introduction of the metal ion or metal-oxo ion.
  • the mertiatide peptide is complexed to the metal ion (or metal-oxo ion), it can be referred to either as “mertiatide complexed to the metal ion (or metal-oxo ion),” or as a group derived from mertiatide. That is, a group bound or complexed to a metal ion or metal-oxo ion which is referred to as “derived” from a specific moiety refers to the group after it has complexed with the metal ion or metal-oxo ion.
  • the group which binds or complexes to the metal ion or metal-oxo ion can be referred to by the same name in its free, uncomplexed form and in its complexed form with the metal; for example, “mertiatide group” can refer to both a mertiatide group without a complexed metal or metal-oxo ion, and also a mertiatide group which has complexed with a metal or metal-oxo ion.
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl,
  • R 9 is H.
  • the substituents R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with fluoro, hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or, independently of the other substituents, (R 10 and R 11 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, (R 12 and R 13 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 14 and R 15 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring
  • TechneScan MAG3TM is a commercially available kit for preparing 99m Tc-mertiatide conjugates, and is sold by Mallinckrodt Pharmaceuticals (catalog number N096B0, National Drug Code 00019N096B0), 675 McDonnell Boulevard., St. Louis, Mo. 63042, USA.
  • the kit vials contain betiatide, stannous chloride dihydrate (SnCl 2 .2H 2 O), sodium tartrate dihydrate, and lactose monohydrate.
  • Betiatide which is N-[(benzoylthio)acetyl]glycylglycylglycine, reacts with sodium pertechnetate 99m Tc to form 99m Tc-mertiatide.
  • Yet another useful chelating group for preparation of conjugates is based on the tetradentate ethylenedicysteine group:
  • carboxylic acid functionalities of the complex allows for a wide range of coupling reactions.
  • One of the carboxylic acid functionalities can be blocked, for example as an amide:
  • carboxylic acid group can be used for attachment to the remainder of the molecule.
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl, R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and
  • R 9 is H.
  • the substituents R 18 , R 19 , R 20 , R 21 , R 22 , R 23 , R 24 , and R 25 are independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with fluoro, hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or, independently of the other substituents, (R 18 and R 19 ) together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, (R 20 and R 21 ) together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 22 and R 23 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • C 10 heterohydrocarbyl group (specifically, C 10 heteroalkyl) with three nitrogen atoms and a sulfur atom in the chain, and five oxo substituents, while the ethylenedicysteine fragment:
  • the ethylenedicysteine fragment has two nitrogen atoms in the chain, two —SH substituents on the first and last carbons in the chain, one —COOH substituent, and a second —COOH substituent which is linked to the remainder of the molecule by removal of the —OH group of the carboxyl.
  • the ethylenedicysteine fragment can be considered as a 3,6-diazaoctane (i.e., heteroalkyl) with thiol substituents on the 1 and 8 carbons, a carboxy substituent on the 7 carbon, and a —C( ⁇ O)—OH or —C( ⁇ O)—H moiety on the 2 carbon, where the —OH or —H, respectively, has been removed for attachment to the remainder of the molecule.
  • a 3,6-diazaoctane i.e., heteroalkyl
  • thiol substituents on the 1 and 8 carbons a carboxy substituent on the 7 carbon
  • a —C( ⁇ O)—OH or —C( ⁇ O)—H moiety on the 2 carbon where the —OH or —H, respectively, has been removed for attachment to the remainder of the molecule.
  • the linker(s) is (are) capable of directly binding to or chelating the metal of the imaging moiety
  • the invention comprises compounds of the formula:
  • NSAID, NSAID residue, or NSAID derivative refers to a NSAID or a residue or derivative of a NSAID
  • M is selected from the group consisting of 99m Tc, 52 Mn, and Re
  • x is an integer between 1 and 6 inclusive
  • z 1 is an integer between 0 and 5 inclusive
  • the sum of x and z1 is less than or equal to 6
  • terminal ligand is a ligand that coordinates to M, but which does not have a NSAID attached to it.
  • the linker or linkers may be monodentate or polydentate for M.
  • the terminal ligand or ligands may be monodentate or polydentate for M.
  • all of the ligands can be identical groups, all of the ligands can be different groups, or some of the ligands can be identical groups and some can be different groups.
  • some monodentate ligands such as the oxo ligand, ⁇ O, can occupy more than one valence on the metal ion; that is, there can be multiple bonds between some monodentate ligands, such as the oxo ligand, ⁇ O, and the metal atom.
  • the linker(s) is (are) capable of directly binding to or chelating the metal of the imaging moiety, and where both the linker(s) and the terminal ligand(s) are monodentate and occupy only one valence per linker and one valence per terminal ligand, the invention comprises compounds of the formula:
  • NSAID, NSAID residue, or NSAID derivative refers to a NSAID or a residue or derivative of a NSAID
  • M is selected from the group consisting of 99m Tc , 52 Mn, and Re
  • x is an integer between 1 and 6 inclusive
  • y is an integer between 0 and 5 inclusive
  • x+y 6
  • terminal ligand is a ligand that coordinates to 99m Tc, 52 Mn, or Re, but which does not have a NSAID or a residue or derivative of a NSAID attached to it.
  • Chelating groups including linkers, where the linker is capable of chelation
  • terminal ligands may be monodentate or polydentate, with the condition that the chelating group or groups and terminal ligand or ligands must together satisfy the valency of the metal atom to which they are bonded.
  • the chelating group or groups and terminal ligand or ligands must together satisfy the valency of the metal atom to which they are bonded.
  • the mertiatide moiety is tetradentate and occupies four valences of the rhenium ion, while the monodentate oxo ligand occupies two valences of the rhenium ion, thus together satisfying the valency of the Re(VI) ion.
  • terminal ligands examples include: halo (—X), fluoro (—F), chloro (—Cl), bromo (—Br), iodo (—I), oxo ( ⁇ O), cyano (—CN), isocyano (—NC), hydroxyl (—OH), with oxo being a preferred terminal ligand; and substituted isocyano ligands of the form:
  • R 1 , R 2 , and R 3 can be independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with hydroxy, fluoro, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl, or R 1 and R 2 together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, such as
  • substituted isocyano ligands are preferred when the NSAID linker is also an isocyano ligand.
  • cyclooxygenase inhibitors with a linker which incorporates a ligand to bind 99m Tc which can be used as the moiety [(NSAID, NSAID residue, or NSAID derivative)-linker] include, but are not limited to:
  • ketorolac where one of the hydrogens on the phenyl ring of ketorolac has been replaced by the linker
  • the encircled portion represents a residue of ibuprofen (where one of the methyl groups of the (2-methylpropyl) group of ibuprofen has been replaced by the linker);
  • the encircled portion represents a residue of indomethacin (where the methyl of the methoxy group of indomethacin has been replaced by the linker).
  • the linkers are attached as indicated above in order to preserve the pharmacophoric portions of the NSAID.
  • all of the NSAID, NSAID residue, or NSAID derivatives in the x subunits [(NSAID, NSAID residue, or NSAID derivative)-linker] are the same NSAID, NSAID residue, or NSAID derivative.
  • at least one of the NSAID, NSAID residue, or NSAID derivatives in the x subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker] is different than the remaining NSAID(s) or NSAID residue(s) in the remaining subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker].
  • each of the NSAID, NSAID residue, or NSAID derivatives in the x subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker] is different than the remaining NSAID(s) or NSAID residue(s) in the other subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker].
  • Exemplary conjugates of the invention can be of the form:
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene and optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • L E is absent or is selected from the group consisting of —NH—and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • L E is absent or is selected from the group consisting of —NH— and —N(R 8 )—, where R 8 is optionally substituted C 1 -C 4 alkyl , R 4 is selected from the group consisting of optionally substituted C 1 -C 30 hydrocarbylene, optionally substituted C 2 -C 30 heterohydrocarbylene group (such as C 1 -C 12 alkylene), C 3 -C 8 cycloalkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 1 -C 6 alkyl-C 3 -C 8 cycloalkyl-C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkyl-C 6 -C 10 aryl, C 6 -C 10 aryl-C 1 -C 6 alkyl, and C 1 -C 6 alkyl
  • R 5 is selected from the group consisting of —NH 2 , —NH(C 1 -C 4 alkyl), —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —OCH 3 , and —OCH 2 CH 3 ; in yet a further embodiment, R 5 is selected from the group consisting of —NH 2 , —OCH 3 , and —OCH 2 CH 3 .
  • the compounds of the invention may be administered in any suitable form that will provide sufficient levels of the compounds for the purposes of imaging.
  • Intravenous administration is a useful route of administration, although other parenteral routes can also be employed, where parenteral as used herein includes subcutaneous injections, intravenous injection, intraarterial injection, intramuscular injection, intrasternal injection, intraperitoneal injection, or infusion techniques.
  • the compounds can also be administered orally or enterally, which is a preferred route when compatible with the absorption of the compound and with imaging requirements.
  • the compounds can also be administered sublingually, by buccal administration, subcutaneously, by spinal administration, by epidural administration, by administration to cerebral ventricles, by inhalation (e.g. as mists or sprays), rectally, or topically in unit dosage formulations containing conventional nontoxic pharmaceutically acceptable carriers, excipients, adjuvants, and vehicles as desired.
  • the compounds may be administered directly to a specific or affected organ or tissue.
  • the compounds are mixed with pharmaceutically acceptable carriers, excipients, adjuvants, and vehicles appropriate for the desired route of administration.
  • the formulations and preparations used in the methods of the invention are sterile.
  • Sterile pharmaceutical formulations are compounded or manufactured according to pharmaceutical-grade sterilization standards (United States Pharmacopeia Chapters 797, 1072, and 1211; California Business & Professions Code 4127.7; 16 California Code of Regulations 1751, 21 Code of Federal Regulations 211) known to those of skill in the art.
  • Oral administration is advantageous due to its ease of implementation and patient compliance. If a patient has difficulty swallowing, introduction of medicine via feeding tube, feeding syringe, or gastrostomy can be employed in order to accomplish enteric administration.
  • the active compound (and, if present, other co-administered agents) can be enterally administered in any other pharmaceutically acceptable carrier suitable for formulation for administration via feeding tube, feeding syringe, or gastrostomy.
  • Intravenous administration can also be used advantageously, for delivery of the conjugates of the invention to the bloodstream as quickly as possible and to circumvent the need for absorption from the gastrointestinal tract.
  • the compounds described for use herein can be administered in solid form, in liquid form, in aerosol form, or in the form of tablets, pills, powder mixtures, capsules, granules, injectables, solutions, suppositories, enemas, colonic irrigations, emulsions, dispersions, food premixes, and in other forms suitable for the route of administration.
  • the compounds can also be administered in liposome formulations.
  • the compounds can also be administered as prodrugs, where the prodrug undergoes transformation in the treated subject to a therapeutically effective form. Additional methods of administration are known in the art.
  • Injectable preparations for example, sterile injectable aqueous or oleaginous suspensions, may be formulated according to methods known in the art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in propylene glycol.
  • a nontoxic parenterally acceptable diluent or solvent for example, as a solution in propylene glycol.
  • the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono or di-glycerides.
  • fatty acids such as oleic acid find use in the preparation of injectables.
  • Solid dosage forms for oral administration may include capsules, tablets, pills, powders, and granules.
  • the active compound may be admixed with at least one inert diluent such as sucrose, lactose, or starch.
  • Such dosage forms may also comprise additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate.
  • the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.
  • Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water. Such compositions may also comprise adjuvants, such as wetting agents, emulsifying and suspending agents, cyclodextrins, and sweetening, flavoring, and perfuming agents. Alternatively, the compound may also be administered in neat form if suitable.
  • liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by mono or multilamellar hydrated liquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used.
  • the present compositions in liposome form can contain, in addition to a compound for use in the present invention, stabilizers, preservatives, excipients, and the like.
  • the preferred lipids are the phospholipids and phosphatidyl cholines (lecithins), both natural and synthetic. Methods to form liposomes are known in the art. See, for example, Prescott, Ed., Methods in Cell Biology, Volume XIV, Academic Press, New York, N.W., p. 33 et seq (1976).
  • the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form can vary depending upon the patient to which the active ingredient is administered and the particular mode of administration. It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the specific compound employed; the age, body weight, body area, body mass index (BMI), general health, sex, and diet of the patient; the time of administration and route of administration used; the rate of excretion; and the drug combination, if any, used.
  • the compounds can be administered in a unit dosage formulation.
  • the pharmaceutical unit dosage chosen is fabricated and administered to provide sufficient concentration of drug for imaging a patient.
  • the compounds for use in the present invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more other agents.
  • additional active agents may generally be employed in therapeutic amounts as indicated in the Physicians' Desk Reference (PDR) 53rd Edition (1999), which is incorporated herein by reference, or such therapeutically useful amounts as would be known to one of ordinary skill in the art, or as are determined empirically for each patient.
  • Combinations of the NSAID conjugates can also be used. Combining two or more conjugates of different NSAIDs or residues or derivative s of NSAIDs can provide advantages over using a single conjugate. Advantages can include the ability to tune pharmacokinetics and pharmacodynamics, to adjust the solubility of the overall composition and/or its components, to adjust the half-life of total conjugate in the body, to enhance imaging contrast and/or definition, to adjust binding kinetics to COX, to adjust binding affinity to COX, or to enhance the stability of the composition either in storage or in use.
  • the two or more conjugates can be combined in solution form such as those solution forms described above (such as in a sterile solution for IV administration), or in solid form such as those solid forms as described above (such as pill or tablet form).
  • the two or more conjugates can be mixed together shortly before administration and administered together.
  • the two or more conjugates can be administered simultaneously, either by the same route of administration or by different routes of administration.
  • the two or more conjugates can be administered consecutively, either by the same route of administration or by different routes of administration.
  • a kit form can contain two or more conjugates as individual conjugates, with printed or electronic instructions for administration either as a mixture of conjugates, as separate conjugates administered simultaneously, or as separate conjugates administered consecutively.
  • conjugates are administered, they can be administered as a mixture of conjugates, as separate conjugates administered simultaneously, as separate conjugates administered consecutively, as separate conjugates where two or more may be administered simultaneously with the remainder administered consecutively before or after the simultaneous administration, or any other possible combination of mixed administration, simultaneous administration, and consecutive administration.
  • the conjugates can be used with any suitable imaging technique. Images of a subject, or of a portion of a subject such as the arm, leg, or any specific region of the body of the subject, can be generated using gamma cameras, planar gamma imaging, scintigraphic imaging, SPECT imaging (single photon emission computed tomography), and other radiographic or tomographic imaging techniques. Exemplary imaging methods that can be used are described in Pacelli et al., J. Label. Compd. Radiopharm. 57:317-322 (2014); de Vries et al., J Nucl. Med.
  • kits which can contain one or more conjugates as disclosed herein.
  • the kit can contain printed or electronic instructions for administration of the conjugate.
  • the kit can contain one or more compounds as disclosed herein which lacks the radioactive agent, with printed or electronic instructions for adding the radioactive agent to constitute one or more conjugates of the invention.
  • Synthesis of (16) is realized by heating a mixture of (15) and freshly crystallized CuCl in degassed dry EtOH at 50° C. in an ampoule for 1 h. A solution of NaBF 4 in water is added in one portion, solvents are removed under vacuum, with the resultant crude product dissolved in EtOH and the NaCl generated was separated by filtration. The solvent was removed to get the product (16).
  • a vial is prepared containing a sterile, non-pyrogenic, lyophilized mixture of:
  • Tin Chloride (stannous and stannic) Dihydrate, maximum (as SnCl 2 .2H 2 O)—0.086 mg.
  • the vial contents should be visually inspected. Use only if the solution is clear and free of particulate matter and discoloration.
  • Assay the reaction vial using a suitable radioactivity calibration system. Record the Technetium Tc99m concentration, total volume, assay time and date, expiration time and lot number on the vial shield label and affix the label to the shield.
  • the pH of the reconstituted product is 5.5 (5.0-6.0). No bacteriostatic preservative is present.
  • the precise structure of the technetium complex (1) is Tc99m[IBN] 6 ⁇ where IBN is (S)-2-(6-((1-isocyano-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoic acid.
  • Hexakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)technetium (17) is prepared using the same procedure as in Example 3, starting from tetrakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)copper (16).
  • Amine 20 is readily synthesized by using protocols available in the following publications: (1) Uddin, Md. Jashim, et al. Bioconjugate Chemistry (2013), 24(4), 712-723; (2) Zlatopolskiy, Boris D., et al. Chemical Communications (2012), 48(57), 7134-7136; (3) U.S. Pat. Appl. Publ. 2005/0002859 (2005); (4) U.S. Pat. Appl. Publ. 2007/0292352 (2007); (5) Uddin, Md. Jashim, et al. Journal of Labelled Compounds and Radiopharmaceuticals (2009), 52(9), 387-393; and (6) Uddin, Md. Jashim, et al. Bioorganic & Medicinal Chemistry Letters (2010), 20(5), 1787-1791.
  • amine 20 can be synthesized by the following procedure:
  • Indomethacin derivative 22 is made following the procedure in: Wang Y, et al. Nat Protoc. (2007), 2(4): 972-8.
  • the reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no.
  • Indomethacin derivative 23 is made following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the reagent Trichlorooxobis(triphenylphosphine)rhenium(V), (PPh3)2ReOCl 3 is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • compound 23 can be synthesized using the following procedure: To a stirred solution of compound 22 (100 mg, 0.14 mmol) in NMP (15 mL), (PPh 3 ) 2 ReOCl 3 (Sigma-Aldrich, Order #370193, 106 mg, 0.127 mmol) was added. The mixture was stirred at 80° C. for 48 h. The solution was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: Water (10 mM NH 4 HCO 3 ), solvent B: MeCN) to give compound 23 as a solid.
  • amine 25 has been reported in the following articles: (1) Uddin, Md. Jashim, et al. Bioconjugate Chemistry (2013), 24(4), 712-723. (2) Hua Zhang, et al. J. Am. Chem. Soc. (2013), 135, 11663-11669 (3) Hua Zhang, et al. J. Am. Chem. Soc. (2013), 135, 17469-17475.
  • amine 25 can be synthesized by the following procedure:To a mixture of indomethacin (11.8 g, 33 mmol), tert-butyl 6-aminohexylcarbamate (CAS No. 51857-17-1) (8.5 g, 39 mmol) and HATU (18.8 g, 50 mmol) in DMF (200 mL) was added TEA (10.1 g, 0.1 mol). The mixture was stirred at rt for 4 h and poured onto ice water (300 mL). The precipitate was collected by filtration and dried to give compound 24 as a solid.
  • Indomethacin derivative 26 is made following the procedure in: Wang Y, et al. Nat Protoc. (2007), 2(4): 972-8.
  • the reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no.
  • Indomethacin derivative 27 is made following the procedure in: Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the reagent Trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • compound 27 can be synthesized using the following procedure: A mixture of compound 26 (200 mg, 0.27 mmol) and (Ph 3 P) 2 ReOCl 3 (337 mg, 0.41 mmol) in NMP (10 mL) was stirred for 16 h at 100° C. The solution was directly purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: water containing 10 mM NH 4 HCO 3 , solvent B: ACN) to give 27 as a solid.
  • Prep-HPLC Column: Acquity BEH C18, Waters Corp, solvent A: water containing 10 mM NH 4 HCO 3 , solvent B: ACN
  • the rhenium-indomethacin derivative 35 is made following the procedure in: Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the reagent trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Compound 39 is prepared by a procedure similar to the one described in Example 7, substituting t BocNH(CH 2 ) 4 Br with t BocNH(CH 2 ) 6 Br.
  • Amine 20 is prepared as described in Example 5.
  • Indomethacin derivative 40 is made from amine 20 by amide coupling with ethylenedicysteine (CAS #14344-48-0). The reaction of ethylenedicysteine with primary amines is described in the literature, see e.g. Yang et al., US 2004/6692724.
  • Derivative 41 is made by reacting 40 with diazomethane or TMS-diazomethane.
  • Analog 42 is made by treating 40 with EtOH/HCl or EtOH/TMSCl.
  • Derivative 43 is made from 40 by reaction with NH 3 in the presence of a dehydrating agent or by a similar method well known to a person skilled in the art.
  • the isocyano compound 45 is prepared by formylating amine 20 to yield 44, followed by dehydration of 44 with POCl 3 to give 45.
  • Compound 50b is prepared from compound 41 in a manner analogous to the procedure in Example 2.
  • Compounds 46, 47, 48, and 49 are prepared from compounds 42, 43, 44, and 45, respectively, by treating with sodium pertechnetate as described in Example 3.
  • Compound 51 is prepared by combining, in a reaction vial, 1 mg of 22, between 0.05 mg (minimum) stannous chloride dihydrate (SnCl 2 .2H 2 O) and 0.2 mg (maximum) total tin expressed as stannous chloride dihydrate (SnCl 2 .2H 2 O), 40 mg sodium tartrate dehydrate (Na 2 C 4 H 2 O 6 .2H 2 O), and 20 mg lactose monohydrate.
  • the pH of the reconstituted drug is between 5.0 and 6.0.
  • a solubilizing agent and a bacteriostatic agent are optionally used depending on the need.
  • Compound 52 is prepared from compound 34 using a procedure similar to the one described in Example 10.
  • Compound 53 is prepared from compound 34 using a procedure similar to the one described in Example 10.
  • Compound 54 is prepared from compound 26 using a procedure similar to the one described in Example 10.
  • Compound 61 is prepared from compound 55 by first protecting the acid functionality of 55 via acid-catalyzed esterification to give 56, and then using a procedure analogous to that given in Example 7.
  • Compound 61 is prepared from compound 55 by first protecting the acid functionality of 55 via acid-catalyzed esterification to give 56, and then using a procedure analogous to that given in Example 7.
  • Compound 67 is prepared from compound 55 by preparation of 57 via a procedure analogous to that given in Example 7 using N-Boc-protected 1-amino-4-bromobutane, and then by following the deprotection and coupling steps given in Example 8.
  • Compound 70 is prepared from compound 68 in a similar manner to Part 1 of this Example.
  • Compound 72 is prepared from compound 58 in a manner similar to Example 8, Part 2.
  • Compounds 73 and 74 are prepared from compounds 67 and 70, respectively, by treating with sodium pertechnetate as described in Example 3, substituting 67 and 70, respectively, for compound 2.
  • Compound 79 is prepared from compound 3 using N 1 -Boc-1,4-diaminobutane.
  • Compound 82 is prepared from compound 79 by using a procedure analogous to the corresponding steps of Example 7.
  • Compound 5 is obtained from the commercial starting material 4 in 82% yield as reported in WO 2013/025790 A2. Alkylation of 5 with t BocNH(CH 2 ) 4 Br and deprotection of the t BOC amine and the t Bu-ester provides amino acid 88 which can be reacted with NHS-S-Acetyl-MAG3 following the procedure in: Wang Y, et al. Nat Protoc. 2007; 2(4), 972-8 to afford 89.
  • the reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no.
  • the rhenium-indomethacin derivative 90 is made following a procedure similar to the one described by Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the reagent Trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Compound 91 is prepared from compound 81 using the procedure of Example 10.
  • the celecoxib analog 95 in which a methyl ester replaces the trifluoromethyl group of celecoxib, is synthesized from 94 using the procedure described in Lill et al., Tetrahedron Letters 54, 6682-6686, (2013). The ester is hydrolyzed to give 96, and coupled with N 1 -Boc-1,6-diaminohexane to yield 97. The corresponding steps of Example 7 are then followed to yield 100.
  • Compound 104 is produced as in Example 25, using N 1 -Boc-1,4-diaminobutane in place of N 1 -Boc-1,6-diaminohexane.
  • Compound 108 is produced as in Example 25, using N 1 -Boc-1,10-diaminodecane in place of N 1 -Boc-1,6-diaminohexane.
  • Compound 109 is prepared from compound 103 using the procedure of Example 10.
  • Compound 110 is prepared from compound 107 using the procedure of Example 10.
  • Compound 178 was prepared by the following procedure: S,S-ethylenedicysteine 172 (CAS #14344-48-0) was prepared according to the procedures described in the literature, see e.g. Blondeau, Berse, Gravel, Can. J. Chem. 45, 49-52, (1967); Ratner, Clarke, J. Am. Chem. Soc. 59, 200-206, (1937).
  • Compound 176 was prepared by a procedure similar to the one described for compounds 20 and 25 in examples 5 and 6. 176 is coupled with acid 173 to give the amide 177 as described in example 5.
  • Compound 177 is dissolved in ethanol and treated with 5 eq of TMSCl at 40° C. for 20 h. Solvent is removed and the product is purified by HPLC to give the target compound 178.
  • Compound 185 was prepared by a procedure similar to the one described in Example 31 by replacing ethanol in the last step with isopropanol (Propan-2-ol).
  • Compound 176 is synthesized as described in Example 31. 176 is coupled with S,S-ethylenedicysteine 172 (CAS #14344-48-0) according to literature procedures, see e.g. Yang et al., US 2006/6692724.
  • the ethylester 192 is obtained by treating 191 with EtOH/TMSCl or EtOH/HCl.
  • Compound 193 is prepared from compound 192 by treating with sodium pertechnetate as described in Example 3.
  • indomethacin 57 mg, 0.16 mmol
  • DCM 20 ml
  • HOBt 22 mg, 0.16 mmol
  • EDCI 31 mg, 0.16 mmol
  • DIEA 62 mg, 0.48 mmol
  • the mixture was stirred at RT for 0.5 h, after which 203 (100 mg, 0.16 mmol) was added.
  • the reaction mixture was stirred at RT overnight.
  • the mixture was then diluted with water (30 ml) and extracted with EtOAc (25 ml ⁇ 3).
  • the following compounds 205-211 can also be prepared according to the procedure given in Example 34 by replacing tert-butyl 2-(2-(2-aminoethoxy)ethoxy)ethylcarbamate 174 with the appropriate reagent given in Table 2.
  • the following compounds 212-219 can also be prepared according to the procedure given in Example 34 and for compounds 204-211, by substituting Re(CO) 5 Br (CAS No. 14220-21-4) in step 1 of example 34 with Re(CO) 5 C1 (CAS No. 14099-01-5).
  • Compound 176 is synthesized as described in Example 31. 176 is coupled with picolinaldehyde to give the imine 220 according to literature procedures or methods well known to a person skilled in the art. For example, dissolving equal amounts in toluene and heating to reflux will accomplish such a transformation.
  • Compound 221 is prepared from compound 220 as described by e.g. Alberto, R., Schibli, R., Schubiger, A. P., J. Am. Chem. Soc., 121, 6076-6077, (1999).
  • the metallated complexes are purified by RP-HPLC and the peaks collected into either 100 ⁇ l of deionized H 2 O containing 100 ⁇ g of bovine serum albumin solution (BSA, in vitro analysis) or 100 ⁇ l of isotonic saline (in vivo analysis). Residual MeCN is evaporated from the solution using a stream of nitrogen.
  • BSA bovine serum albumin solution
  • isotonic saline in vivo analysis
  • Compound 236 is prepared as described in example 38.
  • Cyclopentadienyltricarbonylrhenium(I) carboxylic acid 241 is synthesized as described by Siden Top, Jean-Sébastien Lehn, Pierre Morel, opposition Jaouen, J. Organomet. Chem., 583, 63-68, (1999).
  • Tc complex 254 can be converted into the Tc complex 254 as described in the literature, see e.g. Bioorg. Med. Chem. Letters 22 (2012) 6352-6357; J. Med. Chem. (2007), 50, 543-549; J. Med. Chem. (2013), 56, 471-482; J. Med. Chem. (2014), 57, 7113-7125.
  • Compound 255 is made according to the procedure in: Ziv, Ilan et al., WO 2003/101948 and Mahmood, A., et al., WO 2001/083436.
  • Compound 255 is alkylated with 1-bromo-6-chlorohexane to form 256 as previously described in: Mahmood, A.; et al., “Functionalized tetradentate chelates and their Technetium and Rhenium complexes: synthesis spectroscopy and structural characterization”, in Technetium and Rhenium in chemistry and nuclear medicine 5, pp. 253-257 (Nicolini, M. et al.) and also in Mahmood, A., et al., WO 2001/083436.
  • Compound 256 is treated with ammonia in methanol at rt to give amine 257.
  • Compound 270 is synthesized by reacting 259 (example 42) with 99m Tc-glucoheptonate as described in: Mahmood, A., et al., WO 2001/083436.
  • Compound 255 is made according to the procedure in: Ziv, Ilan et al., WO 2003/101948 and Mahmood, A., et al., WO 2001/083436. 255 is reduced with LiAlH 4 and Boc-protected to give compound 271 according to the procedure described in Ono, M., et al., ACS Chem. Neurosci., 1, 598-607, (2010).
  • the 99m Tc complex 276 is prepared by a ligand exchange reaction employing 99m Tc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci., 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748, (2010).
  • Compound 277 can be transformed to 278 by reacting 277 with di-tert-butyldicarbonate in the presence of a base such as NaHCO 3 or aq. NaOH.
  • a base such as NaHCO 3 or aq. NaOH.
  • the nitrile 279 is obtained using a procedure similar to the one described in: Mizuno, A.; Hamada, Y.; Shioiri, T., Synthesis 1007, (1980).
  • the nitrile is reduced with hydrogen in presence of a catalyst, such as Raney®-Nickel (W.R. Grace and Co.) in a solvent such as methanol or tert-butanol to give amine 280.
  • Indomethacin is coupled to compound 280 as described in example 5 and treated with TFA to give the amide 281.
  • ligand 282 is coupled with the S-benzoyl-protected thioglycolic acid using DCC as the coupling agent to afford ligand 282.
  • 283 is made following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the Technetium complex 284 is prepared from compound 282 (example 46) as described in: Eisenhut, M., et al., J. Med. Chem., 45, 5802-5805, (2002).
  • Compound 282 (Example 46) is reduced with LiAlH 4 in a solvent such as THF to give compound 285.
  • 286 is prepared from 285 following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • the Technetium complex 287 is prepared from compound 285 (example 48) as described in: Eisenhut, M., et al., J. Med. Chem., 45, 5802-5805, (2002).
  • Compound 281 (Example 46) is coupled with tert-butyl bromoacetate in presence of a base, such as NaH, to afford compounds 288 and 289, which are separated by column chromatography on silica gel.
  • 288 is transformed to 290 by treating with TFA in DCM followed by reaction with Re(CO) 5 Cl by a procedure similar to the one described in Example 36.
  • 291 can be obtained form 289.
  • Compound 299 is prepared from compound 296 (example 52) by a procedure similar to the one described in Example 41.
  • Compound 296 is transformed into the imine 300 by a procedure similar to the one described for compound 220 in example 35. 300 is converted into the Rhenium complex 301 as described in example 36.
  • compound 301 can be prepared as follows: A mixture of 296 (100 mg, 0.29 mmol), picolinaldehyde (31 mg, 0.29 mmol) and Re(CO) 5 Cl (105 mg, 0.29 mmol) in MeOH (10 mL) was stirred at 75° C. for 3 h, then cooled to rt. The precipitate was filtered and washed with MeOH (2 ⁇ 20 ml), and dried to give compound 301 as a yellow solid (51 mg, 23%).
  • Compound 300 (example 54) is converted to 302 by a procedure similar to the one described in example 37.
  • tert-butyl (3-aminopropyl)carbamate as a colorless oil (1.8 g, yield: 32%).
  • Compound 328 was obtained from compound 327 by applying procedures similar to the ones described in Example 56 (compound 316 to compound 320).
  • the compound was was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give a light pink solid.
  • Compound 346 was synthesized from 2-(1-(4-chlorobenzoyl)-5-(methoxy-d 3 )-2-methyl-1H-indol-3-yl)acetic acid 345 by a procedure similar to the one described in Example 57, using 6-aminohexan-1-ol instead of intermediate 315.
  • 2-(1-(4-Chlorobenzoyl)-5-methoxy-2-(trifluoromethyl)-1H-indol-3-yl)acetic acid, 350 can be synthesized as described by Anna L. Blobaum, Md. Jashim Uddin, Andrew S. Felts, Brenda C. Crews, Carol A. Rouzer, and Lawrence J. Marnett, ACS Med. Chem. Lett., 4, 486-490, (2013).
  • 350 can be synthesized as outlined below.
  • Compound 351 was synthesized from 2-(1-(4-chlorobenzoyl)-5-methoxy-2-(trifluoromethyl)-1H-indol-3-yl) acetic acid, 350, by a procedure similar to the one described in Example 42.
  • the following compound 352 can also be prepared according to the procedure given in Example 60.
  • the 99m Tc complex 360 is prepared as described in Example 62 using as the last step a ligand exchange reaction employing 99m Tc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci. 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748, (2010).
  • Compound 366 is prepared from compound 364 (Example 64) by a procedure similar to the one described in Example 41.
  • Compound 367 is prepared from compound 364 (Example 64) and compound 358 (Example 62) using a procedure similar to the one described in Example 61.
  • the 99m Tc complex 368 is prepared as described in Example 66 using as the last step a ligand exchange reaction employing 99m Tc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci. 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748,
  • a patient with an undiagnosed cause of pain, or a cause of pain which cannot be localized to a site of pathology, is scheduled for a “pain scan.”
  • the patient refrains from drinking or eating for at least eight hours prior to the pain scan.
  • a compound of the invention is administered to the patient either orally or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The loci are imaged and viewed or photographed as appropriate.
  • Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection.
  • the scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the etiology of the pain and determine appropriate treatment.
  • Tumor Scans to Localize Site(s) of Tumor(s)
  • a patient to be screened for presence of a tumor is scheduled for a “COX scan.”
  • the patient refrains from drinking or eating for at least eight hours prior to the COX scan.
  • a compound of the invention is administered to the patient either orally or parenterally.
  • the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound.
  • the loci are imaged and viewed or photographed as appropriate. Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection.
  • the scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the presence and/or location of the tumor and determine appropriate treatment.
  • a patient to be screened for an asymptomatic infection, or to have the site of a localized infection identified, is scheduled for a “COX scan.”
  • the patient refrains from drinking or eating for at least eight hours prior to the COX scan.
  • a compound of the invention is administered to the patient either orally or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The loci are imaged and viewed or photographed as appropriate.
  • Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection.
  • the scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the presence and/or location of an infection, and to determine appropriate treatment.
  • Animal models can be used to test the conjugates and compounds of the invention for their suitability for clinical use.
  • Animal models of pain (and inflammation related to pain), of infection, and of cancer are well known. See, for example, Handbook of Laboratory Animal Sciense, Second Edition: Animal Models, Volume 2 (Jann Hau, Gerald L. Van Hoosier Jr., editors), Boca Raton: CRC Press, 2003; Animal Models for the Study of Human Disease (P. Michael Conn, editor), San Diego: Academic Press, 2013.
  • a suitable animal model for pain, for cancer, or for infection
  • the appropriate pathology is induced.
  • the site of the induced pain, inflammation, infection, or tumor is recorded by the investigator.
  • One or more candidate conjugates or compounds of the invention is administered to the animal, either by oral gavage or parenterally.
  • the animal is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The location(s) indicated by the scan are compared with the known site or sites at which the pathology was induced, for evaluation of the effectiveness of the conjugate for accumulating at the site of pathology.
  • the carrageenan induced rat paw edema assay can be used as an exemplary model for inflammation; see Shalini, V. et al., Molecular Immunology 66:229-239 (2015); see also Winter, C. et al., Proc. Soc. Exp. Biol. Med. 111:544-547 (1962). Briefly, acute inflammation is induced by aponeurosis injection of 0.1 ml of 1% carrageenan in 0.9% saline. Additional information regarding model assays is described in Guay et al., J. Biol. Chem.
  • the animal is then imaged using the appropriate modality, for example, scintigraphic imaging or SPECT imaging.
  • appropriate modality for example, scintigraphic imaging or SPECT imaging.
  • Exemplary imaging methods that can be used are described in Pacelli et al., J. Label. Compd. Radiopharm. 57:317-322 (2014); de Vries et al., J Nucl. Med. 44:1700-1706 (2003); and Tietz et al., Current Medicinal Chemistry, 20, 4350-4369 (2013).
  • a variety of assays can be used to evaluate inhibition of compounds to cyclooxygenase (COX).
  • COX cyclooxygenase
  • Compounds in the present invention display inhibition of cyclooxygenase in the following assays.
  • RAW264.7 murine macrophages were obtained from the Cell Bank of Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences (Shanghai, China) and cultured in Dulbecco's modified Eagle's medium containing 100 U/ml penicillin and 100 ⁇ m/ml streptomycin at 37° C. in 5% CO 2 .
  • Cell-based COX-2 assay RAW264.7 cells were plated at a density of 2.5 ⁇ 105/ml cells in a 96-well plate with 0.1 ml of culture medium per well and cultured overnight. The cells were pre-incubated for 30 min with various doses of compounds and stimulated for 7 h with 1 ⁇ g/ml LPS and 10 U/ml IFN-g. The cell culture supernatants were collected immediately following treatment and centrifuged at 1,000 rpm for 5 min to remove the particulate matter. PGE2 was determined using a Prostaglandin E2 assay kit (catalog no. 62P2APEB; Cisbio Co.,).
  • COX-1/-2 enzyme assay The ability of compounds to inhibit ovine COX-1 and human COX-2 was determined using a commercially available enzyme immunoassay (EIA) kit (catalog no. 701090(COX-1); 701080 (COX-2) Cayman Chemical Co., Ann Arbor, Mich., USA) according to the manufacturer's protocol. COX catalyzes the first step in the biosynthesis of AA to PGH2. PGF2 ⁇ , produced from PGH2 by reduction with stannous chloride, was measured by EIA (ACETM competitive EIA, Cayman Chemical, Ann Arbor, Mich., USA).
  • EIA enzyme immunoassay
  • reaction buffer solutions [960 ⁇ l 0.1 M Tris-HCl (pH 8.0) containing 5 mM EDTA and 2 mM phenol] with either COX-1 or COX-2 (10 ⁇ l) enzyme in the presence of heme (10 ⁇ l), 10 ⁇ l of various concentrations of test drug solutions were added. These solutions were incubated for 15 min at 37° C. and subsequently 10 ⁇ l AA solution (100 ⁇ M) was added. The COX reaction was stopped by the addition of 30 ⁇ l stannus chloride after 2 min, mixed immediately, supernatants were 2000 fold diluted. The produced PGF2 ⁇ was measured by EIA.
  • This assay is based on the competition between PGs and a PG-acetylcholinesterase conjugate (PG tracer) for a limited amount of PG antiserum.
  • the amount of PG tracer that is able to bind to the PG antiserum is inversely proportional to the concentration of PGs in the wells since the concentration of the PG tracer is held at a constant while the concentration of PGs varies.
  • the specific antiserum-PG complex bound to a mouse anti-rabbit IgG that had been previously attached to the well.
  • the plate was washed to remove any unbound reagents and 200 ⁇ l Ellman's reagent (5,5′-dithiobis-(2-nitrobenzoic acid), which contains the substrate to acetylcholine esterase, was added to the well.
  • the product of this enzymatic reaction generates a distinct yellow color that absorbs at 406 nm.
  • the intensity of this color determined by spectrophotometry, is proportional to the amount of PG tracer bound to the well, which is inversely proportional to the amount of PGs present in the well during the incubation. Percent inhibition was calculated by the comparison of the compounds treated to the various control incubations.
  • Dose-response curves were generated using XLFit (IDBS, Surrey, UK) or Prism (GraphPad Software, La Jolla, Calif., US) to calculate IC 50 values for each compound tested.
  • Embodiment 1 A conjugate comprising: a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt thereof.
  • NSAID non-steroidal anti-inflammatory drug
  • Embodiment 2 The conjugate of embodiment 1, wherein said radioactive agent is 99m Tc.
  • Embodiment 3 The conjugate of embodiment 1, wherein the NSAID or the residue of a NSAID and imaging moiety are bonded or complexed via a linker selected from the group consisting of an optionally substituted C 1 -C 30 hydrocarbylene group and an optionally substituted C 3 -C 30 heterohydrocarbylene group.
  • Embodiment 4 The conjugate of any of embodiments 1-3, wherein the NSAID or the residue of a NSAID is selected from the group consisting of acetylsalicylic acid, diflunisal, salsalate, choline magnesium trisalicylate, ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, nabumetone, piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib, rofecoxib
  • Embodiment 5 The conjugate of any of embodiments 1-3, wherein the optionally substituted C 3 -C 30 heterohydrocarbylene group is
  • R 1 and R 2 are independently selected from hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or R 1 and R 2 together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring; and n is an integer selected from 0 to 4, inclusive.
  • Embodiment 6 The conjugate of embodiment 5, wherein R 1 and R 2 are methyl.
  • Embodiment 7 The conjugate of embodiment 5, wherein the linking group is
  • Embodiment 8 The conjugate of any of embodiments 1-3, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • NSAID non-steroidal anti-inflammatory drug
  • a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • Embodiment 9 The conjugate of embodiment 1, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent is:
  • NSAID non-steroidal anti-inflammatory drug
  • Tc is 99m Tc;or a pharmaceutically acceptable salt thereof.
  • Embodiment 10 The conjugate of embodiment 1, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent is:
  • NSAID non-steroidal anti-inflammatory drug
  • Tc is 99m Tc;or a pharmaceutically acceptable salt thereof.
  • Embodiment 11 A pharmaceutical composition comprising the conjugate of any of embodiments 1-3, 9, or 10, and a pharmaceutically acceptable excipient.
  • Embodiment 12 A method of imaging a site of pathology in a subject, comprising: a) administering a conjugate comprising a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt of said conjugate; or a pharmaceutical composition comprising said conjugate or a pharmaceutically acceptable salt of said conjugate and a pharmaceutically acceptable excipient; and b) generating an image of the subject or an image of a portion of the subject.
  • NSAID non-steroidal anti-inflammatory drug
  • Embodiment 13 The method of embodiment 12, wherein said radioactive agent is 99m Tc.
  • Embodiment 14 The method of embodiment 12, wherein the NSAID or the residue of a NSAID and imaging moiety are bonded or complexed via an optionally substituted C 1 -C 30 hydrocarbylene group or an optionally substituted C 3 -C 30 heterohydrocarbylene group.
  • Embodiment 15 The method of any of embodiments 12-14, wherein the NSAID or the residue of a NSAID is selected from the group consisting of acetylsalicylic acid, diflunisal, salsalate, choline magnesium trisalicylate, ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, nabumetone, piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib, rofecoxib ,
  • Embodiment 16 The method of any of embodiments 12-14, wherein the optionally substituted C 3 -C 30 heterohydrocarbylene group is
  • R 1 and R 2 are independently selected from hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or R 1 and R 2 together with the carbon to which they are attached form a C 3 -C 8s cycloalkyl ring; and n is an integer selected from 0 to 4, inclusive.
  • Embodiment 17 The method of embodiment 16, wherein R 1 and R 2 are methyl.
  • Embodiment 18 The method of embodiment 16, wherein the linking group is
  • Embodiment 19 The method of any of embodiments 12-14, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • NSAID non-steroidal anti-inflammatory drug
  • a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • Embodiment 20 The method of embodiment 12, wherein the conjugate is:
  • Tc is 99m Tc; or a pharmaceutically acceptable salt thereof.
  • Embodiment 21 The method of embodiment 12, wherein the conjugate is:
  • Tc is 99m Tc; or a pharmaceutically acceptable salt thereof.
  • Embodiment 22 The method of any of embodiments 12-14, 20, or 21, wherein the conjugate is administered as a composition additionally comprising a pharmaceutically acceptable excipient.
  • Embodiment 23 A conjugate comprising: a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt thereof.
  • NSAID non-steroidal anti-inflammatory drug
  • Embodiment 24 The conjugate of embodiment 23, wherein said radioactive agent is 99m Tc, 52 Mn, 186 Re or 188 Re.
  • Embodiment 25 The conjugate of embodiment 23, of the form:
  • each “terminal ligand” is independently selected from a ligand that bonds or complexes to M, but which does not have a NSAID or NSAID residue attached to it.
  • Embodiment 26 The conjugate of embodiment 23, wherein the NSAID or the residue of a NSAID and the imaging moiety are bonded or complexed via a linker, wherein the linker is selected from the group consisting of:
  • Embodiment 27 The conjugate of embodiment 26, wherein the linker is selected from the group consisting of: (—CH 2 CH 2 —O—) n and (—CH 2 CH(CH 3 )—O—) n ,
  • n is an integer from 1 to 12 inclusive.
  • Embodiment 28 The conjugate of embodiment 26, wherein the linker is selected from the group consisting of: —(NR a )—(CH 2 ) n —(NR a )—, —(NH)—(CH 2 ) n —(NH)—, —(NR a )—(CH 2 CH 2 )—(OCH 2 CH 2 ) n —(NR a )—, —(NH)—(CH 2 CH 2 )—(OCH 2 CH 2 ) n —(NH)—, where R a is (C 1 -C 4 alkyl) and n is an integer from 1 to 12 inclusive,
  • Embodiment 29 The conjugate of embodiment 23 or embodiment 24, wherein the imaging moiety further comprises a group which bonds or complexes to the radioactive agent.
  • Embodiment 30 The conjugate of embodiment 29, wherein the group which bonds or complexes to the radioactive agent is a chelating group.
  • Embodiment 31 The conjugate of embodiment 30, wherein the chelating group is of the form:
  • each J is independently selected from the group consisting of NH and S,
  • Embodiment 32 The conjugate of embodiment 30, wherein the chelating group is selected from the group consisting of:
  • R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , and R 17 are independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with fluoro, hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or, independently of the other substituents, (R 10 and R 11 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, (R 12 and R 13 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 14 and R 15 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 16 and R 17 )
  • R 18 , R 19 , R 20 , R 21 , R 22 , R 23 , R 24 , and R 25 are independently selected from the group consisting of hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with fluoro, hydroxy, —O—C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; or, independently of the other substituents, (R 18 and R 19 ) together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, (R 20 and R 21 ) together with the carbon to which they are attached form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 22 and R 23 ) together with the carbon to which they are attached independently form a C 3 -C 8 cycloalkyl ring or heterocycloalkyl ring, or (R 24 and R 25 ) together with
  • Embodiment 33 A conjugate of the formula:
  • NSAID or NSAID residue refers to a NSAID or a residue of a NSAID
  • M is selected from the group consisting of 99m Tc , 52 Mn, and Re;

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Optics & Photonics (AREA)
  • Physics & Mathematics (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Conjugates derived from non-steroidal anti-inflammatory drugs (NSAIDs) and methods of use thereof are disclosed, useful for, inter alia, identifying and localizing the site of pathology and/or inflammation responsible for the sensation of pain in a patient; for identifying the sites of primary, secondary, benign, or malignant tumors; and for diagnosing infection or confirming or ruling out suspected infection. The NSAID-based conjugates contain an imaging moiety. The conjugates concentrate at sites of increased cyclooxygenase expression, thus revealing the sites of increased prostaglandin production, which is correlated with pain and inflammation, and correlated with tumor presence and/or location. Identifying areas of increased COX expressing can also aid in screening for infections.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This patent application claims priority benefit of U.S. Provisional Patent Application No. 62/018,397, filed Jun. 27, 2014; of U.S. Provisional Patent Application No. 62/052,928, filed Sep. 19, 2014; and of U.S. Provisional Patent Application No. 62/109,544, filed Jan. 29, 2015. The entire contents of those applications are hereby incorporated by reference herein.
  • FIELD OF THE INVENTION
  • Conjugates derived from non-steroidal anti-inflammatory drugs (NSAIDs) and methods of use thereof are disclosed, useful for, inter alia, identifying and localizing the site of pathology and/or inflammation responsible for the sensation of pain in a patient, sites of infection, and identifying and localizing the sites of tumor pathology, including benign, malignant, primary, and secondary tumors.
  • BACKGROUND OF THE INVENTION
  • It is important in medicine to identify the site of pathology in order to properly screen for and/or treat a disease. Tumor screening for the presence of tumors (e.g. for breast cancer, cervical cancer, colon cancer, prostate cancer, etc.) is very common. Some of the difficulties with tumor screening are expense, patient's time, physician's time, and accuracy. Also, many of the screening tests are not particularly accurate. For example, testing for prostate cancer using serum acid phosphatase or prostate specific antigen (PSA) is non-specific, and elevation of the marker in healthy individuals can be cause for an unnecessary surgery, a prostate biopsy. An additional example is MRI screening for breast tumors, whose value has recently been questioned for both insensitivity and occasional misinterpretation. In addition, the presence or absence of sentinel (metastatic) nodes is critical for the optimal treatment of breast cancer. Low grade chondrosarcomas are notoriously difficult to read by the pathologist, and frequently have to be sent to multiple institutions for a diagnostic consensus. All of these examples suggest the need for improving detection for all benign, malignant, primary and secondary tumors. A rapid and non-invasive method of localizing tumors would aid immensely in diagnosing and treating the underlying cause. The growing tendency to understand tumors at the molecular level may also be guided by such improved non-invasive methods.
  • Localization of pain is another area where identifying the site of pathology is important for treatment; however, such localization is often not straightforward. The unpleasant sensation of pain serves as an indicator of a disease or pathological state. Pain often occurs at the site of pathology, and can be a helpful guide in determining diagnosis and appropriate treatment. However, in many cases, the area where a patient experiences pain may not be coincident with the area where the actual pathology has occurred. A classic example is sciatica, where pressure on the sciatic nerve due to a herniated disc in the lower spine can result in a sensation of pain in the leg, at a significant distance from the site of pathology. Another example is the difficulty in diagnosing pain in the chest or thorax, which can arise from multiple causes, such as cardiac ischemia, gastroesophageal reflux, or pulmonary embolism. In such cases, differential diagnosis requires a systematic process of elimination through tests and procedures until the cause and/or location of pathology is identified.
  • Screening for infectious diseases, particularly when a patient is still asymptomatic, also poses difficulties. Medicaments and methods for such screening would prove useful in limiting outbreaks of diseases; early treatment of infected individuals; and avoiding unnecessary treatment or isolation for individuals who are suspected of being infected, but who in actuality have not been infected, by a disease.
  • Because pathology is often accompanied by inflammation at the site of the pathology (which is not necessarily the site where pain is experienced), rapid and non-invasive methods of localizing inflammation in a patient experiencing pain would aid immensely in diagnosing and treating the underlying cause of the pain.
  • SUMMARY OF THE INVENTION
  • The current invention provides compounds and methods useful for identification of areas of pathology, including tumors and inflammation, and screening for infections and sites of infections, via non-invasive imaging. The compounds and methods can be used in both human and veterinary medicine.
  • In a first embodiment, the invention embraces conjugate comprising a non-steroidal anti-inflammatory drug (NSAID), a residue of a NSAID, or a derivative of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter, an X-ray emitter, and a beta emitter; or a pharmaceutically acceptable salt thereof. In this first embodiment, the imaging moiety can be optionally bonded to the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID via a linker. In a second embodiment, the radioactive agent in the first embodiment can be 99mTc, 52Mn, 186Re or 188Re. In a third embodiment, the imaging moiety of the first or second embodiment can further comprise a chelating group which bonds or complexes to the radioactive agent; and the imaging moiety can be optionally bonded to the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID via a linker.
  • In a fourth embodiment, the imaging moiety comprising a chelating group bonded or complexed to the radioactive agent of the third embodiment is of the form:
  • Figure US20190169084A1-20190606-C00001
  • wherein M is selected from the group consisting of 99mTc, 52Mn, 186Re or 188Re, wherein each J is independently selected from the group consisting of NH and S,
  • R101, R102, and R103 are independently selected from the group consisting of optionally substituted C2-C4 alkyl, and the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group, either through a linker or directly, at
  • a) any J, R101, R102, or R103 atom where a hydrogen atom can be replaced with a bond to the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present; or at
  • b) the nitrogen atom in the —R101—N—R102— portion, forming a bond between that nitrogen and the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present; or at
  • c) the nitrogen atom in the —R102—N—R103— portion, forming a bond between that nitrogen and the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present;
  • or the imaging moiety comprising a chelating group bonded or complexed to the radioactive agent of the third embodiment is of the form:
  • Figure US20190169084A1-20190606-C00002
  • wherein R(ri) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive and the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group either through a linker or directly if no linker is present, at any location on the cyclopentane ring which does not have a (Rri) group.
  • In a fifth embodiment, in any of the first, second, third, or fourth embodiments, the NSAID, residue of an NSAID, or derivative of a NSAID and the imaging moiety are bonded or complexed via a linker, where the linker is selected from the group consisting of an optionally substituted C1-C10 hydrocarbylene group; an optionally substituted C2-C10 heterohydrocarbylene group; and a linker of the form -LE-R4-LF-, where the linker -LE-R4-LF- can be in either orientation with respect to the NSAID, residue of an NSAID, or derivative of a NSAID and the imaging moiety (that is, either LE or LF can be attached to the NSAID, residue of an NSAID, or derivative of a NSAID, and the other of LE or LF is attached to the imaging moiety). In this fifth embodiment, LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —C(═O)—, and R8 is optionally substituted C1-C4 alkyl, R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl, and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)— —N(R9)—(C═O)—(CH2)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—,
  • —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl.
  • In a sixth embodiment, in any of the first, second, third, fourth, or fifth embodiments, the linker is selected from the group consisting of: —(NH)—(CH2)n—, —(NRa)—(CH2)n—, —(NH)—(CH2)n—(NH)—, —(NRa)—(CH2)n—(NRa)—, —(NH)—(CH2CH2)—(OCH2CH2)m—(NH)—, —(NRa)—(CH2CH2)—(OCH2CH2)m—(NRa)—, —(NH)—(CH2CH2)—((NH)CH2CH2)m—(NH)—, —(NRa)—(CH2CH2)—((NH)CH2CH2)m—(NRa)—, (—CH2CH2—O—)n, (—CH2CH(CH3)—O—)q, where Ra is (C1-C4 alkyl), n is an integer from 1 to 10 inclusive, m is an integer from 1 to 4 inclusive, and q is an integer from 1 to 3 inclusive,
    • —NH—(CH2)2—,
    • —NH—(CH2)3—,
    • —NH—(CH2)4—,
    • —NH—(CH2)5—,
    • —NH—(CH2)6—,
    • —NH—(CH2)7—,
    • —NH—(CH2)8—,
    • —NH—(CH2)2—C(H)═C(H)—(CH2)2—,
    • —NH—(CH2)2—NH—,
    • —NH—(CH2)3—NH—,
    • —NH—(CH2)4—NH—,
    • —NH—(CH2)5—NH—,
    • —NH—(CH2)6—NH—,
    • —NH—(CH2)7—NH—,
    • —NH—(CH2)8—NH—,
    • —NH—(CH2)3—C(CH3)2—NH—,
    • —NH—(CH2)4—C(CH3)2—NH—,
    • —NH—(CH2)5—C(CH3)2—NH—,
    • —NH—(CH2)6—C(CH3)2—NH—,
    • —NH—(CH2)7—C(CH3)2—NH—,
    • —NH—(CH2)2—C(CH3)2—(CH2)2—NH—,
    • —NH—(CH2)2—C(CH3)2—(CH2)2—,
    • —NH—C(CH3)2—(CH2)3—,
    • —NH—C(CH3)2—(CH2)4—,
    • —NH—C(CH3)2—(CH2)5—,
    • —NH—C(CH3)2—(CH2)6—,
    • —NH—C(CH3)2—(CH2)7—,
    • —NH—CH(CH3)—(CH2)3—,
    • —NH—CH(CH3)—(CH2)4—,
    • —NH—CH(CH3)—(CH2)5—,
    • —NH—CH(CH3)—(CH2)6—,
    • —NH—CH(CH3)—(CH2)7—,
    • —NH—CH(CF3)—(CH2)3—,
    • —NH—CH(CF3)—(CH2)4—,
    • —NH—CH(CF3)—(CH2)5—,
    • —NH—CH(CF3)—(CH2)6—,
    • —NH—CH(CF3)—(CH2)7—,
    • —NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—,
    • —NH—(CH2)2—NH—(C═O)—,
    • —NH—(CH2)3—NH—(C═O)—,
    • —NH—(CH2)4—NH—(C═O)—,
    • —NH—(CH2)5—NH—(C═O)—,
    • —NH—(CH2)6—NH—(C═O)—,
    • —NH—(CH2)7—NH—(C═O)—,
    • —NH—(CH2)8—NH—(C═O)—,
    • —NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—(C═O)—,
    • —NH—(CH2)2—NH—(C═O)—(CH2)—,
    • —NH—(CH2)3—NH—(C═O)—(CH2)—,
    • —NH—(CH2)4—NH—(C═O)—(CH2)—,
    • —NH—(CH2)5—NH—(C═O)—(CH2)—,
    • —NH—(CH2)6—NH—(C═O)—(CH2)—,
    • —NH—(CH2)7—NH—(C═O)—(CH2)—,
    • —NH—(CH2)8—NH—(C═O)—(CH2)—,
    • —NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—(C═O)—(CH2)—,
    • —C(═O)—(CH2)2—,
    • —C(═O)—(CH2)3—,
    • —C(═O)—(CH2)4—,
    • —C(═O)—(CH2)5—,
    • —C(═O)—(CH2)6—,
    • —C(═O)—(CH2)7—,
    • —C(═O)—(CH2)8—,
    • —C(═O)—(CH2)2—C(H)═C(H)—(CH2)2—,
    • —C(═O)—(CH2)2—NH—,
    • —C(═O)—(CH2)3—NH—,
    • —C(═O)—(CH2)4—NH—,
    • —C(═O)—(CH2)5—NH—,
    • —C(═O)—(CH2)6—NH—,
    • —C(═O)—(CH2)7—NH—,
    • —C(═O)—(CH2)8—NH—,
    • —C(═O)—(CH2)2—C(H)═C(H)—(CH2)2—NH—,
    • —NH—(CH2)2—O—(CH2)2—NH—,
    • —NH—(CH2)2—O—(CH2)2—O—(CH2)2—NH—,
    • —NH—(CH2)2—O—(CH2)2—O—(CH2)2—O—(CH2)2—NH—,
    • —NH—(CH2)2—NH—(CH2)2—NH—,
    • —NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—,
    • —NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—,
    • —NH—(CH2)2—N(CH3)—,
    • —NH—(CH2)3—N(CH3)—,
    • —NH—(CH2)4—N(CH3)—,
    • —NH—(CH2)5—N(CH3)—,
    • —NH—(CH2)6—N(CH3)—,
    • —NH—(CH2)7—N(CH3)—,
    • —NH—(CH2)8—N(CH3)—,
    • —NH—(CH2)3NH—(CH2)3—,
    • —NH—(CH2)2—C(H)═C(H)—(CH2)2—,
    • —NH—CH2—CF2—(CH2)4—,
    • —NH—CH2—CF2—(CH2)5
    • —C(═O)—CF2—(CH2)4—,
    • —C(═O)—CF2—(CH2)5—,
  • Figure US20190169084A1-20190606-C00003
  • In a seventh embodiment, in any of the first, second, third, fourth, fifth, or sixth embodiments, the conjugate is of the formula:
  • Figure US20190169084A1-20190606-C00004
  • or pharmaceutically acceptable salts thereof.
  • In this seventh embodiment, LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —C(═O)—, and R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C 10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 aryl-C1-C6 alkyl, LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)— —N(R9)—(C═O)—(CH2)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl; M is selected from the group consisting of 99mTc, 52Mn, 186Re or 188Re; R10, R1, R12, R13, R14, R15, R16, and R17 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R10 and R11) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R12 and R13) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R14 and R15) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R10 and R11), (R12 and R13), (R14 and R15,) and (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; R18, R19, R20, R21, R22, R23, R24, R25, R26, R27, R28, and R29 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R26 and R27) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25), or (R26 and R27), or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; or, independently of the other substituents, (R22 and R23) together form an oxo group; Q is selected from the group consisting of OH, NH2, NH(C1-C4 alkyl), N(C1-C4 alkyl)(C1-C4 alkyl), OCH3, and OCH2CH3.
  • In an eighth embodiment, the conjugates of the seventh embodiment are of the form:
  • Figure US20190169084A1-20190606-C00005
  • where R38 is —O—(C1-C4) alkyl; R39 is selected from the group consisting of H, F, Cl, Br, I, CH3, and CF3; R40 is selected from the group consisting of H, CH3, and CF3; R41 and R42 are both H, or R41 is H and R42 is OH, or R41 and R42 together form an oxo group; R43 is selected from the group consisting of (C1-C10) hydrocarbylene and (C2-C10) heterohydrocarbylene containing one O atom, two O atoms, one (—S(═O2))— group, two (—S(═O2))— groups, or one O atom and one (—S(═O2))— group, where the O atom or atoms of the heteroalkylene are not bonded directly to a nitrogen atom, and where when more than one heteroatom is present, at least one carbon atom intervenes between the heteroatoms; M is selected from the group consisting of 99mTc, 52Mn, 186Re or 188Re; or pharmaceutically acceptable salts thereof.
  • In a ninth embodiment, the conjugates of the eighth embodiment are of the formula:
  • Figure US20190169084A1-20190606-C00006
  • where Re is 186Re or 188Re; or pharmaceutically acceptable salts thereof.
  • In a tenth embodiment, the conjugates of the eighth embodiment are of the formula:
  • Figure US20190169084A1-20190606-C00007
  • wherein Tc is 99mTc; or pharmaceutically acceptable salts thereof.
  • In an eleventh embodiment, the conjugates of the eighth embodiment can be selected from the group consisting of the compounds:
  • Figure US20190169084A1-20190606-C00008
  • where Re is 186Re or 188Re; where Tc is 99mTc; and pharmaceutically acceptable salts thereof.
  • In a twelfth embodiment, the conjugates of the first or second embodiment can be of the formula

  • (NSAID, NSAID residue, or NSAID derivative)-(linker)-(chelator)-M-(terminal ligand)z1

  • or (NSAID, NSAID residue, or NSAID derivative)-(linker)-M-(terminal ligand)z2
  • where z1 is an integer between 0 and 4 inclusive; z2 is an integer between 0 and 5 inclusive; and -(linker)-(chelator)-M-(terminal ligand)z1 or -(linker)-M-(terminal ligand)z2 is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00009
  • where LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —(C═O)—, and R8 is optionally substituted C1-C4 alkyl , with the proviso that if the LE moiety of the group -LF-R4-LE- would be attached to a nitrogen atom, then LE is absent; LG is absent or is selected from the group consisting of —NH—, —N(R8)—, and —(C═O)—, and R8 is optionally substituted C1-C4 alkyl; R4 is selected from the group consisting of optionally substituted C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 aryl-C1-C6 alkyl; R5 is selected from the group consisting of —OH, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; RN is H or (C1-C4 alkyl); LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)— —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl; and R18, R19, R20, R21, R22, R23, R24, R25, R26, R27, R28, and R29 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R26 and R27) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25), or (R26 and R27), or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; R30, R31, R32, and R33 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R30 and R31), (R31 and R32), or (R32 and R33), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring; R34, R35, R36, and R37 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R34 and R35), (R35 and R36), or (R36 and R37), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring; M is selected from the group consisting of 99mTc, 52Mn, 186Re and 188Re; R(ri) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive; and X is Cl or Br; or pharmaceutically acceptable salts thereof. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • In a thirteenth embodiment, the -(linker)-(chelator)-M-(terminal ligand)z1 or -(linker)-M-(terminal ligand)z2 group of the conjugates of the twelfth embodiment can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00010
  • where the substituents are as indicated in the twelfth embodiment, and pharmaceutically acceptable salts thereof.
  • In a fourteenth embodiment, the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID in any of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, or thirteenth embodiments can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00011
  • where the atom marked with an asterisk * indicates an open valence at that atom at which the NSAID, residue of the NSAID or derivative of the NSAID is attached to the remainder of the conjugate. In a fifteenth embodiment, the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID in any of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, or thirteenth embodiment can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00012
  • where the carbon atom or oxygen atom marked with an asterisk * indicates an open valence at that atom at which the NSAID, residue of a NSAID, or derivative of a NSAID is attached to the remainder of the conjugate.
  • In a sixteenth embodiment, the conjugate of the first, second, third, or fourth embodiments can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00013
    Figure US20190169084A1-20190606-C00014
    Figure US20190169084A1-20190606-C00015
    Figure US20190169084A1-20190606-C00016
    Figure US20190169084A1-20190606-C00017
  • where Tc is 99mTc, Re is 186Re or 188Re; and pharmaceutically acceptable salts thereof.
  • In a seventeenth embodiment, the conjugate of any one of the first, second, or third embodiments can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00018
    Figure US20190169084A1-20190606-C00019
    Figure US20190169084A1-20190606-C00020
    Figure US20190169084A1-20190606-C00021
    Figure US20190169084A1-20190606-C00022
    Figure US20190169084A1-20190606-C00023
  • wherein Tc is 99mTc; and pharmaceutically acceptable salts thereof.
  • In an eighteenth embodiment, the conjugate of any one of the first, second, or third embodiments can be selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00024
    Figure US20190169084A1-20190606-C00025
    Figure US20190169084A1-20190606-C00026
  • wherein Tc is 99mTc; and pharmaceutically acceptable salts thereof.
  • In a nineteenth embodiment, the invention embraces a pharmaceutical composition comprising one or more conjugates of any one of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, thirteenth, fourteenth, fifteenth, sixteenth, seventeenth, or eighteenth embodiments, and a pharmaceutically acceptable excipient.
  • In a twentieth embodiment, the invention embraces a method of imaging a site of pathology or suspected pathology in a subject, comprising:
  • a) administering one or more conjugates of any one of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, thirteenth, fourteenth, fifteenth, sixteenth, seventeenth, or eighteenth embodiments, or the pharmaceutical composition of the nineteenth embodiment, to the subject, where the radioactive agent of the conjugate comprises 99mTc, 52Mn, 186Re or 188Re; and
  • b) generating an image of the subject or an image of a portion of the subject.
  • In a twentieth-first embodiment, the pathology or suspected pathology of the twentieth embodiment is a tumor or a suspected tumor.
  • In a twenty-second embodiment, the pathology or suspected pathology of the twentieth embodiment is pain (that is, the subject is suffering from pain).
  • In a twenty-third embodiment, the pathology or suspected pathology of the twentieth h embodiment is an infection or a suspected infection.
  • In a twenty-fourth embodiment, the invention embraces a conjugate disclosed herein which has an IC50 for inhibition of a cyclooxygenase of less than about 2 micromolar, less than about 1 micromolar, preferably less than about 0.5 micromolar, more preferably less than about 0.3 micromolar, still more preferably less than about 0.1 micromolar, yet more preferably less than about 50 nanomolar; in a twenty-fifth embodiment, the cyclooxygenase is COX-2. In a twenty-sixth embodiment, the invention embraces a conjugate of any one of the first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, tenth, eleventh, twelfth, thirteenth, fourteenth, fifteenth, sixteenth, seventeenth, or eighteenth embodiments which has an IC50 for inhibition of a cyclooxygenase of less than about 2 micromolar, less than about 1 micromolar, preferably less than about 0.5 micromolar, more preferably less than about 0.3 micromolar, still more preferably less than about 0.1 micromolar, yet more preferably less than about 50 nanomolar; in a twenty-seventh embodiment, the cyclooxygenase is COX-2.
  • In some embodiments, the conjugates of the invention can be selected from the group consisting of a conjugate illustrated in FIG. 1, FIG. 2, or FIG. 3; a rhenium-containing conjugate illustrated in FIG. 1, FIG. 2, or FIG. 3; a technetium-containing conjugate illustrated in FIG. 1, FIG. 2, or FIG. 3; a technetium-99m-containing conjugate illustrated in FIG. 1, FIG. 2, or FIG. 3; or a pharmaceutically acceptable salt thereof
  • In further embodiments, the invention embraces a pharmaceutical composition comprising one or more of the foregoing conjugates and a pharmaceutically acceptable excipient.
  • In further embodiments, the invention embraces any of the conjugates disclosed herein, with the substitution of a non-radioactive agent for the radioactive agent. Thus, for any of the generic structures or specific conjugates disclosed herein containing 99mTc, 52Mn, 186Re, or 188Re, the invention also embraces those generic structures or specific conjugates with a non-radioactive metal, such as non-radioactive Re, such as 185Re.
  • In further embodiments, the invention embraces any of the conjugates disclosed herein, with the removal of the radioactive agent. Thus, for any of the generic structures or specific conjugates disclosed herein containing 99mTc, 52Mn, 186Re, or 188Re, the invention also embraces those generic structures or specific conjugates without the metal, that is, with the uncomplexed or free chelator.
  • In further embodiments, the invention embraces the synthesis of any of the conjugates described herein, according to the protocols disclosed herein.
  • The invention also embraces methods of imaging a patient or subject. In one embodiment, the invention embraces a method of imaging a site of pathology or suspected pathology in a subject, comprising administering one or more conjugates or compositions described herein, including any of the foregoing embodiments, to the subject, wherein the radioactive agent of the conjugate comprises 99mTc, 52Mn, 186Re, or 188Re; and generating an image of the subject or an image of a portion of the subject. The pathology or suspected pathology in the subject can be a tumor or a suspected tumor. The pathology or suspected pathology in the subject can be an infection or a suspected infection. The subject can be a subject suffering from pain.
  • In further embodiments, the invention embraces any of the conjugates and compositions as disclosed herein for use in imaging a subject or for diagnosing a subject. In further embodiments, the invention embraces the use in imaging or in diagnosis of any of the conjugates and compositions as disclosed herein. In further embodiments, the invention embraces the use of any of the conjugates and compositions as disclosed herein for the manufacture of a medicament for use in imaging a subject, or for use in diagnostic purposes.
  • In further embodiments, the invention includes conjugates where the ratio of (NSAID, NSAID residue, or NSAID derivative) to (chelating moiety) is 1:1.
  • Some embodiments described herein are recited as “comprising” or “comprises” with respect to their various elements. In alternative embodiments, those elements can be recited with the transitional phrase “consisting essentially of” or “consists essentially of” as applied to those elements. In further alternative embodiments, those elements can be recited with the transitional phrase “consisting of” or “consists of” as applied to those elements. Thus, for example, if a composition or method is disclosed herein as comprising A and B, the alternative embodiment for that composition or method of “consisting essentially of A and B” and the alternative embodiment for that composition or method of “consisting of A and B” are also considered to have been disclosed herein. Likewise, embodiments recited as “consisting essentially of” or “consisting of” with respect to their various elements can also be recited as “comprising” as applied to those elements. Finally, embodiments recited as “consisting essentially of” with respect to their various elements can also be recited as “consisting of” as applied to those elements, and embodiments recited as “consisting of” with respect to their various elements can also be recited as “consisting essentially of” as applied to those elements.
  • When a composition is described as “consisting essentially of” the listed components, the composition contains the components expressly listed, and may contain other components which do not substantially affect the condition being treated. That is, the composition either does not contain any other components which do substantially affect the condition being treated other than those components expressly listed; or, if the composition does contain extra components other than those listed which substantially affect the condition being treated, the composition does not contain a sufficient concentration or amount of those extra components to substantially affect the condition being treated. When a method is described as “consisting essentially of” the listed steps, the method contains the steps listed, and may contain other steps that do not substantially affect the condition being treated, but the method does not contain any other steps which substantially affect the condition being treated other than those steps expressly listed.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 illustrates various 99mTc-containing conjugates useful in the invention.
  • FIG. 2 illustrates various rhenium-containing conjugates.
  • FIG. 3 (3A-3S) illustrates various rhenium-containing and 99mTc-containing conjugates.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Identifying sites of pathology is important for proper diagnosis and treatment of a patient. However, it can often be difficult to pinpoint the precise location of pathology. Extensive imaging and testing may be required to accurately identify the source of pathology.
  • Tumor localization is an example of a condition where it can be difficult to precisely identify the area of pathology, e.g., in a patient with metastatic adenocarcinoma who presents with clear metastasis, but where the primary site of the malignancy is not known. The secondary sites of the tumor (metastases) are difficult to find in many cancer cases. This problem also occurs with “benign tumors” such as giant cell tumors, which rarely metastasize, and “quasi-malignant tumors” such as adamantinomas, which rarely metastasize early, but are known to metastasize late in their course. Because the tumor location can be extremely difficult to find, a new test which could reveal all types of tumor cells would facilitate tumor searches, whether primary tumor sites or metastatic tumor sites, and help determine the appropriate treatment.
  • Pain is a common symptom in medicine, and is another condition where the source of the pathology is not always readily apparent, despite thorough physical exams, laboratory studies, and radiologic studies and analysis. This is especially true for low back pain and abdominal pain. Pain in the body results from various compounds produced and released at the site of the injured area. These pain-producing compounds include bradykinins, prostaglandins, chemokines, histamine, and others. Importantly, the site at which the patient perceives the pain may not be the site of the actual injury or pathology. The term “referred pain” is used to describe pain that is perceived by the patient at a site distinct from the pathology. Referred pain can complicate diagnosis, location of the actual site of pathology, and determination of appropriate treatment.
  • Prostaglandins, especially the PG2 group of prostaglandins, are over-expressed in tumor cells. Prostaglandins (such as the PG2 group of prostaglandins) are also strongly associated with the experience of pain. Because prostaglandins are produced at the site of tumor location, actual injury, or pathology, identifying the site where prostaglandin synthesis occurs will assist in locating the precise area of pathology. Biosynthesis of the PG2 prostaglandins requires the cyclooxygenase (COX) enzyme. The cyclooxygenase enzyme exists in (at least) two isoforms, COX-1, which is expressed constitutively, but which may be upregulated at sites of pain and inflammation, and COX-2, which is inducible by inflammatory stimuli. Both COX-1 and COX-2 are upregulated at tumor sites. Areas of high expression of cyclooxygenase will be associated with areas of high expression of prostaglandins, which in turn are associated with the area of pathology. Thus, pinpointing areas of high cyclooxygenase expression will enable identification of the pathological area.
  • The cyclooxygenase enzymes are readily inhibited by non-steroidal anti-inflammatory drugs (NSAIDs), which are sold over the counter in most countries, and also often frequently prescribed by doctors. These non-steroidal anti-inflammatory medicines include several pharmaceutical classes; each class has a number of specific drugs. If a NSAID drug is bonded or complexed to an imaging moiety, partial or total imaging of the patient provides a method of identifying sites of cyclooxygenase overexpression, prostaglandin synthesis, and inflammation, which determines the site of pathology or injury. Thus, in one embodiment, the invention encompasses conjugates of a NSAID with an imaging moiety, where said conjugate is suitable for imaging with an appropriate imaging modality.
  • In addition to conjugates suitable for imaging, the invention also encompasses conjugates which are not used for imaging, but which are useful surrogates for studying the chemical, biological, and pharmacokinetic properties of the conjugates suitable for imaging. For example, substitution of non-radioactive isotopes of rhenium (Re) for 99mTc results in a conjugate which can be handled without the need for radiation protection (the most abundant rhenium isotope, 187Re, has a half-life of on the order of 1010 years, and the second most abundant rhenium isotope, 185Re, is stable). Accordingly, preparation of conjugates which have non-radioactive rhenium isotopes in place of radioactive technetium isotopes can be useful for chemical, physical, in vitro, and in vivo studies of compound properties in which the imaging properties of the conjugate are not under study, such as studies of toxicity and biological half-life, and the invention embraces both the conjugates suitable for imaging and their analogs which can be handled without radiation precautions.
  • The conjugates are also useful for diagnosis of infections. Infections cause cells to overexpress the COX-1 and COX-2 enzymes. The pattern distribution of the cellular influence for the three major types of infections, bacterial, tuberculosis (TB), or viral, differ in major ways. Bacterial infections (not including TB) affect COX production in the cells of most of the body's organs. The conjugates of the invention can be used for diagnosis of any bacterial infection, and are particularly useful in abscess forming bacteria, in subjects or patients with an organ-specific infection, and in aiding in diagnosis and determination of the cause of a fever of unknown origin (FUO). The organ most involved would produce more COX enzyme than the rest of the body's tissues, even though all tissues may show some increased activity.
  • TB infections can infect almost any organ, such as the lungs, the testes, the spinal column (such as psoas abscess), etc. Scans conducted with conjugates disclosed herein can help pinpoint the major locus of TB infection, which is especially helpful in a subject or patient with a positive skin reaction to TB (such as a positive PPD test). The primary locus for a TB infection would likely be at the site of the highest gamma count on a gamma camera when a gamma-emitting radioactive moiety is used in the conjugate.
  • Viral infections tend to first cause elevated COX production in the spleen to a great extent and in the stomach to a slightly lesser extent. The conjugates disclosed herein can thus be used for the screening of asymptomatic patients infected with a virus. Patients are frequently infectious even before they exhibit symptoms, such as patients with Ebola virus and other viruses. An asymptomatic patient or subject who has been exposed to such viruses, such Ebola virus, influenza viruses, or other viruses deemed sufficiently important for screening, or who has traveled in areas where outbreaks of such viruses have occurred, can be screened by administration of conjugates of the invention, followed by imaging. When a gamma-emitting radioactive moiety is used in the conjugate, a gamma scanner could detect signals above background (and thus increased COX expression) from at least the spleen and probably the stomach, indicating the presence of an infection.
  • Definitions
  • A “residue” of a non-steroidal anti-inflammatory drug (NSAID), referred to as an “NSAID residue” or “residue of a NSAID,” is a portion of the NSAID, where the portion of the NSAID retains its ability to bind to cyclooxygenase. Typically, a residue of a NSAID refers to the portion of the molecule left after removal of a hydrogen, a hydroxyl, a methyl, or a methoxy group from the NSAID. The residue is then bonded or complexed together with an imaging moiety. NSAID residues also include portions of an NSAID that retains its ability to bind to cyclooxygenase, where the portion is further modified by the replacement of a hydrogen with a halogen or a trifluoromethyl group, or by the replacement of a methyl group with a trifluoromethyl group, or by the replacement of a hydroxyl group with a methoxy group. In some embodiments, the residue can be connected to a linker, which linker in turn is attached to a imaging moiety, in order to bond or complex the NSAID residue with the imaging moiety.
  • An NSAID derivative is an NSAID or NSAID residue which has been modified in one or more of the following manners:
  • a hydroxyl group has been replaced with a —O-(C1-C4 alkyl) group, preferably a methoxy group; a halogen; a C1-C4 alkyl group, preferably a methyl group; or a trifluoromethyl group;
  • a methyl group has been replaced with a trifluoromethyl group; a C2-C4 alkyl group; a —O—(C1-C4 alkyl) group, preferably a methoxy group; a halogen; or hydrogen;
  • a methoxy group has been replaced with a hydroxyl group, a —O—(C2-C4 alkyl) group, a C1-C4 alkyl group, preferably a methyl group; a halogen, or a trifluoromethyl group;
  • a halogen has been replaced with a different halogen, a trifluoromethyl group, a —O—(C1-C4 alkyl) group, preferably a methoxy group; a C1-C4 alkyl group, preferably a methyl group; or hydrogen;
  • a hydrogen has been replaced with a halogen, a methyl group, or a trifluoromethyl group;
  • a —COOH group has been replaced with a —NH2 group, or a —C(═O)—O— group has been replaced by a —NH— group;
  • a —COOH group has been replaced with a —CH2NH2 group, or a —C(═O)—O— group has been replaced by an —CH2NH— group;
  • an amino group has been replaced by a carboxyl group;
  • a trifluoromethyl group has been replaced with a —CH2NH2 group or a —CH2NH— group.
  • “Bonded or complexed” indicates that the NSAID, NSAID residue, or NSAID derivative is associated with the imaging moiety in a manner such that the imaging moiety can be localized along with the NSAID, NSAID residue, or NSAID derivative to the intended site, such that the imaging moiety can indicate where the NSAID, NSAID residue, or NSAID derivative bonded or complexed to the imaging moiety has concentrated. “Bonded or complexed” embraces any manner of association sufficiently stable for the foregoing purpose, whether such association is via a covalent bond, an ionic bond, a coordination bond (coordinate covalent bond or dative bond), a donor-acceptor complex, or any other association of NSAID, NSAID residue, or NSAID derivative and imaging moiety which has suitable stability. In one embodiment, “bonded or complexed” can indicate a covalent bond. In another embodiment, “bonded or complexed” can indicate a coordination bond. In another embodiment, “bonded or complexed” can indicate an ionic bond. In another embodiment, “bonded or complexed” can indicate a donor-acceptor complex.
  • “Alkyl” is intended to embrace a univalent saturated linear or branched hydrocarbon chain having the number of carbon atoms specified, or if no number is specified, having 1 to 8 carbon atoms. “Alkylene” refers to a similar group, which is divalent. “Optionally substituted” alkyl refers to either an unsubstituted alkyl group, or an alkyl group substituted with one or more substituents (such as one, two, three, four, or five substituents) selected from the group consisting of —OH, —(C1-C4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C1-C4 alkyl), —(C1-C4) haloalkyl, —(C1-C4) perhaloalkyl, —O—(C1-C4 alkyl), —O—(C1-C4 haloalkyl), —O—(C1-C4 perhaloalkyl), —(C1-C4) perfluoroalkyl, —(C═O)—(C1-C4) alkyl, —(C═O)—(C1-C4) haloalkyl, —(C═O)—(C1-C4) perhaloalkyl, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —NO2, —CN, isocyano (NC—), oxo (═O), —C(═O)H, —C(═O)—(C1-C4 alkyl), —COOH, —C(═O)—O—(C1-C4 alkyl), —C(═O)NH2, —C(═)ONH(C1-C4 alkyl), —C(═O)N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —SH, alkyl)-SH, —S—(C1-C4 alkyl), —S(═O)—(C1-C4 alkyl), —SO2—(C1-C4 alkyl), and —SO2—(C1-C4 perfluoroalkyl). Examples of such substituents are —CH3, —CH2CH3, —CF3, —CH2CF3, —CF2CF3, —OCH3, —NH(CH3), —N(CH3)2, —SCH3, and SO2CH3. “Optionally substituted alkylene” groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups.
  • “Cycloalkyl” is intended to embrace a univalent saturated cyclic hydrocarbon chain having the number of carbon atoms specified, or if no number is specified, having 3 to 10 carbon atoms, or 3 to 8 carbon atoms, preferably 3 to 6 carbon atoms. “Cycloalkylene” refers to a similar group, which is divalent. Cycloalkyl and cycloalkylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups.
  • “Alkenyl” is intended to embrace a univalent linear or branched hydrocarbon chain having at least one carbon-carbon double bond, and having the number of carbon atoms specified, or if no number is specified, having 2 to 8 carbon atoms. “Alkenylene” refers to a similar group, which is divalent. Alkenyl and alkenylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • “Cycloalkenyl” is intended to embrace a univalent cyclic hydrocarbon chain having at least one carbon-carbon double bond and having the number of carbon atoms specified, or if no number is specified, having 4 to 10 carbon atoms, or 4 to 8 carbon atoms, or 4 to 6 carbon atoms. “Cycloalkenylene” refers to a similar group, which is divalent. Cycloalkenyl and cycloalkenylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • “Alkynyl” is intended to embrace a univalent linear or branched hydrocarbon chain having at least one carbon-carbon triple bond, and having the number of carbon atoms specified, or if no number is specified, having 2 to 8 carbon atoms. “Alkynylene” refers to a similar group, which is divalent. Alkynyl and alkynylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • “Aryl” is defined as a univalent aromatic ring system. Aryl groups include monocyclic aromatic rings and polycyclic aromatic ring systems containing the number of carbon atoms specified, or if no number is specified, containing six to twenty carbon atoms. In other embodiments, aryl groups may contain six to ten carbon atoms. In some embodiments, aryl groups can be unsubstituted. In other embodiments, aryl groups can be substituted with, for example, one, two, or three substituents independently selected from the group consisting of —OH, —(C1-C4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C1-C4 alkyl), —(C1-C4) haloalkyl, —(C1-C4) perhaloalkyl, —O—(C1-C4 alkyl), —O—(C1-C4 haloalkyl), —O—(C1-C4 perhaloalkyl), —(C1-C4) perfluoroalkyl, —(C═O)—(C1-C4) alkyl, —(C═O)—(C1-C4) haloalkyl, —(C═O)—(C1-C4) perhaloalkyl, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —NO2, —CN, (NC—), —C(═O)H, —C(═O)—(C1-C4 alkyl), —COOH, —C(═O)—O—(C1-C4 alkyl), —C(═O)NH2, —C(═)ONH(C1-C4 alkyl), —C(═O)N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —SH, —(C1-C4 alkyl)-SH and —S—C1-C4 alkyl. “Arylene” refers to a similar group, which is divalent.
  • “Hydrocarbyl” is defined as a univalent hydrocarbon group, that is, a group comprised of hydrogen and carbon, whether aliphatic or aromatic, acyclic or cyclic, or any combination of, or all of, aliphatic, aromatic, acyclic and cyclic. Hydrocarbyl groups have the number of carbon atoms specified, or if no number is specified, having 1 to 10 carbon atoms. “Hydrocarbylene” refers to a similar group, which is divalent. Hydrocarbyl and hydrocarbylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible.
  • “Heterocycle” or a “heterocyclic group” is defined as a ring system which contains the number of carbon atoms specified, and one or more heteroatoms (such as one to six heteroatoms, or one to three heteroatoms, or one heteroatom), where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus. “Heteroaryl” is defined as an aromatic ring system which contains the number of carbon atoms specified, and one or more heteroatoms (such as one to six heteroatoms, or one to three heteroatoms, or one heteroatom), where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus; heteroaryl groups are a subset of heterocyclic groups. In some embodiments, heteroatoms for heterocyclyl and heteroaryl groups are selected from the group consisting of oxygen and nitrogen. In various embodiments, heterocyclic groups may contain two to twenty carbon atoms and one to six heteroatoms, two to twelve carbon atoms and one to four heteroatoms, two to twelve carbon atoms and one to three heteroatoms, two to ten carbon atoms and one to three heteroatoms, two to six carbon atoms and one to three heteroatoms, or two to six carbon atoms and two to four heteroatoms. In some embodiments, heterocyclic groups can be unsubstituted. In other embodiments, heterocyclic groups can be substituted on any chemically possible valence with for example, one, two, or three substituents independently selected from the group consisting of —OH, —(C1-C4 alkyl)-OH, halo, fluoro, chloro, bromo, iodo, —(C1-C4 alkyl), —(C1-C4) haloalkyl, —(C1-C4) perhaloalkyl, —O—(C1-C4 alkyl), —O—(C1-C4 haloalkyl), —O—(C1-C4 perhaloalkyl), —(C1-C4) perfluoroalkyl, —(C═O)—(C1-C4) alkyl, —(C═O)—(C1-C4) haloalkyl, —(C═O)—(C1-C4) perhaloalkyl, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —NO2, —CN, (NC—), —C(═O)H, —C(═O)—(C1-C4 alkyl), —COOH, —C(═O)—O—(C1-C4 alkyl), —C(═O)NH2, —C(═)ONH(C1-C4 alkyl), —C(═O)N(C1-C4 alkyl)(C1-C4 alkyl) (where each C1-C4 alkyl is chosen independently of the other), —SH, —(C1-C4 alkyl)-SH and —S—C1-C4 alkyl. Examples of heterocycles include aziridine, oxirane, oxetane, azetidine, pyrrolidine, pyrrole, tetrahydrofuran, furan, thiolane, thiophene, imidazolidine, imidazole, pyrazolidine, pyrazole, 1,2,3-triazole, 1,2,4-triazole, piperidine, pyridine, pyran, piperazine, and morpholine.
  • A “heterohydrocarbyl” group is defined as a univalent hydrocarbyl group, where one or more of the carbon atoms have been independently replaced by a heteroatom at any chemically possible location, where heteroatoms include, but are not limited to, oxygen, nitrogen, sulfur, and phosphorus. Heterohydrocarbyl groups have the number of carbon atoms specified, or if no number is specified, having 1 to 10 carbon atoms, and also at least one heteroatom, such as 1 to 5 heteroatoms, 1 to 4 heteroatoms, 1 to 3 heteroatoms, 1 to 2 heteroatoms, or one heteroatom. “Heterohydrocarbylene” refers to a similar group, which is divalent. Heterohydrocarbyl and heterohydrocarbylene groups can be unsubstituted, or substituted in the same manner as substituted alkyl groups where chemically possible. Examples of heterohydrocarbyl and heterohydrocarbylene groups include, but are not limited to, ethylene glycol and polyethylene glycol moieties, such as (—CH2CH2—On)—H (a monovalent heterohydrocarbyl group) and (—CH2CH2—O—)n (a divalent heterohydrocarbylene group) where n is an integer from 1 to 12 inclusive, and propylene glycol and polypropylene glycol moieties, such as (—CH2CH(CH3)—O—)n—H (a monovalent heterohydrocarbyl group) and (—CH2CH(CH3)—O)n— (a divalent heterohydrocarbylene group) where n is an integer from 1 to 12 inclusive. For heterohydrocarbyl groups, when more than one heteroatom is present, at least one carbon atom intervenes between any two heteroatoms.
  • The various groups described above can be attached to the remainder of the molecule at any chemically possible location on the fragment, including attachment via a substituent when the group is substituted. For the purposes of drawing the structures, groups are typically attached by replacement of a hydrogen, hydroxyl, methyl, or methoxy group on a “complete” molecule to generate the appropriate fragment, and a bond is drawn from the open valence on the fragment to the remainder of the molecule. For example, attachment of the heteroalkyl group —CH2—O—CH3 proceeds by removal of a hydrogen from one of the methyl groups of CH3—O—CH3, to generate the heteroalkyl fragment —CH2—O—CH3, from which a bond is drawn from the open valence to the remainder of the molecule.
  • Reference to “about” a value or parameter herein includes (and describes) variations that are directed to that value or parameter per se. For example, description referring to “about X” includes description of “X”.
  • The terms “a” or “an,” as used in herein means one or more, unless the context clearly indicates otherwise.
  • By “subject,” “individual,” or “patient” is meant an individual organism, preferably a vertebrate, more preferably a mammal, most preferably a human.
  • The description is intended to embrace all salts of the compounds described herein, as well as methods of using such salts of the compounds. In one embodiment, the salts of the compounds comprise pharmaceutically acceptable salts. Pharmaceutically acceptable salts are those salts which can be administered as drugs or pharmaceuticals to humans and/or animals and which, upon administration, retain at least some of the biological activity of the free compound (neutral compound or non-salt compound). The desired salt of a basic compound may be prepared by methods known to those of skill in the art by treating the compound with an acid. Examples of inorganic acids include, but are not limited to, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and phosphoric acid. Examples of organic acids include, but are not limited to, formic acid, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, sulfonic acids, and salicylic acid. Salts of basic compounds with amino acids, such as aspartate salts and glutamate salts, can also be prepared. The desired salt of an acidic compound can be prepared by methods known to those of skill in the art by treating the compound with a base. Examples of inorganic salts of acid compounds include, but are not limited to, alkali metal and alkaline earth salts, such as sodium salts, potassium salts, magnesium salts, and calcium salts; ammonium salts; and aluminum salts. Examples of organic salts of acid compounds include, but are not limited to, procaine, dibenzylamine, N-ethylpiperidine, N,N′-dibenzylethylenediamine, and triethylamine salts. Salts of acidic compounds with amino acids, such as lysine salts, can also be prepared. For lists of pharmaceutically acceptable salts, see, for example, P. H. Stahl and C. G. Wermuth (eds.) “Handbook of Pharmaceutical Salts, Properties, Selection and Use” Wiley-VCH, 2011 (ISBN: 978-3-90639-051-2). Several pharmaceutically acceptable salts are also disclosed in Berge, J. Pharm. Sci. 66:1 (1977).
  • The invention also includes, where chemically possible, all stereoisomers and geometric isomers of the compounds, including diastereomers, enantiomers, and cis/trans (E/Z) isomers. The invention also includes mixtures of stereoisomers and/or geometric isomers in any ratio, including, but not limited to, racemic mixtures. Unless stereochemistry is explicitly indicated in a structure, the structure is intended to embrace all possible stereoisomers of the compound depicted. If stereochemistry is explicitly indicated for one portion or portions of a molecule, but not for another portion or portions of a molecule, the structure is intended to embrace all possible stereoisomers for the portion or portions where stereochemistry is not explicitly indicated.
  • Unless a specific isotope is indicated, the invention includes all isotopologues of the compounds disclosed herein, such as, for example, deuterated derivatives of the compounds (where H can be 2H, i.e., D).
  • The following abbreviations may be used herein:
    • ˜ about
    • +ve or pos. ion positive ion
    • Δ heat
    • AA Arachidonic acid
    • Ac Acetyl
    • ACN acetonitrile
    • Ac2O acetic anhydride
    • aq aqueous
    • AcOH acetic acid
    • Bn benzyl
    • Boc tert-butyloxycarbonyl
    • BOP-Cl Bis(2-oxo-3-oxazolidinyl)phosphinic chloride
    • BSA bovine serum albumin
    • Bu butyl
    • Bz benzoyl
    • Calcd or Calc'd calculated
    • Conc. concentrated
    • COX cyclooxygenase, prostaglandin-endoperoxide synthase
    • d day(s)
    • DCE dichloroethane
    • DCM dichloromethane
    • DEA diethylamine
    • DEAD Diethyl azodicarboxylate
    • DIEA or DIPEA diisopropylethylamine
    • DMAP 4-dimethylaminopyridine
    • DME 1,2-dimethoxyethane
    • DMF N,N-dimethylformamide
    • DMSO dimethyl sulfoxide
    • EDC or EDCI N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide
    • EIA Enzyme immunoassay
    • eq equivalent
    • ESI or ES electrospray ionization
    • Et ethyl
    • Et2O diethyl ether
    • Et3N triethylamine
    • EtOAc ethyl acetate
    • EtOH ethyl alcohol
    • g gram(s)
    • h hour(s)
    • HATU O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate
    • HBTU O-benzotriazole-N,N,N′,N′-tetramethyl-uronium-hexafluorophosphate
    • Hex hexanes
    • HMPA hexamethylphosphoramide
    • HOAt 1-hydroxy-7-azabenzotriazole
    • HOBt hydroxybenzotriazole
    • HPLC high pressure liquid chromatography
    • IPA or iPrOH isopropyl alcohol
    • KOAc potassium acetate
    • LCMS, LC-MS or LC/MS liquid chromatography mass spectrometry
    • LDA lithium diisopropylamide
    • LHMDS or LiHMDS lithium hexamethyldisilazide
    • M molar (mol L−1)
    • Me methyl
    • MeCN acetonitrile
    • MeI iodomethane
    • MeOH methyl alcohol
    • mg milligram(s)
    • min minute(s)
    • mL milliliter(s)
    • M mole(s)
    • MS mass spectrometry
    • MsCl methanesulfonyl chloride
    • MTBE or MtBE methyl tert-butyl ether
    • m/z mass-to-charge ratio
    • NaHMDS sodium hexamethyldisilazide
    • NaOtBu sodium tert-butoxide
    • NBS N-bromosuccinimide
    • NCS N-chlorosuccinimide
    • nBuLi n-butyl lithium
    • NMO N-methylmorpholine-N-oxide
    • NMP 1-methyl-2-pyrrolidinone
    • NMR nuclear magnetic resonance
    • PE Petroleum ether, CAS Number: 101316-46-5
    • PG Prostaglandin or prostaglandins
    • PGE2 Prostaglandin E2
    • PGF2α Prostaglandin F2α
    • PGH2 Prostaglandin H2
    • PBS phosphate buffered saline
    • PMB para-methoxybenzyl, 4-methoxybenzyl
    • Pr propyl
    • Prep-HPLC Preparative high pressure liquid chromatography
    • ppm parts per million
    • p-tol para-toluoyl
    • rac racemic
    • RP-HPLC or RPHPLC reversed phase high pressure liquid chromatography
    • RT or rt or r.t. room temperature
    • sat. or sat'd or satd saturated
    • TBAF tetrabutylammonium fluoride
    • TBDMS tert-butyldimethylsily
    • TBDMS-Cl tert-butyidimethylsilyl chloride
    • TBDPS tert-butyldiphenylsilyl
    • TEMPO (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl
    • tert or t tertiary
    • TFA triflouroacetic acid
    • THF tetrahydrofuran
    • TLC thin layer chromatography
    • TMS trimethylsilyl or trimethylsilane
    • tR retention time
    • tBuOH tert-butyl alcohol
    • v/v volume per volume
    Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)
  • Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to treat pain and inflammation, which occur due to many diseases, such as those involving tumors. NSAIDs which can be used in the invention include:
  • salicylates, such as aspirin (acetylsalicylic acid), diflunisal, salsalate, and choline magnesium trisalicylate;
  • propionic acid derivatives, such as ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, and loxoprofen;
  • acetic acid derivatives, such as indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, and nabumetone;
  • enolic acid (oxicam) derivatives, such as piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, and isoxicam;
  • anthranilic acid derivatives (fenamates), such as mefenamic acid, meclofenamic acid, flufenamic acid, and tolfenamic acid;
  • selective COX-2 inhibitors (coxibs, several of which are not approved, or have been withdrawn, in various countries), such as celecoxib, rofecoxib, valdecoxib, parecoxib, lumiracoxib, etoricoxib, and firocoxib (firocoxib approved for equine and canine use only);
  • sulfonanilides such as nimesulide (which should be used cautiously due to the risk of liver damage); and
  • licofelone, which is both a cyclooxygenase and lipoxygenase inhibitor.
  • When forming a conjugate of a NSAID compound, typically a bond to an atom or atoms on the NSAID compound is replaced with a bond to a linking group in order to facilitate bonding or complexing the NSAID, NSAID residue, or NSAID derivative to the imaging moiety. Thus, for example, linking an amine-containing linker to a carboxylic acid-containing NSAID compound can be accomplished by condensing the amine and carboxylic acid to form an amide group. The bond to the —OH portion of the —COOH group has been replaced with a bond to the nitrogen atom of the amine-containing linker. “NSAID residue” refers to the portion of the NSAID molecule that remains and which is attached to the linker, and, as defined previously, retains its ability to bind to cyclooxygenase. The NSAID residue need not bind to COX with the same affinity or specificity as the NSAID from which the residue is derived, as long as sufficient binding affinity remains for the purposes of the invention. A derivative of a NSAID includes an NSAID or NSAID residue that has been modified as defined herein, and the NSAID derivative portion of the conjugate need not bind to COX with the same affinity or specificity as the NSAID which was modified to form the derivative, as long as sufficient binding affinity remains for the purposes of the invention.
  • Linker Groups and Linker/Chelator Groups for Attachment of Imaging Moieties to NSAID Compounds; General and Exemplary Forms of Conjugates
  • An imaging moiety can be bonded or complexed to a NSAID compound by using an appropriate linker (also referred to as a linking group). The linker must be capable of being bonded or complexed to both the NSAID compound, or to a residue or derivative of the NSAID compound, and bonded or complexed to the imaging moiety, for the purpose of localizing the imaging moiety to the site where the NSAID compound or residue or derivative of the NSAID compound concentrates when administered to a patient. In various non-limiting embodiments, a linker group covalently bound to both the NSAID and the imaging moiety, or a linker group covalently bound to the NSAID and bonded or complexed via a coordination bond to the imaging moiety, or a linker group covalently bound to the NSAID and bonded or complexed via an ionic bond to the imaging moiety, can be used. The linker should preferably be bonded or complexed to the NSAID molecule or residue or derivative of the NSAID at a site as distant as possible from the region of the NSAID or residue or derivative of the NSAID that binds to cyclooxygenase, in order to preserve the ability of the NSAID or residue or derivative of the NSAID to bind to cyclooxygenase. However, any attachment to the NSAID molecule or residue or derivative of the NSAID, which attachment does not render the conjugate unsuitable for its purpose, can be used.
  • The linker also needs to bind or complex with the imaging moiety. One particularly useful imaging moiety is the metastable isotope of technetium-99, referred to as 99mTc, Tc99m, or Tc-99m. 99mTc decays to 99Tc with a half-life of about 6 hours, via gamma emission at an energy of about 140 keV. 99mTc is often used in a complex with six methoxyisobutylisonitrile (MIBI) ligands, which is often referred to as 99mTc-MIBI, technetium Tc99m Sestamibi, or 99mTc sestamibi (sold as CARDIOLITE, a registered trademark of Lantheus Medical Imaging, Inc., North Billerica, Mass.). This compound has the following structure:
  • Figure US20190169084A1-20190606-C00027
  • Modification of a NSAID with a linker such as
  • Figure US20190169084A1-20190606-C00028
  • enables the linker to bind to a radioactive tracer moiety, such as 99mTc, via the isocyano group, while the remaining open valence on the linker will allow attachment of a NSAID or a residue or derivative of a NSAID. For example, the structure below can be attached to a radioactive tracer moiety, such as 99mTc:
  • Figure US20190169084A1-20190606-C00029
  • where R1, R2, and R3 can be independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with hydroxy, fluoro, —O—C1-C4 alkyl, or C3-C6 cycloalkyl, or R1 and R2 together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, while n is an integer selected from 0 to 4, inclusive.
  • The linker itself may be capable of bonding to or complexing the radioactive agent, as with the methoxyisobutylisonitrile ligands above which directly bond to 99mTc. In other embodiments, the imaging moiety comprises a chelating group and the radioactive agent, and may further comprise additional groups, such as ligands, bound or complexed to the radioactive agent. Chelating groups can comprise a number of ligand systems known to the skilled artisan, such as those described in e.g. Jürgens, S. et al., J. Organomet. Chem. (2014), 751, 83-89 and Liu, G. et al. Anticancer Agents Med. Chem. (2007), 7(3): 367-377.
  • In some embodiments, when a linker is used to link a NSAID, NSAID residue, or NSAID derivative to an imaging moiety, the linker can be selected from the group consisting of an optionally substituted C1-C40 hydrocarbylene group; an optionally substituted C2-C40 heterohydrocarbylene group; and a linker of the form -LE-R4-LF-, where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene and optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 aryl-C1-C6 alkyl; and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group such as 1,2,3-triazole or 1,2,4-triazole, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl.
  • In other embodiments, when a linker is used to link a NSAID, NSAID residue, or NSAID derivative to an imaging moiety, the linker can be selected from the group consisting of an optionally substituted C1-C10 hydrocarbylene group; an optionally substituted C2-C10 heterohydrocarbylene group; and a linker of the form -LE-R4-LF- ; where LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —C(═O)—, and R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 aryl-C1-C6 alkyl, and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —N(R9)—(C═O)—(CH2)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl.
  • A useful chelating group for preparation of conjugates is the tetradentate mertiatide group (N-[N-[N-[(acetylthio)acetyl]glycyl]glycyl]-glycine; Fritzberg et al., J. Nuclear Medicine (1986) 27(1):111-116), having the structure:
  • Figure US20190169084A1-20190606-C00030
  • For example, the following structure shows metal complexed with a group derived from mertiatide to form an imaging moiety:
  • Figure US20190169084A1-20190606-C00031
  • where M indicates a cationic metal ion, where the metal ion also bears an oxo group (for example, M=O can be 99mTc=O or Re=O). The carboxylic acid functionality of the complex allows for a wide range of coupling reactions in order to attach the imaging moiety to the remainder of the molecule. Typically, the mertiatide peptide is coupled via its carboxylate group prior to introduction of the metal ion or metal-oxo ion. Once the mertiatide peptide is complexed to the metal ion (or metal-oxo ion), it can be referred to either as “mertiatide complexed to the metal ion (or metal-oxo ion),” or as a group derived from mertiatide. That is, a group bound or complexed to a metal ion or metal-oxo ion which is referred to as “derived” from a specific moiety refers to the group after it has complexed with the metal ion or metal-oxo ion. Alternatively, the group which binds or complexes to the metal ion or metal-oxo ion can be referred to by the same name in its free, uncomplexed form and in its complexed form with the metal; for example, “mertiatide group” can refer to both a mertiatide group without a complexed metal or metal-oxo ion, and also a mertiatide group which has complexed with a metal or metal-oxo ion.
  • A mertiatide-based group of the form:
  • Figure US20190169084A1-20190606-C00032
  • such as
  • Figure US20190169084A1-20190606-C00033
  • can be used in conjugates of the invention, where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl; and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl. In one embodiment, R9 is H. The substituents R10, R11, R12, R13, R14, R15, R16 and R17 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R10 and R11) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R12 and R13) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R14 and R15) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring. In some embodiments, only one of (R10 and R11) (R12 and R13), (R14 and R15) and (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; that is, only one of the four pairs of substituents forms a spiro ring, and the remaining three pairs do not form a spiro ring.
  • TechneScan MAG3™ is a commercially available kit for preparing 99mTc-mertiatide conjugates, and is sold by Mallinckrodt Pharmaceuticals (catalog number N096B0, National Drug Code 00019N096B0), 675 McDonnell Blvd., St. Louis, Mo. 63042, USA. The kit vials contain betiatide, stannous chloride dihydrate (SnCl2.2H2O), sodium tartrate dihydrate, and lactose monohydrate. Betiatide, which is N-[(benzoylthio)acetyl]glycylglycylglycine, reacts with sodium pertechnetate 99mTc to form 99mTc-mertiatide.
  • Yet another useful chelating group for preparation of conjugates is based on the tetradentate ethylenedicysteine group:
  • Figure US20190169084A1-20190606-C00034
  • or, in stereospecific form using L-cysteine (having the R configuration at the alpha carbon):
  • Figure US20190169084A1-20190606-C00035
  • The following structure shows a metal ion complexed with a linker derived from ethylenedicysteine:
  • Figure US20190169084A1-20190606-C00036
  • where M indicates a cationic metal ion, where the metal ion also bears an oxo group (for example, M=O can be 99mTc=O or Re=O). Again, the carboxylic acid functionalities of the complex allows for a wide range of coupling reactions. One of the carboxylic acid functionalities can be blocked, for example as an amide:
  • Figure US20190169084A1-20190606-C00037
  • while the remaining carboxylic acid group can be used for attachment to the remainder of the molecule.
  • An ethylenedicysteine-based linker-imaging moiety of the form:
  • Figure US20190169084A1-20190606-C00038
  • can be used in conjugates of the invention, where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl, R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl, R5 is —OH, —OR6, —NH2, —NHR6, or —NR6R7, R6 and R7 are independently selected from C1-C4 alkyl, and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)—(C═O)—N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl. In one embodiment, R9 is H. The substituents R18, R19, R20, R21, R22, R23, R24, and R25 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring. In some embodiments, only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; that is, only one of the four pairs of substituents forms a spiro ring, and the remaining three pairs do not form a spiro ring. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • It should be noted that the mertiatide fragment:
  • Figure US20190169084A1-20190606-C00039
  • is a C10 heterohydrocarbyl group (specifically, C10 heteroalkyl) with three nitrogen atoms and a sulfur atom in the chain, and five oxo substituents, while the ethylenedicysteine fragment:
  • Figure US20190169084A1-20190606-C00040
  • is a C6 heterohydrocarbyl group (specifically, C6 heteroalkyl); following the chain from the first thiol-substituted carbon to the second thiol-substituted carbon, the ethylenedicysteine fragment has two nitrogen atoms in the chain, two —SH substituents on the first and last carbons in the chain, one —COOH substituent, and a second —COOH substituent which is linked to the remainder of the molecule by removal of the —OH group of the carboxyl. Alternatively, the ethylenedicysteine fragment can be considered as a 3,6-diazaoctane (i.e., heteroalkyl) with thiol substituents on the 1 and 8 carbons, a carboxy substituent on the 7 carbon, and a —C(═O)—OH or —C(═O)—H moiety on the 2 carbon, where the —OH or —H, respectively, has been removed for attachment to the remainder of the molecule.
  • In one embodiment, where the linker(s) is (are) capable of directly binding to or chelating the metal of the imaging moiety, the invention comprises compounds of the formula:

  • [(NSAID, NSAID residue, or NSAID derivative)-(linker)]x-M-(terminal ligand)z1
  • where “NSAID, NSAID residue, or NSAID derivative” refers to a NSAID or a residue or derivative of a NSAID, M is selected from the group consisting of 99mTc, 52Mn, and Re, x is an integer between 1 and 6 inclusive, z 1 is an integer between 0 and 5 inclusive, and the sum of x and z1 is less than or equal to 6, and “terminal ligand” is a ligand that coordinates to M, but which does not have a NSAID attached to it. The linker or linkers may be monodentate or polydentate for M. The terminal ligand or ligands may be monodentate or polydentate for M. When more than one terminal ligand is present, all of the ligands can be identical groups, all of the ligands can be different groups, or some of the ligands can be identical groups and some can be different groups. It should be noted that some monodentate ligands, such as the oxo ligand, ═O, can occupy more than one valence on the metal ion; that is, there can be multiple bonds between some monodentate ligands, such as the oxo ligand, ═O, and the metal atom.
  • In one embodiment, where the linker(s) is (are) capable of directly binding to or chelating the metal of the imaging moiety, and where both the linker(s) and the terminal ligand(s) are monodentate and occupy only one valence per linker and one valence per terminal ligand, the invention comprises compounds of the formula:

  • [(NSAID, NSAID residue, or NSAID derivative)-monodentate linker]xM-(terminal monodentate ligand)y
  • where “NSAID, NSAID residue, or NSAID derivative” refers to a NSAID or a residue or derivative of a NSAID, M is selected from the group consisting of 99mTc , 52Mn, and Re, x is an integer between 1 and 6 inclusive, y is an integer between 0 and 5 inclusive, and x+y=6, and “terminal ligand” is a ligand that coordinates to 99mTc, 52Mn, or Re, but which does not have a NSAID or a residue or derivative of a NSAID attached to it.
  • Chelating groups (including linkers, where the linker is capable of chelation) and terminal ligands may be monodentate or polydentate, with the condition that the chelating group or groups and terminal ligand or ligands must together satisfy the valency of the metal atom to which they are bonded. For example, in the following compound:
  • Figure US20190169084A1-20190606-C00041
  • the mertiatide moiety is tetradentate and occupies four valences of the rhenium ion, while the monodentate oxo ligand occupies two valences of the rhenium ion, thus together satisfying the valency of the Re(VI) ion.
  • In the formula:

  • (NSAID, NSAID derivative, or NSAID residue)-(linker)-(chelating group)-M-(terminal ligand)z2,
  • which can be written as the three individual formulas:

  • (NSAID)-(linker)-(chelating group)-M-(terminal ligand)z2

  • (NSAID derivative)-(linker)-(chelating group)-M-(terminal ligand)z2

  • (NSAID residue)-(linker)-(chelating group)-M-(terminal ligand)z2,
  • and where z2 is an integer between 0 and 4 inclusive,
    • the chelating group binds the radioactive agent M by two or more bonds. When two or more terminal ligands are present, two or more of the terminal ligands can be combined to form an additional chelating group or groups.
  • Examples of terminal ligands include: halo (—X), fluoro (—F), chloro (—Cl), bromo (—Br), iodo (—I), oxo (═O), cyano (—CN), isocyano (—NC), hydroxyl (—OH), with oxo being a preferred terminal ligand; and substituted isocyano ligands of the form:
  • Figure US20190169084A1-20190606-C00042
  • where R1, R2, and R3 can be independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with hydroxy, fluoro, —O—C1-C4 alkyl, or C3-C6 cycloalkyl, or R1 and R2 together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, such as
  • Figure US20190169084A1-20190606-C00043
  • These substituted isocyano ligands are preferred when the NSAID linker is also an isocyano ligand.
  • Examples of cyclooxygenase inhibitors with a linker which incorporates a ligand to bind 99mTc, which can be used as the moiety [(NSAID, NSAID residue, or NSAID derivative)-linker] include, but are not limited to:
  • Figure US20190169084A1-20190606-C00044
  • where the encircled portion represents a residue of ketorolac (where one of the hydrogens on the phenyl ring of ketorolac has been replaced by the linker);
  • Figure US20190169084A1-20190606-C00045
  • where the encircled portion represents a residue of naproxen (where the methyl of the methoxy group of naproxen has been replaced by the linker);
  • Figure US20190169084A1-20190606-C00046
  • where the encircled portion represents a residue of ibuprofen (where one of the methyl groups of the (2-methylpropyl) group of ibuprofen has been replaced by the linker); and
  • Figure US20190169084A1-20190606-C00047
  • where the encircled portion represents a residue of indomethacin (where the methyl of the methoxy group of indomethacin has been replaced by the linker). The linkers are attached as indicated above in order to preserve the pharmacophoric portions of the NSAID.
  • In some embodiments, when x is two or greater, all of the NSAID, NSAID residue, or NSAID derivatives in the x subunits [(NSAID, NSAID residue, or NSAID derivative)-linker] are the same NSAID, NSAID residue, or NSAID derivative. In some embodiments, when x is two or greater, at least one of the NSAID, NSAID residue, or NSAID derivatives in the x subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker] is different than the remaining NSAID(s) or NSAID residue(s) in the remaining subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker]. In some embodiments, when x is two or greater, each of the NSAID, NSAID residue, or NSAID derivatives in the x subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker] is different than the remaining NSAID(s) or NSAID residue(s) in the other subunits of [(NSAID, NSAID residue, or NSAID derivative)-linker].
  • Exemplary conjugates of the invention can be of the form:
  • Figure US20190169084A1-20190606-C00048
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene and optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl; LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl (in one embodiment, R9 is H), and M is selected from the group consisting of 99mTc , 52Mn, and Re, where Re can be 186Re or 188Re.
  • Examples of specific conjugates of this form include:
  • Figure US20190169084A1-20190606-C00049
  • Further exemplary conjugates of the invention can be of the form:
  • Figure US20190169084A1-20190606-C00050
  • where LE is absent or is selected from the group consisting of —NH—and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl; R5 is —OH, —NH2, —NH(C1-C4 alkyl), or —N(C1-C4 alkyl)(C1-C4 alkyl), LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl (in one embodiment, R9 is H); and M is selected from the group consisting of 99mTc , 52Mn, and Re, where Re can be 186Re or 188Re. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • Examples of specific conjugates of this form include:
  • Figure US20190169084A1-20190606-C00051
    Figure US20190169084A1-20190606-C00052
    Figure US20190169084A1-20190606-C00053
    Figure US20190169084A1-20190606-C00054
  • Further exemplary conjugates of the invention can be of the form:
  • Figure US20190169084A1-20190606-C00055
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C1-C6 aryl-C1-C6 alkyl; R5 is —OH, —NH2, —NH(C1-C4 alkyl), or —N(C1-C4 alkyl)(C1-C4 alkyl), LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl (in one embodiment, R9 is H); R(n) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive; and M is selected from the group consisting of 99mTc, 52Mn, and Re, where Re can be 186Re or 188Re. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • Examples of specific conjugates of this form include:
  • Figure US20190169084A1-20190606-C00056
    Figure US20190169084A1-20190606-C00057
    Figure US20190169084A1-20190606-C00058
  • Further exemplary conjugates of the invention can be of the form:
  • Figure US20190169084A1-20190606-C00059
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl; R5 is —OH, —NH2, —NH(C1-C4 alkyl), or —N(C1-C4 alkyl)(C1-C4 alkyl), LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl (in one embodiment, R9 is H); and M is selected from the group consisting of 99mTc , 52Mn, and Re, where Re can be 186Re or 188Re. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • Examples of specific conjugates of this form include:
  • Figure US20190169084A1-20190606-C00060
    Figure US20190169084A1-20190606-C00061
    Figure US20190169084A1-20190606-C00062
    Figure US20190169084A1-20190606-C00063
  • Further exemplary conjugates of the invention can be of the form:
  • Figure US20190169084A1-20190606-C00064
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl , R4 is selected from the group consisting of optionally substituted C1-C30 hydrocarbylene, optionally substituted C2-C30 heterohydrocarbylene group (such as C1-C12 alkylene), C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl; R5 is —OH, —NH2, —NH(C1-C4 alkyl), or —N(C1-C4 alkyl)(C1-C4 alkyl), LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —(C═O)N(H)—, —N(H)—(C═O)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, and —O—(C═O)N(R9)— where one valence of LF (when LF is present) is attached to the R4 group and the other valence is attached to the NSAID or residue or derivative of a NSAID; and where each R9 is independently selected from the group consisting of H and optionally substituted C1-C4 alkyl (in one embodiment, R9 is H); and M is selected from the group consisting of 99mTc, 52Mn, and Re, where Re can be 186Re or 188Re. In a further embodiment, R5 is selected from the group consisting of —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3; in yet a further embodiment, R5 is selected from the group consisting of —NH2, —OCH3, and —OCH2CH3.
  • Examples of specific conjugates of this form include:
  • Figure US20190169084A1-20190606-C00065
    Figure US20190169084A1-20190606-C00066
  • All pharmaceutically acceptable salts of all of the above general and specific compounds are also included in this disclosure.
  • Specific exemplary technetium conjugates of the invention are disclosed in the Examples and in FIG. 1. Specific exemplary rhenium conjugates of the invention are disclosed in the Examples and in FIG. 2. Further specific conjugates of the invention are disclosed in the Examples and in FIG. 3.
  • Formulations and Routes of Administration
  • The compounds of the invention, that is, any conjugates of the invention disclosed herein, used in the methods of the invention may be administered in any suitable form that will provide sufficient levels of the compounds for the purposes of imaging. Intravenous administration is a useful route of administration, although other parenteral routes can also be employed, where parenteral as used herein includes subcutaneous injections, intravenous injection, intraarterial injection, intramuscular injection, intrasternal injection, intraperitoneal injection, or infusion techniques. The compounds can also be administered orally or enterally, which is a preferred route when compatible with the absorption of the compound and with imaging requirements. Where the pharmacokinetics of the compounds are suitable, the compounds can also be administered sublingually, by buccal administration, subcutaneously, by spinal administration, by epidural administration, by administration to cerebral ventricles, by inhalation (e.g. as mists or sprays), rectally, or topically in unit dosage formulations containing conventional nontoxic pharmaceutically acceptable carriers, excipients, adjuvants, and vehicles as desired. The compounds may be administered directly to a specific or affected organ or tissue. The compounds are mixed with pharmaceutically acceptable carriers, excipients, adjuvants, and vehicles appropriate for the desired route of administration.
  • In certain embodiments of the invention, especially those embodiments where a formulation is used for injection or other parenteral administration, including the routes listed herein, but also including any other route of administration described herein (such as oral, enteric, gastric, etc.), the formulations and preparations used in the methods of the invention are sterile. Sterile pharmaceutical formulations are compounded or manufactured according to pharmaceutical-grade sterilization standards (United States Pharmacopeia Chapters 797, 1072, and 1211; California Business & Professions Code 4127.7; 16 California Code of Regulations 1751, 21 Code of Federal Regulations 211) known to those of skill in the art.
  • Oral administration is advantageous due to its ease of implementation and patient compliance. If a patient has difficulty swallowing, introduction of medicine via feeding tube, feeding syringe, or gastrostomy can be employed in order to accomplish enteric administration. The active compound (and, if present, other co-administered agents) can be enterally administered in any other pharmaceutically acceptable carrier suitable for formulation for administration via feeding tube, feeding syringe, or gastrostomy.
  • Intravenous administration can also be used advantageously, for delivery of the conjugates of the invention to the bloodstream as quickly as possible and to circumvent the need for absorption from the gastrointestinal tract.
  • The compounds described for use herein can be administered in solid form, in liquid form, in aerosol form, or in the form of tablets, pills, powder mixtures, capsules, granules, injectables, solutions, suppositories, enemas, colonic irrigations, emulsions, dispersions, food premixes, and in other forms suitable for the route of administration. The compounds can also be administered in liposome formulations. The compounds can also be administered as prodrugs, where the prodrug undergoes transformation in the treated subject to a therapeutically effective form. Additional methods of administration are known in the art.
  • Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions, may be formulated according to methods known in the art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in propylene glycol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono or di-glycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.
  • Solid dosage forms for oral administration may include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound may be admixed with at least one inert diluent such as sucrose, lactose, or starch. Such dosage forms may also comprise additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.
  • Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water. Such compositions may also comprise adjuvants, such as wetting agents, emulsifying and suspending agents, cyclodextrins, and sweetening, flavoring, and perfuming agents. Alternatively, the compound may also be administered in neat form if suitable.
  • The compounds for use in the present invention can also be administered in the form of liposomes. As is known in the art, liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by mono or multilamellar hydrated liquid crystals that are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain, in addition to a compound for use in the present invention, stabilizers, preservatives, excipients, and the like. The preferred lipids are the phospholipids and phosphatidyl cholines (lecithins), both natural and synthetic. Methods to form liposomes are known in the art. See, for example, Prescott, Ed., Methods in Cell Biology, Volume XIV, Academic Press, New York, N.W., p. 33 et seq (1976).
  • The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form can vary depending upon the patient to which the active ingredient is administered and the particular mode of administration. It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the specific compound employed; the age, body weight, body area, body mass index (BMI), general health, sex, and diet of the patient; the time of administration and route of administration used; the rate of excretion; and the drug combination, if any, used. The compounds can be administered in a unit dosage formulation. The pharmaceutical unit dosage chosen is fabricated and administered to provide sufficient concentration of drug for imaging a patient.
  • While the compounds for use in the present invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more other agents. When additional active agents are used in combination with the compounds for use in the present invention, the additional active agents may generally be employed in therapeutic amounts as indicated in the Physicians' Desk Reference (PDR) 53rd Edition (1999), which is incorporated herein by reference, or such therapeutically useful amounts as would be known to one of ordinary skill in the art, or as are determined empirically for each patient.
  • Combinations of the NSAID conjugates can also be used. Combining two or more conjugates of different NSAIDs or residues or derivative s of NSAIDs can provide advantages over using a single conjugate. Advantages can include the ability to tune pharmacokinetics and pharmacodynamics, to adjust the solubility of the overall composition and/or its components, to adjust the half-life of total conjugate in the body, to enhance imaging contrast and/or definition, to adjust binding kinetics to COX, to adjust binding affinity to COX, or to enhance the stability of the composition either in storage or in use. The two or more conjugates can be combined in solution form such as those solution forms described above (such as in a sterile solution for IV administration), or in solid form such as those solid forms as described above (such as pill or tablet form). The two or more conjugates can be mixed together shortly before administration and administered together. The two or more conjugates can be administered simultaneously, either by the same route of administration or by different routes of administration. The two or more conjugates can be administered consecutively, either by the same route of administration or by different routes of administration. In one embodiment, a kit form can contain two or more conjugates as individual conjugates, with printed or electronic instructions for administration either as a mixture of conjugates, as separate conjugates administered simultaneously, or as separate conjugates administered consecutively. Where three or more conjugates are administered, they can be administered as a mixture of conjugates, as separate conjugates administered simultaneously, as separate conjugates administered consecutively, as separate conjugates where two or more may be administered simultaneously with the remainder administered consecutively before or after the simultaneous administration, or any other possible combination of mixed administration, simultaneous administration, and consecutive administration.
  • Imaging techniques
  • The conjugates can be used with any suitable imaging technique. Images of a subject, or of a portion of a subject such as the arm, leg, or any specific region of the body of the subject, can be generated using gamma cameras, planar gamma imaging, scintigraphic imaging, SPECT imaging (single photon emission computed tomography), and other radiographic or tomographic imaging techniques. Exemplary imaging methods that can be used are described in Pacelli et al., J. Label. Compd. Radiopharm. 57:317-322 (2014); de Vries et al., J Nucl. Med. 44:1700-1706 (2003); Tietz et al., Current Medicinal Chemistry, 20, 4350-4369 (2013); Sogbein et al., Biomed. Res. Int. , Sogbein, Oyebola O. et al., BioMed Research International, 2014:942960, doi: 10.1155/2014/942960; and Wernick, Minn. and Aarsvold, J. N., Emission Tomography: The Fundamentals of PET and SPECT, San Diego: Elsevier Academic Press, 2004.
  • Kits
  • Further embodiments of the invention embrace one or more kit forms which can contain one or more conjugates as disclosed herein. The kit can contain printed or electronic instructions for administration of the conjugate. In further embodiments, the kit can contain one or more compounds as disclosed herein which lacks the radioactive agent, with printed or electronic instructions for adding the radioactive agent to constitute one or more conjugates of the invention.
  • The following examples are intended to illustrate, but not limit, the invention.
  • EXAMPLES Synthetic Examples Example 1 General method for the synthesis of tetrakis(((2-((6-((S)-1-carboxyethyl)naphthalen-2-yl)oxy)-2-methylpropyl)-14-azanylidyne)methyl)copper (2)
  • Figure US20190169084A1-20190606-C00067
  • Synthesis of (S)-2-(6-hydroxynaphthalen-2-yl)propanoic acid (4) As described in del Amo, V., McGlone, A. P., Soriano, J. M. & Davis, A. P. “Two-colour screening in combinatorial chemistry: prospecting for enantioselectivity in a library of steroid-based receptors.” Tetrahedron 65, 6370-6381 (2009), (S)-2-(6-methoxynaphthalen-2-yl)propanoic acid (Naproxen) (3) (3.0 g, 13.0 mmol) is suspended in HBr (48% w/w in water, 120 mL) and heated at reflux for 2 h. The mixture is allowed to warm to room temperature and filtered. The solid is washed with chilled water to afford the title product (S)-2-(6-hydroxynaphthalen-2-yl)propanoic acid (4).
  • Synthesis of tert-butyl (S)-2-(6-hydroxynaphthalen-2-yl)propanoate (5) As described in del Amo, V., McGlone, A. P., Soriano, J. M. & Davis, A. P. “Two-colour screening in combinatorial chemistry: prospecting for enantioselectivity in a library of steroid-based receptors.” Tetrahedron 65, 6370-6381 (2009), the carboxylic acid (4) (2.39 g, 11.05 mmol) is dissolved in dry THF (110 mL) under a nitrogen atmosphere. The solution is cooled to 0° C., then trifluoroacetic anhydride (13.93 g, 9.42 mL, 66.32 mmol) is added drop wise and the mixture is further stirred for 4 h maintaining the temperature below 5° C. tert-Butanol (32 mL) is added drop wise and the resulting mixture is then allowed to rise to room temperature and is vigorously stirred overnight. The reaction is cooled again to ice-bath temperature and NH4OH (35% in water, 6 mL) is added drop wise. When the addition is finished the mixture is allowed to rise to room temperature again and is finally stirred for a further 30 min before the volatiles are evaporated under vacuum. The crude residue is triturated with boiling DCM and the crystalline solid formed is removed by filtration. The filtrate is washed with saturated aqueous NaHCO3 and dried over MgSO4, then the solvent is evaporated under reduced pressure to give the tert-butyl ester (5). An analytical sample can be prepared by crystallizing (5) from hot benzene/hexane.
  • Synthesis of tert-butyl (S)-2-(6-((1-formamido-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoate (6) Using the method of Al-Ktaifani, M. M., Nakawa, A. a., Tabbaa, Z. a. & Namou, A. a. “Synthesis of 2-methyl-2-propoxypropyl isocyanide and its Cu(I) tetrafluoroborate complex.” Chem. Pap. 62, 329-333 (2008): in general, mercuric(II)trifluoroacetate and N-(2-methyl-2-propenyl)formamide (Synthesized by the method of van Wyk, A. J. et al. “Synthesis and 99mTc labelling of MMI (MIBI) and its ethyl analogue EMI.” Int. J. Radiat. Appl. Instrumentation. Part A. Appl. Radiat. Isot. 42, 687-689 (1991)) and tert-butyl (S)-2-(6-hydroxynaphthalen-2-yl)propanoate (5) are dissolved in THF and stirred at room temperature. The mixture is cooled down in an ice bath and NaOH pellets in isopropanol are added slowly. Subsequently, NaBH4 was added to the mixture, which was stirred for 18 h. The solution was passed through a column of Celite® (J. T. Baker, Phillipsberg, N.J., diatomaceous earth) to remove elemental Hg to yield tert-butyl (S)-2-(6-((1-formamido-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoate (6).
  • Synthesis of (S)-2-(6-((1-isocyano-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoic acid (7) tert-Butyl (S)-2-(6-((1-formamido-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoate (6) is dissolved in pyridine and benzene. The solution is cooled to 0° C. and POCl3 is subsequently added drop wise. The reaction is quenched by pouring over ice and the product is extracted into CH2Cl2.
  • Synthesis of tetrakis(((2-((6-((S)-1-carboxyethyl)naphthalen-2-yl)oxy)-2-methylpropyl)-14-azanylidyne) methyl)copper (2) Based on the method of Al-Ktaifani, M. M., Nakawa, A. a., Tabbaa, Z. a. & Namou, A. a. “Synthesis of 2-methyl-2-propoxypropyl isocyanide and its Cu(I) tetrafluoroborate complex.” Chem. Pap. 62, 329-333 (2008): synthesis of (2) is realized by heating a mixture of (7) and freshly crystallized CuCl in degassed dry EtOH at 50° C. in an ampoule for 1 h. A solution of NaBF4 in water is added in one portion, solvents are removed under reduced pressure, and the resultant crude product is dissolved in EtOH and the NaCl generated is separated by filtration. The solvent is removed to get the product (2).
  • Example 2 Synthesis of tetrakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)copper (16)
  • Figure US20190169084A1-20190606-C00068
  • Synthesis of 4-(2-((tert-butyldimethylsilyl)oxy)ethyl)benzoic acid (9) Commercially available 4-(2-hydroxyethyl)benzoic acid (8) is protected as the TBDMS ether using standard conditions (see, for example, Greene's Protective Groups in Organic Synthesis, 4th Edition. Peter G. M. Wuts, Theodora W. Greene; John Wiley & Sons, Inc.; ISBN: 978-0-471-69754-1).
  • Synthesis of 4-(2-((tert-butyldimethylsilyl)oxy)ethyl)benzoyl chloride (10) 4-(2-((tert-butyldimethylsilyl)oxy)ethyl)benzoic acid (9) is converted to its acid chloride using standard conditions.
  • Synthesis of tert-butyl (S)-5-(4-(2-((tert-butyldimethylsilyl)oxy)ethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (12) Components (10) and tert-butyl (S)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (11) are coupled using the methods of either Muchowski et al. or Baran et al. (for the chiral synthesis) of (12) (Muchowski, J. M. et al., “Synthesis and antiinflammatory and analgesic activity of 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids and related compounds,” J. Med. Chem. 28, 1037-49 (1985); Baran, P. S., Richter, J. M. and Lin, D. W., “Direct coupling of pyrroles with carbonyl compounds: short enantioselective synthesis of (S)-ketorolac,” Angew. Chem. Int. Ed. Engl. 44, 609-12 (2005)).
  • Synthesis of tert-butyl (S)-5-(4-(2-hydroxyethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (13) Compound (12) is deprotected with TBAF using standard methods to yield (13).
  • tert-butyl (S)-5-(4-(2-((1-formamido-2-methylpropan-2-yl)oxy)ethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (14) Using the method of Al-Ktaifani, M. M., Nakawa, A. A., Tabbaa, Z. A. and Namou, A. A., “Synthesis of 2-methyl-2-propoxypropyl isocyanide and its Cu(I) tetrafluoroborate complex,” Chem. Pap. 62, 329-333 (2008).
  • In general, mercuric(II)trifluoroacetate and N-(2-methyl-2-propenyl)formamide (Synthesized by the method of van Wyk, A. J. et al. “Synthesis and 99mTc labelling of MMI (MIBI) and its ethyl analogue EMI.” Int. J. Radiat. Appl. Instrumentation. Part A. Appl. Radiat. Isot. 42, 687-689 (1991)) and tert-butyl (S)-5-(4-(2-hydroxyethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (13) are dissolved in THF and stirred at room temperature. The mixture is cooled down in an ice bath and NaOH pellets in isopropanol are added slowly. Subsequently, NaBH4 was added to the mixture, which was stirred for 18 h. The solution was passed through a column of Celite® (J. T. Baker, Phillipsberg, N.J., diatomaceous earth) to remove elemental Hg to yield tert-butyl (S)-5-(4-(2-((1-formamido-2-methylpropan-2-yl)oxy)ethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (14). Synthesis of (S)-5-(4-(2-((1-isocyano-2-methylpropan-2-yl)oxy)ethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid (15) tert-butyl (S)-5-(4-(2-((1-formamido-2-methylpropan-2-yl)oxy)ethyl)benzoyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylate (14) is dissolved in pyridine and benzene. The solution is cooled to 0° C. and POCl3 is subsequently added drop wise. The reaction is quenched by pouring over ice and extracting the product into CH2Cl2.
  • Synthesis of tetrakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)copper (16) Based on the method of Al-Ktaifani, M. M., Nakawa, A. A., Tabbaa, Z. A. and Namou, A. A., “Synthesis of 2-methyl-2-propoxypropyl isocyanide and its Cu(I) tetrafluoroborate complex.” Chem. Pap. 62, 329-333 (2008). Synthesis of (16) is realized by heating a mixture of (15) and freshly crystallized CuCl in degassed dry EtOH at 50° C. in an ampoule for 1 h. A solution of NaBF4 in water is added in one portion, solvents are removed under vacuum, with the resultant crude product dissolved in EtOH and the NaCl generated was separated by filtration. The solvent was removed to get the product (16).
  • Example 3 Synthesis of hexakis(((2-((6-((S)-1-carboxyethyl)naphthalen-2-yl)oxy)-2-methylpropyl)-14-azanylidyne)methyl)technetium (1)
  • Figure US20190169084A1-20190606-C00069
  • A vial is prepared containing a sterile, non-pyrogenic, lyophilized mixture of:
  • Tetrakis(((2-((6-((S)-1-carboxyethyl)naphthalen-2-yl)oxy)-2-methylpropyl)-14-azanylidyne)methyl) Copper (I) tetrafluoroborate—1.0 mg
  • Sodium Citrate Dihydrate—2.6 mg
  • L-Cysteine Hydrochloride Monohydrate—1.0 mg
  • Mannitol—20 mg
  • Stannous Chloride, Dihydrate, minimum (SnCl2.2H2O)—0.025 mg
  • Stannous Chloride, Dihydrate, (SnCl2.2H2O)—0.075 mg
  • Tin Chloride (stannous and stannic) Dihydrate, maximum (as SnCl2.2H2O)—0.086 mg.
  • Prior to lyophilization the pH is 5.3 to 5.9. The contents of the vial are lyophilized and stored under nitrogen.
  • Reconstitution with sterile, non-pyrogenic, oxidant-free Sodium Pertechnetate Tc99m Injection forms the compound (1), which is administered by intravenous injection for diagnostic use (see Scheme 2). The specific steps for reconstitution are:
  • Place the vial in a suitable radiation shield with a fitted radiation cap.
  • With a sterile shielded syringe, aseptically obtain additive-free, sterile, non-pyrogenic Sodium Pertechnetate Tc99m Injection [925-5550 MBq, (25-150 mCi)] in approximately 1 to 3 mL.
  • Aseptically add the Sodium Pertechnetate Tc99m Injection to the vial in the lead shield. Without withdrawing the needle, remove an equal volume of headspace to maintain atmospheric pressure within the vial.
  • Shake vigorously, about 5 to 10 quick upward-downward motions.
  • Remove the vial from the lead shield and place upright in an appropriately shielded and contained boiling water bath, such that the vial is suspended above the bottom of the bath, and boil for 10 minutes. Timing for 10 minutes is begun as soon as the water begins to boil again. Do not allow the boiling water to come in contact with the aluminum crimp.
  • Remove the vial from the water bath, place in the lead shield and allow to cool for fifteen minutes.
  • Using proper shielding, the vial contents should be visually inspected. Use only if the solution is clear and free of particulate matter and discoloration.
  • Assay the reaction vial using a suitable radioactivity calibration system. Record the Technetium Tc99m concentration, total volume, assay time and date, expiration time and lot number on the vial shield label and affix the label to the shield.
  • Store the reaction vial containing the Technetium Tc99m (1) at 15° C. to 25° C. until use; at such time the product should be aseptically withdrawn. Technetium Tc99m (1) should be used within six hours of preparation. The vial contains no preservative.
  • The pH of the reconstituted product is 5.5 (5.0-6.0). No bacteriostatic preservative is present. The precise structure of the technetium complex (1) is Tc99m[IBN]6 where IBN is (S)-2-(6-((1-isocyano-2-methylpropan-2-yl)oxy)naphthalen-2-yl)propanoic acid.
  • Example 4 Synthesis of Hexakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)technetium (17)
  • Figure US20190169084A1-20190606-C00070
    Figure US20190169084A1-20190606-C00071
  • Hexakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)technetium (17) is prepared using the same procedure as in Example 3, starting from tetrakis(((2-(4-((S)-1-carboxy-2,3-dihydro-1H-pyrrolizine-5-carbonyl)phenethoxy)-2-methylpropyl)-14-azanylidyne)methyl)copper (16).
  • Example 5 Synthesis of Indomethacin Derivatives
  • Figure US20190169084A1-20190606-C00072
  • Amine 20 is readily synthesized by using protocols available in the following publications: (1) Uddin, Md. Jashim, et al. Bioconjugate Chemistry (2013), 24(4), 712-723; (2) Zlatopolskiy, Boris D., et al. Chemical Communications (2012), 48(57), 7134-7136; (3) U.S. Pat. Appl. Publ. 2005/0002859 (2005); (4) U.S. Pat. Appl. Publ. 2007/0292352 (2007); (5) Uddin, Md. Jashim, et al. Journal of Labelled Compounds and Radiopharmaceuticals (2009), 52(9), 387-393; and (6) Uddin, Md. Jashim, et al. Bioorganic & Medicinal Chemistry Letters (2010), 20(5), 1787-1791.
  • Alternatively, amine 20 can be synthesized by the following procedure:
  • To a stirred solution of indomethacin 18 (2 g, 5.6 mmol) in DMF (50 mL) was added tert-butyl 4-aminobutylcarbamate (2 g, 11.2 mmol), HOBt (2.3 g , 16.8 mmol), DIPEA (3.6 g, 28 mmol) and EDCI (2.1 g, 11.2 mmol, 2 eq) at rt. The resultant mixture was stirred at rt for 16 h. The mixture was washed with 100 mL saturated LiCl solution and extracted with EtOAc (3×100 mL). The organic layers were combined, concentrated and crystallized from n-hexane to give 19 as a yellow solid. LC-MS: m/z=428 (M-100+H)+; H-NMR (400 MHz, CDCl3) δ: 7.68 (d, 2H, J=8.8 Hz), 7.50 (d, 2H, J=8.4 Hz), 6.90 (m, 2H), 6.71 (d, 2H, J=2.4 Hz), 5.79 (s, 1H), 4.59 (s, 1H), 3.82 (s, 3H), 3.63 (s, 2H), 3.22 (m, 2H), 3.06 (m, 2H), 2.39 (s, 3H), 1.41(m, 12H).
  • To a stirred solution of 19 (2 g, 3.7 mmol) in DCM (20 mL), a solution of HCl in dioxane (4M, 7.5 mL) was added dropwise. The resultant solution was stirred at rt for 2 h. Removal of solvent under reduced pressure afforded 20 as a yellow residue, which was used without further purification. LC-MS: m/z=428 (M-36+H)+; H-NMR (400 MHz, DMSO-d6) δ: 8.26 (s, 1H), 8.07 (s, 3H), 7.68 (m, 4H), 7.18 (d, 1H, J=2.4 Hz), 6.94 (d, 2H, J=8 Hz 6.71 (d, 1H, J=2.8 Hz), 3.77 (s, 3H), 3.56 (s, 2H), 3.07 (d, 2H, J=6 Hz 2.76(d, 2H, J=6.4 Hz), 2.24 (s, 3H), 1.57 (m, 2H), 1.48 (m, 2H).
  • Indomethacin derivative 22 is made following the procedure in: Wang Y, et al. Nat Protoc. (2007), 2(4): 972-8. The reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no. ES1001; see the supplier web site: www.kerafast.com/p-1447-s-acetyl-mag3-nhs-ester.aspx?gclid=Cj0KEQjwur2eBRDtvMS0gIuS-dYBEiQANBPMR3SKY-ABw0HCC08Gud53dB29ws1dYYU13UeQFvVxc_gaAiIA8P8HAQ; see also Winnard P. et al., Nucl Med Biol. (1997), 24(5): 425-32; Wang Y. et al., Nat. Protoc. (2007) 2(4): 972-8; Rusckowski M. et al., Cancer Biotherapy & Radiopharmaceuticals (2007), 22(4): 564-72; and Wang Y. et al., European J. Nucl. Med. Mol. Imag. (2009), 36(12): 1977-86).
  • Indomethacin derivative 23 is made following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748. The reagent Trichlorooxobis(triphenylphosphine)rhenium(V), (PPh3)2ReOCl3, is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Alternatively, compound 23 can be synthesized using the following procedure: To a stirred solution of compound 22 (100 mg, 0.14 mmol) in NMP (15 mL), (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 106 mg, 0.127 mmol) was added. The mixture was stirred at 80° C. for 48 h. The solution was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: Water (10 mM NH4HCO3), solvent B: MeCN) to give compound 23 as a solid. LC-MS: m/z=871 (M+H)+; H-NMR (400 MHz, DMSO-d6) δ: 8.00 (m, 1H), 7.70˜7.63 (m, 4H), 7.20 (m, 1H), 7.11 (m, 1H), 6.95 (d, 1H, J=8.8 Hz), 6.71 (d, 1H, J=2 Hz), 4.82 (d, 1H, J=16 Hz), 4.55 (d, 1H, J=17.6 Hz), 4.41 (d, 1H, J=16 Hz), 3.80 (m, 4H), 3.65 (d, 1H, J=16.8 Hz), 3.48 (s, 2H), 3.03 (m, 4H), 2.22 (s, 3H), 1.36 (s, 4H). 13C-NMR (400 MHz, DMSO-d6) δ: 192.27, 191.61, 188.45, 170.13, 169.65, 168.32, 156.01, 137.97, 135.53, 134.77, 131.61, 130.72, 129.49, 115.00, 111.76, 102.30, 58.45, 56.21, 55.90, 53.08, 39.94, 38.53, 31.61, 27.12, 26.91, 13.84.
  • Example 6 Synthesis of Indomethacin Derivatives
  • Figure US20190169084A1-20190606-C00073
    Figure US20190169084A1-20190606-C00074
  • Similarly as Example 5, amine 25 has been reported in the following articles: (1) Uddin, Md. Jashim, et al. Bioconjugate Chemistry (2013), 24(4), 712-723. (2) Hua Zhang, et al. J. Am. Chem. Soc. (2013), 135, 11663-11669 (3) Hua Zhang, et al. J. Am. Chem. Soc. (2013), 135, 17469-17475.
  • Alternatively, amine 25 can be synthesized by the following procedure:To a mixture of indomethacin (11.8 g, 33 mmol), tert-butyl 6-aminohexylcarbamate (CAS No. 51857-17-1) (8.5 g, 39 mmol) and HATU (18.8 g, 50 mmol) in DMF (200 mL) was added TEA (10.1 g, 0.1 mol). The mixture was stirred at rt for 4 h and poured onto ice water (300 mL). The precipitate was collected by filtration and dried to give compound 24 as a solid. LC-MS: m/z=456.3 (M-100+H; H-NMR (400 MHz, DMSO-d6)δ: 8.00 (br s, 1H), 7.77-7.63 (m, 4H), 7.11 (d, J=2.4 Hz, 1H), 6.95-6.93 (m, 1H), 6.74-6.69 (m, 2H), 3.76 (s, 3H), 3.48 (s, 2H), 3.06-3.01 (m, 2H), 2.88-2.83 (m, 2H), 2.23 (s, 3H), 1.36 (s, 9H), 1.33-1.18 (m, 8H).
  • A mixture of compound 24 (10 g, 18 mmol) in HC1/dioxane (3M, 150 mL) was stirred at rt for 2 h. The mixture was concentrated to give compound 25 as white solid, which was in the next step without further purification. LC-MS: m/z=456.3 (M+H)+; H NMR (400 MHz, CD3OD) δ: 7.72 (d, J=8.4 Hz, 2H), 7.59 (d, J=8.4 Hz, 2H), 7.03 (d, J=2.4 Hz, 1H), 6.95 (d, J=9.2 Hz, 1H), 6.73-6.70 (m, 1H), 3.83 (s, 3H), 3.63 (s, 2H), 3.34-3.23 (m, 2H), 2.91-2.85 (m, 2H), 2.34 (s, 3H), 1.62-1.37 (m, 8H).
  • Indomethacin derivative 26 is made following the procedure in: Wang Y, et al. Nat Protoc. (2007), 2(4): 972-8. The reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no. ES1001; see the supplier web site: www.kerafast.com/p-1447-s-acetyl-mag3-nhs-ester.aspx?gclid=Cj0KEQwur2eBRDtvMSOgIuS-dYBEiQANBPMR3SKY-ABw0HCC08Gud53dB29ws1dYYU13UeQFvVxc_gaAiIA8P8HAQ; see also Winnard P. et al., Nucl. Med Biol. (1997), 24(5): 425-32; Wang Y. et al., Nat. Protoc. (2007), 2(4): 972-8; Rusckowski M. et al., Cancer Biotherapy & Radiopharmaceuticals (2007), 22(4): 564-72; and Wang Y. et al., European J. Nucl. Med. Mol. Imag.; (2009), 36(12): 1977-86).
  • Indomethacin derivative 27 is made following the procedure in: Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748. The reagent Trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Alternatively, compound 27 can be synthesized using the following procedure: A mixture of compound 26 (200 mg, 0.27 mmol) and (Ph3P)2ReOCl3 (337 mg, 0.41 mmol) in NMP (10 mL) was stirred for 16 h at 100° C. The solution was directly purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: water containing 10 mM NH4HCO3, solvent B: ACN) to give 27 as a solid. LC-MS: m/z=899.2 MS (M−H); H-NMR (400 MHz, DMSO-d6) δ: 8.00 (s, 1H), 7.70-7.63 (m, 4H), 7.16-7.11 (m, 2H), 6.94 (d, J=8.8 Hz, 1H), 6.71-6.69 (m, 1H), 4.78 (d, J=16.4 Hz, 1H), 4.52(d, J=18.0 Hz, 1H), 4.38 (d, J=16.0 Hz, 1H), 4.16-4.10 (m, 3H), 3.79-3.75 (m, 4H), 3.63 (d, J=17.2 Hz, 1H), 3.47(s, 2H), 3.03-2.98 (m, 4H), 2.22 (s, 3H), 1.36-1.20 (m, 8H).
  • Example 7 Synthesis of Indomethacin Derivatives
  • Figure US20190169084A1-20190606-C00075
    Figure US20190169084A1-20190606-C00076
  • Compound 31 has been reported by Yoriko Iwata, et al. J. Med. Chem. (2001), 44, 1718-1728 and is readily synthesized from the commercially available hydrazine 28 through the Fisher indole synthesis with levulinic acid. Alkylation of 31 with tBocNH(CH2)4Br and deprotection of the tBOC amine and the tBu-ester leads to amino acid 33 which can be reacted with NHS-S-Acetyl-MAG3 following the procedure in: Wang Y, et al. Nat Protoc. 2007; 2(4), 972-8 to afford 34. The reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no. ES1001; see the supplier web site: www.kerafast.com/p-1447-s-acetyl-mag3-nhs-ester.aspx?gclid=Cj0KEQjwur2eBRDtvMS0gIuS-dYBEiQANBPMR3 SKY-ABw0HCC08Gud53dB29ws1dYYU13UeQFvVxc_gaAiIA8P8HAQ; see also Winnard P. et al., Nucl. Med. Biol. (1997), 24(5): 425-32; Wang Y. et al., Nat. Protoc. (2007), 2(4): 972-8; Rusckowski M. et al., Cancer Biotherapy & Radiopharmaceuticals (2007), 22(4): 564-72; and Wang Y. et al., European J. Nucl. Med. Mol. Imag. (2009), 36(12): 1977-86).
  • The rhenium-indomethacin derivative 35 is made following the procedure in: Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748. The reagent trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Example 7b Synthesis of Indomethacin Derivatives
  • Figure US20190169084A1-20190606-C00077
  • Compound 39 is prepared by a procedure similar to the one described in Example 7, substituting tBocNH(CH2)4Br with tBocNH(CH2)6Br.
  • Example 8 Synthesis of ethylenedicysteine Indomethacin Derivatives 40, 41, 42, and 43
  • Figure US20190169084A1-20190606-C00078
    Figure US20190169084A1-20190606-C00079
  • Part 1: Synthesis of Ethylenedicysteine Indomethacin derivatives D40, 41, 42, and 43
  • Amine 20 is prepared as described in Example 5.
  • Indomethacin derivative 40 is made from amine 20 by amide coupling with ethylenedicysteine (CAS #14344-48-0). The reaction of ethylenedicysteine with primary amines is described in the literature, see e.g. Yang et al., US 2004/6692724.
  • Derivative 41 is made by reacting 40 with diazomethane or TMS-diazomethane. Analog 42 is made by treating 40 with EtOH/HCl or EtOH/TMSCl. Derivative 43 is made from 40 by reaction with NH3 in the presence of a dehydrating agent or by a similar method well known to a person skilled in the art.
  • Example 8b Synthesis of Isocyano Indomethacin Derivative 45
  • Figure US20190169084A1-20190606-C00080
  • The isocyano compound 45 is prepared by formylating amine 20 to yield 44, followed by dehydration of 44 with POCl3 to give 45.
  • Example 8c Synthesis of 99mTc Indomethacin Derivative 50b
  • Figure US20190169084A1-20190606-C00081
  • Compound 50b is prepared from compound 41 in a manner analogous to the procedure in Example 2.
  • Example 9 Synthesis of 99mTc Indomethacin Derivatives: 46, 47, 48, and 49
  • Figure US20190169084A1-20190606-C00082
  • Compounds 46, 47, 48, and 49 are prepared from compounds 42, 43, 44, and 45, respectively, by treating with sodium pertechnetate as described in Example 3.
  • Example 10 Synthesis of 99mTc Indomethacin MAG3 Analog (51)
  • Figure US20190169084A1-20190606-C00083
  • Compound 51 is prepared by combining, in a reaction vial, 1 mg of 22, between 0.05 mg (minimum) stannous chloride dihydrate (SnCl2.2H2O) and 0.2 mg (maximum) total tin expressed as stannous chloride dihydrate (SnCl2.2H2O), 40 mg sodium tartrate dehydrate (Na2C4H2O6.2H2O), and 20 mg lactose monohydrate. The pH of the reconstituted drug is between 5.0 and 6.0. A solubilizing agent and a bacteriostatic agent are optionally used depending on the need.
  • The preparation of compound 51 is analogous to the preparation of Technetium Tc 99m Mertiatide using the TechneScan MAG3™ Kit. Details of the preparation are at URL www.mallinckrodt.com/WorkArea/DownloadAsset.aspx?id=616 .
  • Example 11 Synthesis of 99mTc Indomethacin MAG3 Analog (52)
  • Figure US20190169084A1-20190606-C00084
  • Compound 52 is prepared from compound 34 using a procedure similar to the one described in Example 10.
  • Example 11b Synthesis of 99mTc Indomethacin MAG3 Analog (53)
  • Figure US20190169084A1-20190606-C00085
  • Compound 53 is prepared from compound 34 using a procedure similar to the one described in Example 10.
  • Example 12 Synthesis of 99mTc Indomethacin MAG3 Analog (54)
  • Figure US20190169084A1-20190606-C00086
  • Compound 54 is prepared from compound 26 using a procedure similar to the one described in Example 10.
  • Example 13 Synthesis of Ketorolac MAG3 ligand Part 1
  • Figure US20190169084A1-20190606-C00087
  • Compound 61 is prepared from compound 55 by first protecting the acid functionality of 55 via acid-catalyzed esterification to give 56, and then using a procedure analogous to that given in Example 7.
  • Example 14 Synthesis of Ketorolac Hexanoic MAG Re Ligand
  • Figure US20190169084A1-20190606-C00088
  • Compound 61 is prepared from compound 55 by first protecting the acid functionality of 55 via acid-catalyzed esterification to give 56, and then using a procedure analogous to that given in Example 7.
  • Example 15 Synthesis of Ketorolac ethylenedicysteine Ligand Part 1
  • Figure US20190169084A1-20190606-C00089
  • Compound 67 is prepared from compound 55 by preparation of 57 via a procedure analogous to that given in Example 7 using N-Boc-protected 1-amino-4-bromobutane, and then by following the deprotection and coupling steps given in Example 8.
  • Part 2
  • Figure US20190169084A1-20190606-C00090
  • Compound 70 is prepared from compound 68 in a similar manner to Part 1 of this Example.
  • Part 3
  • Figure US20190169084A1-20190606-C00091
  • Compound 72 is prepared from compound 58 in a manner similar to Example 8, Part 2.
  • Example 16 Synthesis of Ketorolac 9m Tc Complex Part 1
  • Figure US20190169084A1-20190606-C00092
  • Compounds 73 and 74 are prepared from compounds 67 and 70, respectively, by treating with sodium pertechnetate as described in Example 3, substituting 67 and 70, respectively, for compound 2.
  • Part 2
  • Figure US20190169084A1-20190606-C00093
  • Compound 76 is prepared from compound 72 using procedures analogous to those of Example 2 and Example 3.
  • Example 17 Synthesis of 99mTc Ketorolac MAG3 Analog (77)
  • Figure US20190169084A1-20190606-C00094
  • Compound 77 is prepared from compound 60 using the procedure of Example 10.
  • Example 18 Synthesis of 99mTc Ketorolac MAG3 Analog (78)
  • Figure US20190169084A1-20190606-C00095
  • Compound 78 is prepared from compound 65 using the procedure of Example 10.
  • Example 19 Synthesis of Naproxen butanyl MAG3 Ligand
  • Figure US20190169084A1-20190606-C00096
  • Compound 79 is prepared from compound 3 using N1-Boc-1,4-diaminobutane. Compound 82 is prepared from compound 79 by using a procedure analogous to the corresponding steps of Example 7.
  • Example 20 Synthesis of Naproxen Hexanyl Ligand
  • Figure US20190169084A1-20190606-C00097
  • Compound 86 is prepared from compound 3 using the procedure of Example 19.
  • Example 21 Synthesis of Naproxen Derivatives
  • Figure US20190169084A1-20190606-C00098
  • Compound 5 is obtained from the commercial starting material 4 in 82% yield as reported in WO 2013/025790 A2. Alkylation of 5 with tBocNH(CH2)4Br and deprotection of the tBOC amine and the tBu-ester provides amino acid 88 which can be reacted with NHS-S-Acetyl-MAG3 following the procedure in: Wang Y, et al. Nat Protoc. 2007; 2(4), 972-8 to afford 89. The reagent S-Acetyl-MAG3-NHS ester is available commercially (KeraFAST Inc., Boston, Mass., USA; catalog no. ES1001; see the supplier web site: www.kerafast.com/p-1447-s-acetyl-mag3-nhs-ester.aspx?gclid=Cj0KEQjwur2eBRDtvMS0gIuS-dYBEiQANBPMR3 SKY-ABw0HCC08Gud53dB29ws1dYYU13UeQFvVxc_gaAiIA8P8HAQ; see also Winnard P. et al., Nucl Med Biol. 1997 July; 24(5):425-32; Wang Y. et al., Nat. Protoc. 2007; 2(4):972-8; Rusckowski M. et al., Cancer Biotherapy & Radiopharmaceuticals 2007; 22(4): 564-72; and Wang Y. et al., European J Nucl Med Mol Imag 2009; 36(12): 1977-86).
  • The rhenium-indomethacin derivative 90 is made following a procedure similar to the one described by Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748. The reagent Trichlorooxobis(triphenylphosphine)rhenium(V) is commercially available (Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 370193).
  • Example 22 Synthesis of 99mTc Naproxen Butanyl MAG3 Analog (91)
  • Figure US20190169084A1-20190606-C00099
  • Compound 91 is prepared from compound 81 using the procedure of Example 10.
  • Example 23 Synthesis of 99mTc Naproxen Hexanyl MAG3 Analog (92)
  • Figure US20190169084A1-20190606-C00100
  • Compound 92 is prepared from compound 85 using the procedure of Example 10.
  • Example 24 Synthesis of 99mTc Naproxen MAG3 Analog (93)
  • Figure US20190169084A1-20190606-C00101
  • Compound 93 is prepared from compound 89 using the procedure of Example 10.
  • Example 25 Synthesis of Celecoxib Hexanyl MAG3 Ligand
  • Figure US20190169084A1-20190606-C00102
    Figure US20190169084A1-20190606-C00103
  • The celecoxib analog 95, in which a methyl ester replaces the trifluoromethyl group of celecoxib, is synthesized from 94 using the procedure described in Lill et al., Tetrahedron Letters 54, 6682-6686, (2013). The ester is hydrolyzed to give 96, and coupled with N1-Boc-1,6-diaminohexane to yield 97. The corresponding steps of Example 7 are then followed to yield 100.
  • Example 26 Synthesis of Celecoxib Butanyl MAG3 Ligand
  • Figure US20190169084A1-20190606-C00104
    Figure US20190169084A1-20190606-C00105
  • Compound 104 is produced as in Example 25, using N1-Boc-1,4-diaminobutane in place of N1-Boc-1,6-diaminohexane.
  • Example 27 Synthesis of Celecoxib Decanyl MAG3 Ligand
  • Figure US20190169084A1-20190606-C00106
    Figure US20190169084A1-20190606-C00107
  • Compound 108 is produced as in Example 25, using N1-Boc-1,10-diaminodecane in place of N1-Boc-1,6-diaminohexane.
  • Example 28 Synthesis of 99mTc Celecoxib MAG3 Analog (109)
  • Figure US20190169084A1-20190606-C00108
  • Compound 109 is prepared from compound 103 using the procedure of Example 10.
  • Example 29 Synthesis of 99mTc Celecoxib MAG3 Analog (110)
  • Figure US20190169084A1-20190606-C00109
  • Compound 110 is prepared from compound 107 using the procedure of Example 10.
  • Example 30 Synthesis of 99mTc Celecoxib MAG3 Analog (111)
  • Figure US20190169084A1-20190606-C00110
  • Compound 111 is prepared from compound 99 using the procedure of Example 10.
  • Example 31 Synthesis of Compound 178
  • Figure US20190169084A1-20190606-C00111
    Figure US20190169084A1-20190606-C00112
  • Compound 178 was prepared by the following procedure: S,S-ethylenedicysteine 172 (CAS #14344-48-0) was prepared according to the procedures described in the literature, see e.g. Blondeau, Berse, Gravel, Can. J. Chem. 45, 49-52, (1967); Ratner, Clarke, J. Am. Chem. Soc. 59, 200-206, (1937). Compound 176 was prepared by a procedure similar to the one described for compounds 20 and 25 in examples 5 and 6. 176 is coupled with acid 173 to give the amide 177 as described in example 5. Compound 177 is dissolved in ethanol and treated with 5 eq of TMSCl at 40° C. for 20 h. Solvent is removed and the product is purified by HPLC to give the target compound 178.
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.3 Hz, 2H), 7.49 (d, J=8.3 Hz, 2H), 7.00-6.80 (m, 1H), 6.84-6.47 (m, 2H), 6.16 (s, 1H), 5.90 (s, 1H), 4.67 (d, J=7.1 Hz, 1H), 4.44-4.26 (m, 2H), 3.96-3.76 (m, 5H), 3.65 (s, 2H), 3.61-3.26 (m, 13H), 3.23-3.05 (m, 2H), 3.05-2.83 (m, 2H), 2.38 (s, 3H), 1.34 (t, J=7.1 Hz, 3H). MS (ESI) m/z: 966.1 (M+H+).
  • The following compounds 179-185 can also be prepared according to the procedure given in Example 31 by replacing tert-butyl 2-(2-(2-aminoethoxy)ethoxy)ethylcarbamate 174 with the appropriate reagent shown in Table 1.
  • Figure US20190169084A1-20190606-C00113
  • TABLE 1
    Compound Y = Reagent used
    179
    Figure US20190169084A1-20190606-C00114
    tert-butyl (2-aminoethyl)carbamate
    180
    Figure US20190169084A1-20190606-C00115
    tert-butyl (2-(2-aminoethoxy)ethyl)carbamate
    181
    Figure US20190169084A1-20190606-C00116
    tert-butyl (6-aminohexyl)carbamate
    182
    Figure US20190169084A1-20190606-C00117
    tert-butyl (7-aminoheptyl)carbamate
    183
    Figure US20190169084A1-20190606-C00118
    tert-butyl (8-aminooctanyl)carbamate
    184
    Figure US20190169084A1-20190606-C00119
    tert-butyl (2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)eth- yl)carbamate
  • Compound 181
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=7.3 Hz, 2H), 7.49 (d, J=7.1 Hz, 2H), 6.89 (d, J=6.9 Hz, 2H), 6.70 (d, J=8.8 Hz, 1H), 6.48 (s, 1H), 5.72 (s, 1H), 4.67 (s, 1H), 4.36 (s, 2H), 4.08-3.72 (m, 5H), 3.70-3.28 (m, 5H), 3.27-2.87 (m, 5H), 2.78 (s, 1H), 2.37 (s, 3H), 1.51-0.91 (m, 11H). MS (ESI) m/z: 934.1(M+H+).
  • Compound 182
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.50 (t, J=9.2 Hz, 2H), 6.90 (d, J=9.1 Hz, 2H), 6.70 (dd, J=9.0, 2.5 Hz, 1H), 6.57 (s, 1H), 5.69 (d, J=26.8 Hz, 2H), 4.67 (d, J=6.1 Hz, 1H), 4.43-4.26 (m, 2H), 4.03-3.75 (m, 5H), 3.70-3.33 (m, 5H), 3.32-3.10 (m, 4H), 3.03 (dd, J=12.9, 6.4 Hz, 2H), 2.75 (s, 1H), 2.37 (s, 3H), 1.32 (dd, J=41.6, 34.4 Hz, 13H). MS (ESI) m/z: 948.1 (M+H+).
  • Compound 183
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.4 Hz, 2H), 7.50 (t, J=8.6 Hz, 2H), 7.00-6.83 (m, 2H), 6.70 (dd, J=9.0, 2.4 Hz, 1H), 6.58 (s, 1H), 5.73 (s, 1H), 5.62 (s, 1H), 4.68 (d, J=7.1 Hz, 1H), 4.37 (qd, J=10.7, 3.5 Hz, 2H), 3.99-3.76 (m, 5H), 3.63 (s, 2H), 3.59-3.32 (m, 3H), 3.30-2.86 (m, 6H), 2.84-2.65 (m, 1H), 2.37 (s, 3H), 1.55-0.93 (m, 15H). MS (ESI) m/z: 962.1 (M+H+).
  • Compound 185
  • Figure US20190169084A1-20190606-C00120
  • Compound 185 was prepared by a procedure similar to the one described in Example 31 by replacing ethanol in the last step with isopropanol (Propan-2-ol).
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=7.8 Hz, 2H), 7.49 (d, J=8.0 Hz, 2H), 6.89 (d, J=7.1 Hz, 2H), 6.70 (d, J=8.3 Hz, 1H), 6.58 (s, 1H), 5.73 (s, 2H), 5.28 (d, J=57.0 Hz, 2H), 4.68 (s, 1H), 4.01-3.75 (m, 5H), 3.74-3.34 (m, 5H), 3.32-2.93 (m, 5H), 2.74 (s, 1H), 2.38 (s, 3H), 2.02 (s, 1H), 1.48-1.13 (m, 15H). MS (ESI) m/z: 474.7[(M+2H+)/2]
  • Example 32 Synthesis of Compound 190
  • Figure US20190169084A1-20190606-C00121
  • 186 is coupled with indomethacin to give the amide 187 as described in example 5. Compound 187 is dissolved in methanol and hydrogenated over Pd/C to give compound 188. Compound 188 is then coupled with acid 173 and esterified to give compound 190 as described in example 31.
  • Example 33 Synthesis of compound 193
  • Figure US20190169084A1-20190606-C00122
  • Compound 176 is synthesized as described in Example 31. 176 is coupled with S,S-ethylenedicysteine 172 (CAS #14344-48-0) according to literature procedures, see e.g. Yang et al., US 2006/6692724. The ethylester 192 is obtained by treating 191 with EtOH/TMSCl or EtOH/HCl. Compound 193 is prepared from compound 192 by treating with sodium pertechnetate as described in Example 3.
  • The following compounds 194-201 can also be prepared according to the procedure given in Example 33 by replacing compound 176 with the appropriate intermediate (synthesis described in examples 31-32.
  • Figure US20190169084A1-20190606-C00123
  • Example Y =
    194
    Figure US20190169084A1-20190606-C00124
    195
    Figure US20190169084A1-20190606-C00125
    196
    Figure US20190169084A1-20190606-C00126
    197
    Figure US20190169084A1-20190606-C00127
    198
    Figure US20190169084A1-20190606-C00128
    199
    Figure US20190169084A1-20190606-C00129
    200
    Figure US20190169084A1-20190606-C00130
    201
    Figure US20190169084A1-20190606-C00131
  • Example 34 Synthesis of Compound 204
  • Figure US20190169084A1-20190606-C00132
  • Compound 204 was prepared by the following procedure:
  • A solution of tert-butyl 2-(2-(2-aminoethoxy)ethoxy)ethylcarbamate 174 (50 mg, 0.2 mmol), Re(CO)5Br (82 mg, 0.2 mmol), and picolinaldehyde (22 mg, 0.2 mmol) in methanol (20 ml) was stirred at 80° C. for 12 h under nitrogen. The reaction mixture was then concentrated and purified by column chromatography to give compound 202 (110 mg, 79%). A solution of HCl in dioxane (4N, 10 ml) and compound 202 (110 mg, 0.16 mmol) was stirred at rt for 2 h, and then concentrated in vacuo to give crude product 203 (100 mg), which was used directly in the next step.
  • To a solution of indomethacin (57 mg, 0.16 mmol) in DCM (20 ml) was added HOBt (22 mg, 0.16 mmol), EDCI (31 mg, 0.16 mmol), and DIEA (62 mg, 0.48 mmol). The mixture was stirred at RT for 0.5 h, after which 203 (100 mg, 0.16 mmol) was added. The reaction mixture was stirred at RT overnight. The mixture was then diluted with water (30 ml) and extracted with EtOAc (25 ml×3). The combined organic layers were washed with brine (15 ml×2), dried over Na2SO4, filtered and the filtrate was concentrated and purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp.; solvent A: water, solvent B: MeCN) to give the desired product 204.
  • 1H NMR (400 MHz, CDCl3) δ 9.00 (d, J=5.3 Hz, 1H), 8.66 (s, 1H), 8.09-7.97 (m, 1H), 7.88 (d, J=7.6 Hz, 1H), 7.67 (d, J=8.5 Hz, 2H), 7.60-7.44 (m, 3H), 6.98-6.84 (m, 2H), 6.69 (dd, J=9.0, 2.5 Hz, 1H), 6.00 (s, 1H), 4.32-4.11 (m, 2H), 4.04-3.89 (m, 2H), 3.86-3.76 (m, 3H), 3.61 (s, 2H), 3.57-3.38 (m, 6H), 3.38-3.22 (m, 2H), 2.39 (d, J=7.7 Hz, 3H). MS (ESI) m/z: 927.2 (M+H+).
  • The following compounds 205-211 can also be prepared according to the procedure given in Example 34 by replacing tert-butyl 2-(2-(2-aminoethoxy)ethoxy)ethylcarbamate 174 with the appropriate reagent given in Table 2.
  • Figure US20190169084A1-20190606-C00133
  • TABLE 2
    Compound Y = Reagent used
    205
    Figure US20190169084A1-20190606-C00134
    tert-butyl (2-aminoethyl)carbamate
    206
    Figure US20190169084A1-20190606-C00135
    tert-butyl (2-(2-aminoethoxy)ethyl)carbamate
    207
    Figure US20190169084A1-20190606-C00136
    tert-butyl (6-aminohexyl)carbamate
    208
    Figure US20190169084A1-20190606-C00137
    tert-butyl (7-aminoheptyl)carbamate
    209
    Figure US20190169084A1-20190606-C00138
    tert-butyl (8-aminooctanyl)carbamate
    210
    Figure US20190169084A1-20190606-C00139
    tert-butyl (2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)eth- yl)carbamate
    211
    Figure US20190169084A1-20190606-C00140
    tert-butyl (4-(aminomethyl)benzyl)carbamate
  • Compound 207
  • 1H NMR (400 MHz, DMSO-d6) δ 9.19 (s, 1H), 9.03 (d, J=5.0 Hz, 1H), 8.43-8.20 (m, 2H), 8.06 (s, 1H), 7.86-7.73 (m, 1H), 7.66 (dd, J=18.1, 8.4 Hz, 4H), 7.13 (s, 1H), 6.93 (d, J=8.9 Hz, 1H), 6.70 (d, J=9.0 Hz, 1H), 4.29-4.07 (m, 1H), 4.06-3.92 (m, J=6.5 Hz, 2H), 3.75 (s, 3H), 3.48 (s, 2H), 3.17 (d, J=5.2 Hz, 2H), 2.22 (s, 3H), 1.90 (s, 2H), 1.52-1.14 (m, J=36.9 Hz, 6H). MS (ESI) m/z: 851.2 (M+H+).
  • Compound 208
  • 1H NMR (400 MHz, CDCl3) δ 9.04 (d, J=5.1 Hz, 1H), 8.71 (s, 1H), 8.05 (dd, J=7.7, 6.5 Hz, 1H), 7.92 (d, J=7.6 Hz, 1H), 7.67 (d, J=8.5 Hz, 2H), 7.58-7.53 (m, 1H), 7.50 (t, J=8.0 Hz, 2H), 6.87 (t, J=5.3 Hz, 2H), 6.69 (dd, J=9.0, 2.5 Hz, 1H), 5.59 (s, 1H), 4.37-4.14 (m, 1H), 4.07-3.97 (m, 1H), 3.94-3.71 (m, 3H), 3.62 (s, 2H), 3.20 (dd, J=13.0, 6.7 Hz, 2H), 2.37 (s, 3H), 2.15-1.92 (m, 2H), 1.52-1.14 (m, 8H). MS (ESI) m/z: 910.2(M+H+).
  • Compound 209
  • 1H NMR (400 MHz, CDCl3) δ 9.04 (d, J=5.1 Hz, 1H), 8.70 (s, 1H), 8.12-8.00 (m, 1H), 7.90 (d, J=7.7 Hz, 1H), 7.67 (d, J=8.4 Hz, 2H), 7.61-7.53 (m, 1H), 7.49 (d, J=8.4 Hz, 2H), 6.87 (t, J=5.7 Hz, 2H), 6.70 (dd, J=9.0, 2.5 Hz, 1H), 5.59 (t, J=5.8 Hz, 1H), 4.34-4.12 (m, 1H), 4.02 (dt, J=11.8, 7.4 Hz, 1H), 3.82 (s, 3H), 3.62 (s, 2H), 3.34-3.13 (m, 2H), 2.38 (s, 3H), 2.23-1.85 (m, 2H), 1.47-1.11 (m, 10H). MS (ESI) m/z: 923.2 (M+H+).
  • Compound 210
  • 1H NMR (400 MHz, CDCl3) δ 9.08-8.96 (m, 1H), 8.75 (s, 1H), 8.01 (td, J=7.8, 1.4 Hz, 1H), 7.88 (d, J=7.7 Hz, 1H), 7.67 (d, J=8.5 Hz, 2H), 7.54 (dd, J=9.5, 3.8 Hz, 1H), 7.49 (d, J=8.5 Hz, 2H), 7.01-6.81 (m, 2H), 6.68 (dd, J=9.0, 2.5 Hz, 1H), 6.07 (s, 1H), 4.25 (ddd, J=16.8, 16.2, 8.2 Hz, 2H), 4.03 (dt, J=8.7, 6.3 Hz, 2H), 3.83 (d, J=11.1 Hz, 3H), 3.70-3.59 (m, 3H), 3.55-3.34 (m, 8H). MS (ESI) m/z: 971.2(M+H+).
  • Compound 211
  • 1H NMR (400 MHz, DMSO-d6) δ 9.37 (s, 1H), 9.01 (d, J=5.2 Hz, 1H), 8.55 (t, J=5.7 Hz, 1H), 8.31 (d, J=3.2 Hz, 2H), 7.77 (dd, J=8.8, 5.2 Hz, 1H), 7.66 (dd, J=24.0, 8.4 Hz, 4H), 7.36 (d, J=7.9 Hz, 2H), 7.27 (d, J=7.9 Hz, 2H), 7.14 (d, J=2.0 Hz, 1H), 6.96 (d, J=9.0 Hz, 1H), 6.71 (dd, J=8.9, 2.1 Hz, 1H), 5.76 (s, 2H), 5.37 (d, J=13.6 Hz, 1H), 5.09 (d, J=13.3 Hz, 1H), 4.31 (d, J=5.6 Hz, 2H), 3.73 (s, 3H), 3.59 (s, 2H), 2.22 (s, 3H). MS (ESI) m/z: 915.2(M+H+).
  • The following compounds 212-219 can also be prepared according to the procedure given in Example 34 and for compounds 204-211, by substituting Re(CO)5Br (CAS No. 14220-21-4) in step 1 of example 34 with Re(CO)5C1 (CAS No. 14099-01-5).
  • Figure US20190169084A1-20190606-C00141
  • Compound Y =
    212
    Figure US20190169084A1-20190606-C00142
    213
    Figure US20190169084A1-20190606-C00143
    214
    Figure US20190169084A1-20190606-C00144
    215
    Figure US20190169084A1-20190606-C00145
    216
    Figure US20190169084A1-20190606-C00146
    217
    Figure US20190169084A1-20190606-C00147
    218
    Figure US20190169084A1-20190606-C00148
    219
    Figure US20190169084A1-20190606-C00149
  • Compound 219
  • 1H NMR (400 MHz, CDCl3) δ 8.98 (d, J=5.2 Hz, 1H), 8.69 (s, 1H), 8.03 (t, J=7.7 Hz, 1H), 7.87 (d, J=7.7 Hz, 1H), 7.68 (d, J=8.5 Hz, 2H), 7.63-7.52 (m, 1H), 7.49 (d, J=8.4 Hz, 2H), 6.89 (dd, J=11.2, 5.7 Hz, 2H), 6.69 (dd, J=9.0, 2.4 Hz, 1H), 6.05 (s, 1H), 4.33-4.15 (m, 2H), 3.95 (qd, J=10.8, 4.3 Hz, 2H), 3.81 (s, 3H), 3.61 (s, 2H), 3.58-3.23 (m, 8H), 2.38 (s, 3H). MS (ESI) m/z: 883 .2(M+H+).
  • Example 35 Synthesis of Compound 221
  • Figure US20190169084A1-20190606-C00150
  • Compound 176 is synthesized as described in Example 31. 176 is coupled with picolinaldehyde to give the imine 220 according to literature procedures or methods well known to a person skilled in the art. For example, dissolving equal amounts in toluene and heating to reflux will accomplish such a transformation. Compound 221 is prepared from compound 220 as described by e.g. Alberto, R., Schibli, R., Schubiger, A. P., J. Am. Chem. Soc., 121, 6076-6077, (1999).
  • The following compounds 222-229 can also be prepared according to the procedure given in Example 35 by replacing compound 176 with the appropriate intermediate (synthesis described in examples 5, 6, 31-32.
  • Figure US20190169084A1-20190606-C00151
  • Compound Y =
    222
    Figure US20190169084A1-20190606-C00152
    223
    Figure US20190169084A1-20190606-C00153
    224
    Figure US20190169084A1-20190606-C00154
    225
    Figure US20190169084A1-20190606-C00155
    226
    Figure US20190169084A1-20190606-C00156
    227
    Figure US20190169084A1-20190606-C00157
    228
    Figure US20190169084A1-20190606-C00158
    229
    Figure US20190169084A1-20190606-C00159
    230
    Figure US20190169084A1-20190606-C00160
  • Example 36 Synthesis of Compound 234
  • Figure US20190169084A1-20190606-C00161
  • The synthesis of compound 25 is described in Example 6.
  • Intermediate 231:
  • To a solution of 25 (400 mg, 0.81 mmol) and picolinaldehyde (87 mg, 0.81 mmol, 1 eq) in MeOH (10 ml) was added AcOH (0.3 ml), the mixture was stirred at RT for 30min, NaBH(OAC)3 (687 mg, 3.24 mmol, 4 eq) was added, the mixture was stirred at RT overnight. Water (20 ml) was added and extracted with ethyl acetate (30 ml×3), the combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product which was purified by column chromatography (DCM:MeOH=10:1) to get the product (120 mg, 27%) as a yellow solid. LC-MS: m/z=547.3 [M+1]+
  • Intermediate 232:
  • To a solution of 231 (120 mg, 0.22 mmol) and TEA (45 mg, 0.44 mmol) in THF (10 mL) was added tert-butyl 2-bromoacetate (64 mg, 0.33 mmol). The mixture was stirred at 60° C. for 2 h. Water (10 ml) was added and extracted with ethyl acetate (3 x 30 ml), the combined organic layers were washed with brine, dried over Na2SO4, concentrated to get the crude product (130 mg, 90%) as yellow oil, which was used in the next step without further purification. LC-MS: m/z=661.3 [M+1]
  • Intermediate 233:
  • To a solution of 232 (130 mg, 0.20 mmol) in DCM (10 ml) was added TFA (2 ml), the mixture was stirred at RT for 4 h and then evaporated the solvent to give the crude product (110 mg, 92%) as a yellow oil, which was used directly in the next step. LC-MS: m/z=605.3 [M+1]+.
  • 233 (100 mg, 0.16 mmol) was dissolved in MeOH (5 ml), Re(CO)5Cl (90 mg, 0.25 mmol) was added and the mixture was stirred at 80° C. overnight. The solvent was evaporated and the residue was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to get the product 234 (20 mg, 14%) as a white solid. LC-MS: m/z=875.0[M+1]+. 1H NMR (400 MHz, MeOD) δ 8.83 (d, J=5.2 Hz, 1H), 8.10 (td, J=7.8, 1.3 Hz, 1H), 7.72 (d, J=8.5 Hz, 3H), 7.56 (dd, J=13.3, 7.5 Hz, 3H), 7.07 (d, J=2.4 Hz, 1H), 6.97 (d, J=9.0 Hz, 1H), 6.71 (dd, J=9.0, 2.5 Hz, 1H), 4.67 (d, J=15.6 Hz, 1H), 4.51 (d, J=15.5 Hz, 1H), 3.89 (d, J=17.3 Hz, 1H), 3.84 (s, 3H), 3.63 (s, 2H), 3.52 (ddd, J=31.5, 18.4, 11.2 Hz, 3H), 3.26 (t, J=6.8 Hz, 2H), 2.35 (s, 3H), 1.91-1.67 (m, 2H), 1.65-1.53 (m, 2H), 1.39 (d, J=3.1 Hz, 4H). 13C NMR (101 MHz, MeOD) δ 196.76, 195.90, 181.92, 171.87, 168.59, 159.46, 156.23, 152.15, 140.25, 138.81, 135.75, 134.32, 130.98, 130.82, 128.83, 125.57, 123.60, 114.62, 113.52, 111.33, 101.17, 100.15, 69.68, 67.91, 60.58, 54.85, 38.88, 31.11, 28.89, 26.17, 26.05, 24.79, 12.18.
  • Example 37 Synthesis of Compound 235
  • Figure US20190169084A1-20190606-C00162
  • Compound 233 is prepared as described in Example 36.
  • 233 is converted to 235 via the addition of [99mTc-(H2O)3(CO)3]+ (Isolink® kit; Mallinckrodt, St. Louis, Mo., USA) to a vial containing 100 μg of compound 235 dissolved in 100 μl of water. The yield of radiolabeled conjugate is maximized by adjusting the pH to 7 using 0.1 M HCl prior to heating at 80° C. for 1 hour. After incubation, the metallated complexes are purified by RP-HPLC and the peaks collected into either 100 μl of deionized H2O containing 100 μg of bovine serum albumin solution (BSA, in vitro analysis) or 100 μl of isotonic saline (in vivo analysis). Residual MeCN is evaporated from the solution using a stream of nitrogen.
  • Example 38 Synthesis of Compound 237
  • Figure US20190169084A1-20190606-C00163
  • Intermediate 236:
  • To a solution of 25 (400 mg, 0.81 mmol) and picolinaldehyde (520 mg, 4.86 mmol, 6 eq) in MeOH (20 ml) was added AcOH (0.3 ml), the mixture was stirred at RT for 30 min. NaBH(OAc)3 (687 mg, 3.24 mmol, 4 eq) was added and the mixture was stirred at RT overnight. Water (20 ml) was added and the mixture was extracted with ethyl acetate (3×30 ml). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product, which was purified by column chromatography on silica gel (DCM:MeOH=10:1) to get the product (150 mg, 34%) as a yellow solid. LC-MS: m/z=638.0 [M+1].
  • To a solution of 236 (64 mg, 0.1 mmol) in MeOH (5 ml) was added Re(CO)5Cl (54.3 mg, 0.15 mmol, 1.5 eq), the mixture was stirred at 80° C. overnight. The mixture was then concentrated and purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give the product 237 (20 mg, 23%) as a white solid. LC-MS: m/z=908.1 [M+H]+. 1H NMR (400 MHz, MeOD): δ 8.77-8.76 (d, J=5.5 Hz, 2H), 7.84-7.81 (m, 2H), 7.60 (d, J=8.6 Hz, 2H), 7.48-7.42 (dd, J=20.2, 8.2 Hz, 4H), 7.32-7.21 (m, 2H), 6.96 (d, J=2.4 Hz, 1H), 6.86 (d, J=9.0 Hz, 1H), 6.60-6.57 (dd, J=9.0, 2.5 Hz, 1H), 4.78-4.63 (m, 4H), 3.73 (s, 3H), 3.69-3.59 (m, 2H), 3.52 (s, 2H), 3.16-3.14 (t, J=6.9 Hz, 2H), 2.23 (s, 3H), 1.76 (s, 2H), 1.56-1.42 (m, 2H), 1.32 (s, 4H).
  • Example 39 Synthesis of Compound 238
  • Figure US20190169084A1-20190606-C00164
  • Compound 236 is prepared as described in example 38.
  • 236 is converted to 238 by a procedure similar to the one described in example 37.
  • Example 40 Synthesis of Compound 242
  • Figure US20190169084A1-20190606-C00165
  • Cyclopentadienyltricarbonylrhenium(I) carboxylic acid 241 is synthesized as described by Siden Top, Jean-Sébastien Lehn, Pierre Morel, Gérard Jaouen, J. Organomet. Chem., 583, 63-68, (1999). To a solution of compound 25 (example 6) (0.16 mmol) in DCM (20 ml) was added HOBt (22 mg, 0.16 mmol), EDCI (31 mg, 0.16 mmol), and DIEA (62 mg, 0.48 mmol). The mixture was stirred at RT for 0.5 h, after which 241 (0.16 mmol) was added. The reaction mixture was stirred at RT overnight. The mixture was then diluted with water (30 ml) and extracted with EtOAc (25 ml×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated and purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water, B: MeCN) to give the desired product 242.
  • 1H NMR (400 MHz, MeOD) δ 8.03 (s, 1H), 7.72 (d, J=8.5 Hz, 2H), 7.58 (d, J=8.5 Hz, 2H), 7.04 (d, J=2.4 Hz, 1H), 6.95 (d, J=9.0 Hz, 1H), 6.69 (dd, J=9.0, 2.4 Hz, 1H), 6.17 (t, J=4.0 Hz, 2H), 5.57 (t, J=4.0 Hz, 2H), 3.82 (s, 3H), 3.63 (s, 2H), 3.24-3.18 (m, 4H), 2.34 (s, 3H), 1.61-1.44 (m, 4H), 1.41-1.27 (m, 4H). MS (ESI) m/z: 818.0[M+H+].
  • The following compounds 243-251 can also be prepared according to the procedure given in Example 40 by replacing compound 25 with the appropriate intermediate (synthesis described in examples 5, 31, and 32).
  • Figure US20190169084A1-20190606-C00166
  • Compound Y =
    243
    Figure US20190169084A1-20190606-C00167
    244
    Figure US20190169084A1-20190606-C00168
    245
    Figure US20190169084A1-20190606-C00169
    246
    Figure US20190169084A1-20190606-C00170
    247
    Figure US20190169084A1-20190606-C00171
    248
    Figure US20190169084A1-20190606-C00172
    249
    Figure US20190169084A1-20190606-C00173
    250
    Figure US20190169084A1-20190606-C00174
    251
    Figure US20190169084A1-20190606-C00175
  • Compound 243
  • 1H NMR (400 MHz, DMSO-d6) δ 8.31 (t, J=5.2 Hz, 1H), 8.07 (t, J=5.2 Hz, 1H), 7.67 (dd, J=22.2, 8.6 Hz, 4H), 7.09 (d, J=2.4 Hz, 1H), 6.94 (d, J=9.0 Hz, 1H), 6.70 (dd, J=9.0, 2.5 Hz, 1H), 6.20 (t, J=2.2 Hz, 2H), 5.76-5.68 (m, 2H), 3.76 (s, 3H), 3.50 (s, 2H), 3.23-3.09 (m, 4H), 2.22 (s, 3H). MS (ESI) m/z: 762.0 [M+H+].
  • Compound 244
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.5 Hz, 2H), 7.50 (d, J=6.9 Hz, 2H), 6.91 (d, J=2.3 Hz, 1H), 6.88 (d, J=9.0 Hz, 1H), 6.71 (dd, J=9.0, 2.3 Hz, 2H), 6.12 (t, J=2.0 Hz, 2H), 5.95 (s, 1H), 5.34 (t, J=2.0 Hz, 2H), 3.83 (s, 3H), 3.68 (s, 2H), 3.53-3.35 (m, 8H), 2.39 (s, 3H). MS (ESI) m/z: 806.0[M+H+].
  • Compound 245
  • 1H NMR (400 MHz, CDCl3) δ 7.63 (d, J=8.2 Hz, 3H), 7.50 (d, J=8.3 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 7.04 (d, J=8.9 Hz, 1H), 6.84-6.73 (m, 4H), 6.12 (s, 2H), 5.45 (s, 2H), 5.32 (s, 1H), 3.83 (s, 3H), 3.55 (s, 2H), 3.44 (s, 2H), 2.66 (s, 2H), 2.14 (s, 3H). MS (ESI) m/z: 860.0 [M+H+].
  • Compound 246
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.4 Hz, 2H), 7.50 (d, J=8.4 Hz, 2H), 6.87 (d, J=9.3 Hz, 2H), 6.71 (dd, J=9.0, 2.2 Hz, 1H), 6.01 (s, 1H), 5.96 (s, 2H), 5.61 (s, 1H), 5.34 (s, 2H), 3.82 (s, 3H), 3.64 (s, 2H), 3.31 (d, J=5.7 Hz, 2H), 3.21 (d, J=5.9 Hz, 2H), 2.39 (s, 3H), 1.42 (m, 4H), 1.22 (m, 6H). MS (ESI) m/z: 832.2 [M+H+].
  • Compound 247
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=7.9 Hz, 2H), 7.49 (d, J=7.7 Hz, 2H), 6.87 (d, J=9.1 Hz, 2H), 6.70 (d, J=8.0 Hz, 1H), 5.90 (s, 2H), 5.61 (s, 1H), 5.32 (d, J=16.8 Hz, 3H), 3.82 (s, 3H), 3.64 (s, 2H), 3.25 (dd, J=41.8, 5.8 Hz, 4H), 2.39 (s, 3H), 1.59-1.23 (m, 8H). MS (ESI) m/z: 846.2[M+H+].
  • Compound 248
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.5 Hz, 2H), 7.50 (t, J=7.8 Hz, 2H), 6.93-6.86 (m, 2H), 6.70 (dd, J=9.0, 2.4 Hz, 1H), 6.61 (s, 1H), 6.08 (s, 1H), 5.96 (s, 2H), 5.31 (t, J=4.0 Hz, 2H), 3.82 (s, 3H), 3.65 (s, 2H), 3.59-3.37 (m, 16H), 2.38 (s, 3H). MS (ESI) m/z: 894.2 [M+H+].
  • Compound 249
  • 1H NMR (400 MHz, CDCl3) δ 7.64 (d, J=8.5 Hz, 2H), 7.47 (d, J=8.5 Hz, 2H), 7.17 (d, J=8.0 Hz, 2H), 7.09 (d, J=8.0 Hz, 2H), 6.84 (dd, J=5.7, 3.2 Hz, 2H), 6.68 (dd, J=9.1, 2.4 Hz, 1H), 6.09 (t, J=4.0 Hz, 1H), 5.96-5.89 (m, 3H), 5.35 (t, J=4.0 Hz, 2H), 4.46 (d, J=5.6 Hz, 2H), 4.35 (d, J=5.9 Hz, 2H), 3.78 (s, 3H), 3.68 (s, 2H), 2.36 (s, 3H). MS (ESI) m/z: 838.0 [M+H+].
  • Compound 250
  • 1H NMR (400 MHz, CDCl3) 6 7.68 (d, J=8.3 Hz, 2H), 7.50 (d, J=8.3 Hz, 2H), 7.04 (s, 1H), 6.87 (d, J=9.6 Hz, 2H), 6.72 (d, J=9.1 Hz, 1H), 6.10 (s, 2H), 5.83 (s, 1H), 5.34 (s, 2H), 3.83 (s, 3H), 3.67 (s, 2H), 3.39 (s, 2H), 3.26 (s, 2H), 2.39 (s, 3H), 1.51 (s, 3H). MS (ESI) m/z: 790.0 [M+H+].
  • Compound 251
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.50 (d, J=8.5 Hz, 2H), 6.91 (d, J=2.3 Hz, 1H), 6.86 (d, J=9.0 Hz, 1H), 6.70 (dd, J=9.0, 2.4 Hz, 1H), 6.60 (s, 1H), 6.00 (m, 3H), 5.33 (t, J=4.0 Hz, 2H), 3.82 (s, 3H), 3.65 (s, 2H), 3.46 (m, 12H), 2.40 (s, 3H). MS (ESI) m/z: 850.1 [M+H+].
  • Example 41 Synthesis of Compound 254
  • Figure US20190169084A1-20190606-C00176
  • To a solution of compound 25 (example 6) (0.16 mmol) in DCM (20 ml) is added HOBt (22 mg, 0.16 mmol), EDCI (31 mg, 0.16 mmol), and DIEA (62 mg, 0.48 mmol). The mixture was stirred at RT for 0.5 h, after which 252 (CAS No. 1271-42-7, Sigma-Aldrich, Saint Louis, Mo., USA; catalog no. 106887; 0.16 mmol) is added. The reaction mixture is stirred at RT overnight. The mixture is then diluted with water and extracted with EtOAc (25 ml×3). The combined organic layers are washed with brine (15 ml×2), dried over Na2SO4, filtered and the filtrate is concentrated and purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water, B: MeCN) to give the desired product 253.
  • 253 can be converted into the Tc complex 254 as described in the literature, see e.g. Bioorg. Med. Chem. Letters 22 (2012) 6352-6357; J. Med. Chem. (2007), 50, 543-549; J. Med. Chem. (2013), 56, 471-482; J. Med. Chem. (2014), 57, 7113-7125.
  • Example 42 Synthesis of Compound 260
  • Figure US20190169084A1-20190606-C00177
  • Compound 255 is made according to the procedure in: Ziv, Ilan et al., WO 2003/101948 and Mahmood, A., et al., WO 2001/083436. Compound 255 is alkylated with 1-bromo-6-chlorohexane to form 256 as previously described in: Mahmood, A.; et al., “Functionalized tetradentate chelates and their Technetium and Rhenium complexes: synthesis spectroscopy and structural characterization”, in Technetium and Rhenium in chemistry and nuclear medicine 5, pp. 253-257 (Nicolini, M. et al.) and also in Mahmood, A., et al., WO 2001/083436. Compound 256 is treated with ammonia in methanol at rt to give amine 257.
  • To a solution of indomethacin (57 mg, 0.16 mmol) in DCM (20 ml) was added HOBt (22 mg, 0.16 mmol), EDCI (31 mg, 0.16 mmol), and DIEA (62 mg, 0.48 mmol). The mixture was stirred at RT for 0.5 h, after which (257) (85 mg, 0.16 mmol) was added. The reaction mixture was stirred at RT overnight. The mixture was then diluted with water (30 ml) and extracted with EtOAc (25 ml×3). The combined organic layers were washed with brine (15 ml×2), dried over Na2SO4, filtered and the filtrate was concentrated to give the free dithiol 259.
  • Compound 259 is dissolved in DCM and treated with TFA in presence of 5 eq. of Et3SiH at 80° C. for 4 h. The volatiles are removed by lyophilizing overnight. To a stirred solution of the residue (100 mg, 0.14 mmol) in NMP (15 mL), (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 106 mg, 0.127 mmol) was added. The mixture was stirred at 80° C. for 16 h. The solution was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: Water, NH4HCO3, solvent B: MeCN) to give compound 260 as a solid.
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.5 Hz, 2H), 7.50 (d, J=8.5 Hz, 2H), 6.91-6.83 (m, 2H), 6.71 (d, J=9.0, 2.4 Hz, 1H), 5.60 (s, 1H), 4.65-4.53 (m, 2H), 4.15-4.03 (m, 2H), 3.94-3.86 (m, 1H), 3.83 (s, 3H), 3.65 (s, 2H), 3.49-3.39 (m, 1H), 3.40-3.11 (m, 6H), 2.85 (dd, J=13.4, 4.2 Hz, 1H), 2.40 (s, 3H), 1.62-1.51 (m, 2H), 1.48-1.38 (m, 2H), 1.37-1.19 (m, 4H). MS (ESI) m/z: 855.0 (M+Na+)
  • The following compounds 261-269 can also be prepared according to the procedure given in Example 42 by replacing 1-bromo-6-chloro-hexane in Example 42 with the appropriate dihalide.
  • Figure US20190169084A1-20190606-C00178
  • Compound Y =
    261
    Figure US20190169084A1-20190606-C00179
    262
    Figure US20190169084A1-20190606-C00180
    263
    Figure US20190169084A1-20190606-C00181
    264
    Figure US20190169084A1-20190606-C00182
    265
    Figure US20190169084A1-20190606-C00183
    266
    Figure US20190169084A1-20190606-C00184
    267
    Figure US20190169084A1-20190606-C00185
    268
    Figure US20190169084A1-20190606-C00186
    269
    Figure US20190169084A1-20190606-C00187
  • Compound 261
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.4 Hz, 2H), 7.50 (d, J=8.3 Hz, 2H), 6.87 (d, J=9.5 Hz, 1H), 6.78-6.64 (m, 1H), 5.77 (s, 1H), 4.70-4.42 (m, 2H), 4.07 (dd, J=10.8, 4.5 Hz, 1H), 3.97 (d, J=16.5 Hz, 1H), 3.83 (s, 3H), 3.67 (s, 2H), 3.56-3.42 (m, 1H), 3.38-2.95 (m, 6H), 2.81 (dd, J=13.6, 4.1 Hz, 1H), 2.40 (s, 3H), 1.85-1.40 (m, 5H). MS (ESI) m/z: 805.0(M+H+)
  • Compound 262
  • 1H NMR (400 MHz, CDCl3) δ 7.69 (d, J=8.2 Hz, 2H), 7.50 (d, J=8.3 Hz, 2H), 6.92-6.85 (m, 2H), 6.72 (s, 1H), 6.02 (s, 1H), 4.57-4.55 (m, 1H), 4.46-4.41 (m, 1H), 4.11-4.08 (m, 1H), 3.84-3.80 (m, 5H), 3.68-3.52 (m, 5H), 3.51-3.41 (m, 4H), 3.41-3.09 (m, 4H), 2.66 (d, J=12.8 Hz, 1H), 2.42 (d, J=4.1 Hz, 3H). MS (ESI) m/z: 843.0 (M+Na+).
  • Compound 263
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.3 Hz, 2H), 7.50 (d, J=8.4 Hz, 2H), 6.90-6.78 (m, 2H), 6.72 (d, J=9.1 Hz, 1H), 5.73 (s, 1H), 4.70-4.49 (m, 2H), 4.19-4.00 (m, 2H), 3.83 (s, 3H), 3.78 (s, 1H), 3.69 (s, 2H), 3.45-3.05 (m, 7H), 2.85 (dd, J=13.2, 4.1 Hz, 1H), 2.41 (s, 3H), 1.87-1.66 (m, 2H), 1.62-1.45 (m, 2H), 1.31-1.15 (m, 2H). MS (ESI) m/z: 840.9 (M+Na+).
  • Compound 264
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.2 Hz, 2H), 7.50 (d, J=7.8 Hz, 2H), 6.96-6.79 (m, 2H), 6.71 (d, J=8.8 Hz, 2H), 5.58 (s, 1H), 4.70-4.51 (m, 2H), 4.20-4.01 (m, 2H), 3.98-3.88 (m, 1H), 3.82 (s, 1H), 3.64 (s, 1H), 3.52-3.41 (m, 1H), 3.40-3.04 (m, 6H), 2.85 (d, J=9.7 Hz, 1H), 2.40 (s, 3H), 1.85-1.67 (m, 2H), 1.47-1.37 (m, 2H), 1.37-1.12 (m, 6H). MS (ESI) m/z: 847.1 (M+H+).
  • Compound 265
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.49 (d, J=8.5 Hz, 2H), 6.87 (dd, J=8.8, 5.7 Hz, 2H), 6.70 (dd, J=9.0, 2.4 Hz, 1H), 5.58 (t, J=5.7 Hz, 1H), 4.71-4.51 (m, 2H), 4.16-4.02 (m, 2H), 4.00-3.88 (m, 1H), 3.82 (s, 3H), 3.64 (s, 2H), 3.55-3.42 (m, 1H), 3.41-3.30 (m, 1H), 3.29-3.08 (m, 5H), 2.85 (dd, J=13.4, 4.3 Hz, 1H), 2.39 (s, 3H), 1.85-1.66 (m, 2H), 1.64-1.56 (m, 2H), 1.46-1.35 (m, 2H), 1.36-1.12 (m, 8H). MS (ESI) m/z: 883.4 (M+Na+).
  • Compound 266
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.2 Hz, 2H), 7.54-7.44 (m, 2H), 6.99-6.85 (m, 2H), 6.74 (d, J=9.3 Hz, 1H), 6.11 (s, 1H), 4.70-4.49 (m, 2H), 4.22-4.01 (m, 4H), 3.84 (d, J=3.3 Hz, 4H), 3.71 (s, 2H), 3.59-3.12 (m, 10H), 2.87 (d, J=13.5 Hz, 1H), 2.35 (s, 3H), 1.91 (s, 2H), 1.66-1.54 (m, 2H). MS (ESI) m/z: 849.1 (M+H+).
  • Compound 267
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.50 (d, J=7.8 Hz, 2H), 6.92-6.81 (m, 2H), 6.71 (dd, J=9.0, 2.5 Hz, 1H), 5.88 (s, 1H), 4.75 (d, J=16.9 Hz, 1H), 4.63-4.51 (m, 1H), 4.20 (d, J=16.8 Hz, 1H), 4.14-4.05 (m, 1H), 4.04-3.94 (m, 1H), 3.84 (s, J=16.4 Hz, 3H), 3.78 (s, 1H), 3.72-3.57 (m, 5H), 3.55-3.06 (m, 8H), 2.97-2.69 (m, 1H), 2.40 (s, 3H), 1.86-1.68 (m, 2H). MS (ESI) m/z: 835.1(M+H+).
  • Compound 268
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=7.5 Hz, 2H), 7.50 (d, J=7.6 Hz, 2H), 7.03-6.93 (m, 1H), 6.90 (s, 1H), 6.73 (d, J=8.6 Hz, 1H), 4.72 (d, J=11.8 Hz, 1H), 4.59 (d, J=6.4 Hz, 1H), 4.22-3.94 (m, 3H), 3.83 (s, 3H), 3.66 (s, 3H), 3.45 (d, J=38.6 Hz, 3H), 3.33-3.06 (m, 3H), 2.88 (s, 3H), 2.37 (s, 5H), 2.01 (s, 2H), 1.66 (s, 2H). MS (ESI) m/z: 897.1(M+H+).
  • Compound 269
  • 1H NMR (400 MHz, CDCl3) 6 7.65 (d, J=8.4 Hz, 2H), 7.47 (d, J=8.4 Hz, 2H), 6.95 (s, 2H), 6.89 (d, J=9.0 Hz, 1H), 6.69 (dd, J=8.9, 2.1 Hz, 1H), 4.68 (d, J=17.4 Hz, 1H), 4.43-4.32 (m, 1H), 4.17 (d, J=17.4 Hz, 1H), 4.09-3.98 (m, 1H), 3.95-3.76 (m, 6H), 3.76-3.70 (m, 1H), 3.66 (d, J=6.5 Hz, 2H), 3.62-3.41 (m, 7H), 3.36-3.21 (m, 3H), 3.17-3.05 (m, 2H), 2.80 (dd, J=12.8, 4.0 Hz, 1H), 2.37 (s, 1H). MS (ESI) m/z: 886.9 (M+Na+).
  • Example 43 Synthesis of Compound 270
  • Figure US20190169084A1-20190606-C00188
  • Compound 270 is synthesized by reacting 259 (example 42) with 99mTc-glucoheptonate as described in: Mahmood, A., et al., WO 2001/083436.
  • Example 44 Synthesis of Compound 275
  • Figure US20190169084A1-20190606-C00189
  • Compound 255 is made according to the procedure in: Ziv, Ilan et al., WO 2003/101948 and Mahmood, A., et al., WO 2001/083436. 255 is reduced with LiAlH4 and Boc-protected to give compound 271 according to the procedure described in Ono, M., et al., ACS Chem. Neurosci., 1, 598-607, (2010).
  • Intermediate 272
  • To a solution of indomethacin (2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid, 1.5 g, 4.2 mmol) in DMF (20 mL) was added 6-aminohexan-1-ol (589 mg, 5.04 mmol), HOBt (1.02 g, 7.56 mmol), EDCI (1.45 g, 7.56 mmol) and DIPEA (2.16 g, 16.8 mmol). The resulting solution was stirred RT overnight by which time LCMS showed completion of the reaction. Then water was added (80 mL), and the mixture was extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine, dried over Na2SO4 filtered and the filtrate was concentrated to obtain the product (1.5 g, yield: 78%) as a light yellow solid.
  • Intermediate 273
  • To a solution of 272 (1.5 g, 3.28 mmol) in DCM (30 ml) was added Dess-Martin periodinane (1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benziodoxol-3-(1H)-one, 2.09 g, 4.93 mmol) at 0° C. The resulting solution was stirred RT for 2 h, then a sat'd. aq. solution of Na2S2O3 (10 mL), was added. The mixture was extracted with DCM (20 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to get the crude product 273 (1.2 g, yield: 81%) as a yellow solid which was used in the next step without further purification.
  • Intermediate 274
  • To a solution of 273 (1.2 g, 2.64 mmol) in MeOH (30 mL) was added compound 271 (1.0 g, 1.98 mmol), and 1 mL of CH3COOH. The resulting solution was stirred at rt for 0.5 h. Then, NaBH3CN (332 mg, 5.28 mmol) was added and the mixture was stirred for another 2 h. Then the reaction was quenched with water (20 mL) and extracted with DCM (30 mL×4). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product, which was purified by chromatography on silica gel (DCM:MeOH=50:1) to get the product 274 (1.2 g yield: 63%) as a yellow oil.
  • Compound 275
  • To a solution of 274 (1.2 g, 1.26 mmol) in TFA (20 mL) was added Et3SiH (220 mg, 1.9 mmol). The resulting mixture was stirred at 80° C. for 2 h. Then volatiles were removed and the residue was dissolved in NMP (10 mL). (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 1.0 eq) was added and the mixture was stirred at 80° C. overnight. The reaction was concentrated and the residue was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give 275 as a light pink solid (80 mg, 8% yield over both steps).
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.4 Hz, 2H), 7.50 (d, J=8.4 Hz, 2H), 6.98-6.80 (m, 2H), 6.70 (dd, J=9.0, 2.3 Hz, 1H), 5.61 (s, 1H), 4.12 (dt, J=12.7, 6.3 Hz, 2H), 3.99 (dd, J=18.6, 7.5 Hz, 2H), 3.91-3.73 (m, 5H), 3.64 (s, 2H), 3.51-3.16 (m, 7H), 3.11-2.88 (m, 2H), 2.82-2.61 (m, 1H), 2.40 (s, 3H), 1.69 (dd, J=11.9, 7.1 Hz, 2H), 1.51-1.36 (m, 2H), 1.29 (s, 4H). MS (ESI) m/z: 818.9 [M+H+].
  • Example 45 Synthesis of Compound 276
  • Figure US20190169084A1-20190606-C00190
  • 274 is converted into the dithiol by reacting with TFA and Et3SiH as described for compound 275. The 99mTc complex 276 is prepared by a ligand exchange reaction employing 99mTc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci., 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748, (2010).
  • Example 46 Synthesis of Compound 283
  • Figure US20190169084A1-20190606-C00191
  • Compound 277 can be transformed to 278 by reacting 277 with di-tert-butyldicarbonate in the presence of a base such as NaHCO3 or aq. NaOH. The nitrile 279 is obtained using a procedure similar to the one described in: Mizuno, A.; Hamada, Y.; Shioiri, T., Synthesis 1007, (1980). The nitrile is reduced with hydrogen in presence of a catalyst, such as Raney®-Nickel (W.R. Grace and Co.) in a solvent such as methanol or tert-butanol to give amine 280. Indomethacin is coupled to compound 280 as described in example 5 and treated with TFA to give the amide 281. 281 is coupled with the S-benzoyl-protected thioglycolic acid using DCC as the coupling agent to afford ligand 282. 283 is made following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • Example 47 Synthesis of Compound 284
  • Figure US20190169084A1-20190606-C00192
  • The Technetium complex 284 is prepared from compound 282 (example 46) as described in: Eisenhut, M., et al., J. Med. Chem., 45, 5802-5805, (2002).
  • Example 48 Synthesis of compound 286
  • Figure US20190169084A1-20190606-C00193
  • Compound 282 (Example 46) is reduced with LiAlH4 in a solvent such as THF to give compound 285. 286 is prepared from 285 following the procedure in Ono, et al. Bioorg. Med. Chem. Lett. (2010), 20, 5743-5748.
  • Example 49 Synthesis of Compound 287
  • Figure US20190169084A1-20190606-C00194
  • The Technetium complex 287 is prepared from compound 285 (example 48) as described in: Eisenhut, M., et al., J. Med. Chem., 45, 5802-5805, (2002).
  • Example 50 Synthesis of Compounds 290 and 291
  • Figure US20190169084A1-20190606-C00195
  • Compound 281 (Example 46) is coupled with tert-butyl bromoacetate in presence of a base, such as NaH, to afford compounds 288 and 289, which are separated by column chromatography on silica gel. 288 is transformed to 290 by treating with TFA in DCM followed by reaction with Re(CO)5Cl by a procedure similar to the one described in Example 36. Similarly, 291 can be obtained form 289.
  • Example 51 Synthesis of Compounds 292 and 293
  • Figure US20190169084A1-20190606-C00196
  • 288 and 289 are converted to 292 and 293, respectively, by a procedure similar to the one described in example 37.
  • Example 52 Synthesis of Compound 297
  • Figure US20190169084A1-20190606-C00197
  • Intermediate 294
  • To the mixture of 18 (1.07 g, 3 mmol) and NH4Cl (318 mg, 6 mmol) in DMF (40 ml) was added HOBt (607 mg, 4.5 mmol), EDCI (864 mg, 4.5 mmol) and DIPEA (1.6 ml, 9 mmol). The resulting mixture was stirred at room temperature overnight. Water (100 ml) was added and the product was extracted with EtOAc (2×100 ml). The combined organic layers were dried over Na2SO4, and the solvent was removed under reduced pressure to give the product without further purification as a yellow oil (1 g, 93.6%). LC-MS: m/z=357.1 [M+H]+
  • Intermediate 295
  • To the solution of compound 294 (1 g, 2.8 mmol) in DCM (20 ml) was added TEA (606 mg, 6 mmol) and TFAA (2.1 g, 10 mmol) at 0° C. The resulting solution was stirred at RT for 1 h. The reaction solution was concentrated under reduced pressure to give a yellow solid. The crude solid was washed with hexane (50 ml) to give the product 295 as a yellow solid (700 mg, 74%). LC-MS: m/z=339.2 [M+H]+
  • Intermediate 296
  • The mixture of compound 295 (700 mg, 2.07 mmol) and Raney®-Nickel (W.R. Grace and Co., 100 mg) in THF/MeOH (5 ml/20 ml) was stirred under a hydrogen atmosphere overnight. The catalyst was removed by filtering through a column of Celite® (J.T. Baker, Phillipsberg, N.J., diatomaceous earth) and the filtrate was concentrated under reduced pressure to give the crude product, which was purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: water/solvent B: MeCN) to give the product as light yellow solid (500 mg, 70%). LC-MS: m/z=343.1 [M+H]+.
  • To a solution of compound 296 (171 mg, 0.5 mmol) and compound 241 (191 mg, 0.5 mmol) in DMF (15 ml) was added HOBt (135 mg, 1 mmol), EDCI (192 mg, 1 mmol) and DIPEA (258 mg, 2 mmol). The resulting solution was stirred at rt overnight. The reaction was quenched with saturated NaHCO3 solution (30 ml) and extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with brine (30 ml), dried over Na2SO4, concentrated, and purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: water/solvent B: MeCN) to give the compound 297 as a light yellow solid (20 mg, 6%). LC-MS: m/z=343.2 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ 8.42 (t, J=5.8 Hz, 1H), 7.65 (q, J =8.6 Hz, 3H), 7.10 (d, J=2.3 Hz, 1H), 7.01 (d, J=9.0 Hz, 1H), 6.72 (dd, J=9.0, 2.4 Hz, 1H), 6.23 (t, J=2.1 Hz, 2H), 5.93-5.55 (m, 2H), 3.78 (s, 3H), 3.46-3.33 (m, 2H), 2.82 (t, J=6.8 Hz, 2H), 2.15 (s, 3H).
  • Example 53 Synthesis of Compound 299
  • Figure US20190169084A1-20190606-C00198
  • Compound 299 is prepared from compound 296 (example 52) by a procedure similar to the one described in Example 41.
  • Example 54 Synthesis of Compound 301
  • Figure US20190169084A1-20190606-C00199
  • Compound 296 is transformed into the imine 300 by a procedure similar to the one described for compound 220 in example 35. 300 is converted into the Rhenium complex 301 as described in example 36.
  • Alternatively, compound 301 can be prepared as follows: A mixture of 296 (100 mg, 0.29 mmol), picolinaldehyde (31 mg, 0.29 mmol) and Re(CO)5Cl (105 mg, 0.29 mmol) in MeOH (10 mL) was stirred at 75° C. for 3 h, then cooled to rt. The precipitate was filtered and washed with MeOH (2×20 ml), and dried to give compound 301 as a yellow solid (51 mg, 23%). LC-MS: m/z=759.9 [M+H]; 1H NMR (400 MHz, DMSO-d6) δ 9.32 (s, 1H), 9.06 (d, J=5.2 Hz, 1H), 8.36 (t, J=7.7 Hz, 1H), 8.27 (d, J=7.5 Hz, 1H), 7.92-7.76 (m, 1H), 7.68 (dd, J=28.7, 8.4 Hz, 4H), 7.23 (d, J=2.1 Hz, 1H), 7.03 (d, J=9.0 Hz, 1H), 6.76 (dd, J=9.0, 2.2 Hz, 1H), 4.21 (t, J=7.9 Hz, 2H), 3.77 (s, 3H), 3.43-3.02 (m, 2H), 2.27 (s, 3H).
  • Example 55 Synthesis of Compound 302
  • Figure US20190169084A1-20190606-C00200
  • Compound 300 (example 54) is converted to 302 by a procedure similar to the one described in example 37.
  • The following compounds 303-307 can be prepared according to the procedure given in Example 44 by replacing 6-aminohexan-1-ol with the appropriate aminoalcohol.
  • Figure US20190169084A1-20190606-C00201
  • Compound Y =
    303
    Figure US20190169084A1-20190606-C00202
    304
    Figure US20190169084A1-20190606-C00203
    305
    Figure US20190169084A1-20190606-C00204
    306
    Figure US20190169084A1-20190606-C00205
    307
    Figure US20190169084A1-20190606-C00206
  • Compound 303
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.2 Hz, 2H), 7.50 (d, J=8.3 Hz, 2H), 7.01-6.83 (m, 2H), 6.77-6.63 (m, 1H), 5.78 (s, 1H), 4.22-4.00 (m, 2H), 3.98-3.58 (m, 8H), 3.59-3.06 (m, 8H), 2.96 (td, J=11.7, 6.5 Hz, 1H), 2.81 (d, J=11.4 Hz, 1H), 2.74-2.52 (m, 1H), 2.39 (s, 3H), 1.78-1.64 (m, 2H), 1.46 (d, J=22.8 Hz, 2H). MS (ESI) m/z: 791.0 [M+H].
  • Compound 304
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.3 Hz, 2H), 7.49 (d, J=8.2 Hz, 2H), 6.99-6.77 (m, 2H), 6.71 (dd, J=9.0, 1.9 Hz, 1H), 5.71 (d, J=5.5 Hz, 1H), 4.26-4.07 (m, 2H), 4.02-3.89 (m, 1H), 3.85 -3.71 (m, 5H), 3.64 (s, 2H), 3.51 -3.13 (m, 8H), 3.09-2.87 (m, 2H), 2.71 (dd, J=13.1, 3.2 Hz, 1H), 2.40 (s, 3H), 1.89-1.70 (m, 2H), 1.59-1.46 (m, 2H), 1.32-1.19 (m, 2H). MS (ESI) m/z: 805.0 [M+H].
  • Compound 305
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.49 (d, J=8.5 Hz, 2H), 6.99-6.78 (m, 2H), 6.70 (dd, J=9.1, 2.3 Hz, 1H), 5.59 (s, 1H), 4.27 -3.92 (m, 4H), 3.90-3.71 (m, 5H), 3.64 (s, 2H), 3.55-3.14 (m, 7H), 3.06-2.88 (m, 2H), 2.79-2.65 (m, 1H), 2.39 (s, 3H), 1.81-1.68 (m, 2H), 1.41 (dt, J=14.5, 7.3 Hz, 2H), 1.35-1.13 (m, 6H). MS (ESI) m/z: 833.2 [M+H+].
  • Compound 306
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.4 Hz, 2H), 7.49 (d, J=8.4 Hz, 2H), 7.10-6.79 (m, 2H), 6.71 (dd, 1H), 5.89 (s, 1H), 4.22 -3.97 (m, 3H), 3.97 -3.74 (m, 5H), 3.63 (s, 2H), 3.58 -3.07 (m, 11H), 3.05 -2.94 (m, 1H), 2.89 (d, J=11.6 Hz, 1H), 2.71 (d, J=9.5 Hz, 2H), 2.36 (s, 3H), 1.98-1.83 (m, 2H), 1.78-1.66 (m, 2H). MS (ESI) m/z: 835.1 [M+H+].
  • Compound 307
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.3 Hz, 2H), 7.50 (d, J=8.3 Hz, 2H), 7.05-6.78 (m, 2H), 6.71 (d, J=8.9 Hz, 1H), 5.60 (s, 1H), 4.36-3.94 (m, 3H), 3.94-3.71 (m, 5H), 3.64 (s, 2H), 3.58-3.43 (m, 1H), 3.40-3.08 (m, 6H), 3.09-2.89 (m, 2H), 2.84-2.65 (m, 1H), 2.40 (s, 3H), 2.13-1.88 (m, 1H), 1.85-1.60 (m, 2H), 1.44-1.34 (m, 2H), 1.14-0.90 (m, 6H). MS (ESI) m/z: 833.1 [M+H+].
  • The following compounds 308-313 can also be prepared according to the procedure given in Example 40 by replacing compound 25 with the appropriate intermediate (synthesis described in examples 5, 31, and 32).
  • Figure US20190169084A1-20190606-C00207
  • Compound Y =
    308
    Figure US20190169084A1-20190606-C00208
    309
    Figure US20190169084A1-20190606-C00209
    310
    Figure US20190169084A1-20190606-C00210
    311
    Figure US20190169084A1-20190606-C00211
    312
    Figure US20190169084A1-20190606-C00212
    313
    Figure US20190169084A1-20190606-C00213
  • Compound 308
  • 1H NMR (400 MHz, CDCl3) δ 7.66 (d, J=8.1 Hz, 2H), 7.49 (d, J=8.1 Hz, 2H), 6.88 (d, J=8.8 Hz, 2H), 6.71 (d, J=8.8 Hz, 1H), 6.48 (s, 1H), 6.09 (s, 2H), 5.81 (s, 1H), 5.33 (s, 2H), 3.82 (s, 3H), 3.65 (s, 2H), 3.33-3.19 (m, 4H), 2.38 (s, 3H), 1.61-1.51 (m, 2H), 1.48-1.40 (m, 2H), 1.36-1.23 (m, 2H). MS (ESI) m/z: 804.0 [M+H+].
  • Compound 309
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.1 Hz, 2H), 7.49 (d, J=8.1 Hz, 2H), 6.87 (d, J=9.4 Hz, 2H), 6.71 (d, J=8.1 Hz, 2H), 6.00 (s, 2H), 5.85 (s, 1H), 5.31 (s, 2H), 3.83 (s, 3H), 3.64 (s, 2H), 3.32 (s, 2H), 3.19 (s, 2H), 2.39 (s, 3H), 1.50 (s, 2H), 1.44-1.37 (m, 2H), 0.87 (s, 6H). MS (ESI) m/z: 832.2 [M+H].
  • Compound 310
  • 1H NMR (400 MHz, CDCl3) 6 7.67 (d, J=8.2 Hz, 2H), 7.49 (d, J=8.3 Hz, 2H), 7.41 (s, 1H), 6.91 (d, J=9.2 Hz, 2H), 6.72 (d, J=8.9 Hz, 1H), 6.20 (s, 2H), 5.99 (s, 1H), 5.30 (s, 2H), 3.82 (s, 3H), 3.67 (s, 2H), 3.48-3.33 (m, 8H), 2.38 (s, 3H), 1.66 (d, J=23.4 Hz, 4H). MS (ESI) m/z: 834.2 [M+H+].
  • Compound 311
  • 1H NMR (400 MHz, CDCl3) δ 7.71 (d, J=8.5 Hz, 2H), 7.50 (d, J=8.5 Hz, 2H), 6.93-6.89 (m, 2H), 6.72 (dd, J=9.0, 2.4 Hz, 1H), 5.84 (t, J=2.2 Hz, 2H), 5.77 (s, 1H), 5.57 (s, 1H), 5.34 (t, J=2.2 Hz, 2H), 3.84 (s, 3H), 3.66 (s, 2H), 3.23 (dd, J=12.8, 6.7 Hz, 2H), 2.41 (s, 3H), 1.46-1.24 (m, 10H). MS (ESI) m/z: 818.1 [M+H+].
  • Compound 312
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.5 Hz, 2H), 7.49 (d, J=8.5 Hz, 2H), 6.88 (t, J=5.5 Hz, 2H), 6.70 (dd, J=9.0, 2.4 Hz, 1H), 6.10 (s, 2H), 5.92 (s, 1H), 5.76 (s, 1H), 5.34 (d, J=1.9 Hz, 2H), 3.82 (s, 3H), 3.65 (s, 2H), 3.24 (d, J=6.1 Hz, 2H), 2.39 (s, 3H), 1.71-1.63 (m, 2H), 1.58 (s, 2H), 1.46-1.38 (m, 1H), 1.36-1.23 (m, 8H). MS (ESI) m/z: 832.1 [M+H+].
  • Compound 313
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=7.6 Hz, 2H), 7.49 (d, J=7.6 Hz, 2H), 6.87 (d, J=9.0 Hz, 2H), 6.70 (d, J=8.9 Hz, 1H), 5.87 (s, 2H), 5.71 (s, 1H), 5.44 (s, 1H), 5.32 (s, 2H), 3.83 (s, 3H), 3.65 (s, 2H), 3.32 (s, 2H), 2.40 (s, 3H), 1.40 (m, 14H). MS (ESI) m/z: 846.1 [M+H+].
  • Example 56 Synthesis of Compound 320
  • Figure US20190169084A1-20190606-C00214
    Figure US20190169084A1-20190606-C00215
  • Intermediate 314
  • To a solution of propane-1,3-diamine (5.0 g, 67.5 mmol) in 100 mL of MeOH:THF (2:1) was slowly added a solution of Boc2O (7.4 g, 33.8 mmol) in THF (20 mL) at 0° C. The reaction mixture was allowed to stir at room temperature overnight. LCMS showed the reaction was completed, the solvent was evaporated, water (100 mL) was added, and the mixture was extracted with DCM (100 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated in vacuum to give tert-butyl (3-aminopropyl)carbamate as a colorless oil (1.8 g, yield: 32%). A mixture of tert-butyl (3-aminopropyl)carbamate (5.22 g, 30 mmol), 3-chloropropan-1-ol (11.28 g, 120 mmol), K2CO3 (24.84g, 180 mmol) and KI (996 mg, 6 mmol) in MeCN (300 mL) was stirred at 80° C. overnight. The solvent was evaporated and the residue was washed with water (300 mL) and extracted with EtOAc (200 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give compound 314 (6.5 g, 93%) as a yellow oil.
  • Intermediate 315
  • To a solution of compound 314 (6.5 g, 28 mmol) in dioxane (100 mL) was added NaOH (4 M, 21 mL) followed by CbzCl (4.76 g, 28 mmol) at 0° C. The resulting mixture was stirred at rt overnight. The pH was adjusted to pH=6 with HCl (1 N), and the mixture was extracted with EtOAc (100 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (eluent: PE/EtOAc: 8/1) to give tert-butyl (3-((3-hydroxypropyl) (2-oxo-2-phenyl-1λ2-ethyl)amino)propyl) carbamate as a colorless oil (7 g, 74%). This was dissolved in a solution of HCl in Dioxane (4M, 5m1) and stirred at rt for 2 h. The volatiles were removed to yield compound 315 (2-((3-aminopropyl) (3-hydroxypropyl)amino)-1-phenyl-2λ2-ethan-1-one) which was used in subsequent reactions without further purification.
  • Intermediate 316
  • To a solution of indomethacin (366 mg, 0.93 mmol) in DMF (5 mL) was added compound 315 (300 mg, 1.12 mmol), HOBt (228 mg, 1.69 mmol), EDCI (323 mg, 1.69 mmol) and DIPEA (479 mg, 3.72 mmol) at 0° C. The resulting solution was stirred at room temperature for 3.0 h. Then water was added (20 mL) and the mixture was extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to get the intermediate 316 (500 mg, yield: 89%) as a light yellow solid.
  • Intermediate 317
  • To a solution of 316 (500 mg, 0.83 mmol) in DCM (20 ml) at 0° C. was added Dess-Martin periodinane (385 mg, 0.91 mmol). The resulting solution was stirred rt for 1.5 h, saturated Na2S2O3 (10 mL) was added and the mixture was stirred for 10 min, then washed with aqueous Na2CO3 solution, extracted with DCM (30 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give compound 317 (490 mg, yield: 95%) as a yellow solid.
  • Intermediate 318
  • To a solution of compound 317 (490 mg, 0.81 mmol) in MeOH (10 mL) was added 255 (352 mg, 0.81 mmol), and 0.5 mL of acetic acid. The resulting solution was stirred at room temperature for 0.5 h. Then NaBH3CN (256 mg, 4.06 mmol) was added to the reaction mixture, which was stirred for 2. h. Then water (20 mL) was added and the mixture was extracted with DCM (30 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product 318, which was purified by chromatography on silica gel (DCM/MeOH: 50/1) to give the product (360 mg, yield: 45%) as yellow oil.
  • Intermediate 319
  • 318 (360 mg, 0.35 mmol) was dissolved in a solution of HBr in AcOH (40%, 5 mL) and was stirred at room temperature for 2 h. The reaction was concentrated to give 319, which was used in the next step without purification (290 mg, crude).
  • Compound 320
  • To a solution of 319 (290 mg, 0.32 mmol) in TFA (8 mL) was added Et3SiH (68 mg, 0.59 mmol). The resulting mixture was stirred at 80° C. for 1.5 h. The volatiles were removed and the residue was dissolved in NMP and (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 1.0 eq) was added. The mixture was stirred at 80° C. overnight. The reaction was concentrated and the residue was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give compound 320 as a light pink solid (16 mg, yield: 6%)
  • 1H NMR (400 MHz, CDCl3) δ 8.29 (s, 1H), 7.67 (d, J=8.5 Hz, 2H), 7.49 (d, J=8.6 Hz, 2H), 6.97-6.82 (m, 2H), 6.74-6.57 (m, 2H), 4.76 (d, J=16.3 Hz, 1H), 4.60-4.48 (m, 1H), 4.16-4.03 (m, 2H), 4.01-3.89 (m, 2H), 3.82 (s, 3H), 3.75-3.61 (m, 3H), 3.56-3.43 (m, 1H), 3.38-3.05 (m, 5H), 2.98-2.65 (m, 5H), 2.42-2.11 (m, 5H), 1.75-1.50 (m, 2H). MS (ESI) m/z: 848.1(M+H+).
  • Example 57 Synthesis of Compounds 328 and 329
  • Figure US20190169084A1-20190606-C00216
    Figure US20190169084A1-20190606-C00217
  • Intermediate 322
  • To a solution of oxalyl chloride (3.1 g, 24.5 mmol) in dry DCM (200 mL) was added DMSO (2.9 mL, 40.8 mmol) at −60° C. The mixture was stirred for 30 min. Then a solution of tert-butyl (R)-(1-hydroxypropan-2-yl)carbamate (3.5 g, 20 mmol) in DCM (20 mL) was added at −60° C. The resulting solution was stirred for another 30 min. Triethylamine (11.1 mL, 80 mmol) was added at −60° C., and the mixture was stirred for 2 h at room temperature. Water (100 mL) was added and the mixture was extracted with DCM (3×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the aldehyde 322 as a light yellow oil (3.2 g, 94%), which was used in the next step without further purification.
  • Intermediate 323
  • To a solution of (4-methoxy-4-oxobutyl) triphenylphosphonium brominde (8.2 g, 18.5 mmol) in dry THF (150 mL) was added LiHMDS (1 M in THF, 20 mL) dropwise. The resulting reaction was stirred at 0° C. for 30 min. Then the reaction was recooled to −60° C. A solution of compound 322 (3.2 g, 18.5 mmol) in dry THF (50 mL) was added to the reaction. The solution was slowly warmed to RT and stirred overnight. The reaction was quenched with NH4Cl (aq.), extracted with EtOAc (100 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica gel (eluent: PE/EtOAc=10/1) to give the compound 323 as a colorless oil (1.9 g, yield: 40%).
  • Intermediate 324
  • A mixture of compound 323 (1.9 g, 7.4 mmol) and Pd/C (200 mg) in MeOH (50 mL) was stirred under an atmosphere of H2 overnight. The catalyst was filtered off, the filtrate was washed with MeOH (30 mL×3), and concentrated to give 324 as a light yellow oil (1.9 g, yield: 99%) which was used without further purification.
  • Intermediate 325
  • To a solution of compound 324 (518 mg, 2 mmol) in dry THF (15 mL) was added LiAlH4 (114 mg, 3 mmol) slowly at 0° C. The resulting reaction was stirred at room temperature for another 2 h. The reaction was quenched with H2O (15 ml), extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (eluent: PE/EtOAc=4/1) to give the Boc-protected product as a colorless oil (270 mg, yield: 58%). This was dissolved in HCl (4M in dioxane, 5 mL) and stirred at rt for 2 h, after which time LCMS showed the reaction was completed. The reaction was concentrated to give 325, which was used without further purification (150 mg, yield: 99%).
  • Intermediate 326
  • 326 was obtained by a sequence similar to the one described for intermediate 325, starting with (S)-(1-hydroxypropan-2-yl)carbamate.
  • Intermediate 327
  • To a solution of indomethacin (341 mg, 0.95 mmol) in DMF (5 mL) was added 325 (150 mg, 1.14 mmol), HOBt (230 mg, 1.71 mmol), EDCI (327 mg, 1.71 mmol) and DIPEA (490 mg, 3.8 mmol) at 0° C. The resulting solution was stirred room temperature for 3.0 h. Then water was added (20 mL) and the mixture was extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give 327 (300 g, yield: 67%) as a light yellow solid.
  • Compound 328
  • Compound 328 was obtained from compound 327 by applying procedures similar to the ones described in Example 56 (compound 316 to compound 320). The compound was was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give a light pink solid.
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=7.4 Hz, 2H), 7.50 (d, J=5.4 Hz, 2H), 6.93-6.81 (m, 2H), 6.75-6.67 (m, 1H), 5.29 (d, J=8.4 Hz, 1H), 4.69-4.52 (m, 2H), 4.14-3.95 (m, 3H), 3.94-3.85 (m, 1H), 3.83 (s, 3H), 3.63 (s, 2H), 3.55-3.06 (m, 6H), 2.91-2.78 (m, 1H), 2.40 (d, J=1.8 Hz, 3H), 1.60-1.52 (m, 1H), 1.38-1.15 (m, 7H), 1.05 (d, J=6.6 Hz, 3H). MS (ESI) m/z: 847.1 (M+H+).
  • Compound 329
  • Figure US20190169084A1-20190606-C00218
  • Compound 329 was obtained by procedures similar to the ones described for compound 328, using intermediate 326.
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5, 1.0 Hz, 2H), 7.50 (d, J=8.6 Hz, 2H), 6.92-6.82 (m, 2H), 6.74-6.67 (m, 1H), 5.30 (d, J=8.5 Hz, 1H), 4.67-4.52 (m, 2H), 4.14-3.95 (m, 3H), 3.95-3.75 (m, 4H), 3.63 (s, 2H), 3.54-3.02 (m, 6H), 2.89-2.78 (m, 1H), 2.40 (d, J=1.8 Hz, 3H), 1.61-1.55 (m, 1H), 1.48-1.13 (m, 7H), 1.05 (d, J=6.6 Hz, 3H). MS (ESI) m/z: 847.1 (M+H+).
  • The following compounds 330-333 can also be prepared according to the procedure given in Example 57 by replacing intermediates 325/326 with the appropriate aminoalcohol.
  • Figure US20190169084A1-20190606-C00219
  • Compound Y =
    330
    Figure US20190169084A1-20190606-C00220
    331
    Figure US20190169084A1-20190606-C00221
    332
    Figure US20190169084A1-20190606-C00222
    333
    Figure US20190169084A1-20190606-C00223
  • Example 58 Synthesis of Compound 341
  • Figure US20190169084A1-20190606-C00224
  • Intermediate 335
  • To a solution of 334 (CAS No.: 25126-93-6, 3.45 g, 20.08 mmol) in THF (100 ml) was added lithium aluminum hydride (2.27 g, 60 mmol) at −78° C. After an hour the mixture was warmed to room temperature and stirred under nitrogen for 4 h. The reaction was then quenched by the slow addition of cold ethyl acetate. The white precipitate that formed was then filtered off and washed with cold ether to give the diol 335 3.2 g (100%) as a colorless oil.
  • Intermediate 336
  • To a solution of triphenylphosphine (2.0 g, 7.50 mmol) in THF (10 mL) was added N-chlorosuccinimide (1.0 g, 7.50 mmol). The reaction mixture was allowed to stir at room temperature for 10 min, then 331 (400 mg, 3.4 mmol) was added. The mixture was stirred overnight. Then water (20 mL) was added. The mixture was extracted with EtOAc (30 mL×3), the combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product, which was purified by chromatography on silica gel (EtOAc/hexanes) to give the dichloride 336 (260 mg yield: 50%) as a colorless oil.
  • Intermediate 337
  • To a solution of 336 (900 mg, 5.92 mmol) in DMF (15 mL) compound 255 (850 mg, 1.97 mmol), K2CO3 (543 mg, 3.94 mmol) and KI (327 mg, 1.97 mmol) were added. The mixture was heated to 80° C. overnight. Then water (50 mL) was added. The mixture was extracted with EtOAc (40 mL×3), the combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product which was purified by chromatography on silica gel (DCM/MeOH=50/1) to give 337 (400 mg, yield: 37%) as yellow oil.
  • Intermediate 338
  • Compound 337 (400 mg, 0.72 mmol) was dissolved in a solution of NH3 in MeOH (7M, 15 mL) and was heated to 110° C. in an autoclave overnight. The volatiles were removed and the crude product was purified by chromatography on silica gel (DCM/MeOH/H2O=100:5:1) to give the intermediate 338 (240 mg, yield: 63%) as yellow oil.
  • Intermediate 339
  • To the solution of 338 (240 mg, 0.45 mmol) in DMF (10 mL) was added indomethacin (2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid, 134 mg, 0.37 mmol), HOBt (92 mg, 0.68 mmol), EDCI (130 mg, 0.68 mmol) and DIPEA (190 mg, 1.48 mmol) at) 0° C. The resulting solution was stirred at rt for 3 h. Water (20 mL) was added and the mixture was extracted with EtOAc (20 mL×4). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. Chromatography on silica gel (DCM:MeOH=50:1) afforded the product 339 (300 mg, yield: 93%) as a white solid.
  • Intermediate 340
  • To a solution of 339 (300 mg, 0.34 mmol) in TFA (2.0 mL) was added Et3SiH (75 mg, 0.68 mmol). The resulting mixture was stirred at 80° C. for 1.5 h. The reaction was concentrated to give 340 which was used without further purification.
  • Compound 341
  • To a solution of 340 in NMP was added (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 1.0 eq) and the mixture was stirred at 80° C. overnight. The reaction was concentrated and the residue was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give compound 341 as a light pink solid (35 mg, yield: 10%).
  • 1H NMR (400 MHz, CDCl3) δ 7.67 (d, J=8.5 Hz, 2H), 7.50 (d, J=8.5 Hz, 2H), 6.95-6.85 (m, 2H), 6.73 (dd, J=9.0, 2.5 Hz, 1H), 5.63 (t, J=5.5 Hz, 1H), 5.49-5.36 (m, 1H), 5.18-5.08 (m, 1H), 4.70-4.53 (m, 2H), 4.13-4.03 (m, 2H), 3.84 (s, 3H), 3.83-3.74 (m, 1H), 3.64 (s, 2H), 3.51-3.04 (m, 8H), 2.86 (dd, J=13.5, 4.3 Hz, 1H), 2.36 (s, 3H), 2.34-2.21 (m, 2H), 2.17-2.06 (m, 2H). MS (ESI) m/z: 831.1 (M+H+).
  • Example 59 Synthesis of Compound 346
  • Figure US20190169084A1-20190606-C00225
  • Intermediate 342
  • To a solution of indomethacin (2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid, 3.57 g, 10 mmol) in dry DCM (50 mL) was added a solution of BBr3 in DCM (1M, 13 mL) dropwise at −78° C. The resulting solution was stirred at room temperature for another 1 h. LCMS showed the reaction was completed. Water (100 mL) was added to the reaction slowly, and the mixture was extracted with DCM (70 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the product (2.4 g, yield: 70%) as light yellow solid.
  • Intermediate 343
  • To a solution of 342 (2.4 g, 4.86 mmol) and K2CO3 (520 mg, 4.86 mmol) in DMF (30 mL) was added BnBr (0.3 mL) dropwise. The mixture was stirred at room temperature for 1.0 h, then water (50 mL) was added and the mixture was extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (PE/EA=2/1) to give the benzyl ester 343 (2.5 g yield: 83%) as a white solid.
  • Intermediate 344
  • To a solution of 343 (800 mg, 2.54 mmol) and PPh3 (1.45 g, 7.62 mmol) in THF (30 ml) was added CD3OD (135 mg, 5.08 mmol) under N2 at 0° C. The mixture was stirred for 20 min, and then DEAD (964 mg, 7.62 mmol) was added dropwise at 0° C. The mixture was stirred at room temperature overnight. Then water (30 mL) was added and the mixture was extracted with EtOAc (40 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (PE/EA=10/1) to get the product 344 (450 mg, yield: 40%) as a white solid.
  • Intermediate 345
  • A mixture of compound 344 (300 mg, 0.66 mmol) and Pd/C (60 mg) in THF (20 mL) was stirred under H2 for 3 h. The catalyst was filtered off, the filtrate was washed with THF (10 mL×3), and concentrated to give 2-(1-(4-chlorobenzoyl)-5-(methoxy-d3)-2-methyl-1H-indol-3-yl)acetic acid 345 (240 mg, 98%) which was used without further purification.
  • Compound 346 was synthesized from 2-(1-(4-chlorobenzoyl)-5-(methoxy-d3)-2-methyl-1H-indol-3-yl)acetic acid 345 by a procedure similar to the one described in Example 57, using 6-aminohexan-1-ol instead of intermediate 315.
  • 1H NMR (400 MHz, CDCl3) δ 7.68 (d, J=8.5 Hz, 2H), 7.50 (d, J=8.5 Hz, 2H), 6.93-6.79 (m, 2H), 6.71 (dd, J=9.0, 2.5 Hz, 1H), 5.60 (t, J=5.7 Hz, 1H), 4.67-4.51 (m, 2H), 4.17-4.01 (m, 2H), 3.97-3.81 (m, 1H), 3.65 (s, 2H), 3.53-3.41 (m, 1H), 3.39-3.07 (m, 6H), 2.85 (dd, J=13.4, 4.2 Hz, 1H), 2.40 (s, 3H), 1.80-1.63 (m, 2H), 1.50-1.38 (m, 2H), 1.36-1.20 (m, 4H). MS (ESI) m/z: 836.0 (M+H).
  • Example 60 Synthesis of Compound 351
  • Figure US20190169084A1-20190606-C00226
  • 2-(1-(4-Chlorobenzoyl)-5-methoxy-2-(trifluoromethyl)-1H-indol-3-yl)acetic acid, 350, can be synthesized as described by Anna L. Blobaum, Md. Jashim Uddin, Andrew S. Felts, Brenda C. Crews, Carol A. Rouzer, and Lawrence J. Marnett, ACS Med. Chem. Lett., 4, 486-490, (2013). Alternatively, 350 can be synthesized as outlined below.
  • Intermediate 347
  • 2-(5-methoxy-1H-indol-3-yl)acetic acid (5 g, 24.4 mmol) and BOP-Cl (7.4 g, 29 mmol) were suspended in DCM (100 mL), and Et3N (5.4 g, 53.7 mmol) was slowly added. The resulting solution was stirred for 30 min. Benzyl alcohol (2.9 g, 26.8 mmol) was added and the mixture was stirred for 12 h. DCM (100 mL) was added, the layers were separated and the organic layer was washed with water (200 mL) and brine. The organic layer was concentrated and purified by chromatography on silica gel (eluent: PE/EtOAc=2/1) to give 347 as a white solid (6.1 g, 85%).
  • Intermediate 348
  • A mixture of compound 347 (4.7 g, 15.82 mmol) and Togni's reagent (1-Trifluoromethyl-1,2-benziodoxol-3-(1H)-one, 6.5 g, 20.56 mmol) in MeOH (100 mL) was degassed for 15 min, then CuOAc (1.4 g, 11 mmol) was added. The resulting mixture was stirred at rt overnight. The solvent was removed; water (100 mL) was added, extracted with EtOAc (100 mL×2). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (eluent: PE/EtOAc=5/1) to give the product as a white solid (4 g, 70%).
  • Intermediate 349
  • To a solution of compound 348 (4 g, 11 mmol) in dry DMF (50 mL) was added NaH (750 mg, 18.7 mmol). The reaction was stirred for another 30 min, and then 4-chlorobenzoyl chloride (2.9 g, 16.5 mmol) was added. The resulting mixture was stirred at room temperature overnight. The reaction was quenched by addition of sat'd aq, NH4Cl solution (100 mL), extracted with EtOAc (100 mL×3). The combined organic layers were washed brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (eluent: PE/EtOAc=2/1) to give the product as a yellow solid (3.3 g, 50%).
  • Intermediate 350
  • A mixture of compound 349 (3.3 g, 6.5 mmol) and Pd/C (1 g) in THF (30 mL) was stirred at 40° C. for 1 h under H2 atmosphere. The catalyst was filtered off and washed with MeOH (30 mL×3). The filtrate was concentrated in vacuo to give the crude product which was purified by chromatography on silica gel (eluent: DCM/MeOH=40/1) to give 2-(1-(4-chlorobenzoyl)-5-methoxy-2-(trifluoromethyl)-1H-indol-3-yl) acetic acid, 350, as a solid (1.6 g, yield: 60%).
  • Compound 351 was synthesized from 2-(1-(4-chlorobenzoyl)-5-methoxy-2-(trifluoromethyl)-1H-indol-3-yl) acetic acid, 350, by a procedure similar to the one described in Example 42.
  • 1H NMR (400 MHz, CDCl3) δ 7.83 (d, J=8.7 Hz, 2H), 7.56 (d, J=7.7 Hz, 2H), 7.15 (s, 1H), 6.91 (d, J=9.0 Hz, 1H), 6.73 (d, J=9.2 Hz, 1H), 5.60 (s, 1H), 4.74-4.54 (m, 2H), 4.23-4.04 (m, 2H), 4.00-3.74 (m, 6H), 3.49 (s, 1H), 3.42-3.06 (m, 6H), 2.89 (s, 1H), 1.69-1.44 (m, 4H), 1.42-1.25 (m, 4H). MS (ESI) m/z: 887.1 (M+H+).
  • The following compound 352 can also be prepared according to the procedure given in Example 60.
  • Figure US20190169084A1-20190606-C00227
  • 1H NMR (400 MHz, CDCl3) δ 7.80 (d, J=8.5 Hz, 2H), 7.53 (d, J=8.4 Hz, 2H), 7.11 (d, J=2.2 Hz, 1H), 6.88 (dd, J=9.2, 2.3 Hz, 1H), 6.71 (d, J=9.2 Hz, 1H), 5.62 (s, 1H), 4.76-4.51 (m, 1H), 4.20-4.02 (m, 2H), 4.02-3.79 (m, 6H), 3.60-3.42 (m, 1H), 3.41-3.09 (m, 7H), 2.86 (dd, J=13.4, 4.2 Hz, 1H), 1.60-1.38 (m, 2H), 1.41-1.09 (m, 8H). MS (ESI) m/z: 901.1 (M+H+).
  • Example 61 Synthesis of Compound 356
  • Figure US20190169084A1-20190606-C00228
  • Synthesis of Intermediate 353
  • A mixture of compound 255 (1.3 g, 3 mmol), 3-chloropropanoic acid (1.3 g, 12 mmol) and TEA (1.52 g, 15 mmol) in MeCN (30 mL) was stirred at 80° C. overnight. LCMS showed the reaction was completed. The reaction was concentrated in vacuo, washed with water (50 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were washed brine, dried over Na2SO4, filtered and the filtrate was concentrated to give 353 as a yellow oil (1.4 g, 92%).
  • Synthesis of Intermediate 354
  • To a solution of 353 (1.4 g, 2.77 mmol) in DMF (20 mL) were added compound 296 (Example 52, 950 mg, 2.77 mmol), HOBt (560 mg, 4.15 mmol), EDCI (792 mg, 4.15 mmol) and DIPEA (1.8 g, 13.8 mmol) at 0° C. The resulting solution was stirred rt overnight. Then water (40 mL) was added and the mixture was extracted with EtOAc (50 mL×4). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (eluent: DCM/MeOH=40/1) to give the product (1 g, 43%) as light yellow solid.
  • Synthesis of Intermediate 355
  • At 0° C., to a solution of compound 3 (300 mg, 0.36 mmol) in TFA (2 mL) was added anisole (0.1 mL). MeSO3H (1 mL) was added dropwise. The resulting reaction was stirred at room temperature for another 1 h. When LCMS showed completion of the reaction, the mixture was concentrated to give the crude product 355 (310 mg) which was used without further purification.
  • A solution of 355 (310 mg) and (PPh3)2ReOCl3 (Sigma-Aldrich, Order #370193, 300 mg, 0.36 mmol) was stirred at 80° C. for 16 h. The reaction was concentrated and purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp, A: water/B: MeCN) to give 356 as a light pink solid (30 mg, yield: 10%).
  • 1H NMR (400 MHz, CDCl3) δ 7.71-7.59 (m, 2H), 7.55-7.43 (m, 2H), 6.94 (s, 1H), 6.86 (d, J=9.0 Hz, 1H), 6.67 (d, J=9.0 Hz, 1H), 5.90 (s, 1H), 4.61 (d, J=16.5 Hz, 1H), 4.51 (dd, J=11.6, 5.1 Hz, 1H), 4.07 (dd, J=10.5, 3.9 Hz, 1H), 4.03-3.74 (m, 6H), 3.63-3.36 (m, 3H), 3.29-3.04 (m, 3H), 2.98-2.78 (m, 3H), 2.65 (t, J=6.6 Hz, 2H), 2.36 (s, 3H). MS (ESI) m/z: 790.8 (M+H+)
  • Example 62 Synthesis of Compound 359
  • Figure US20190169084A1-20190606-C00229
  • Synthesis of Intermediate 357
  • A mixture of 255 (868 mg, 2 mmol), methyl 6-bromohexanoate (1.3 g, 6 mmol), K2CO3 (1.3 g, 10 mmol) and KI (500 mg, 3 mmol) in MeCN (50 mL) was stirred at 80° C. overnight. Then water (40 mL) was added and the mixture was extracted with EtOAc (50 mL×4). The combined organic layers were washed brine, dried over Na2SO4, filtered and the filtrate was concentrated to give 357 as a white solid (1.1 g, yield: 92%).
  • Synthesis of Intermediate 358
  • A mixture of 357 (1.1g, 1.95 mmol) and NaOH (156 mg, 3.9 mmol) in THF/MeOH/H2O (10 mL/10 mL/4 mL) was stirred at rt. Once LCMS showed the reaction to be completed, the pH was adjusted to 4 and the mixture was extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give 358 as light yellow solid (850 mg, 79%).
  • Compound 359 was synthesized from intermediate 358 by a procedure similar to the one described in Example 61.
  • 1H NMR (400 MHz, CDCl3) δ 7.66 (d, J=8.4 Hz, 2H), 7.48 (d, J=8.3 Hz, 2H), 6.98 (d, J=16.3 Hz, 1H), 6.86 (d, J=9.0 Hz, 1H), 6.68 (d, J=9.0 Hz, 1H), 5.53 (s, 1H), 4.82-4.33 (m, 2H), 4.07 (dd, J=21.9, 13.1 Hz, 2H), 3.98-3.72 (m, 4H), 3.58-3.05 (m, 7H), 2.88 (dt, J=13.7, 5.4 Hz, 3H), 2.45 (d, J=63.8 Hz, 3H), 2.16 (dd, J=17.8, 10.6 Hz, 2H), 1.95-1.56 (m, 4H), 1.38 (dd, J=15.1, 7.5 Hz, 2H). MS (ESI) m/z: 833.1 (M+H+).
  • Example 63
  • Figure US20190169084A1-20190606-C00230
  • The 99mTc complex 360 is prepared as described in Example 62 using as the last step a ligand exchange reaction employing 99mTc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci. 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748, (2010).
  • Example 64 Synthesis of Compound 365
  • Figure US20190169084A1-20190606-C00231
  • Intermediate 361
  • To a solution of 4-fluorophenyl methyl ketone (8.28 g, 60 mmol) in dry THF (200 mL) was added NaH (3.12 g, 78 mmol), followed by dimethyl oxalate (7.8 g, 66 mmol). The resulting solution was stirred at 70° C. overnight. LCMS showed the reaction was completed. The reaction was quenched by addition of sat'd aq. NH4Cl solution and extracted with EtOAc (200 mL×3). The combined organic layers washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product which was purified by chromatography on silica gel (eluent: PE/EtOAc=8/1) to give 361 (10g, yield: 75%) as a colorless oil.
  • Intermediate 362
  • A solution of 361 (10 g, 44.6 mmol) and 4-hydrazinylbenzenesulfonamide (8.34 g, 44.6 mmol) in MeOH (150 mL) was stirred at 70° C. overnight. LCMS showed the reaction was completed. The reaction was concentrated, washed with water (150 mL) and extracted with EtOAc (150 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give 362 (15 g, 90%) as a white solid.
  • Intermediate 363
  • To a solution of 362 (15 g, 40 mmol) in dry THF (200 mL) at 0° C. was slowly added LiAlH4 (1.82g, 48 mmol). The resulting reaction was stirred at room temperature for 1 h. LCMS showed the reaction was completed. The reaction was quenched with 2 mL of water at 0° C., then 150 mL water was added thereto. The mixture was extracted with EtOAc (150 mL×3) and the combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give the crude product, which was purified by chromatography on silica gel (eluent: DCM/MeOH=40/1) to give 363 (9.5 g, yield: 68%).
  • Intermediate 364
  • To a solution of compound 4 (500 mg, 1.44 mmol) in dry THF (20 mL) at 0° C. was added MsCl (248 mg, 2.16 mmol), followed by TEA (363 mg, 3.6 mmol). The resulting mixture was stirred at room temperature for another 1 h. The reaction was judged complete by TLC and H2O (20 mL) was added. The mixture was extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated to give a colorless oil. This was dissolved in a solution of NH3 in MeOH (7 M, 5 mL) and stirred at room temperature for 1 h. LCMS showed the reaction was completed. The reaction was concentrated in vacuo to give 364 (450 mg, yield: 93%).
  • To a solution of 364 (450 mg, 1.3 mmol) in DMF (10 mL) acid 241 (580 mg, 1.5 mmol), HOBt (350 mg, 2.6 mmol), EDCI (497 mg, 2.6 mmol) and DIPEA (671 mg, 5.2 mmol) were added at 0° C. The resulting solution was stirred room temperature overnight. The reaction was quenched with saturated NaHCO3 solution (30 ml) and extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with brine (30 ml), dried over Na2SO4, concentrated, and purified by prep-HPLC (Column: Acquity BEH C18, Waters Corp, solvent A: water/solvent B: MeCN) to give the compound 365 (90 mg, yield: 10%).
  • 1H NMR (400 MHz, CDCl3) δ 7.65 (d, J=8.0 Hz, 2H), 7.21-6.89 (m, 7H), 6.55 (s, 1H), 6.07 (d, J=39.8 Hz, 4H), 5.36 (s, 2H), 4.62 (d, J=4.9 Hz, 2H). MS (ESI) m/z: 709.0 (M+H+)
  • Example 65 Synthesis of Compound 366
  • Figure US20190169084A1-20190606-C00232
  • Compound 366 is prepared from compound 364 (Example 64) by a procedure similar to the one described in Example 41.
  • Example 66 Synthesis of Compound 367
  • Figure US20190169084A1-20190606-C00233
  • Compound 367 is prepared from compound 364 (Example 64) and compound 358 (Example 62) using a procedure similar to the one described in Example 61.
  • Example 67 Synthesis of Compound 368
  • Figure US20190169084A1-20190606-C00234
  • The 99mTc complex 368 is prepared as described in Example 66 using as the last step a ligand exchange reaction employing 99mTc-glucoheptonate as described in e.g.: Ono, M., et al., ACS Chem. Neurosci. 1, 598, (2010) and Ono, M., et al., Bioorg. Med. Chem. Lett., 20, 5743-5748,
  • Example 68 Synthesis of Compound 371
  • Figure US20190169084A1-20190606-C00235
  • Intermediate 369
  • To a solution of 296 (170 mg, 0.5 mmol) and picolinaldehyde (54 mg, 0.5 mmol) in DCM (15 ml) was added AcOH (0.2 ml). The mixture was stirred at room temperature for 30 min, NaBH(OAc)3 (422 mg, 2.0 mmol) was added, the mixture was stirred at room temperature overnight, then water (20 mL) was added and the mixture was extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (DCM/MeOH =10/1) to give 369 (60 mg yield: 28%).
  • Intermediate 370
  • To a solution of 369 (120 mg, 0.3 mmol) and 2-oxoacetic acid (50% in water, 133 mg. 0.9 mmol) in MeOH (10 mL) was added AcOH (0.1 mL). The mixture was stirred at room temperature for 30 min, then NaCNBH3 (93 mg, 1.5 mmol) was added and the mixture was stirred at room temperature overnight. Water (20 mL) was added and the mixture was extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (DCM/MeOH=3/1) to give 370 (30 mg yield: 20%).
  • To a solution of compound 370 (30 mg, 0.065 mmol) in MeOH (3 mL) was added Re(CO)5Cl (36 mg, 0.1 mmol). The resulting mixture was refluxed overnight. LCMS showed the reaction to be complete. The reaction mixture was concentrated in vacuo to give the crude product, which was purified by Prep-HPLC (Column: Acquity BEH C18, Waters Corp.) to give 371 (10 mg yield: 20%) as a white solid.
  • 1H NMR (400 MHz, DMSO-d6) δ 8.80 (d, J=5.3 Hz, 1H), 8.20 (t, J=7.6 Hz, 1H), 7.79 (d, J=7.9 Hz, 1H), 7.72 (d, J=8.4 Hz, 2H), 7.63 (dd, J=18.1, 7.5 Hz, 3H), 7.25 (d, J=2.1 Hz, 1H), 6.91 (d, J=9.0 Hz, 1H), 6.74 (dd, J=9.0, 2.1 Hz, 1H), 4.94 (dd, J=35.8, 15.8 Hz, 2H), 4.14 (d, J=16.7 Hz, 1H), 3.79 (s, 3H), 3.72-3.48 (m, 3H), 3.25-3.09 (m, 2H), 2.33 (s, 3H). MS (ESI) m/z: 762.0 [M+H+].
  • CLINICAL AND SCREENING EXAMPLES Example A “Pain Scans” to Localize Site(s) of Inflammation
  • A patient with an undiagnosed cause of pain, or a cause of pain which cannot be localized to a site of pathology, is scheduled for a “pain scan.” The patient refrains from drinking or eating for at least eight hours prior to the pain scan. A compound of the invention is administered to the patient either orally or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The loci are imaged and viewed or photographed as appropriate. Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection. The scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the etiology of the pain and determine appropriate treatment.
  • Example B “Tumor Scans” to Localize Site(s) of Tumor(s)
  • A patient to be screened for presence of a tumor is scheduled for a “COX scan.” The patient refrains from drinking or eating for at least eight hours prior to the COX scan. A compound of the invention is administered to the patient either orally or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The loci are imaged and viewed or photographed as appropriate. Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection. The scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the presence and/or location of the tumor and determine appropriate treatment.
  • Example C Scans to Screen for Asymptomatic Infections or Localized Infections
  • A patient to be screened for an asymptomatic infection, or to have the site of a localized infection identified, is scheduled for a “COX scan.” The patient refrains from drinking or eating for at least eight hours prior to the COX scan. A compound of the invention is administered to the patient either orally or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the patient is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The loci are imaged and viewed or photographed as appropriate. Scans of the patient can be repeated at various intervals after ingestion or injection of the compound of the invention, for example, at two hours, three hours, and four hours after ingestion or injection. The scan findings are correlated with the patient's medical history, physical examination and other information to assist in diagnosis of the presence and/or location of an infection, and to determine appropriate treatment.
  • Example D Scans to Screen Candidate Compounds for Imaging
  • Animal models can be used to test the conjugates and compounds of the invention for their suitability for clinical use. Animal models of pain (and inflammation related to pain), of infection, and of cancer are well known. See, for example, Handbook of Laboratory Animal Sciense, Second Edition: Animal Models, Volume 2 (Jann Hau, Gerald L. Van Hoosier Jr., editors), Boca Raton: CRC Press, 2003; Animal Models for the Study of Human Disease (P. Michael Conn, editor), San Diego: Academic Press, 2013.
  • A suitable animal model (for pain, for cancer, or for infection) is selected and the appropriate pathology is induced. The site of the induced pain, inflammation, infection, or tumor is recorded by the investigator. One or more candidate conjugates or compounds of the invention is administered to the animal, either by oral gavage or parenterally. After an appropriate period of time determined by the pharmacokinetics of the compound of the invention, during which the compound of the invention binds to cyclooxygenase, the animal is scanned with the appropriate modality to determine the locus or loci of the greatest concentration of the compound. The location(s) indicated by the scan are compared with the known site or sites at which the pathology was induced, for evaluation of the effectiveness of the conjugate for accumulating at the site of pathology.
  • The carrageenan induced rat paw edema assay can be used as an exemplary model for inflammation; see Shalini, V. et al., Molecular Immunology 66:229-239 (2015); see also Winter, C. et al., Proc. Soc. Exp. Biol. Med. 111:544-547 (1962). Briefly, acute inflammation is induced by aponeurosis injection of 0.1 ml of 1% carrageenan in 0.9% saline. Additional information regarding model assays is described in Guay et al., J. Biol. Chem. 279:24866-24872 (2004); Nantel et al., British Journal of Pharmacology 128:853-859 (1999); Siebert et al., Proc. Natl. Acad. Sci. USA 91:12013-12017 (1994); de Vries et al., J Nucl. Med. 44:1700-1706 (2003); and Uddin et al., Cancer Prev. Res. 4:1536-1545 (2011).
  • The animal is then imaged using the appropriate modality, for example, scintigraphic imaging or SPECT imaging. Exemplary imaging methods that can be used are described in Pacelli et al., J. Label. Compd. Radiopharm. 57:317-322 (2014); de Vries et al., J Nucl. Med. 44:1700-1706 (2003); and Tietz et al., Current Medicinal Chemistry, 20, 4350-4369 (2013).
  • Example E COX Inhibition Assay
  • A variety of assays can be used to evaluate inhibition of compounds to cyclooxygenase (COX). Compounds in the present invention display inhibition of cyclooxygenase in the following assays.
  • Cell culture: RAW264.7 murine macrophages were obtained from the Cell Bank of Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences (Shanghai, China) and cultured in Dulbecco's modified Eagle's medium containing 100 U/ml penicillin and 100 μm/ml streptomycin at 37° C. in 5% CO2.
  • Cell-based COX-2 assay: RAW264.7 cells were plated at a density of 2.5×105/ml cells in a 96-well plate with 0.1 ml of culture medium per well and cultured overnight. The cells were pre-incubated for 30 min with various doses of compounds and stimulated for 7 h with 1 μg/ml LPS and 10 U/ml IFN-g. The cell culture supernatants were collected immediately following treatment and centrifuged at 1,000 rpm for 5 min to remove the particulate matter. PGE2 was determined using a Prostaglandin E2 assay kit (catalog no. 62P2APEB; Cisbio Co.,). 10 μL of cell supernatant was transferred to a 384-well low volume plate (e.g. Corning® 3544), 5 μL of PGE2-d2 was added, followed by 5 μL anti-PGE2 Cryptate as a negative control. Replace the standard by 10 ∞L of diluent and PGE2-d2 by 5 μL of reconstitution buffer, Cal0 (for positive control), replace the standard by 10 μL of diluent. Incubate at 4° C. overnight. After centrifuging at 1,000 rpm for 1 min, the dual fluorescence emissions of 615 and 665 nm with a 320 nm excitation were measured using an Envision plate reader (Perkin Elmer, Shelton, Conn.). The results are expressed as the ratio of 665 nm/615 nm emissions.
  • COX-1/-2 enzyme assay: The ability of compounds to inhibit ovine COX-1 and human COX-2 was determined using a commercially available enzyme immunoassay (EIA) kit (catalog no. 701090(COX-1); 701080 (COX-2) Cayman Chemical Co., Ann Arbor, Mich., USA) according to the manufacturer's protocol. COX catalyzes the first step in the biosynthesis of AA to PGH2. PGF2α, produced from PGH2 by reduction with stannous chloride, was measured by EIA (ACE™ competitive EIA, Cayman Chemical, Ann Arbor, Mich., USA). Briefly, to a series of supplied reaction buffer solutions [960 μl 0.1 M Tris-HCl (pH 8.0) containing 5 mM EDTA and 2 mM phenol] with either COX-1 or COX-2 (10 μl) enzyme in the presence of heme (10 μl), 10 μl of various concentrations of test drug solutions were added. These solutions were incubated for 15 min at 37° C. and subsequently 10 μl AA solution (100 μM) was added. The COX reaction was stopped by the addition of 30 μl stannus chloride after 2 min, mixed immediately, supernatants were 2000 fold diluted. The produced PGF2α was measured by EIA. This assay is based on the competition between PGs and a PG-acetylcholinesterase conjugate (PG tracer) for a limited amount of PG antiserum. The amount of PG tracer that is able to bind to the PG antiserum is inversely proportional to the concentration of PGs in the wells since the concentration of the PG tracer is held at a constant while the concentration of PGs varies. The specific antiserum-PG complex bound to a mouse anti-rabbit IgG that had been previously attached to the well. The plate was washed to remove any unbound reagents and 200 μl Ellman's reagent (5,5′-dithiobis-(2-nitrobenzoic acid), which contains the substrate to acetylcholine esterase, was added to the well. The product of this enzymatic reaction generates a distinct yellow color that absorbs at 406 nm. The intensity of this color, determined by spectrophotometry, is proportional to the amount of PG tracer bound to the well, which is inversely proportional to the amount of PGs present in the well during the incubation. Percent inhibition was calculated by the comparison of the compounds treated to the various control incubations.
  • Dose-response curves were generated using XLFit (IDBS, Surrey, UK) or Prism (GraphPad Software, La Jolla, Calif., US) to calculate IC50 values for each compound tested.
  • Representative results for COX-2 inhibition are provided in Table 3 below. IC50 values are given in micromolar units.
  • TABLE 3
    COX-2
    IC50 (μM)
    Compound enzyme cell
    23 12.0
    27 0.6 12.7
    35 1.6
    39 1.1
    178 0.2 1.8
    181 1.0 1.5
    182 0.8 0.6
    183 0.4 0.7
    185 1.2 0.5
    204 0.2 0.9
    207 0.6 0.8
    208 0.3 0.6
    209 2.4 0.7
    210 0.3 0.6
    211 2.2 1.6
    219 4.0 2.1
    234 1.7 3.7
    237 4.5 >1
    242 0.3 0.4
    243 0.5 0.7
    244 >30 1.5
    245 >30 0.3
    246 0.1 0.2
    247 0.2 2.6
    248 0.2 >30
    249 1.1 4.4
    250 0.2 0.3
    251 0.3 >30
    260 0.3 0.2
    261 0.8 1.8
    262 0.9 1.7
    263 0.3 0.3
    264 0.3 0.1
    265 2.1 0.1
    266 0.6 0.2
    267 >30 0.3
    268 >30 >10
    269 0.5 0.9
    275 0.7 0.2
    297 0.5 0.8
    301 >30 >1
    303 >30 0.9
    304 >30 0.9
    305 0.3 0.1
    306 0.7 0.2
    307 >30 0.5
    308 0.9 0.2
    309 0.5 0.3
    310 >30 0.2
    311 0.4
    312 0.1 0.4
    313 0.2
    320 5.0
    328 0.6 0.1
    329 0.6 0.1
    341 0.8 0.3
    346 0.3 0.2
    351 >30 0.4
    352 >30 0.3
    356 1.6
    359 0.6 0.2
    365 7.9 1.1
    367 4.5 >10
    371 0.1 2.1
  • Representative results for COX-1 inhibition are provided in Table 4 below. IC50 values are given in micromolar units.
  • TABLE 4
    COX-1 IC50 (μM)
    Compound enzyme
    242 >30
    246 >30
    260 >30
    264 >30
    275 >30
    305 >30
    306 >30
    275 >30
    369 >30
  • Example F: Pharmacokinetic Data
  • In vitro data of metabolic stability and protein binding as well as in vivo pharmacokinetic data for the conjugates of the invention can be generated using the techniques disclosed in Silber, B. M. et al., Pharm. Res. 30(4):932-950 (2013), which is hereby incorporated by reference in its entirety. Various biological, pharmacokinetic and other properties of the conjugates, including hepatic microsomal stability, determination of metabolites, binding to proteins such as plasma protein binding, and in vivo studies, including single-dose and multi-dose pharmacokinetic studies, are determined using the protocols described in that publication and the publications cited therein.
  • Exemplary Embodiments
  • The invention is further described by the following exemplary embodiments. The features of each of the embodiments are combinable with any of the other embodiments where appropriate and practical.
  • Embodiment 1. A conjugate comprising: a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt thereof.
  • Embodiment 2. The conjugate of embodiment 1, wherein said radioactive agent is 99mTc.
  • Embodiment 3. The conjugate of embodiment 1, wherein the NSAID or the residue of a NSAID and imaging moiety are bonded or complexed via a linker selected from the group consisting of an optionally substituted C1-C30 hydrocarbylene group and an optionally substituted C3-C30 heterohydrocarbylene group.
  • Embodiment 4. The conjugate of any of embodiments 1-3, wherein the NSAID or the residue of a NSAID is selected from the group consisting of acetylsalicylic acid, diflunisal, salsalate, choline magnesium trisalicylate, ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, nabumetone, piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib, rofecoxib , valdecoxib, parecoxib, lumiracoxib, etoricoxib, firocoxib, nimesulide, and licofelone, and a residue of any of the foregoing compounds.
  • Embodiment 5. The conjugate of any of embodiments 1-3, wherein the optionally substituted C3-C30 heterohydrocarbylene group is
  • Figure US20190169084A1-20190606-C00236
  • where R1 and R2 are independently selected from hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or R1 and R2 together with the carbon to which they are attached form a C3-C8 cycloalkyl ring; and n is an integer selected from 0 to 4, inclusive.
  • Embodiment 6. The conjugate of embodiment 5, wherein R1 and R2 are methyl.
  • Embodiment 7. The conjugate of embodiment 5, wherein the linking group is
  • Figure US20190169084A1-20190606-C00237
  • Embodiment 8. The conjugate of any of embodiments 1-3, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • Embodiment 9. The conjugate of embodiment 1, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent is:
  • Figure US20190169084A1-20190606-C00238
  • wherein Tc is 99mTc;or a pharmaceutically acceptable salt thereof.
  • Embodiment 10. The conjugate of embodiment 1, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent is:
  • Figure US20190169084A1-20190606-C00239
  • wherein Tc is 99mTc;or a pharmaceutically acceptable salt thereof.
  • Embodiment 11. A pharmaceutical composition comprising the conjugate of any of embodiments 1-3, 9, or 10, and a pharmaceutically acceptable excipient.
  • Embodiment 12. A method of imaging a site of pathology in a subject, comprising: a) administering a conjugate comprising a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which is a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt of said conjugate; or a pharmaceutical composition comprising said conjugate or a pharmaceutically acceptable salt of said conjugate and a pharmaceutically acceptable excipient; and b) generating an image of the subject or an image of a portion of the subject.
  • Embodiment 13. The method of embodiment 12, wherein said radioactive agent is 99mTc.
  • Embodiment 14. The method of embodiment 12, wherein the NSAID or the residue of a NSAID and imaging moiety are bonded or complexed via an optionally substituted C1-C30 hydrocarbylene group or an optionally substituted C3-C30 heterohydrocarbylene group.
  • Embodiment 15. The method of any of embodiments 12-14, wherein the NSAID or the residue of a NSAID is selected from the group consisting of acetylsalicylic acid, diflunisal, salsalate, choline magnesium trisalicylate, ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, nabumetone, piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib, rofecoxib , valdecoxib, parecoxib, lumiracoxib, etoricoxib, firocoxib, nimesulide, and licofelone, and a residue of any of the foregoing compounds.
  • Embodiment 16. The method of any of embodiments 12-14, wherein the optionally substituted C3-C30 heterohydrocarbylene group is
  • Figure US20190169084A1-20190606-C00240
  • where R1 and R2 are independently selected from hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or R1 and R2 together with the carbon to which they are attached form a C3-C8s cycloalkyl ring; and n is an integer selected from 0 to 4, inclusive.
  • Embodiment 17. The method of embodiment 16, wherein R1 and R2 are methyl.
  • Embodiment 18. The method of embodiment 16, wherein the linking group is
  • Figure US20190169084A1-20190606-C00241
  • Embodiment 19. The method of any of embodiments 12-14, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of naproxen, ketorolac, a residue of naproxen, and a residue of ketorolac.
  • Embodiment 20. The method of embodiment 12, wherein the conjugate is:
  • Figure US20190169084A1-20190606-C00242
  • wherein Tc is 99mTc; or a pharmaceutically acceptable salt thereof.
  • Embodiment 21. The method of embodiment 12, wherein the conjugate is:
  • Figure US20190169084A1-20190606-C00243
  • wherein Tc is 99mTc; or a pharmaceutically acceptable salt thereof.
  • Embodiment 22. The method of any of embodiments 12-14, 20, or 21, wherein the conjugate is administered as a composition additionally comprising a pharmaceutically acceptable excipient.
  • Embodiment 23. A conjugate comprising: a non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter and an X-ray emitter; or a pharmaceutically acceptable salt thereof.
  • Embodiment 24. The conjugate of embodiment 23, wherein said radioactive agent is 99mTc, 52Mn, 186Re or 188Re.
  • Embodiment 25. The conjugate of embodiment 23, of the form:

  • (NSAID or NSAID residue)-(linker)-(chelating group)-M-(terminal ligand)z
  • where z is an integer between 0 and 5 inclusive; and each “terminal ligand” is independently selected from a ligand that bonds or complexes to M, but which does not have a NSAID or NSAID residue attached to it.
  • Embodiment 26. The conjugate of embodiment 23, wherein the NSAID or the residue of a NSAID and the imaging moiety are bonded or complexed via a linker, wherein the linker is selected from the group consisting of:
      • an optionally substituted C1-C40 hydrocarbylene group;
      • an optionally substituted C2-C40 heterohydrocarbylene group; and
      • a linker of the form -LE-R4-LF-,
        • where LE is absent or is selected from the group consisting of —NH—and —N(R8)—, and R8 is optionally substituted C1-C4 alkyl,
        • R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene, optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl,
        • and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl.
  • Embodiment 27. The conjugate of embodiment 26, wherein the linker is selected from the group consisting of: (—CH2CH2—O—)n and (—CH2CH(CH3)—O—)n,
  • where n is an integer from 1 to 12 inclusive.
  • Embodiment 28. The conjugate of embodiment 26, wherein the linker is selected from the group consisting of: —(NRa)—(CH2)n—(NRa)—, —(NH)—(CH2)n—(NH)—, —(NRa)—(CH2CH2)—(OCH2CH2)n—(NRa)—, —(NH)—(CH2CH2)—(OCH2CH2)n—(NH)—, where Ra is (C1-C4 alkyl) and n is an integer from 1 to 12 inclusive,
  • Figure US20190169084A1-20190606-C00244
    Figure US20190169084A1-20190606-C00245
  • Embodiment 29. The conjugate of embodiment 23 or embodiment 24, wherein the imaging moiety further comprises a group which bonds or complexes to the radioactive agent.
  • Embodiment 30. The conjugate of embodiment 29, wherein the group which bonds or complexes to the radioactive agent is a chelating group.
  • Embodiment 31. The conjugate of embodiment 30, wherein the chelating group is of the form:
  • Figure US20190169084A1-20190606-C00246
  • wherein each J is independently selected from the group consisting of NH and S,
    • R101, R102, and R103 are independently selected from the group consisting of optionally substituted C2-C4 alkyl, and
    • the NSAID or NSAID residue is attached to the H-J-R101-J-R102-J-R103-J-H, either directly or through a linker, at any J, R101, R102, or R103 atom where a hydrogen atom can be replaced with a bond to the NSAID or NSAID residue, or to the linker.
  • Embodiment 32. The conjugate of embodiment 30, wherein the chelating group is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00247
  • where R10, R11, R12, R13, R14, R15, R16, and R17 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R10 and R11) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R12 and R13) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R14 and R15) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R10 and R11), (R12 and R13), (R14 and R15), and (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; and wherein the bond marked with an asterisk * indicates the attachment of the chelating group to the remainder of the conjugate;
    • and
  • Figure US20190169084A1-20190606-C00248
  • R18, R19, R20, R21, R22, R23, R24, and R25 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; and wherein the bond marked with an asterisk * indicates the attachment of the chelating group to the remainder of the conjugate.
  • Embodiment 33. A conjugate of the formula:

  • [(NSAID or NSAID residue)-(linker)]x-M-(terminal ligand)z
  • where “NSAID or NSAID residue” refers to a NSAID or a residue of a NSAID; M is selected from the group consisting of 99mTc , 52Mn, and Re;
    • x is an integer between 1 and 6 inclusive, z is an integer between 0 and 5 inclusive, and the sum of x and z is less than or equal to 6; and
    • “terminal ligand” is a ligand that coordinates to M, but which does not have a NSAID attached to it; or a pharmaceutically acceptable salt thereof.
  • Embodiment 34. The conjugate of embodiment 33, wherein said conjugate is of the formula:
  • Figure US20190169084A1-20190606-C00249
  • where LE is absent or is selected from the group consisting of —NH—and —N(R8)—, where R8 is optionally substituted C1-C4 alkyl;
    • R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene, optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl;
    • LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl;
    • where R10, R11, R12, R13, R14, R15, R16, and R17 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R10 and R11) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R12 and R13) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R14 and R15) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R10 and R11), (R12 and R13), (R14 and R15), and (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; and
    • M is selected from the group consisting of 99mTc and Re;
    • or a pharmaceutically acceptable salt thereof.
  • Embodiment 35. The conjugate of embodiment 33, wherein said conjugate is of the formula:

  • (NSAID or NSAID residue)-(linker)-M-(terminal ligand)z
  • and -(linker)-M-(terminal ligand)z is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00250
    Figure US20190169084A1-20190606-C00251
    Figure US20190169084A1-20190606-C00252
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, and R8 is optionally substituted C1-C4 alkyl , with the proviso that if the LE moiety of the group -LF-R4-LE- would be attached to a nitrogen atom, then LE is absent;
  • where LG is absent or is selected from the group consisting of —NH— and —N(R8)—, and R8 is optionally substituted C1-C4 alkyl;
  • R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene, optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl;
  • LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl; and
    • R18, R19, R20, R21, R22, R23, R24, R25, R26, R27, R28, and R29 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R26 and R27) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25), or (R26 and R27), or (R28 and R29) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring;
    • R30, R31, R32, and R33 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R30 and R31), (R31 and R32), or (R32 and R33), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring;
    • R34, R35, R36, and R37 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R34 and R35), (R35 and R36), or (R36 and R37), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring;
    • R(ri) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive;
      and
    • X is Cl or Br;
    • or a pharmaceutically acceptable salt thereof.
  • Embodiment 36. The conjugate of embodiment 33, wherein said conjugate is of the formula:

  • (NSAID or NSAID residue)-(linker)-M-(terminal ligand)z
  • and -(linker)-M-(terminal ligand)z is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00253
    Figure US20190169084A1-20190606-C00254
    Figure US20190169084A1-20190606-C00255
  • where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, and R8 is optionally substituted C1-C4 alkyl , with the proviso that if the LE moiety of the group -LF-R4-LE- would be attached to a nitrogen atom, then LE is absent;
  • R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene, optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl;
  • LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl; and
    • X is Cl or Br;
    • or a pharmaceutically acceptable salt thereof.
  • Embodiment 37. The conjugate of embodiment 33, wherein said conjugate is of the formula:
  • Figure US20190169084A1-20190606-C00256
    • where LE is absent or is selected from the group consisting of —NH—and —N(R8)—,
    • where R8 is optionally substituted C1-C4 alkyl,
    • R4 is selected from the group consisting of optionally substituted C1-C40 hydrocarbylene, optionally substituted C2-C40 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 aryl-C1-C6 alkyl;
    • R5 is selected from the group consisting of —OH, —NH2, —NH(C1-C4 alkyl), and —N(C1-C4 alkyl)(C1-C4 alkyl);
    • LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl;
    • M is selected from the group consisting of 99mTc and Re; and
    • R18, R19, R20, R21, R22, R23, R24, and R25 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring;
    • or a pharmaceutically acceptable salt thereof.
  • Embodiment 38. The conjugate of any one of embodiments 23-26, wherein the linker is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00257
    • where R1, R2, and R3 can be independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with hydroxy, fluoro, —O—C1-C4 alkyl, or C3-C6 cycloalkyl;
    • or R1 and R2 together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring; and
    • n is an integer selected from 0 to 4, inclusive.
  • Embodiment 39. The conjugate of any one of embodiments 23-38, wherein the NSAID or the residue of a NSAID is selected from the group consisting of acetylsalicylic acid, diflunisal, salsalate, choline magnesium trisalicylate, ibuprofen, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, aceclofenac, nabumetone, piroxicam, meloxicam, tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib, rofecoxib, valdecoxib, parecoxib, lumiracoxib, etoricoxib, firocoxib, nimesulide, and licofelone, and a residue of any of the foregoing compounds.
  • Embodiment 40. The conjugate of any one of embodiments 23-38, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of indomethacin, naproxen, ketorolac, celecoxib, rofecoxib, a residue of indomethacin, a residue of naproxen, a residue of ketorolac, a residue of celecoxib, and a residue of rofecoxib.
  • Embodiment 41. The conjugate of embodiment 40, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is a residue of a NSAID selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00258
    Figure US20190169084A1-20190606-C00259
  • where the carbon atom or oxygen atom marked with an asterisk * indicates an open valence at that atom at which the residue of the NSAID is attached to the remainder of the conjugate.
  • Embodiment 42. The conjugate of embodiment 40, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is selected from the group consisting of indomethacin and a residue of indomethacin.
  • Embodiment 43. The conjugate of embodiment 40, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID is a residue of a NSAID selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00260
  • where the carbon atom or oxygen atom marked with an asterisk * indicates an open valence at that atom at which the residue of the NSAID is attached to the remainder of the conjugate.
  • Embodiment 44. The conjugate of embodiment 23, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00261
    Figure US20190169084A1-20190606-C00262
    Figure US20190169084A1-20190606-C00263
    Figure US20190169084A1-20190606-C00264
    Figure US20190169084A1-20190606-C00265
    Figure US20190169084A1-20190606-C00266
    Figure US20190169084A1-20190606-C00267
    Figure US20190169084A1-20190606-C00268
    Figure US20190169084A1-20190606-C00269
    Figure US20190169084A1-20190606-C00270
    Figure US20190169084A1-20190606-C00271
    Figure US20190169084A1-20190606-C00272
  • wherein Tc is 99mTc;
    • and pharmaceutically acceptable salts thereof.
  • Embodiment 45. The conjugate of embodiment 23, wherein the non-steroidal anti-inflammatory drug (NSAID) or a residue of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent is selected from the group consisting of:
  • Figure US20190169084A1-20190606-C00273
    Figure US20190169084A1-20190606-C00274
    Figure US20190169084A1-20190606-C00275
    Figure US20190169084A1-20190606-C00276
    Figure US20190169084A1-20190606-C00277
  • wherein Tc is 99mTc;
    • and pharmaceutically acceptable salts thereof
  • Embodiment 46. A pharmaceutical composition comprising one or more conjugates of any one of embodiments 23-45, and a pharmaceutically acceptable excipient.
  • Embodiment 47. A method of imaging a site of pathology or suspected pathology in a subject, comprising:
    • a) administering one or more conjugates of any one of embodiments 23-45 or the composition of embodiment 46 to the subject, wherein the radioactive agent of the conjugate comprises 99mTc, 52Mn, 186Re or 188Re; and
    • b) generating an image of the subject or an image of a portion of the subject.
  • Embodiment 48. The method of embodiment 47, wherein the pathology or suspected pathology in the subject is a tumor or a suspected tumor.
  • Embodiment 49. The method of embodiment 47, wherein the subject is suffering from pain.
  • Embodiment 50. The method of embodiment 47, wherein the pathology or suspected pathology in the subject is an infection or a suspected infection.
  • The disclosures of all publications, patents, patent applications and published patent applications referred to herein by an identifying citation are hereby incorporated herein by reference in their entirety.
  • The present invention has been described in terms of specific embodiments incorporating details to facilitate the understanding of principles of construction and operation of the invention. Such reference herein to specific embodiments and details thereof is not intended to limit the scope of the claims appended hereto. It will be readily apparent to one skilled in the art that other various modifications can be made in the embodiments chosen for illustration without departing from the spirit and scope of the invention. Therefore, the description and examples should not be construed as limiting the scope of the invention.

Claims (22)

1. A conjugate of the formula:
Figure US20190169084A1-20190606-C00278
where LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —C(═O)—, and R8 is optionally substituted C1-C4 alkyl,
R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl,
LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —N(R9)—(C═O)—(CH2)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl;
M is selected from the group consisting of 99mTc 52Mn, 186Re or 188Re,
where R10, R11, R12, R13, R14, R15, R16, and R17 are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R10 and R11) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R12 and R13) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R14 and R15) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R10 and R11), (R12 and R13), (R14 and R15), and (R16 and R17) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring;
where Q is selected from the group consisting of OH, NH2, NH(C1-C4 alkyl), N(C1-C4 alkyl)(C1-C4 alkyl), OCH3, and OCH2CH3;
or a pharmaceutically acceptable salt thereof.
2-5. (canceled)
6. A conjugate comprising: a non-steroidal anti-inflammatory drug (NSAID), a residue of a NSAID, or a derivative of a NSAID bonded or complexed to an imaging moiety which comprises a radioactive agent, wherein the radioactive agent is selected from the group consisting of a gamma-ray emitter, an X-ray emitter, and a beta emitter; or a pharmaceutically acceptable salt thereof.
7. The conjugate of claim 6, wherein said radioactive agent is 99mTc, 52Mn, 186Re or 188Re.
8. The conjugate of claim 7, wherein the imaging moiety further comprises a chelating group which bonds or complexes to the radioactive agent; and where the imaging moiety is optionally bonded to the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID via a linker.
9. The conjugate of claim 8, wherein the imaging moiety comprising a chelating group bonded or complexed to the radioactive agent is of the form:
Figure US20190169084A1-20190606-C00279
wherein M is selected from the group consisting of 99mTc 52Mn, 186Re or 188Re,
wherein each J is independently selected from the group consisting of NH and S,
R101, R102m and R103 are independently selected from the group consisting of optionally substituted C2-C4 alkyl, and
the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group, either through a linker or directly, at
a) any J, R101, R102, or R103 atom where a hydrogen atom can be replaced with a bond to the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present; or at
b) the nitrogen atom in the —R101—N—R102— portion, forming a bond between that nitrogen and the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present; or at
c) the nitrogen atom in the —R102—N—R102— portion, forming a bond between that nitrogen and the linker (if present) or to the NSAID, NSAID residue, or NSAID derivative if no linker is present;
or wherein the imaging moiety comprising a chelating group bonded or complexed to the radioactive agent is of the form:
Figure US20190169084A1-20190606-C00280
wherein M is selected from the group consisting of 99mTc 52Mn, 186Re or 188Re, wherein R(ri) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive, and the NSAID, NSAID residue, or NSAID derivative is attached to the chelating group either through a linker or directly if no linker is present, at any location on the cyclopentane ring which does not have a (Rri) group.
10. The conjugate of claim 8, wherein the NSAID, residue of an NSAID, or derivative of a NSAID and the imaging moiety are bonded or complexed via a linker, wherein the linker is selected from the group consisting of:
an optionally substituted C1-C10 hydrocarbylene group;
an optionally substituted C2-C10 heterohydrocarbylene group; and
a linker of the form -LE-R4-LF-;
where LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —C(═O)—, and R8 is optionally substituted C1-C4 alkyl ,
R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl,
and LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, -(C=O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—,—N(R9)—(C═O)—(CH2)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl.
11. The conjugate of claim 8, wherein the linker is selected from the group consisting of: —(NH)—(CH2)n—, —(NRa)—(CH2)n—, —(NH)—(CH2)n—(NH)—, —(NRa)—(CH2)n—(NRa)—, —(NH)—(CH2CH2)—(OCH2CH2)m—(NH)—, —(NRa)—(CH2CH2)—(OCH2CH2)m—(NRa)—, —(NH)—(CH2CH2)—((NH)CH2CH2)m—(NH)—, —(NRa)—(CH2CH2)—((NH)CH2CH2)m—(NRa)—, (—CH2CH2—O—)n, (—CH2CH(CH3)—O—)q, where Ra is (C1-C4 alkyl), n is an integer from 1 to 10 inclusive, m is an integer from 1 to 4 inclusive, and q is an integer from 1 to 3 inclusive,
—NH—(CH2)2—,
—NH—(CH2)3—,
—NH—(CH2)4—,
—NH—(CH2)5—,
—NH—(CH2)6—,
—NH—(CH2)7—,
—NH—(CH2)8—,
—NH—(CH2)2—C(H)═C(H)—(CH2)2—,
—NH—(CH2)2—NH—,
—NH—(CH2)3—NH—,
—NH—(CH2)4—NH—,
—NH—(CH2)5—NH—,
—NH—(CH2)6—NH—,
—NH—(CH2)7—NH—,
—NH—(CH2)8—NH—,
—NH—(CH2)3—C(CH3)2—NH—,
—NH—(CH2)4—C(CH3)2—NH—,
—NH—(CH2)5—C(CH3)2—NH—,
—NH—(CH2)6—C(CH3)2—NH—,
—NH—(CH2)7—C(CH3)2—NH—,
—NH—(CH2)2—C(CH3)2—(CH2)2—NH—,
—NH—(CH2)2—C(CH3)2—(CH2)2—,
—NH—C(CH3)2—(CH2)3—,
—NH—C(CH3)2—(CH2)4—,
—NH—C(CH3)2—(CH2)5—,
—NH—C(CH3)2—(CH2)6—,
—NH—C(CH3)2—(CH2)7—,
—NH—CH(CH3)—(CH2)3—,
—NH—CH(CH3)—(CH2)4—,
—NH—CH(CH3)—(CH2)5—,
—NH—CH(CH3)—(CH2)6—,
—NH—CH(CH3)—(CH2)7—,
—NH—CH(CF3)—(CH2)3—,
—NH—CH(CF3)—(CH2)4—,
—NH—CH(CF3)—(CH2)5—,
—NH—CH(CF3)—(CH2)6—,
—NH—CH(CF3)—(CH2)7—,
—NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—,
—NH—(CH2)2—NH—(C═O)—,
—NH—(CH2)3—NH—(C═O)—,
—NH—(CH2)4—NH—(C═O)—,
—NH—(CH2)5—NH—(C═O)—,
—NH—(CH2)6—NH—(C═O)—,
—NH—(CH2)7—NH—(C═O)—,
—NH—(CH2)8—NH—(C═O)—,
—NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—(C═O)—,
—NH—(CH2)2—NH—(C═O)—(CH2)—,
—NH—(CH2)3—NH—(C═O)—(CH2)—,
—NH—(CH2)4—NH—(C═O)—(CH2)—,
—NH—(CH2)5—NH—(C═O)—(CH2)—,
—NH—(CH2)6—NH—(C═O)—(CH2)—,
—NH—(CH2)7—NH—(C═O)—(CH2)—,
—NH—(CH2)8—NH—(C═O)—(CH2)—,
—NH—(CH2)2—C(H)═C(H)—(CH2)2—NH—(C═O)—(CH2)—,
—C(═O)—(CH2)2—,
—C(═O)—(CH2)3—,
—C(═O)—(CH2)4—,
—C(═O)—(CH2)5—,
—C(═O)—(CH2)6—,
—C(═O)—(CH2)7—,
—C(═O)—(CH2)8—,
—C(═O)—(CH2)2—C(H)═C(H)—(CH2)2—,
—C(═O)—(CH2)2—NH—,
—C(═O)—(CH2)3—NH—,
—C(═O)—(CH2)4—NH—,
—C(═O)—(CH2)5—NH—,
—C(═O)—(CH2)6—NH—,
—C(═O)—(CH2)7—NH—,
—C(═O)—(CH2)8—NH—,
—C(═O)—(CH2)2—C(H)═C(H)—(CH2)2—NH—,
—NH—(CH2)2—O—(CH2)2—NH—,
—NH—(CH2)2—O—(CH2)2—O—(CH2)2—NH—,
—NH—(CH2)2—O—(CH2)2—O—(CH2)2—O—(CH2)2—NH—,
—NH—(CH2)2—NH—(CH2)2—NH—,
—NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—,
—NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—(CH2)2—NH—,
—NH—(CH2)2—N(CH3)—,
—NH—(CH2)3—N(CH3)—,
—NH—(CH2)4—N(CH3)—,
—NH—(CH2)5—N(CH3)—,
—NH—(CH2)6—N(CH3)—,
—NH—(CH2)7—N(CH3)—,
—NH—(CH2)8—N(CH3)—,
—NH—(CH2)3NH—(CH2)3—,
—NH—(CH2)2—C(H)═C(H)—(CH2)2—,
—NH—CH2—CF2—(CH2)4—,
—NH—CH2—CF2—(CH2)5
—C(═O)—CF2—(CH2)4—,
—C(═O)—CF2—(CH2)5—,
Figure US20190169084A1-20190606-C00281
12. The conjugate of claim 1, wherein said conjugate is of the formula:

(NSAID, NSAID residue, or NSAID derivative)-(linker)-(chelator)-M-(terminal ligand)z1

or

(NSAID, NSAID residue, or NSAID derivative)-(linker)-M-(terminal ligand)z2
where z1 is an integer between 0 and 4 inclusive; z2 is an integer between 0 and 5 inclusive;
and -(linker)-(chelator)-M-(terminal ligand)z1 or -(linker)-M-(terminal ligand)z2 is selected from the group consisting of:
Figure US20190169084A1-20190606-C00282
Figure US20190169084A1-20190606-C00283
where LE is absent or is selected from the group consisting of —NH—, —N(R8)—, and —(C═O)—, and R8 is optionally substituted C1-C4 alkyl , with the proviso that if the LE moiety of the group -LF-R4-LE- would be attached to a nitrogen atom, then LE is absent;
where LG is absent or is selected from the group consisting of —NH—, —N(R8)—, and —(C═O)—, and R8 is optionally substituted C1-C4 alkyl;
R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl;
R5 is selected from the group consisting of —OH, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3;
RN is H or (C1-C4 alkyl);
LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C═O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl; and
R18, R19, R20, R21, R22, R23, R24, and R25, are independently selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkyl substituted with fluoro, hydroxy, —O—C1-C4 alkyl, or C3-C6 cycloalkyl; or, independently of the other substituents, (R18 and R19) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, (R20 and R21) together with the carbon to which they are attached form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R22 and R23) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, or (R24 and R25) together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring, with the proviso that only one of (R18 and R19), (R20 and R21), or (R22 and R23), or (R24 and R25), together with the carbon to which they are attached independently form a C3-C8 cycloalkyl ring or heterocycloalkyl ring;
R30, R31, R32, and R33 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R30 and R31), (R31 and R32), or (R32 and R33), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring;
R34, R35, R36, and R37 are independently selected from hydrogen and C1-C4 alkyl, or one pair of (R34 and R35), (R35 and R36), or (R36 and R37), together with the atoms to which they are attached, form a six-membered aryl ring or a five-to-six membered heteroaryl ring;
M is selected from the group consisting of 99mTc, 52Mn, 186Re and 188Re;
R(ri) is —CH3 or —CH2CH3 and p is an integer between 0 and 4 inclusive;
and
X is Cl or Br;
or a pharmaceutically acceptable salt thereof.
13. The conjugate of claim 12, wherein -(linker)-(chelator)-M-(terminal ligand)z1 or -(linker)-M-(terminal ligand)z2 is selected from the group consisting of:
Figure US20190169084A1-20190606-C00284
Figure US20190169084A1-20190606-C00285
where LE is absent or is selected from the group consisting of —NH— and —N(R8)—, and R8 is optionally substituted C1-C4 alkyl , with the proviso that if the LE moiety of the group -LF-R4-LE- would be attached to a nitrogen atom, then LE is absent;
R4 is selected from the group consisting of optionally substituted C1-C10 hydrocarbylene, optionally substituted C2-C10 heterohydrocarbylene, C3-C8 cycloalkyl, C1-C6 alkyl-C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C6 alkyl, C1-C6 alkyl-C3-C8 cycloalkyl-C1-C6 alkyl, C6-C10 aryl, C1-C6 alkyl-C6-C10 aryl, C6-C10 aryl-C1-C6 alkyl, and C1-C6 alkyl-C6-C10 aryl-C1-C6 alkyl;
R5 is selected from the group consisting of —OH, —NH2, —NH(C1-C4 alkyl), —N(C1-C4 alkyl)(C1-C4 alkyl), —OCH3, and —OCH2CH3;
LF is absent or is a functional group selected from the group consisting of —(C═O)—, —O—, —N(R9)—, —(C═O)N(R9)—, —N(R9)—(C═O)—, —(C=O)N(H)—, —N(H)—(C═O)—, —(SO2)N(R9)—, —N(R9)—(SO2)—, —N(R9)(C═O)N(R9)—, —N(R9)—(C═O)—O—, —O—(C═O)N(R9)—, —(CH═CH)—, or a divalent cycloalkyl or heterocyclic group, where R9 is selected from the group consisting of H and optionally substituted C1-C4 alkyl;
M is selected from the group consisting of 99mTc, 52Mn, 186Re and 188Re; and
X is Cl or Br;
or a pharmaceutically acceptable salt thereof.
14. The conjugate of claim 1, wherein the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID is selected from the group consisting of:
Figure US20190169084A1-20190606-C00286
Figure US20190169084A1-20190606-C00287
Figure US20190169084A1-20190606-C00288
where the atom marked with an asterisk * indicates an open valence at that atom at which the NSAID, residue of the NSAID or derivative of the NSAID is attached to the remainder of the conjugate.
15. The conjugate of claim 14, wherein the non-steroidal anti-inflammatory drug (NSAID), residue of a NSAID, or derivative of a NSAID is selected from the group consisting of:
Figure US20190169084A1-20190606-C00289
where the carbon atom or oxygen atom marked with an asterisk * indicates an open valence at that atom at which the NSAID, residue of a NSAID, or derivative of a NSAID is attached to the remainder of the conjugate.
16. The conjugate of claim 3 claim 6, which is selected from the group consisting of:
Figure US20190169084A1-20190606-C00290
Figure US20190169084A1-20190606-C00291
Figure US20190169084A1-20190606-C00292
Figure US20190169084A1-20190606-C00293
Figure US20190169084A1-20190606-C00294
Figure US20190169084A1-20190606-C00295
Figure US20190169084A1-20190606-C00296
Figure US20190169084A1-20190606-C00297
Figure US20190169084A1-20190606-C00298
Figure US20190169084A1-20190606-C00299
Figure US20190169084A1-20190606-C00300
where Tc is 99mTc, Re is 186Re or 188Re;
and pharmaceutically acceptable salts thereof.
17. The conjugate of claim 1, which is selected from the group consisting of:
Figure US20190169084A1-20190606-C00301
Figure US20190169084A1-20190606-C00302
Figure US20190169084A1-20190606-C00303
Figure US20190169084A1-20190606-C00304
Figure US20190169084A1-20190606-C00305
Figure US20190169084A1-20190606-C00306
Figure US20190169084A1-20190606-C00307
Figure US20190169084A1-20190606-C00308
Figure US20190169084A1-20190606-C00309
Figure US20190169084A1-20190606-C00310
Figure US20190169084A1-20190606-C00311
wherein Tc is 99mTc;
and pharmaceutically acceptable salts thereof.
18. The conjugate of claim 1, which is selected from the group consisting of:
Figure US20190169084A1-20190606-C00312
Figure US20190169084A1-20190606-C00313
Figure US20190169084A1-20190606-C00314
Figure US20190169084A1-20190606-C00315
wherein Tc is 99mTc;
and pharmaceutically acceptable salts thereof.
19. A pharmaceutical composition comprising one or more conjugates of claim 1, and a pharmaceutically acceptable excipient.
20. A method of imaging a site of pathology or suspected pathology in a subject, comprising:
a) administering one or more conjugates of claim 1 to the subject, wherein the radioactive agent of the conjugate comprises 99mTc, 52Mn, 186Re or 188Re; and
b) generating an image of the subject or an image of a portion of the subject.
21. The method of claim 20, wherein the pathology or suspected pathology in the subject is a tumor or a suspected tumor.
22. The method of claim 20, wherein the subject is suffering from pain.
23. The method of claim 20, wherein the pathology or suspected pathology in the subject is an infection or a suspected infection.
24. The conjugate of claim 1, wherein said conjugate has an IC50 for cyclooxygenase inhibition of less than about 0.5 micromolar.
25. The conjugate of claim 24, wherein the cyclooxygenase is COX-2.
US16/025,826 2014-06-27 2018-07-02 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging Abandoned US20190169084A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US16/025,826 US20190169084A1 (en) 2014-06-27 2018-07-02 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US17/158,967 US20220017432A1 (en) 2014-06-27 2021-01-26 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US18/207,628 US20240190790A1 (en) 2014-06-27 2023-06-08 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201462018397P 2014-06-27 2014-06-27
US201462052928P 2014-09-19 2014-09-19
US201562109544P 2015-01-29 2015-01-29
US14/746,349 US9850183B2 (en) 2014-06-27 2015-06-22 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US15/808,493 US20180162784A1 (en) 2014-06-27 2017-11-09 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US16/025,826 US20190169084A1 (en) 2014-06-27 2018-07-02 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US15/808,493 Continuation US20180162784A1 (en) 2014-06-27 2017-11-09 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/158,967 Continuation US20220017432A1 (en) 2014-06-27 2021-01-26 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Publications (1)

Publication Number Publication Date
US20190169084A1 true US20190169084A1 (en) 2019-06-06

Family

ID=54929372

Family Applications (5)

Application Number Title Priority Date Filing Date
US14/746,349 Active 2035-11-05 US9850183B2 (en) 2014-06-27 2015-06-22 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US15/808,493 Abandoned US20180162784A1 (en) 2014-06-27 2017-11-09 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US16/025,826 Abandoned US20190169084A1 (en) 2014-06-27 2018-07-02 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US17/158,967 Abandoned US20220017432A1 (en) 2014-06-27 2021-01-26 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US18/207,628 Pending US20240190790A1 (en) 2014-06-27 2023-06-08 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US14/746,349 Active 2035-11-05 US9850183B2 (en) 2014-06-27 2015-06-22 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US15/808,493 Abandoned US20180162784A1 (en) 2014-06-27 2017-11-09 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Family Applications After (2)

Application Number Title Priority Date Filing Date
US17/158,967 Abandoned US20220017432A1 (en) 2014-06-27 2021-01-26 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
US18/207,628 Pending US20240190790A1 (en) 2014-06-27 2023-06-08 Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging

Country Status (3)

Country Link
US (5) US9850183B2 (en)
EP (1) EP3160514B1 (en)
WO (1) WO2015200187A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022076741A1 (en) * 2020-10-07 2022-04-14 Reiley Pharmaceuticals, Inc. Coxib-derived conjugate compounds and methods of use thereof

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105732643A (en) * 2016-04-18 2016-07-06 苏州大学 Conjugate and preparation method thereof and application to preparation of IDO enzyme inhibitor and non-steroidal anti-inflammatory drugs
WO2024118818A1 (en) * 2022-11-30 2024-06-06 Reiley Pharmaceuticals, Inc. Nsaid-derived conjugate compounds for imaging

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100111858A1 (en) * 2007-01-19 2010-05-06 Howard Carol P Diangostic and Therapeutic Cyclooxygenase-2 Binding Ligands

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5279811A (en) * 1987-02-18 1994-01-18 The Du Pont Merck Pharmaceutical Company Ester-substituted diaminedithiols and radiolabeled complexes thereof
JP2860157B2 (en) 1990-10-31 1999-02-24 日本メジフィジックス株式会社 Method for producing radioactively labeled technetium chelate injection for renal function measurement
AU7960094A (en) 1993-10-04 1995-05-01 Mallinckrodt Medical, Inc. Compositions and methods for magnetic resonance imaging, x-ray imaging and radiopharmaceuticals
EP0859642A2 (en) 1995-10-17 1998-08-26 G.D. Searle & Co. Method of detecting cyclooxygenase-2
DE60041386D1 (en) 1999-01-19 2009-03-05 Molecular Insight Pharm Inc CONJUGATES OF THE GRANULOCYTE COLONY OF STIMULATING FACTOR FOR THE TARGETED IMAGING OF INFECTIONS AND INFLAMMATION
US6306890B1 (en) 1999-08-30 2001-10-23 Vanderbilt University Esters derived from indolealkanols and novel amides derived from indolealkylamides that are selective COX-2 inhibitors
US6692724B1 (en) 1999-10-25 2004-02-17 Board Of Regents, The University Of Texas System Ethylenedicysteine (EC)-drug conjugates, compositions and methods for tissue specific disease imaging
US7067111B1 (en) * 1999-10-25 2006-06-27 Board Of Regents, University Of Texas System Ethylenedicysteine (EC)-drug conjugates, compositions and methods for tissue specific disease imaging
AU4308001A (en) 1999-12-03 2001-06-12 Yale University Transition metal-cyclopentadienyl-tropane conjugates
DE60127951T2 (en) * 2000-04-28 2008-01-17 President And Fellows Of Harvard College, Cambridge SMALL TECHNETIUM 99M AND RHENIUM-MARKED MEANS AND METHOD FOR TUMOR IMAGING
CN101979095A (en) * 2001-05-02 2011-02-23 普渡研究基金会 Treatment and diagnosis of macrophage mediated disease
AU2003224747A1 (en) 2002-04-08 2003-10-27 Biostream, Inc. Technetium-labeled rotenone derivatives, and methods of use thereof
ATE448799T1 (en) 2002-05-06 2009-12-15 Endocyte Inc FOLATE RECEPTOR TARGETED IMAGING CONJUGATES
IL153183A (en) 2002-06-04 2010-05-17 Aposense Ltd Agents for imaging and diagnostic methods using them
AU2003290673B2 (en) * 2002-11-08 2011-01-06 Massachusetts Institute Of Technology Small technetium-99m and rhenium labeled agents and methods for imaging tissues, organs and tumors
EP1638612A4 (en) 2003-06-25 2010-09-29 Univ Vanderbilt Cox-2-targeted imaging agents
WO2005086612A2 (en) 2003-07-29 2005-09-22 Immunomedics, Inc. Fluorinated carbohydrate conjugates
US9050378B2 (en) 2003-12-10 2015-06-09 Board Of Regents, The University Of Texas System N2S2 chelate-targeting ligand conjugates
US20080260650A1 (en) 2004-10-28 2008-10-23 The General Hospital Corporation Methods of Detection and Therapy of Inflamed Tissues Using Immune Modulation
JP2008531755A (en) 2005-01-05 2008-08-14 ボード オブ リージェンツ, ザ ユニバーシティ オブ テキサス システム Conjugates for dual imaging and radiation chemotherapy: composition, manufacture and indication
CA2623648C (en) 2005-09-21 2018-05-22 The Regents Of The University Of California Systems, compositions, and methods for local imaging and treatment of pain
US7871623B2 (en) 2005-12-21 2011-01-18 The Board Of Trustees Of The Leland Stanford Junior University Compositions and methods for imaging pain and stress in vivo
CA2657691A1 (en) 2006-06-19 2007-12-27 Vanderbilt University Methods and compositions for diagnostic and therapeutic targeting of cox-2
US10925977B2 (en) 2006-10-05 2021-02-23 Ceil>Point, LLC Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
US20080241256A1 (en) 2007-03-30 2008-10-02 Liisa Kuhn Targeted active agent delivery system based on calcium phosphate nanoparticles
US20090180951A1 (en) 2007-12-12 2009-07-16 Molecular Insight Pharmaceuticals, Inc. Inhibitors of integrin vla-4
EP2307032A4 (en) 2008-05-22 2014-08-20 Univ Ramot Novel conjugates of polymers having a therapeutically active agent and an angiogenesis targeting moiety attached thereto and uses thereof in the treatment of angiogenesis related diseases
CU23844B1 (en) 2009-04-17 2012-10-15 Ct De Neurociencias De Cuba PROCEDURE FOR OBTAINING NEW DERIVATIVES OF NAFTALENE FOR THE LIVE DIAGNOSIS OF ALZHEIMER'S DISEASE
WO2011008985A2 (en) 2009-07-15 2011-01-20 Georgia Tech Research Corporation Methods and compositions for improved delivery of therapeutic and diagnostic agents
WO2011016376A1 (en) 2009-08-03 2011-02-10 独立行政法人理化学研究所 Isotope–labeled 2-arylpropionic acid compounds and process for production of same, and molecular probe for positron emission tomography and method for imaging of cyclooxygenase and the like using same
BR112013026680A2 (en) 2011-08-15 2016-12-27 Univ City New York Res Found compound, method of treating an inflammatory disease and pharmaceutical composition
EP3693022A3 (en) 2015-01-09 2020-09-16 Reiley Pharmaceuticals, Inc. Cox-2-targeting, platinum-containing conjugates and their use in the treatment of tumors and cancers

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100111858A1 (en) * 2007-01-19 2010-05-06 Howard Carol P Diangostic and Therapeutic Cyclooxygenase-2 Binding Ligands

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022076741A1 (en) * 2020-10-07 2022-04-14 Reiley Pharmaceuticals, Inc. Coxib-derived conjugate compounds and methods of use thereof

Also Published As

Publication number Publication date
US20240190790A1 (en) 2024-06-13
US20180162784A1 (en) 2018-06-14
US9850183B2 (en) 2017-12-26
EP3160514A1 (en) 2017-05-03
WO2015200187A1 (en) 2015-12-30
US20220017432A1 (en) 2022-01-20
EP3160514B1 (en) 2024-07-31
EP3160514A4 (en) 2018-02-28
US20150374858A1 (en) 2015-12-31

Similar Documents

Publication Publication Date Title
US20240190790A1 (en) Conjugates derived from non-steroidal anti-inflammatory drugs and methods of use thereof in imaging
JP6177832B2 (en) Arginase inhibitors and methods of use
JP6724115B2 (en) Arginase inhibitors and their use
KR20200124706A (en) Chemical conjugates of Evans blue derivatives and use as radiotherapy and contrast agents for targeting prostate cancer
US20220133918A1 (en) Coxib-derived conjugate compounds and methods of use thereof
JP7264489B2 (en) Radiolabeled fluorescent PARP inhibitors for imaging and radiotherapy
AU2010206535B2 (en) Arginase inhibitors and methods of use

Legal Events

Date Code Title Description
STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

AS Assignment

Owner name: REILEY PHARMACEUTICALS, INC., CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:REILEY, MARK A.;SILBER, B. MICHAEL;MEDINA, JULIO;AND OTHERS;SIGNING DATES FROM 20150929 TO 20160113;REEL/FRAME:049961/0932

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION