WO1995022341A1 - Labelled peptide compounds - Google Patents
Labelled peptide compounds Download PDFInfo
- Publication number
- WO1995022341A1 WO1995022341A1 PCT/US1995/002131 US9502131W WO9522341A1 WO 1995022341 A1 WO1995022341 A1 WO 1995022341A1 US 9502131 W US9502131 W US 9502131W WO 9522341 A1 WO9522341 A1 WO 9522341A1
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- WIPO (PCT)
- Prior art keywords
- group
- peptide
- labelled
- isotope
- compound
- Prior art date
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- 125000000430 tryptophan group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations 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
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations 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
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/085—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins the peptide being neurotensin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations 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
- A61K51/04—Organic compounds
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/088—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins conjugates with carriers being peptides, polyamino acids or proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
- C07K7/083—Neurotensin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2121/00—Preparations for use in therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2123/00—Preparations for testing in vivo
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- the present invention relates to labelled peptide compounds, to a method of preparing these compounds, to a pharmaceutical composition comprising these compounds, to the use of this composition for diagnosis and therapy, and to a kit for preparing a radiopharmaceutical composition.
- Neurotensin is a thirteen amino acid peptide, in 1973 isolated from bovine hypothalamus. It has the following structure: pGlu-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH
- neurotensin High concentrations of neurotensin are found in discrete regions of the mammalian central nervous system. In addition, neurotensin interacts with specific receptors in the periphery. During the last decade, neurotensin receptors were found in several tumour cells, like small cell lung carcinoma, human colon carcinoma and human meningiomas.
- [Trp"] neurotensin [Trp"] neurotensin. Iodination (with 125-iodide under electrophilic conditions on the aromatic ring of tyrosine-3) results in a mono-iodo derivative showing a K d of 0.1 nM for binding on rat brain synaptic membranes. Preliminary experiments from the same group of researchers (Sadoul et al.; Biochem. Biophys. Res. Commun. 1984, 120, 812-819) indicated that neurotensin receptors in human brain showed a low affinity for monoiodo-[Trp" ] -neurotensin, making this compound unsuitable for binding experiments. The same group of researchers succeeded later on in preparing a mono-iodo derivative of neurotensin itself; only tyrosine-3 was iodinated with 125-iodide in this method.
- This radioiodinated analogue has a K d of 0.2 nM for binding on rat brain synaptic membranes and a K d of 0.26 nM for binding to human brain neurotensin receptors.
- the labelled natural neurotensin as well as the labelled try ⁇ tophan-11 neurotensin analogue suffers from an enzymatic breakdown due to cleavage of peptide bonds, resulting in an in vivo half-life of only a few minutes.
- This analogue contains one remaining tyrosine residue which can be readily radioiodinated using electrophilic substitution of the hydrogen in the ortho position of the phenolic group. Structure-activity studies revealed, however, that iodination in the 3-position of said tyrosine residue of this analogue results in a remarkable loss of receptor affinity, viz. with a factor of 20 (Mazella et al.; see above).
- a labelled peptide compound wherein the peptide has a selective neurotensin receptor affinity and is represented by the general formula
- R 1 is a (C 1 -C 3 )alkanoyl group, an arylcarbonyl group, an aryl- (C 1 -C 3 )alkanoyl group, or a chelating group attached by an amide bond or through a spacing group to the peptide molecule;
- Xaa and Xbb are each individually Arg or Lys;
- Xcc is an unsubstituted or substituted cyclic amino acid, preferably selected from Pro and Hyp;
- Xdd is Tyr, Trp or Phe
- Xee is Leu, Ile or t.-butylalanine
- n 0 or 1
- a metal isotope selected from the group consisting of 99m Tc, 203 Pb, 67 Ga, 68 Ga, 72 As, 111 In, 113m In, 97 Ru, 62 Cu, 64 Cu, 52 Fe, 52m Mn, 51 Cr, 186 Re, 188 Re, 77 As, 90 Y, 67 Cu, 169 Er, 121 Sn, 127 Te, 142 Pr, 143 Pr, 198 Au, 199 Au, 161 Tb, 109 Pd, 165 Dy, 149 Pm, 151 Pm, 153 Sm, 157 Gd, 159 Gd, 166 Ho, 172 Tm,
- R 1 represents a chelating group for chelating said isotope
- halogen isotope is attached to 4 Tyr in the 2-position of the phenyl ring, to 4 Trp, or to the aryl group of substituent R 1 .
- aryl groups in R 1 are: phenyl, halo-substituted phenyl or indolyl; preferably phenyl, 4-fluorophenyl, 2- or 4-bromophenyl, 2-iodophenyl, 4-fluoro-2-bromophenyl and 4-fluoro-2-iodophenyl.
- radioactive halogen isotopes are: 123 I , 124 I , 125 I, 131 I, 75 Br, 76 Br, 77 Br and 82 Br.
- the amino acids may have the D-configuration instead of the normal L-configuration.
- the labelled peptide compounds of the invention may also comprise socalled pseudo peptide bonds, viz. -CH 2 -NH- bonds, in addition to the natural amide bonds, viz. -CO-NH- bonds. Such modifications of the amino acids naturally occurring in peptides are within the scope of the present invention.
- Peptide compounds which, according to the invention, are labelled with a metal isotope as indicated above, are provided, directly or through a spacing group, with a chelating group, said chelating group being attached by an amide bond to an amino group of said peptide compound.
- Said chelating group is preferably derived from ethylene diamine tetraacetic acid (EDTA), diethylene triamine penta-acetic acid (DTPA), cyclohexyl 1,2-diamine tetra-acetic acid (CDTA) , ethyleneglycol-0,0'bis(2-aminoethyl)-N,N,N',N'-tetra-acetic acid (EGTA), N,N-bis(hydroxybenzyl)-ethylenediamine-N,N'-diacetic acid (HBED), triethylene tetramine hexa-acetic acid (TTHA), 1,4,7,10-tetraazacyclododecane-N,N'- ,N'',N'''-tetra-acetic acid (DOTA), hydroxyethyldiamine triacetic acid (HEDTA), 1,4,8,11-tetra-azacyclotetradecane-N,N',N'',N''
- R is a branched or non-branched, optionally substituted
- hydrocarbyl radical which may be interrupted by one or more heteroatoms selected from N, O and S and/or by one or more NH groups
- Y is a group which is capable of reacting with an amino group of the peptide and which is preferably selected from the group consisting of carbonyl, carbimidoyl, N-(C 1 -C 6 )alkylcarbimidoyl, N-hydroxycarbimidoyl and N-(C 1 -C 6 )alkoxycarbimidoyl.
- Suitable chelators of the general formula III are unsubstituted or substituted 2-iminothiolanes and 2- iminothiacyclohexanes, in particular 2-imino-4-mercaptomethylthiolane.
- Said optionally present spacing group has preferably the general formula or
- R 5 is a C 1 -C 10 alkylene group, a C 1 -C 10 alkylidene group or a C 2 -C 10 alkenylene group
- X is a thiocarbonyl group or a methylcarbonyl group.
- *I is 123 I, 125 I or 131 I
- *M is 111 In, 99m Tc, 186 Re, 166 Ho, 153 Sm or 161 Tb.
- the above labelled peptide compounds have been tested in a number of suitable model experiments that are predictive for in vivo application. These experiments are described in the Examples. From the results of these experiments it will be evident, that the labelled peptide compounds of the present invention have properties which make them suitable for diagnostic and therapeutic purposes. If labelled with a suitable isotope for diagnostic purposes, the peptide compound remains sufficiently long intact after administration to permit imaging of the target organ or tissue without presenting a disturbing background, for example, due to detached label. If labelled with a suitable radioisotope for therapy, such-labelled peptides are promising therapeutic agents for the treatment of a number of malignant tumours that are related to neurotensin binding places, such as small cell lung carcinoma, colon carcinoma and meningiomas.
- the new radiohalogenated peptide compounds of the invention can be prepared in a manner known per se for related compounds. So the invention also relates to a method of preparing a radiohalogenated peptide compound as defined hereinbefore,
- a water-soluble halogenide selected from 123 I-, 124 I-, 125 I-,
- Such a halogen exchange reaction is described in European patent no. 165630.
- An example of a suitable water-soluble acid is citric acid;
- suitable reducing agents are Sn(II) salts, gentisic acid, isoascorbic acid, a monosaccharide and a sulphite.
- the new metal-labelled peptide compounds of the invention can also be prepared in a manner known per se for related compounds.
- the peptide molecule is derivatized with the desired chelating agent as defined hereinbefore, e.g. EDTA, DTPA, etc., directly or after introduction of a spacing group as defined above, after which the compound obtained, having the general formula
- Xaa, Xbb, Xcc, Xdd, Xee and n have the meanings given above, and R 2 is a chelating group attached by an amide bond or through a spacing group to the peptide molecule;
- a metal isotope as defined hereinbefore, in the form of a salt or of a chelate bonded to a comparatively weak chelator, in order to form a complex.
- a metal isotope as defined hereinbefore
- salts or chelates of the desired metal isotope are: 111 In-oxinate, 99m Tc-tartrate, etc.
- the complex-forming reaction can generally be carried out in a simple manner and under conditions that are not detrimental to the peptide.
- the invention further relates to a pharmaceutical composition, comprising in addition to a pharmaceutically acceptable carrier material and, if desired, at least one pharmaceutically acceptable adjuvant, as the active substance a labelled peptide compound as defined hereinbefore.
- the invention also relates to a method for detecting and locating tissues having neurotensin receptors in the body of a warm-blooded living being, which comprises (i) administering to said being a composition comprising, in a quantity sufficient for external imaging, a labelled peptide compound as defined hereinbefore, wherein said peptide is labelled with (a) a metal isotope selected from the group consisting of 99m Tc, 203 Pb, 67 Ga, 68 Ga, 72 As, 111 In, 113m In, 97 Ru, 62 Cu, 64 Cu, 52 Fe, 52m Mn, 51 Cr, or (b) with a radioactive halogen isotope, selected from 123 I, 131 I, 73 Br, 76 Br and 77 Br, and thereupon (ii) subjecting said being to external imaging to determine the targeted sites in the body of said being in relation to the background activity.
- a metal isotope selected from the group consisting of 99m Tc, 203 Pb,
- the invention also relates to a method of intraoperatively detecting and locating tissues having neurotensin receptors in the body of a warm-blooded living being, which comprises (1) administering to said being a composition comprising, in a quantity sufficient for detection by a gamma detecting probe, a peptide compound as defined above, labelled with a radioisotope, selected from 161 Tb, 123 I and 125 I, preferably 161 Tb or 125 I, and thereupon (ii), after allowing the active substance to be taken up in said tissues and after blood clearance of radioactivity, subjecting said being to a radioimmunodetection technique in the relevant area of the body of said being, by using a gamma detecting probe.
- a composition comprising, in a quantity sufficient for detection by a gamma detecting probe, a peptide compound as defined above, labelled with a radioisotope, selected from 161 Tb, 123 I and 125 I, preferably 161
- the above radioisotope viz. in particular 161 Tb or 125 I, allows the use of a such-labelled peptide compound in the technique of radioguided surgery, wherein relevant tissues in the body of a patient can be detected and located intraoperatively by means of a gamma detecting probe.
- the surgeon can, intraoperatively, use this probe to find the lesions in which uptake of the compound labelled with said radioisotope, which is a low-energy gamma photon emittor, has taken place.
- tumour cells such as small cell lung carcinoma, colon carcinoma and meningiomas
- the peptide compounds of the present invention provided they are radiolabelled with isotopes suitable for the purpose, can be used for the therapeutic treatment of these tumours.
- the invention further relates to a method for the therapeutic treatment of tumours, having on their surface a high density of neurotensin receptor sites, in the body of a warm-blooded living being, which comprises administering to said being a composition comprising, in a quantity effective for combating or controling tumours, a peptide compound as defined above, said peptide compound being labelled with a metal isotope selected from the group consisting of 186 Re, 188 Re, 77 As, 90 Y, 67 Cu, 169 Er, 121 Sn, 127 Te, 142 Pr, 143 Pr, 198 Au, 199 Au, 161 Tb, 109 Pd, 165 Dy, 149 Pm, 151 Pm, 153 Sm, 157 Gd, 159 Gd, 166 Ho, 172 Tm, 169 Yb, 175 Yb, 177 Lu , 105 Rh and 111 Ag .
- a metal isotope selected from the group consisting of 186 Re, 188 Re,
- the invention also relates to a kit for preparing a radiopharmaceutical composition.
- kit may comprise (i) a peptide compound having a selective affinity to neurotensin receptors and having the general formula II as presented hereinbefore, to which substance, if desired, an inert pharmaceutically acceptable carrier and/or formulating agents and/or adjuvants is/are added, (ii) a solution of a salt or chelate of a suitable radionuclide, and (iii) instructions for use with a prescription for reacting the ingredients present in the kit.
- Suitable radionuclides for the above kit are the following metal isotopes: 203 Pb, 67 Ga, 68 Ga, 72 As, 111 In, 113m In, 97 Ru, 62 Cu, 99m Tc, 186 Re, 188 Re, 64 Cu, 52 Fe, 52m Mn, 51 Cr, 77 As, 90 Y, 67 Cu, 169 Er, 121 Sn, 127 Te, 142 Pr, 143 Pr, 198 Au, 199 Au, 161 Tb, 109 Pd, 165 Dy, 149 Pm, 151 Pm, 153 Sm, 157 Gd, 159 Gd, 166 Ho, 172 Tm, 169 Yb, 175 Yb, 177 Lu,
- the peptide compound to be used as an ingredient of the above kit has been modified by a reaction with a chelating agent as defined hereinbefore.
- the resulting peptide conjugate provides a facility for firmly attaching the radionuclide in a simple manner.
- Suitable chelating agents for modifying the peptide are described in detail hereinbefore.
- kits to be supplied to the user may also comprise the ingredient (s) defined sub (i) above, together with instructions for use, whereas the solution of a salt or chelate of the radionuclide, defined sub (ii) above, which solution has a limited shelf life, may be put to the disposal of the user separately.
- kits may comprise, in addition to the ingredient (s) defined sub (i) above, (ii) a reducing agent and, if desired, a chelator, and (iii) instructions for use with a prescription for reacting the ingredients of the kit with Tc-99m in the form of a pertechnetate solution, or with Re-186 or Re-188 in the form of a perrhenate solution.
- the ingredients of the kit may be combined, provided they are compatible.
- the kit should comprise a reducing agent to reduce the pertechnetate or perrhenate, for example, a dithionite, a metallic reducing agent or a complex-stabilizing reducing agent, e.g. SnCl 2 , Sn(II)-tartrate, Sn(II)-phosphonate or -pyrophosphate, or Sn(II)- glucoheptonate.
- a reducing agent to reduce the pertechnetate or perrhenate for example, a dithionite, a metallic reducing agent or a complex-stabilizing reducing agent, e.g. SnCl 2 , Sn(II)-tartrate, Sn(II)-phosphonate or -pyrophosphate, or Sn(II)- glucoheptonate.
- the pertechnetate or perrhenate solution can simply be obtained by the user from a suitable generator.
- the kit according to the present invention comprises a modified peptide or a peptide conjugate, obtained by modifying the peptide as defined hereinbefore by a treatment with a chelating agent.
- a chelating agent Suitable chelating agents have been described hereinbefore.
- the complex forming reaction with the peptide conjugate can simply be produced by combining the components in a neutral medium and causing them to react.
- the radionuclide may be presented to the peptide conjugate in the form of a chelate bonded to a comparatively weak chelator, as described hereinbefore.
- the radionuclide will preferably be added separately in the form of a pertechnetate or perrhenate solution.
- the kit will comprise a suitable reducing agent and, if desired, a chelator, the former to reduce the pertechnetate or the perrhenate.
- a suitable reducing agent may be used, for example, a dithionite or a metallic reducing agent.
- the ingredients may optionally be combined, provided they are compatible.
- Such a monocomponent kit in which the combined ingredients are preferably lyophilized, is excellently suitable for being reacted, by the user, with the radionuclide solution.
- a metallic reducing agent for example, Sn(II), Ce(III), Fe(II), Cu(I), Ti(III) or Sb(III); Sn(II) is excellently suitable.
- the peptide constituent of the above-mentioned kits i.e.
- the peptide conjugate may be supplied as a solution, for example, in the form of a physiological saline solution, or in some buffer solution, but is preferably present in a dry condition, for example, in the lyophilized condition.
- a component for an injection liquid it should be sterile, in which, when the constituent is in the dry state, the user should preferably use a sterile physiological saline solution as a solvent.
- the above-mentioned constituent may be stabilized in the conventional manner with suitable stabilizers, for example, ascorbic acid, gentisic acid or salts of these acids, or it may comprise other auxiliary agents, for example, fillers, such as glucose, lactose, mannitol, and the like.
- the first amino acid is attached to a resin (chloromethylpolystyrene, crosslinked with 1% of 1,4-divinylbenzene) via a Cs-salt of the desired amino acid, i.e. leucine.
- the substitution grade (0.60 mmol/g resin) is determined via the picric acid method.
- the peptide is assembled using a repetitive cycle, as follows:
- DIEA diisopropylethylamine
- DCC N,N'-dicyclohexylcarbodiimide
- HOBt 1- hydroxybenzotriazole
- the peptide is cleaved from the resin by reaction with liquid HF. Acetic acid extraction is used to separate the peptide from the resin.
- the peptides are radioiodinated by nucleophilic displacement of bromine by iodine-131, according to the procedure as described in European patent no. 165630.
- nucleophilic displacement of bromine by iodine-131 according to the procedure as described in European patent no. 165630.
- the peptide (1 mg) is dissolved in 500 ⁇ l of stock solution and 60 ⁇ l of
- the desired radioiodinated peptides (1), (2), (3) and (4) are obtained in yields of 84%, 54%, 86% and 55%, respectively (not optimized).
- Binding assays are performed by studying the inhibition of [ 3 H]neurotensin binding to guinea pig forebrain membranes. The following results are obtained, using the unlabelled acetyl compound Ac-Arg-Arg-Pro-Tyr-Ile-Leu-OH (a) as the reference.
- the affinity is expressed as the pIC 50 value (i.e. the concentration of peptide analogue yielding 50% inhibition).
- radioiodinated analogues (1) through (4) show affinities to neurotensin receptor sites in this binding assay which are comparable with that of the unlabelled compound.
- the enzymatic stability of the four radioiodinated analogues (1), (2), (3) and (4) is determined in vitro in human serum in a conventional manner, showing that this stability is sufficient.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7521978A JPH11514329A (en) | 1994-02-18 | 1995-02-21 | Labeled peptide compounds |
EP95911829A EP0752873A4 (en) | 1994-02-18 | 1995-02-21 | Labelled peptide compounds |
US08/737,299 US5952464A (en) | 1994-02-18 | 1995-02-21 | Labelled peptide compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP94200409.4 | 1994-02-18 | ||
EP94200409 | 1994-02-18 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/334,254 Division US6194386B1 (en) | 1994-02-18 | 1999-06-16 | Labelled peptide compounds |
Publications (1)
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WO1995022341A1 true WO1995022341A1 (en) | 1995-08-24 |
Family
ID=8216649
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US1995/002131 WO1995022341A1 (en) | 1994-02-18 | 1995-02-21 | Labelled peptide compounds |
Country Status (5)
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US (1) | US6194386B1 (en) |
EP (1) | EP0752873A4 (en) |
JP (1) | JPH11514329A (en) |
CA (1) | CA2183421A1 (en) |
WO (1) | WO1995022341A1 (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996031531A2 (en) * | 1995-04-04 | 1996-10-10 | Advanced Bioconcept, Inc. | Fluorescent peptides |
US5693679A (en) * | 1995-04-04 | 1997-12-02 | Advanced Bioconcept, Inc. | Fluorescent somatostatin |
WO1998033531A1 (en) * | 1997-02-03 | 1998-08-06 | Mallinckrodt Medical, Inc. | Method for the detection and localization of malignant human tumours |
US5824772A (en) * | 1995-04-04 | 1998-10-20 | Advanced Bioconcept, Inc. | Fluorescent somatostatin |
US5919797A (en) * | 1996-04-24 | 1999-07-06 | Emory University | Halogenated naphthyl methoxy piperidines for mapping serotonin transporter sites |
US6054557A (en) * | 1995-04-04 | 2000-04-25 | Advanced Bioconcept (1994) Ltd. | Fluorescent peptides |
WO2000078796A2 (en) * | 1999-06-24 | 2000-12-28 | Mallinckrodt Inc. | Labeled neurotensin derivatives with improved resistance to enzymatic degradation |
WO2001030398A2 (en) * | 1999-10-22 | 2001-05-03 | Insight Neuroimaging Systems, Llc | Ligand chelated paramagnetic mri contrast agents |
US6677430B1 (en) | 1995-07-20 | 2004-01-13 | Advanced Bioconcept Company | Fluorescent motilin peptides |
WO2005116065A1 (en) * | 2004-05-24 | 2005-12-08 | Institut De Cardiologie De Montréal | Labelled adrenomedullin derivatives and their use for imaging and therapy |
EP2383289A1 (en) | 2006-10-16 | 2011-11-02 | The Salk Institute for Biological Studies | Receptor (SSTR2)-selective somatostatin antagonists |
WO2012113775A1 (en) | 2011-02-21 | 2012-08-30 | University Of Zurich | Ankyrin g and modulators thereof for the treatment of neurodegenerative disorders |
US8691761B2 (en) | 2006-10-16 | 2014-04-08 | Jean E. F. Rivier | Somatostatin receptor 2 antagonists |
EP2740726A1 (en) | 2012-12-07 | 2014-06-11 | 3B Pharmaceuticals GmbH | Neurotensin receptor ligands |
EP2954934A1 (en) | 2014-06-11 | 2015-12-16 | 3B Pharmaceuticals GmbH | Conjugate comprising a neurotensin receptor ligand and use thereof |
EP2954933A1 (en) | 2014-06-10 | 2015-12-16 | 3B Pharmaceuticals GmbH | Conjugate comprising a neurotensin receptor ligand |
WO2015188934A1 (en) | 2014-06-10 | 2015-12-17 | 3B Pharmaceuticals Gmbh | Conjugate comprising a neurotensin receptor ligand and use thereof |
US11279732B2 (en) | 2016-02-09 | 2022-03-22 | Cdrd Ventures Inc. | Somatostatin receptor antagonist compounds and methods of using the same |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7507547B2 (en) * | 2004-09-09 | 2009-03-24 | University Of Massachusetts | Screening assays for antioxidants and antiproliferative compounds |
US20060062729A1 (en) * | 2004-09-09 | 2006-03-23 | Carraway Robert E | Enhanced ligand binding to neurotensin receptors |
US20070231833A1 (en) * | 2005-05-23 | 2007-10-04 | Arcidiacono Steven M | Labeled antimicrobial peptides and method of using the same to detect microorganisms of interest |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2687680A1 (en) * | 1992-02-20 | 1993-08-27 | Centre Nat Rech Scient | Process for labelling proteins and peptides by acylation of their alpha amino functional group by a reagent containing an activated carboxylic functional group |
EP0636032A1 (en) * | 1992-03-25 | 1995-02-01 | Mallinckrodt Medical, Inc. | Method of intraoperatively detecting and locating tumoral tissues |
-
1995
- 1995-02-21 WO PCT/US1995/002131 patent/WO1995022341A1/en not_active Application Discontinuation
- 1995-02-21 JP JP7521978A patent/JPH11514329A/en not_active Ceased
- 1995-02-21 CA CA002183421A patent/CA2183421A1/en not_active Abandoned
- 1995-02-21 EP EP95911829A patent/EP0752873A4/en not_active Withdrawn
-
1999
- 1999-06-16 US US09/334,254 patent/US6194386B1/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
SADOUL J.-L., ET AL.: "PREPARATION OF NEUROTENSIN SELECTIVELY IODINATED ON THE TYROSINE 3 RESIDU. BIOLOGICAL ACTIVITY AND BINDING PROPERTIES ON MAMMALIAN NEUROTENSIN RECEPTORS.", BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, ACADEMIC PRESS INC. ORLANDO, FL, US, vol. 120., no. 03., 1 June 1984 (1984-06-01), US, pages 812 - 819., XP000619657, ISSN: 0006-291X, DOI: 10.1016/S0006-291X(84)80179-5 * |
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JPH11514329A (en) | 1999-12-07 |
EP0752873A4 (en) | 2002-05-15 |
EP0752873A1 (en) | 1997-01-15 |
US6194386B1 (en) | 2001-02-27 |
CA2183421A1 (en) | 1995-08-24 |
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