US20060069047A1 - Antibiotic conjugates - Google Patents
Antibiotic conjugates Download PDFInfo
- Publication number
- US20060069047A1 US20060069047A1 US10/504,792 US50479205A US2006069047A1 US 20060069047 A1 US20060069047 A1 US 20060069047A1 US 50479205 A US50479205 A US 50479205A US 2006069047 A1 US2006069047 A1 US 2006069047A1
- Authority
- US
- United States
- Prior art keywords
- alkyl
- independently
- alkenyl
- aryl
- heteroaryl
- 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
Links
- 230000003115 biocidal effect Effects 0.000 title claims abstract description 41
- 239000003814 drug Substances 0.000 claims abstract description 63
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- 229940124597 therapeutic agent Drugs 0.000 claims abstract description 42
- MQTOSJVFKKJCRP-BICOPXKESA-N azithromycin Chemical class O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)N(C)C[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 MQTOSJVFKKJCRP-BICOPXKESA-N 0.000 claims abstract description 14
- 150000003983 crown ethers Chemical class 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 51
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- 229940039790 sodium oxalate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 208000017810 streptobacillary rat-bite fever Diseases 0.000 description 1
- 229940031000 streptococcus pneumoniae Drugs 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
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- 208000006379 syphilis Diseases 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- LJVAJPDWBABPEJ-PNUFFHFMSA-N telithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)[C@@H](C)C(=O)O[C@@H]([C@]2(OC(=O)N(CCCCN3C=C(N=C3)C=3C=NC=CC=3)[C@@H]2[C@@H](C)C(=O)[C@H](C)C[C@@]1(C)OC)C)CC)[C@@H]1O[C@H](C)C[C@H](N(C)C)[C@H]1O LJVAJPDWBABPEJ-PNUFFHFMSA-N 0.000 description 1
- 229960003250 telithromycin Drugs 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 229940040944 tetracyclines Drugs 0.000 description 1
- MHXBHWLGRWOABW-UHFFFAOYSA-N tetradecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC MHXBHWLGRWOABW-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- OHKOGUYZJXTSFX-KZFFXBSXSA-N ticarcillin Chemical compound C=1([C@@H](C(O)=O)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)C=CSC=1 OHKOGUYZJXTSFX-KZFFXBSXSA-N 0.000 description 1
- 229960004659 ticarcillin Drugs 0.000 description 1
- 208000016523 tick-borne infectious disease Diseases 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 206010044008 tonsillitis Diseases 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 206010044325 trachoma Diseases 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 230000026683 transduction Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229950001272 viomycin Drugs 0.000 description 1
- GXFAIFRPOKBQRV-GHXCTMGLSA-N viomycin Chemical compound N1C(=O)\C(=C\NC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)C[C@@H](N)CCCN)CNC(=O)[C@@H]1[C@@H]1NC(=N)N[C@@H](O)C1 GXFAIFRPOKBQRV-GHXCTMGLSA-N 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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- 150000003751 zinc Chemical class 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- 229940126085 β‑Lactamase Inhibitor Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
- A61K47/552—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds one of the codrug's components being an antibiotic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
Definitions
- Phagocytic white blood cells and antimicrobial agents have been recognized as having several potential interactions that may be synergistic for combating infection. Phagocytic killing by polymorphonuclear leukocytes (PMNs), monocytes, and macrophages is the primary host defense against bacterial infections. Antimicrobial agents make bacteria more susceptible to killing by neutrophils even at subinhibitory concentrations (Adinolfi & Bonventre (1988) Antimicrob Agents Chemother 32: 1012-8). Neutrophils migrate to sites of infection, concentrate at these sites, and thus may serve as an antimicrobial agent delivery mechanism.
- PMNs polymorphonuclear leukocytes
- monocytes monocytes
- macrophages macrophages
- Antimicrobial agents make bacteria more susceptible to killing by neutrophils even at subinhibitory concentrations (Adinolfi & Bonventre (1988) Antimicrob Agents Chemother 32: 1012-8). Neutrophils migrate to sites of infection, concentrate at these sites, and thus
- Salmonella and other intracellular pathogens can invade phagocytes and survive inside them, avoiding the lysosomal compartment.
- Cellular invasion is an important step in the progression of many serious bacterial infections because it allows pathogens to evade host defense mechanisms and benefit from a rich nutrient supply.
- the agent should not interfere with neutrophil migration, the agent should be concentrated in the neutrophil, and the agent should be released in an active form at the site of infection.
- 4,474,768 is more stable than erythromycin in the presence of acids, and has very low plasma concentrations owing to its concentration to a large extent in cells, often achieving a C/E of ⁇ 500 (Bouvier d'Yvoire et al. (1998) J. Antimicrob. Chemother. 41: Suppl. B, 63-68). Its stability, accumulation in phagocytes and long half-life (t 1/2 ⁇ 68 hours), make azithromycin an ideal antibiotic in terms of in vivo distribution.
- successful therapy with a pharmaceutical agent requires that the agent satisfy numerous requirements imposed by the physiology of the host and of the disease or condition. These include: (i) adequate ability to interact with the target; (ii) appropriate physical properties for presence at the location of the receptors in concentrations that permit the interactions noted above; (iii) appropriate physical properties to allow the agent to enter the body and distribute to the location of the receptors by any means; (iv) Sufficient stability in fluids of the body; (v) the absence of toxic effects in compartments where the drug is most concentrated, or in any other compartment where the drug is located; and (vi) the absence of sequestration into non-physiological compartments and so on.
- U.S. Pat. No. 5,434,147 describes a process for conjugation of antibiotics with transferrin or low density lipoprotein for treating intracellular pathogens.
- the coupled transferrin molecules are claimed to be selectively taken up by phagosomes to target membrane-bound pathogens.
- transferrin, and therefore molecules attached to it do not traffic through the lysosomal compartment.
- This process therefore, is of limited utility in areas where the antibiotic is to provide synergistic activity with phagocytic immune cells in neutralising non-intracellular pathogens.
- the molecular weight of transferrin (76,000-81,000 daltons), as well as its polypeptide composition precludes oral delivery of such compositions.
- Oral absorption of drugs is the most desirable method of drug administration in the treatment of human diseases, particularly in prolonged therapeutical treatments.
- 4,474,768 is more stable than erythromycin in the presence of acids, and has very low plasma concentrations owing to its concentration to a large extent in cells, often achieving a C/E of ⁇ 500 (Bouvier d'Yvoire et al., supra). Its stability, accumulation in phagocytes and long half-life (t1 ⁇ 2 ⁇ 68 hours), make azithromycin an ideal antibiotic in terms of in vivo distribution.
- the invention relates to a conjugate useful for enhancing efficacy of a therapeutic agent, and a method of treating diseases including infection diseases (e.g., bacterial diseases).
- infections diseases e.g., bacterial diseases.
- this invention features a compound of the following formula: T L-C) m , wherein T is a transportophore, L is a bond or linker, C is an antibiotic therapeutic agent, and m is 1-8, the transportophore is covalently bonded to the antibiotic therapeutic agent via the bond or the linker, and the transportophore is an azithromycin derivative or crown ether derivative.
- T is a transportophore
- L is a bond or linker
- C is an antibiotic therapeutic agent
- m 1-8
- the transportophore is covalently bonded to the antibiotic therapeutic agent via the bond or the linker
- the transportophore is an azithromycin derivative or crown ether derivative.
- the transportophore can be a metabolite, a natural product, a metabolite mimic, a metabolite derivative (e.g., a sugar, amino, or peptide derivative), a fatty acid, a bile acid, a vitamin, a nucleobase, an alcohol, or an organic acid or base, a portion of which resembles and is recognized as a substrate for transport protein(s).
- It can be an amphiphilic molecule having a pKa value of 6.5 to 9.5, or a cyclic or heterocyclic molecule (e.g., lactone, lactam, ether, cyclic acetal or hemi-acetal).
- the cyclic or heterocyclic molecule can have an attached sugar.
- the cyclic or heterocyclic molecule can be a macrolactone or macroether, including a macrolactone or macroether having an attached sugar.
- the cyclic or heterocyclic molecule can also be a macrolide or ketolide having an amino sugar, including a macrolide having mono-, di-, or tri-basic groups (e.g., an amine).
- the macrolide has no intrinsic antibacterial activity (determined by, e.g., an antibiotic sensitivity test) at 10 ⁇ M in solution and a pKa value between 6.5 and 9.0
- the transportophore is an azithromycin derivative
- the conjugate has the formula (in which a bond, drawn without any attached groups, means a methyl group. The same rule applies to other similar situations):
- Y independently, a bond or a linker (alkylating residue or neighbouring a carbonyl)
- R 13 independently, an antibiotic therapeutic agent
- R 17 (O—R 20 -aryliden)(C 1 -C 10 )alkyl
- the transportophore is a crown ether derivative
- the conjugate has the formula:
- the transportophore is covalently bonded to an antibiotic therapeutic agent.
- the linker can be (C 1 -C 8 )alkyl, (C 1 -C 8 )alkenyl, (C 1 -C 8 )alkynyl, (C 3 -C 10 )cycloalkyl, (C 6 -C 10 )aryl, (C 2 -C 9 )heteroalkyl, or (C 2 -C 9 )heteroaryl; wherein alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl is optionally substituted by (C 1 -C 6 )alkyl, 1-4 halogens, (C 1 -C 4 )alkoxy, (C 1 -C 4 )alkoxycarbonyl, hydroxy, amino, (C 1 -C 4 )alkylamino, (C 1 -C 4 )dialkylamino, (C 3 -C 10
- the linker can be added in one or more positions via one or more linking groups of the same or differing formula.
- the linker can be many other molecules that, to date, have not been classified as pharmacological agents and commercialised as such due to inadequate pharmacokinetic properties including one or more of those listed below. Given the data presented herein, it would be desirable to attach a novel agent potentially active in the indication areas cited herein to a linker in an attempt to capture the in vivo benefits that the linker may confer.
- a “therapeutic agent,” as used herein, is a molecule with pharmacological activity (e.g., a drug, medicine, medicament, or active agent), a disease modification agent, or any other molecule that can be covalently attached to a transportophore via a bond or a linker which may have a desirable mode of action in bacterial cells.
- a therapeutic agent may be released from a compound described above in response to the enzyme activity or the physicochemical environment of the targeted cells.
- the therapeutic agent is selectively accumulated in a cell due to specific characteristics of the cell membranes, specific expression of membrane proteins, specific conditions within the cell, notably to expression of specific proteins such as granule proteins, binding sites in the cytoplasm, or other membrane bound or soluble proteins, and is thus trapped in the cell and therefore exhibits an enhanced or desired activity therein.
- An “amphiphilic molecule,” as used herein, is a molecule having a hydrophilic (polar) and hydrophobic (non-polar) functional groups (e.g., atoms) or a combination of groups (or atoms). The pKa of this molecule is in the range of 6.5 to 9.5.
- sugar refers to a mono-, di-, or tri-saccharide including deoxy-, thio-, and amino-saccharides.
- sugar include, but are not limited to, furanose and pyranose.
- macrolactone refers to a large lactone ring (i.e., cyclic ester) having at least 10 (e.g., 10 to 25) ring atoms.
- crocyclic ether refers to an ether having at least 10 (e.g., 10 to 25) ring atoms.
- macrorolide refers to a chemical compound characterized by a large lactone ring (having at least 10, e.g., 10 to 25, ring atoms) containing one or more keto and hydroxyl groups, or to any of a large group of antibacterial antibiotics containing a large lactone ring linked glycosidically to one or more sugars; they are produced by certain species of Streptomyces and inhibit protein synthesis by binding to the 50S subunits of 70S ribosomes. Examples include erythromycin, azithromycin , and clarithromycin.
- ketolide refers to a chemical compound characterized by a large lactone ring (having at least 10, e.g., 10 to 25, ring atoms) containing one or more keto groups.
- phagocytic cell refers to a cell, especially a leukocyte, that ingests and destroys other cells, microorganisms, or other foreign matter in the blood and tissues.
- heteroatom is a nitrogen, sulfur or oxygen atom.
- Groups containing one or more heteroatoms may contain different heteroatoms.
- Alkyl is an unsubstituted or substituted saturated hydrocarbon chain radical having from 1 to 8 carbon atoms, preferably from 1 to 4 carbon atoms.
- Preferred alkyl groups include (for example) methyl, ethyl, propyl, isopropyl, and butyl.
- Heteroalkyl is an unsubstituted or substituted saturated chain radical having from 3 to 8 members comprising carbon atoms and one or two heteroatoms.
- Alkenyl is an unsubstituted or substituted hydrocarbon chain radical having from 2 to 8 carbon atoms, preferably from 2 to 4 carbon atoms, and having at least one olefinic double bond. alkynyl groups have one or more triple carbon-carbon bonds in the chain.
- Cycloalkyl is a saturated carbocyclic ring radical.
- Preferred cycloalkyl groups include (for example) cyclopropyl, cyclobutyl and cyclohexyl.
- Heterocyclic ring is an unsubstituted or substituted, saturated, unsaturated or aromatic ring radical comprised of carbon atoms and one or more heteroatoms in the ring. Heterocyclic rings are monocyclic or are fused, bridged or spiro polycyclic ring systems. Monocyclic rings contain from 3 to 9 atoms, preferably 3 to 6 atoms. Polycyclic rings contain from 7 to 17 atoms, preferably from 7 to 13 atoms.
- Aryl is an aromatic carbocyclic ring radical.
- Preferred aryl groups include (for example) phenyl, tolyl, xylyl, cumenyl and naphthyl.
- Heteroaryl is an aromatic heterocyclic ring radical.
- Preferred heteroaryl groups include (for example) thienyl, furyl, pyrrolyl, pyridinyl, pyrazinyl, thiazolyl, pyrimidinyl, quinolonyl, and tetrazolyl.
- Alkoxy is an oxygen radical having a hydrocarbon chain substituent, where the hydrocarbon chain is an alkyl or alkenyl (i.e., —O-alkyl or —O-alkenyl).
- Preferred alkoxy groups include (for example) methoxy, ethoxy, propoxy and allyloxy.
- Alkylamino is an amino radical having one or two alkyl substituents (i.e., —N-alkyl).
- Arylalkyl is an alkyl radical substituted with an aryl group. Preferred arylalkyl groups include benzyl and phenylethyl.
- Arylamino is an amine radical substituted with an aryl group (i.e., —NH-aryl).
- Aryloxy is an oxygen radical having a aryl substituent (i.e., —O-aryl).
- alkyl or “carbonyl” is a radical formed by removal of the hydroxy from an carboxylic acid (i.e., R—C( ⁇ O)—).
- Preferred alkylacyl groups include (for example) acetyl, and propionyl.
- “Acyloxy” is an oxygen radical having an acyl substituent (i.e., —O-acyl); for example, —O—C( ⁇ O)-alkyl.
- “Acylamino” is an amino radical having an acyl substituent (i.e., —N-acyl); for example, —NH—C( ⁇ O)-alkyl.
- Alkyliden is a bivalent alkyl group.
- Aryliden is a bivalent aryl group.
- Halo is a chloro, bromo, fluoro or iodo atom radical. Chloro and fluoro are preferred halides.
- a “lower” hydrocarbon moiety is a hydrocarbon chain comprised of from 1 to 6, preferably from 1 to 4, carbon atoms.
- a particular radical may be defined for use as a substituent in multiple locations.
- the R 10 a substituent is defined as a potential substituent of R 1 , but is also incorporated into the definition of other substituents (such as R 3 , R 8 , and R 9 ).
- such a radical is independently selected each time it is used (e.g., R 10a need not be alkyl in all occurrences in defining a given compound of this invention).
- the antibiotic therapeutic agent includes an anti-infectious agent (e.g., anti-bacterial).
- the compounds described above include the compounds themselves, as well as their salts, if applicable.
- Such salts can be formed between a positively charged substituent (e.g., amino) on a compound and an anion.
- Suitable anions include, but are not limited to, chloride, bromide, iodide, sulfate, nitrate, phosphate, citrate, methanesulfonate, trifluoroacetate, and acetate.
- a negatively charged substituent (e.g., carboxylate) on a compound can form a salt with a cation.
- Suitable cations include, but are not limited to, sodium ion, potassium ion, magnesium ion, calcium ion, and an ammonium cation such as tetramethylammonium ion.
- some of the compounds of this invention have one or more double bonds, or one or more asymmetric centers. Such compounds can occur as racemates, racemic mixtures, single enantiomers, individual diastereomers, diastereomeric mixtures, and cis- or trans- or E- or Z-double isomeric forms.
- N-oxides refers to one or more nitrogen atoms, when present in a compound, are in N-oxide form, i.e., N ⁇ O.
- stable refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., treating a disease).
- this invention features a method for treating an infectious disease (e.g., bacterial disease).
- the method includes administering to a subject (e.g., mammal, human, dog, cat, horse, cow, chicken, or pig) in need thereof an effective amount of a just-described compound, wherein the compound contains an antibiotic therapeutic agent that is an anti-infectious agent.
- a subject e.g., mammal, human, dog, cat, horse, cow, chicken, or pig
- the method includes co-usage with other anti-infectious agents or therapeutic agents.
- the present invention also features a pharmaceutical composition including at least one compound of this invention and a pharmaceutically acceptable carrier.
- the pharmaceutical composition includes one or more other therapeutic agents.
- This invention further features a method for making any of the compounds described above.
- the method includes taking any intermediate compound delineated herein, reacting it with any one or more reagents to form a compound of this invention including any processes specifically delineated herein.
- the method includes delivering a conjugate described above to a cell (e.g., a phagocytic cell).
- the conjugate contains a transportophore and an antibiotic therapeutic agent, and in the cell, the transportophore is not covalently bonded to the therapeutic agent.
- the present invention is a widely applicable, pharmacologically viable, method for making prodrugs and the products of this process which will allow the intracellular accumulation of antibiotic compounds.
- the invention involves the use of azithromycin-derived and crown ether-derived molecules as carriers to provide enhanced intracellular accumulation of antibiotics into phagocytic cells among other cell types. These carriers have been shown to exhibit remarkable accumulation in cells, especially in phagocytic cells.
- the present invention represents a significant advancement over conventional administration of antibiotics, as it permits the treatment of intracellular pathogens with a wider array of antibiotics than is currently feasible, and, when accumulated within certain cell types, it will have a synergistic effect with the phagocytic killing by polymorphonuclear leukocytes (PMNs), monocytes, and macrophages.
- PMNs polymorphonuclear leukocytes
- monocytes monocytes
- macrophages macrophages.
- Antibiotics previously identified through high-throughput screens which are not in use because of sub-optimal pharmacokinetic behaviour may serve as a suitable drug in this invention, as the pharmacokinetic properties of the carrier is expected to supersede that of the drug.
- the broadened range of antibiotics which can be intracellularly accumulated using this invention facilitates the management of troublesome infections caused by pathogens resistant to a restricted set of antibiotics. Intracellular accumulation in the order of C/E ⁇ 100 also means that intracellular pathogens will receive a correspondingly higher dose of the antibiotic.
- the present invention relates novel conjugates of antibiotics to carriers consisting of azithromycin-derived or crown ether-derived compounds, as well as methods for synthesising such derivatives of antibiotics are disclosed.
- the carrier-conjugated antibiotics accumulate intracellularly, especially in phagocytic cells. Upon internalisation, the conjugates are capable of slowly hydrolysing to the original active drug molecule under physiological conditions, retaining the spectrum, efficacy and pharmacokinetic properties of the parental molecule.
- the composition is therefore especially effective against numerous bacterial pathogens.
- the conjugate described in the “Summary” section can be prepared by methods known in the art, as well as by the synthetic routes disclosed herein. For example, one can react a transportophore having a reactive moiety with a therapeutic agent having another reactive moiety.
- One of the two reactive moieties is a leaving group (e.g., —Cl, OR) and the other is a derivatizable group (e.g., —OH, or —NH—). Then, the transportophore is covalently bonded to the therapeutic agent via a reaction between the two reactive moieties.
- each of the two reactive moieties is a leaving group or a derivatizable group, and each reacts with its reactive counterpart in the linker to form a covalent bond.
- Detailed routes including various intermediates are illustrated in the examples herein.
- a transportophore and a therapeutic agent can be directly connected or via a linking element.
- This element typically is a bifunctional molecule of low molecular mass, which can react subsequently with the transportophore and the therapeutic agent.
- the therapeutic agent can be released from this linker under physiological conditions. This may be achieved oxidatively (e.g., by action of a cytochrome C), reductively (e.g., by action of NADH), hydrolytically (e.g., by action of a protease), or initiated by radicals (e.g., by the action of superoxide radicals).
- the mechanisms of therapeutic agent release are not limited to the above examples.
- Linkers have the formula: F 1 -L-F 2
- F 1 , F 2 independently a functional groups, suitable to react with a counterpart in the drug or in the carrier.
- F 1 and F 2 are, but are not limited to
- X 1 is a halogen atom or a sulfonate ester or another suitable leaving group
- R a is (C 1 -C 4 )alkyl or aryl, optionally substituted by 1-5 halogen atoms;
- R b is (C 1 -C 5 )alkyl or (C 1 -C 5 )alkenyl;
- R c is H, (C 1 -C 4 )alkyl
- R and R′ are independently —H, —CH 3 , —Cl, —Br, —F, —O(C 1 -C 4 )alkyl, —C( ⁇ O)O(C 1 -C 4 )alkyl, —NO 2 , —S( ⁇ O) k (O) l (C 1 -C 4 )alkyl wherein k is 0, 1 or 2 and 1 can be 0 or 1, SiR 1 R 2 R 3 wherein R 1 ,R 2 and R 3 independently are (C 1 -C 4 )alkyl;
- X 4 is —H, —Cl, —S k (C 1 -C 4 )alkyl, S k (C 6 -C 10 )aryl wherein k is 1 or 2.
- F 1 and F 2 can be connected to form a cyclic anhydride or di- or trisulfide.
- L is a spacing element which is, but is not limited to,
- alkyl-, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl spacing elements are optionally substituted by (C 1 -C 6 )alkyl, 1-4 halogens, (C 1 -C 4 )alkoxy, (C 1 -C 4 )alkoxycarbonyl, hydroxy, amino, (C 1 -C 4 )alkylamino, (C 1 -C 4 )dialkylamino, (C 3 -C 10 )cycloalkyl, (C 1 -C 6 )alkylcarbonyloxy, (C 1 -C 6 )alkylcarbonylamido, (C 1 -C 4 )alkylamidocarbonyl, (C 1 -C 4 )dialkylamidocarbonyl, nitro, cyano, (C 1 -C 4 )alkylimino, mercapto and (C 1 -C 4 )alkylmercapto functions.
- the chemicals used in the afore-mentioned methods may include, for example, solvents, reagents, catalysts, protecting group and deprotecting group reagents and the like.
- the methods described above may also additionally comprise steps, either before or after the steps described specifically herein, to add or remove suitable protecting groups in order to ultimately allow synthesis of the compound of the formulae described herein.
- antibiotic therapeutic activity includes any with modes of action that includes anti-bacterial agent.
- the antibiotics include, but are not limited to, ⁇ -lactams (including amoxicillin, ampicillin, bacampicillin, carbenicillin, cloxacillin, dicloxacillin, flucloxacillin, methicillin, mezlocillin, nafcillin, oxacillin, penicillin G, penicillin V, piperacillin, pivampicillin, pivmecillinam, ticarcillin, sulbactam, tazobactam, clavulanate), cephalosporins (cefaclor, cefadroxil, cefamandole, cefazolin, cefdinir, cefditoren, cefepime, cefixime, cefonicid, cefoperazone, cefotaxime, cefotetan, cefoxitin, cefpodoxime, cefprozil, cefta
- composition that contains an effective amount of at least one of the conjugate of this present invention and a pharmaceutically acceptable carrier.
- Pharmaceutically acceptable salts of the conjugate of this invention include those derived from pharmaceutically acceptable inorganic and organic acids and bases.
- suitable acid salts include acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptanoate, glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, palmoate, pectinate, pers
- Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N-(alkyl) 4 + salts.
- alkali metal e.g., sodium
- alkaline earth metal e.g., magnesium
- ammonium e.g., ammonium
- N-(alkyl) 4 + salts e.g., sodium
- alkali metal e.g., sodium
- alkaline earth metal e.g., magnesium
- ammonium e.g., sodium
- N-(alkyl) 4 + salts e.g., sodium
- this invention covers a method of administering an effective amount of one or more conjugates of this invention to a subject (a human, a mammal, or an animal) in need of treating a disease (e.g., an infectious disease).
- a disease e.g., an infectious disease.
- the methods delineated herein can also include the step of identifying that the subject is in need of treatment of disorders and condition in a subject. The identification can be in the judgment of a subject or a health professional and can be subjective (e.g., opinion) or objective (e.g., measurable by a test or a diagnostic method).
- treating refers to administering a conjugate of this invention to a subject with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve, or affect a disease, the symptoms of the disease or the predisposition toward the disease.
- An effective amount refers to an amount of a conjugate which confers a therapeutic effect on the treated subject.
- the therapeutic effect may be objective (i.e., measurable by some test or marker) or subjective (i.e., subject gives an indication of or feels an effect).
- An effective amount of the conjugate described above may range from about 0.1 mg/Kg to about 20 mg/Kg. Effective doses will also vary, as recognized by those skilled in the art, depending on route of administration, excipient usage, and the possibility of co-usage with other agents for treating a disease, including an infectious disease.
- Respiratory diseases of diverse origin including:
- Pharyngitis (“sore throat”), Tonsilitis, Sinusitis & Otitis Media, Influenza, Laryngo-Tracheo Bronchitis (Croup), Acute Bronchiolitis, Pneumonia, Bronchopneumonia, Bronchiolitis, Bronchitis, Acute pharyngitis with fever, Pharyngoconjunctival fever, Acute follicular conjunctivitis, Pneumonia (and pneumonitis in children), COPD, asthma,
- Escherichia coli Infections E. coli 0157:H7, Shigella dysenteriae , agent of bacillary dysentery, Salmonella Infections, Salmonella typhimurium, Salmonella typhi, Klebsiella Infections, Yaws, Brucellosis. Spirilla, Campylobacter jejuni, Helicobacter pylori.
- Neisseria gonorrhoeae and Neisseria meningitides agents of gonorrhea and certain types of meningitis respectively; Neisseria species are also implicated in acute and potentially chronic arthritis. Meningococcal Meningitis, Haemophilus influenzae
- Mycoplasma Infections Mycoplasma pneumoniae, Ureaplasma Urealyticum, Mycoplasma genitalium -, Legionellosis (Legionaires' pneumonia, Legionella pneumophilia ), Yersinia pestis (Plague), Leptospirosis (Weil's Disease) Leptospira , Rat-Bite Fever (Haverhill Fever), Streptobacillus moniliformis , Tick-Borne Diseases, Spirochetes: Borrelia burgdorferi , (Lyme disease), Erythema migrans, Acrodermatitis Atrophicans, Borrelial Lymphocytoma), Relapsing Fever, Human Ehrlichiosis & Human Granulocytic Erlichiosis-, Tularemia, Chlamydia Infections, Chlamydia pneumoniae and Cardiovascular Disease, Ornithosis, Psittacosis (Ornit
- Staphylococcal Infections Staphylococcus aureus
- Streptococcal Infections Streptococcus pyogenes
- Fasciitis necrotizing Scarlet Fever
- Rheumatic Fever Streptococcus pneumoniae
- pneumonia osteomyelitis, septicemia, food intoxication, toxic shock syndrome, Otitis media, meningitis, glomerulonephritis and other post-streptococcal sequelae.
- Chlamydia are also intracellular pathogens: Chlamydia trachomatis is the agent of trachoma, pelvic inflammatory disease, lymphogranuloma venereum; Chlamydia are also implicated in the etiology of atherosclerolis and arthritis. L. Bartonella bacilliformis . Mycoplasmas; Mycoplasma pneumoniae , Toxoplasmosis.
- the compounds of this invention can be administered to a patient, for example, in order to treat a disease described above.
- the compound can, for example, be administered in a pharmaceutically acceptable carrier such as physiological saline, in combination with other drugs, and/or together with appropriate excipients.
- the compound described herein can, for example, be administered by injection, intravenously, intraarterially, subdermally, intraperitoneally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, topically, in an ophthalmic preparation, by inhalation, by intracranial injection or infusion techniques, with a dosage ranging from about 0.1 to about 20 mg/kg of body weight, preferably dosages between 10 mg and 1000 mg/dose, every 4 to 120 hours, or according to the requirements of the particular drug.
- the methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect. Lower or higher doses than those recited above may be required.
- Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.
- compositions of this invention comprise a compound of this invention or a pharmaceutically acceptable salt thereof; and any pharmaceutically acceptable carrier, adjuvant or vehicle. Such compositions may optionally comprise additional therapeutic agents.
- the compositions delineated herein include the compounds of the formulae delineated herein, as well as additional therapeutic agents if present, in amounts effective for achieving a modulation of a disease.
- pharmaceutically acceptable carrier or adjuvant refers to a carrier or adjuvant that may be administered to a patient, together with a compound of this invention, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.
- Pharmaceutically acceptable carriers, adjuvants and vehicles that may be used in the pharmaceutical compositions of this invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d- ⁇ -tocopherol polyethyleneglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-
- Cyclodextrins such as ⁇ , ⁇ -, and ⁇ -cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3-hydroxypropyl- ⁇ -cyclodextrins, or other solubilized derivatives may also be advantageously used to enhance delivery of compounds of the formulae described herein.
- Oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions.
- compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions.
- carriers which are commonly used include lactose and corn starch.
- Lubricating agents such as magnesium stearate, are also typically added.
- useful diluents include lactose and dried corn starch.
- compositions of this invention may also be administered in the form of suppositories for rectal administration.
- These compositions can be prepared by mixing a compound of this invention with a suitable non-irritating excipient which is solid at room temperature but liquid at the rectal temperature and therefore will melt in the rectum to release the active components.
- suitable non-irritating excipient include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.
- Topical administration of the pharmaceutical compositions of this invention is especially useful when the desired treatment involves areas or organs readily accessible by topical application.
- the pharmaceutical composition should be formulated with a suitable ointment containing the active components suspended or dissolved in a carrier.
- Carriers for topical administration of the compounds of this invention include, but are not limited to, mineral oil, liquid petroleum, white petroleum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water.
- the pharmaceutical composition can be formulated with a suitable lotion or cream containing the active compound suspended or dissolved in a carrier with suitable emulsifying agents.
- Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
- the pharmaceutical compositions of this invention may also be topically applied to the lower intestinal tract by rectal suppository formulation or in a suitable enema formulation. Topically-transdermal patches are also included in this invention.
- compositions of this invention may be administered by nasal aerosol or inhalation.
- Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
- a suitable in vitro assay can be used to preliminarily evaluate a compound of this invention in treating a disease.
- In vivo screening can also be performed by following procedures well known in the art.
- a macrophage phagocytosis assay can be performed as follows:
- the RAW264.7 cells (from ATCC) were seeded at a density of ⁇ 2.5 ⁇ 10 5 Macrophage/well of 24 well microtiter plates 1 day prior to assay. Assay was initiated by addition of 2.5 ⁇ 10 6 of freshly grown Yersinia cells (in 2xYT, 20 mM Sodium Oxalate, 20 mM MgCl 2 ). After 90 min incubation at 37° C. in 5% CO 2 , the supernatant was aspirated and 1 ml of pre-warmed DMEM containing 100 mg/ml gentamicin to each sample. After a further 90 min.
- the TC 50 or MIC procedure for antibiotic sensitivity testing involves an antibiotic dilution assay, which can be performed in microtitre plates. A series of twofold dilutions of each antibiotic are made in the wells, and then all wells are inoculated with a standard amount of the same test organism. After incubation, growth in the presence of the various antibiotics is observed by measuring turbidity. Antibiotic sensitivity is expressed as the concentration of the antibiotic that inhibits 50% of the growth (TC 50 ). Alternatively it could be expressed as the highest dilution of antibiotic that completely inhibits growth (MIC).
- ⁇ -lactams are by far the most widely used class of antibiotics and make up approximately 50% of the market. This class of compounds includes the penicillins, cephalosporins and carbanepems. There are numerous advantages of beta-lactams, including low-toxicity, broad-spectrum activity and good distribution within the body.
- ⁇ -lactam antibiotics act through inhibiting the essential penicillin binding proteins (PBPs) in bacteria, which are responsible for cell wall synthesis.
- PBPs essential penicillin binding proteins
- ⁇ -lactam antibiotics interfere with the transpeptidase enzymes which cleave an alanine from the peptide chain through the action of a serine on the enzyme, and then finish the cross-line by making an amide bond to a lysine NH 2 .
- Penicillin is a substrate for the enzyme and becomes covalently bound to it.
- ⁇ -lactamases penicillinase
- MRSA methicillin-resistant staphylococci
- clavulanic acid sulbactam and tazobactam
- these drugs are not useful therapeutic agents, but they bind ⁇ -lactamases irreversibly and with high affinity preventing them from destroying the antimicrobial agent.
- One effective ⁇ -lactase inhibitor/s lactam antimicrobial combination is amoxicillin-clavulanic acid.
- Imipenem/cilastatin can be administered intravenously.
- a suspension form of the drug is available for intramuscular use.
- the more soluble meropenem can be diluted in smaller amounts of fluid and administered intramuscularly or intravenously, by bolus or short-term infusion.
- Azithromycin 5 g Azithromycin are mixed with 1.5 g p-toluol sulfonic acid chloride in 20 ml dry pyridine at 0° C. and stirred at room temperature for 72 h. The mixture is concentrated at RT in vacuo and the residue is dissolved in 30 ml dimethylsulfoxide (Hutchins et al., 1969). 750 mg of sodium borohydride are added and the mixture is heated for 8 h to 100° C.
- Penicillin G (3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid) are dissolved in 8 ml dichloromethane and activated by the addition of 330 mg DCC. 1.2 g desoxyazithromycin are subjoined and the mixture is stirred at RT for 8 h. A second portion of 650 mg Penicillin G and 330 mg DCC in 8 ml dichloromethane is added and stirring is continued over night.
- the present invention relates generally to the delivery of antibiotics to mammals for use in the treatment of bacterial pathogens. More particularly, the present invention involves the coupling of antibiotics to a macrolide to form antibiotic-macrolide conjugates which target pathogens.
- the present invention overcomes problems encountered by several classes of antibiotics which do not efficiently penetrate cells, for the treatment of, among others, intracellular pathogens.
- Macrolides were selected which have been shown to have high cumulative capacity in macrophages, but which have no anti-microbial activity.
- the proposed oxazolidinone structures are therefore enhanced in efficacy, particularly in the treatment of intracellular pathogens.
- Oxazolidinones are an appealing class of antimicrobials due to their unique bacteriostatic mechanism of action, lack of cross-resistance with other agents, good oral bioavailability, potential for structure modification, and broad spectrum of activity.
- Oxazolidinones with antibacterial activity are a novel class of antibiotics whose mode of action is to block protein synthesis, in particular by binding to the 50s ribosomal subunit, thereby blocking intiation of protein biosynthesis.
- linezolid In in vitro susceptibility studies, linezolid was shown to have activity against a wide variety of organisms, including graph-positive cocci, gram-negative anaerobes, and mycobacteria. With few exceptions, gram-negative bacteria are resistant due to efflux. Linezolid, the first new oxazolidinone class of antibiotics, is well distributed in the body when administered orally, with virtually complete bioavailability. Good tissue penetration is achieved, with high levels in the skin structure. Metabolism yields two primary derivatives, which may accumulate in those patients with renal insufficiency. There are no major toxicity problems which emerged during clinical trials.
- 620 mg of 410b are hydrolyzed by heating it with 5 ml of 0.1N HCl for 30 min to 60° C.
- the aqueous phase is removed by evaporation under reduced pressure to yield 720 mg of the hydrochloride (410c) after drying in vacuo.
- 100 mg of 410c are activated in 5 ml trichloromethane by addition of 50 mg of carbonyldiimidazole. Subsequently 80 mg 3-[4-(1-Benzyl-1,2,3,6-tetrahydro-pyridin-4-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one (U.S. Pat. No. 6,271,383) are added, and the mixture is stirred for 1 h.
- eperezolide (412a) (U-100592, Ford et al., 1996) are dissolved in 15 ml of dry dichloromethane, and 250 mg of triethylamine are added. 230 mg of acroylchloride are added. After stirring for 12 h the volatile compounds are removed by evaporation and the residue is dissolved in 20 ml of dry ethanol. 1.9 g iso-desmethyl-azithromycin are added. After stirring for 46 h, the mixture is evaporated to dryness, filtered over a short column of silica gel and chromatographed to yield 900 mg of the michael-adduct 412c.
- the mycobacterial cell wall is an effective barrier that contributes to drug resistance.
- Inhibitors of cell wall biosyn-thesis not only are potential antimycobacterial agents but also increase mycobacterial susceptibility to other antimicrobial agents.
- One inhibitor of cell wall synthesis is D-cycloserine (D-4-amino-isoxazolidone [DCS]), a cyclic structural analog of D-alanine.
- D-Amino acids especially D-alanine, D-gluta-mate, and D-aminopimelate, are important components of all bacterial cell walls, including those of mycobacteria.
- Alanine is usually available as the L stereoisomer, and the conversion to D-alanine by the cytoplasmic enzyme D-alanine racemase is required for the initial step in the alanine branch of peptidoglycan biosynthesis.
- D-Alanine is converted to the dipeptide D-alanyl-D-alanine in a reaction catalyzed by D-alanyl:alanine synthetase (D-alanine ligase).
- D-alanine ligase D-alanine synthetase
- both D-alanine racemase and D-alanine ligase are targets of DCS.
- the biosynthesis of mycolyl-arabinogalactan-peptidoglycan complex is inhibited by DCS in M.
- DCS D-alanine ligase is one of the targets in mycobacteria.
- DCS is an effective antimycobacterial agent but is rarely prescribed and used only in combined therapies due to its adverse effects. These side effects are due to binding of DCS to neuronal N-methyl aspartate receptors and inhibition of enzymes that metabolize and synthesize the neurotransmitter g-aminobutyric acid. Nevertheless, DCS is an excellent candidate for the development of a new generation of antibiotics. Two important considerations predict that rationally designed derivatives of DCS may be more efficacious antimicrobial agents. First, DCS targets participate in essential steps of cell wall synthesis. Second, DCS resistance has not yet become an important clinical problem. I. Coupling of 1,7-Diaza-15-crown-5 with Cycloserine:
- 410c 100 mg are activated in 5 ml trichloromethane by addition of 45 mg DCC. After 5 min, 21 mg cycloserine and a few crystals 4-N,N-dimethylaminopyridin are added. The mixture is stirred for 1 h, filtered, concentrated and purified by flash-chromatography to yield 72 mg of the cycloserine derivative (411).
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012051126A3 (en) * | 2010-10-10 | 2012-08-16 | Synovo Gmbh | Anti-inflammatory macrolides |
US20140066623A1 (en) * | 2001-08-03 | 2014-03-06 | Yale University | Ribosome Structure and Protein Synthesis Inhibitors |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2476423A1 (en) * | 2002-02-15 | 2003-08-28 | Sympore Gmbh | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
US20040005641A1 (en) * | 2002-02-15 | 2004-01-08 | Michael Burnet | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
PL375162A1 (en) | 2002-07-08 | 2005-11-28 | Pliva-Istrazivacki Institut D.O.O. | Novel compounds, compositions as carriers for steroid/non-steroid anti-inflammatory, antineoplastic and antiviral active molecules |
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EP1682563A1 (en) * | 2003-10-30 | 2006-07-26 | Rib-X Pharmaceuticals, Inc. | Bifunctional macrolide heterocyclic compounds and mehtods of making and using the same |
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US7468428B2 (en) * | 2004-03-17 | 2008-12-23 | App Pharmaceuticals, Llc | Lyophilized azithromycin formulation |
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US20060105941A1 (en) * | 2004-11-12 | 2006-05-18 | Allergan, Inc. | Mixed antibiotic codrugs |
RU2008106915A (ru) * | 2005-07-26 | 2009-09-10 | Меркле Гмбх (De) | Макролидные конъюгаты пирролиновых и индолизиновых соединений |
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WO2013085152A1 (en) * | 2011-12-07 | 2013-06-13 | Union Korea Pharm Co., Ltd. | Combined antibiotics comprising cephalosporins and beta-lactamase inhibitors |
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EP4051687A4 (en) * | 2020-01-08 | 2022-12-21 | Beijing Continent Pharmaceuticals Co., Ltd. | MACROLIDE COMPOUND AND USE THEREOF FOR THE TREATMENT OF CHRONIC RESPIRATORY DISEASE |
CN117222433A (zh) * | 2020-10-01 | 2023-12-12 | 密西西比州立大学 | 与磷酸己糖缀合的药物及其制备和使用方法 |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3417077A (en) * | 1966-05-16 | 1968-12-17 | Lilly Co Eli | Erythromycin derivative and process for the preparation thereof |
US3884903A (en) * | 1973-06-21 | 1975-05-20 | Abbott Lab | 4{41 -Deoxy-4{41 -oxoerythromycin B derivatives |
US4328334A (en) * | 1979-04-02 | 1982-05-04 | Pliva Pharmaceutical And Chemical Works | 11-Aza-10-deoxo-10-dihydroerythromycin A and derivatives thereof as well as a process for their preparation |
US4382086A (en) * | 1982-03-01 | 1983-05-03 | Pfizer Inc. | 9-Dihydro-11,12-ketal derivatives of erythromycin A and epi-erythromycin A |
US4474768A (en) * | 1982-07-19 | 1984-10-02 | Pfizer Inc. | N-Methyl 11-aza-10-deoxo-10-dihydro-erytromycin A, intermediates therefor |
US4517359A (en) * | 1981-03-06 | 1985-05-14 | Sour Pliva Farmaceutska, Kemijska Prehrambena I Kozmeticka Industrija, N.Sol.O. | 11-Methyl-11-aza-4-0-cladinosyl-6-0-desosaminyl-15-ethyl-7,13,14-trihydroxy-3,5,7,9,12,14-hexamethyl-oxacyclopentadecane-2-one and derivatives thereof |
US4834973A (en) * | 1971-05-20 | 1989-05-30 | Meir Strahilevitz | Immunological methods for treating mammals |
US5516864A (en) * | 1993-03-29 | 1996-05-14 | Molecular Probes, Inc. | Fluorescent ion-selective diaryldiaza crown ether conjugates |
US5676971A (en) * | 1988-08-11 | 1997-10-14 | Terumo Kabushiki Kaisha | Agents for inhibiting adsorption of proteins on the liposome surface |
US5750493A (en) * | 1995-08-30 | 1998-05-12 | Raymond F. Schinazi | Method to improve the biological and antiviral activity of protease inhibitors |
US5827533A (en) * | 1997-02-06 | 1998-10-27 | Duke University | Liposomes containing active agents aggregated with lipid surfactants |
US6043227A (en) * | 1998-08-19 | 2000-03-28 | Pfizer Inc. | C11 carbamates of macrolide antibacterials |
US6300316B1 (en) * | 1997-08-06 | 2001-10-09 | Pfizer Inc | C-4 substituted macrolide antibiotics |
US6562796B2 (en) * | 2000-01-14 | 2003-05-13 | Micrologix Biotech Inc. | Derivatives of polyene macrolides and preparation and use thereof |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0055991A3 (en) | 1978-10-02 | 1982-08-11 | Merck & Co. Inc. | Lysosomotropic detergent therapeutic agents, compositions containing them and their uses |
US4518590A (en) | 1984-04-13 | 1985-05-21 | Pfizer Inc. | 9α-Aza-9α-homoerythromycin compounds, pharmaceutical compositions and therapeutic method |
US4585759A (en) | 1985-01-22 | 1986-04-29 | Pfizer Inc. | Antibacterial derivatives of a neutral macrolide |
US5466681A (en) * | 1990-02-23 | 1995-11-14 | Microcarb, Inc. | Receptor conjugates for targeting penicillin antibiotics to bacteria |
SI9011409A (en) | 1990-07-18 | 1995-10-31 | Pliva Pharm & Chem Works | O-methyl azitromycin derivates, methods and intermediates for their preparation and methods for preparation of pharmaceuticals products which comprise them |
JPH07103148B2 (ja) | 1991-12-16 | 1995-11-08 | 株式会社ディ・ディ・エス研究所 | アントラサイクリン−マクロライド複合体 |
US20030068362A1 (en) * | 1993-02-22 | 2003-04-10 | American Bioscience, Inc. | Methods and formulations for the delivery of pharmacologically active agents |
US5486536A (en) * | 1994-08-15 | 1996-01-23 | The Regents Of The University Of Michigan | Sulfatides as anti-inflammatory compounds |
ES2183166T3 (es) * | 1996-04-26 | 2003-03-16 | Massachusetts Inst Technology | Ensayo de cribado por triple hibrido. |
PT1437359E (pt) | 1997-10-16 | 2007-04-30 | Glaxosmithkline Zagreb | Novos 3,6-hemicetais da classe dos 9a-azalidos |
HRP980189B1 (en) | 1998-04-06 | 2004-04-30 | Pliva Pharm & Chem Works | Novel 15-membered lactams ketolides |
JP2002517458A (ja) | 1998-06-08 | 2002-06-18 | アドバンスド メディスン インコーポレーテッド | 多結合ライブラリーのコンビナトリアル合成 |
CA2319495A1 (en) | 1998-06-08 | 1999-12-16 | Advanced Medicine, Inc. | Multibinding inhibitors of microsomal triglyceride transferase protein |
WO1999064040A1 (en) | 1998-06-08 | 1999-12-16 | Advanced Medicine, Inc. | Novel polyene macrolide compounds and uses |
US6100240A (en) | 1998-10-09 | 2000-08-08 | Pfizer Inc | Macrolide derivatives |
ID27331A (id) | 1999-09-29 | 2001-03-29 | Pfizer Prod Inc | Pembuatan antibiotik-antibiotik ketolida karbamat |
EP1122261A3 (en) | 2000-01-31 | 2001-09-26 | Pfizer Products Inc. | 13 and 14-membered antibacterial macrolides |
DK1167376T3 (da) | 2000-06-30 | 2004-10-25 | Pfizer Prod Inc | Makrolidantibiotika |
HRP20010018A2 (en) | 2001-01-09 | 2002-12-31 | Pliva D D | Novel anti-inflammatory compounds |
WO2003045319A2 (en) * | 2001-11-21 | 2003-06-05 | Activbiotics, Inc. | Targeted therapeutics and uses thereof |
US20040005641A1 (en) * | 2002-02-15 | 2004-01-08 | Michael Burnet | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
CA2476423A1 (en) * | 2002-02-15 | 2003-08-28 | Sympore Gmbh | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
-
2003
- 2003-02-14 EP EP03742793A patent/EP1482957A4/en not_active Withdrawn
- 2003-02-14 CA CA002476448A patent/CA2476448A1/en not_active Abandoned
- 2003-02-14 WO PCT/US2003/004714 patent/WO2003070254A1/en active IP Right Grant
- 2003-02-14 AU AU2003211113A patent/AU2003211113B2/en not_active Ceased
- 2003-02-14 US US10/367,104 patent/US7271154B2/en not_active Expired - Fee Related
- 2003-02-14 US US10/504,792 patent/US20060069047A1/en not_active Abandoned
- 2003-02-14 NZ NZ535355A patent/NZ535355A/en unknown
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3417077A (en) * | 1966-05-16 | 1968-12-17 | Lilly Co Eli | Erythromycin derivative and process for the preparation thereof |
US4834973A (en) * | 1971-05-20 | 1989-05-30 | Meir Strahilevitz | Immunological methods for treating mammals |
US3884903A (en) * | 1973-06-21 | 1975-05-20 | Abbott Lab | 4{41 -Deoxy-4{41 -oxoerythromycin B derivatives |
US4328334A (en) * | 1979-04-02 | 1982-05-04 | Pliva Pharmaceutical And Chemical Works | 11-Aza-10-deoxo-10-dihydroerythromycin A and derivatives thereof as well as a process for their preparation |
US4517359A (en) * | 1981-03-06 | 1985-05-14 | Sour Pliva Farmaceutska, Kemijska Prehrambena I Kozmeticka Industrija, N.Sol.O. | 11-Methyl-11-aza-4-0-cladinosyl-6-0-desosaminyl-15-ethyl-7,13,14-trihydroxy-3,5,7,9,12,14-hexamethyl-oxacyclopentadecane-2-one and derivatives thereof |
US4382086A (en) * | 1982-03-01 | 1983-05-03 | Pfizer Inc. | 9-Dihydro-11,12-ketal derivatives of erythromycin A and epi-erythromycin A |
US4474768A (en) * | 1982-07-19 | 1984-10-02 | Pfizer Inc. | N-Methyl 11-aza-10-deoxo-10-dihydro-erytromycin A, intermediates therefor |
US5676971A (en) * | 1988-08-11 | 1997-10-14 | Terumo Kabushiki Kaisha | Agents for inhibiting adsorption of proteins on the liposome surface |
US5846458A (en) * | 1988-08-11 | 1998-12-08 | Terumo Kabushiki Kaisha | Inhibition adsorption of proteins on the liposome surface |
US5516864A (en) * | 1993-03-29 | 1996-05-14 | Molecular Probes, Inc. | Fluorescent ion-selective diaryldiaza crown ether conjugates |
US5750493A (en) * | 1995-08-30 | 1998-05-12 | Raymond F. Schinazi | Method to improve the biological and antiviral activity of protease inhibitors |
US5827533A (en) * | 1997-02-06 | 1998-10-27 | Duke University | Liposomes containing active agents aggregated with lipid surfactants |
US6300316B1 (en) * | 1997-08-06 | 2001-10-09 | Pfizer Inc | C-4 substituted macrolide antibiotics |
US6043227A (en) * | 1998-08-19 | 2000-03-28 | Pfizer Inc. | C11 carbamates of macrolide antibacterials |
US6562796B2 (en) * | 2000-01-14 | 2003-05-13 | Micrologix Biotech Inc. | Derivatives of polyene macrolides and preparation and use thereof |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20140066623A1 (en) * | 2001-08-03 | 2014-03-06 | Yale University | Ribosome Structure and Protein Synthesis Inhibitors |
US8912150B2 (en) * | 2001-08-03 | 2014-12-16 | Melinta Therapeutics, Inc. | Ribosome structure and protein synthesis inhibitors |
WO2012051126A3 (en) * | 2010-10-10 | 2012-08-16 | Synovo Gmbh | Anti-inflammatory macrolides |
US9145436B2 (en) | 2010-10-10 | 2015-09-29 | Michael W. Burnet | Anti-inflammatory macrolides |
Also Published As
Publication number | Publication date |
---|---|
EP1482957A4 (en) | 2006-07-19 |
NZ535355A (en) | 2007-09-28 |
EP1482957A1 (en) | 2004-12-08 |
US7271154B2 (en) | 2007-09-18 |
AU2003211113B2 (en) | 2007-08-09 |
US20040033969A1 (en) | 2004-02-19 |
AU2003211113A1 (en) | 2003-09-09 |
WO2003070254A1 (en) | 2003-08-28 |
CA2476448A1 (en) | 2003-08-28 |
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