CA2369711A1 - Macrocyclic peptides active against the hepatitis c virus - Google Patents
Macrocyclic peptides active against the hepatitis c virus Download PDFInfo
- Publication number
- CA2369711A1 CA2369711A1 CA002369711A CA2369711A CA2369711A1 CA 2369711 A1 CA2369711 A1 CA 2369711A1 CA 002369711 A CA002369711 A CA 002369711A CA 2369711 A CA2369711 A CA 2369711A CA 2369711 A1 CA2369711 A1 CA 2369711A1
- Authority
- CA
- Canada
- Prior art keywords
- mmol
- compound
- alkyl
- mixture
- solution
- 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
- 241000711549 Hepacivirus C Species 0.000 title abstract description 51
- 108090000765 processed proteins & peptides Proteins 0.000 title description 18
- 102000004196 processed proteins & peptides Human genes 0.000 title description 11
- 150000001875 compounds Chemical class 0.000 claims description 182
- 125000000217 alkyl group Chemical group 0.000 abstract description 63
- 229920006395 saturated elastomer Polymers 0.000 abstract description 32
- 101800001838 Serine protease/helicase NS3 Proteins 0.000 abstract description 29
- 125000001424 substituent group Chemical group 0.000 abstract description 26
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract description 24
- 150000002148 esters Chemical class 0.000 abstract description 23
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 19
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 17
- 150000003839 salts Chemical class 0.000 abstract description 17
- 150000001408 amides Chemical class 0.000 abstract description 16
- 125000003118 aryl group Chemical group 0.000 abstract description 15
- 229910052799 carbon Inorganic materials 0.000 abstract description 15
- 125000005842 heteroatom Chemical group 0.000 abstract description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 13
- 229910052760 oxygen Inorganic materials 0.000 abstract description 13
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 11
- 229910052717 sulfur Chemical group 0.000 abstract description 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 10
- 150000002678 macrocyclic compounds Chemical class 0.000 abstract description 10
- 125000005843 halogen group Chemical group 0.000 abstract description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 8
- 125000002947 alkylene group Chemical group 0.000 abstract description 7
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract description 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 7
- 125000004001 thioalkyl group Chemical group 0.000 abstract description 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract description 5
- 125000003710 aryl alkyl group Chemical group 0.000 abstract description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 5
- 238000000423 cell based assay Methods 0.000 abstract description 5
- 239000001301 oxygen Chemical group 0.000 abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract description 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 4
- 125000004043 oxo group Chemical group O=* 0.000 abstract description 4
- 239000011593 sulfur Chemical group 0.000 abstract description 4
- 238000000338 in vitro Methods 0.000 abstract description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract description 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 260
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- 239000000243 solution Substances 0.000 description 155
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 116
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- 238000003786 synthesis reaction Methods 0.000 description 83
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 71
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- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 51
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- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 44
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 43
- 238000003818 flash chromatography Methods 0.000 description 42
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 42
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 42
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- 239000003112 inhibitor Substances 0.000 description 33
- -1 particularly Proteins 0.000 description 33
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 30
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 29
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- 239000000725 suspension Substances 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 19
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 18
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- 238000003556 assay Methods 0.000 description 18
- 239000000758 substrate Substances 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 17
- 125000005647 linker group Chemical group 0.000 description 17
- 239000003054 catalyst Substances 0.000 description 16
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
- 125000003545 alkoxy group Chemical group 0.000 description 15
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
- 229910052739 hydrogen Inorganic materials 0.000 description 15
- 230000007062 hydrolysis Effects 0.000 description 14
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 14
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- PHVXTQIROLEEDB-UHFFFAOYSA-N n-[2-(2-chlorophenyl)ethyl]-4-[[3-(2-methylphenyl)piperidin-1-yl]methyl]-n-pyrrolidin-3-ylbenzamide Chemical compound CC1=CC=CC=C1C1CN(CC=2C=CC(=CC=2)C(=O)N(CCC=2C(=CC=CC=2)Cl)C2CNCC2)CCC1 PHVXTQIROLEEDB-UHFFFAOYSA-N 0.000 description 1
- RCSBCWXPGSPJNF-UHFFFAOYSA-N n-[4-[5-[3-chloro-4-(trifluoromethoxy)phenyl]-1,3,4-oxadiazol-2-yl]butyl]-4-(1,8-naphthyridin-2-yl)butanamide Chemical compound C1=C(Cl)C(OC(F)(F)F)=CC=C1C(O1)=NN=C1CCCCNC(=O)CCCC1=CC=C(C=CC=N2)C2=N1 RCSBCWXPGSPJNF-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 210000004897 n-terminal region Anatomy 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229940127073 nucleoside analogue Drugs 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- UXGHWJFURBQKCJ-UHFFFAOYSA-N oct-7-ene-1,2-diol Chemical compound OCC(O)CCCCC=C UXGHWJFURBQKCJ-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000005897 peptide coupling reaction Methods 0.000 description 1
- 239000000816 peptidomimetic Substances 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002064 post-exposure prophylaxis Effects 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000003757 reverse transcription PCR Methods 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- TZSZZENYCISATO-WIOPSUGQSA-N rodatristat Chemical compound CCOC(=O)[C@@H]1CC2(CN1)CCN(CC2)c1cc(O[C@H](c2ccc(Cl)cc2-c2ccccc2)C(F)(F)F)nc(N)n1 TZSZZENYCISATO-WIOPSUGQSA-N 0.000 description 1
- OHRURASPPZQGQM-GCCNXGTGSA-N romidepsin Chemical compound O1C(=O)[C@H](C(C)C)NC(=O)C(=C/C)/NC(=O)[C@H]2CSSCC\C=C\[C@@H]1CC(=O)N[C@H](C(C)C)C(=O)N2 OHRURASPPZQGQM-GCCNXGTGSA-N 0.000 description 1
- 102220008337 rs1437698471 Human genes 0.000 description 1
- 102220083971 rs34543395 Human genes 0.000 description 1
- 102220024172 rs397515479 Human genes 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
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- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
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- 238000010561 standard procedure Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- FRGKKTITADJNOE-UHFFFAOYSA-N sulfanyloxyethane Chemical compound CCOS FRGKKTITADJNOE-UHFFFAOYSA-N 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- LFKDJXLFVYVEFG-UHFFFAOYSA-N tert-butyl carbamate Chemical group CC(C)(C)OC(N)=O LFKDJXLFVYVEFG-UHFFFAOYSA-N 0.000 description 1
- XBXCNNQPRYLIDE-UHFFFAOYSA-N tert-butylcarbamic acid Chemical compound CC(C)(C)NC(O)=O XBXCNNQPRYLIDE-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000003548 thiazolidines Chemical class 0.000 description 1
- DUYAAUVXQSMXQP-UHFFFAOYSA-M thioacetate Chemical compound CC([S-])=O DUYAAUVXQSMXQP-UHFFFAOYSA-M 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 125000004035 thiopropyl group Chemical group [H]SC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 206010043778 thyroiditis Diseases 0.000 description 1
- 210000001519 tissue Anatomy 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
- 108091006106 transcriptional activators Proteins 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- ZGYICYBLPGRURT-UHFFFAOYSA-N tri(propan-2-yl)silicon Chemical compound CC(C)[Si](C(C)C)C(C)C ZGYICYBLPGRURT-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 238000010200 validation analysis Methods 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 201000001862 viral hepatitis Diseases 0.000 description 1
- 230000008957 viral persistence Effects 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Priority Applications (28)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002369711A CA2369711A1 (en) | 2002-01-30 | 2002-01-30 | Macrocyclic peptides active against the hepatitis c virus |
| US10/320,978 US20030181363A1 (en) | 2002-01-30 | 2002-12-17 | Macrocyclic peptides active against the hepatitis C virus |
| CNA038054841A CN1639187A (zh) | 2002-01-30 | 2003-01-24 | 有效抗c型肝炎病毒的大环肽 |
| CA2474035A CA2474035C (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitis c virus |
| EP03700743A EP1472278B1 (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitis c virus |
| PL03371007A PL371007A1 (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitis c virus |
| JP2003564075A JP4040578B2 (ja) | 2002-01-30 | 2003-01-24 | Ｃ型肝炎ウイルスに対して活性な大環状ペプチド |
| KR10-2004-7011682A KR20040077899A (ko) | 2002-01-30 | 2003-01-24 | Ｃ형 간염 바이러스에 대해 활성인 마크로사이클릭 펩티드 |
| EA200400886A EA007738B1 (ru) | 2002-01-30 | 2003-01-24 | Макроциклические пептиды, обладающие активностью в отношении вируса гепатита с |
| UA20040807068A UA78014C2 (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against hepatitis c virus |
| HR20040689A HRP20040689A2 (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitisc virus |
| NZ534929A NZ534929A (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitis C virus |
| AT03700743T ATE414098T1 (de) | 2002-01-30 | 2003-01-24 | Makrozyklische peptide mit anti-hepatitis c virus wirkung |
| YU67004A RS67004A (sr) | 2002-01-30 | 2003-01-24 | Makrociklični peptidi aktivni prema virusu hepatitisa c |
| BR0307297-5A BR0307297A (pt) | 2002-01-30 | 2003-01-24 | Peptìdeos macrocìclicos ativos contra o vìrus de hepatite c |
| ES03700743T ES2316718T3 (es) | 2002-01-30 | 2003-01-24 | Peptidos macrociclicos activos contra el virus de la hepaitis c. |
| DE60324660T DE60324660D1 (de) | 2002-01-30 | 2003-01-24 | Makrozyklische peptide mit anti-hepatitis c virus wirkung |
| PCT/CA2003/000089 WO2003064455A2 (en) | 2002-01-30 | 2003-01-24 | Macrocyclic peptides active against the hepatitis c virus |
| MXPA04007462A MXPA04007462A (es) | 2002-01-30 | 2003-01-24 | Peptidos macrociclicos activos contra el virus de la hepatitis c. |
| TW092101813A TW200307692A (en) | 2002-01-30 | 2003-01-28 | Macrocyclic peptides active against the hepatitis C virus |
| PE2003000095A PE20030818A1 (es) | 2002-01-30 | 2003-01-29 | Peptidos macrociclicos activos contra el virus de la hepatitis c |
| ARP030100252A AR038330A1 (es) | 2002-01-30 | 2003-01-29 | Peptidos macrociclicos activos contra el virus de la hepatitis c |
| UY27630A UY27630A1 (es) | 2002-01-30 | 2003-01-29 | Péptidos macrocíclicos activos contrael virus de la hepatitis c. |
| US10/353,894 US7119072B2 (en) | 2002-01-30 | 2003-01-29 | Macrocyclic peptides active against the hepatitis C virus |
| SA03230569A SA03230569B1 (ar) | 2002-01-30 | 2003-03-02 | ببتيدات ضخمة الحلقة فعالة ضد فيروس c |
| ZA200405639A ZA200405639B (en) | 2002-01-30 | 2004-07-15 | Macrocyclic peptides active against the hepatitis C virus. |
| EC2004005243A ECSP045243A (es) | 2002-01-30 | 2004-08-20 | Péptidos macrocíclicos activos contra el virus de la hepatitis C |
| NO20043591A NO20043591L (no) | 2002-01-30 | 2004-08-27 | Makrosykliske peptider aktive mot hepatitt C virus |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002369711A CA2369711A1 (en) | 2002-01-30 | 2002-01-30 | Macrocyclic peptides active against the hepatitis c virus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2369711A1 true CA2369711A1 (en) | 2003-07-30 |
Family
ID=27626541
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002369711A Abandoned CA2369711A1 (en) | 2002-01-30 | 2002-01-30 | Macrocyclic peptides active against the hepatitis c virus |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US20030181363A1 (https=) |
| EP (1) | EP1472278B1 (https=) |
| JP (1) | JP4040578B2 (https=) |
| KR (1) | KR20040077899A (https=) |
| CN (1) | CN1639187A (https=) |
| AR (1) | AR038330A1 (https=) |
| AT (1) | ATE414098T1 (https=) |
| BR (1) | BR0307297A (https=) |
| CA (1) | CA2369711A1 (https=) |
| DE (1) | DE60324660D1 (https=) |
| EA (1) | EA007738B1 (https=) |
| EC (1) | ECSP045243A (https=) |
| ES (1) | ES2316718T3 (https=) |
| HR (1) | HRP20040689A2 (https=) |
| MX (1) | MXPA04007462A (https=) |
| NO (1) | NO20043591L (https=) |
| NZ (1) | NZ534929A (https=) |
| PE (1) | PE20030818A1 (https=) |
| PL (1) | PL371007A1 (https=) |
| RS (1) | RS67004A (https=) |
| SA (1) | SA03230569B1 (https=) |
| TW (1) | TW200307692A (https=) |
| UA (1) | UA78014C2 (https=) |
| UY (1) | UY27630A1 (https=) |
| WO (1) | WO2003064455A2 (https=) |
| ZA (1) | ZA200405639B (https=) |
Families Citing this family (138)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AP1019A (en) | 1996-10-18 | 2001-10-16 | Vertex Pharma | Inhibitors of serinre proteases, particularly hepatitis C virus NS3 protease. |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| ES2263687T3 (es) | 2000-11-20 | 2006-12-16 | Bristol-Myers Squibb Company | Inhibidores tripeptidicos de la hepatitis c. |
| US6867185B2 (en) * | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| ATE481106T1 (de) | 2002-05-20 | 2010-10-15 | Bristol Myers Squibb Co | Heterocyclische sulfonamid-hepatitis-c-virus- hemmer |
| DE60324552D1 (en) | 2002-05-20 | 2008-12-18 | Bristol Myers Squibb Co | Substituierte cycloalkyl p1' hepatitis c virus inhibitoren |
| ES2361011T3 (es) | 2002-05-20 | 2011-06-13 | Bristol-Myers Squibb Company | Inhibidores del virus de la hepatitis c. |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US20050075279A1 (en) * | 2002-10-25 | 2005-04-07 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| US20050159345A1 (en) * | 2002-10-29 | 2005-07-21 | Boehringer Ingelheim International Gmbh | Composition for the treatment of infection by Flaviviridae viruses |
| US7176208B2 (en) * | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| AU2004240704B9 (en) | 2003-05-21 | 2009-10-22 | Boehringer Ingelheim International Gmbh | Hepatitis C inhibitor compounds |
| US7521420B2 (en) | 2003-06-18 | 2009-04-21 | Tranzyme Pharma, Inc. | Macrocyclic antagonists of the motilin receptor |
| UY28500A1 (es) | 2003-09-05 | 2005-04-29 | Vertex Pharma | Inhibidores de proteasas de serina, en particular proteasa ns3-ns4a del vhc. |
| RS20060197A (sr) * | 2003-09-22 | 2008-09-29 | Boehringer Ingelheim International Gmbh., | Makrociklični peptidi koji su aktivni protiv hepatitisa c virusa |
| HRP20130098T1 (hr) | 2003-10-14 | 2013-02-28 | F. Hoffmann - La Roche Ag | MAKROCIKLIÄŚKE KARBOKSILNE KISELINE I ACILSULFONAMIDNI SPOJEVI KAO INHIBITORI REPLIKACIJE HCV-a |
| US7491794B2 (en) * | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| US7132504B2 (en) | 2003-11-12 | 2006-11-07 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CA2539575C (en) | 2003-11-20 | 2015-01-20 | Boehringer Ingelheim International Gmbh | Method of removing transition metals, especially from metathesis reaction products |
| US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7135462B2 (en) | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| ES2320776T3 (es) * | 2003-12-08 | 2009-05-28 | Boehringer Ingelheim International Gmbh | Eliminacion de subproductos de rutenio por tratamiento con fluidos supercriticos. |
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| US6608027B1 (en) * | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
| UA74546C2 (en) * | 1999-04-06 | 2006-01-16 | Boehringer Ingelheim Ca Ltd | Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition |
| US6867185B2 (en) * | 2001-12-20 | 2005-03-15 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
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2002
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- 2002-12-17 US US10/320,978 patent/US20030181363A1/en not_active Abandoned
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- 2003-01-24 BR BR0307297-5A patent/BR0307297A/pt not_active IP Right Cessation
- 2003-01-24 DE DE60324660T patent/DE60324660D1/de not_active Expired - Lifetime
- 2003-01-24 EA EA200400886A patent/EA007738B1/ru not_active IP Right Cessation
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- 2003-01-24 JP JP2003564075A patent/JP4040578B2/ja not_active Expired - Fee Related
- 2003-01-24 AT AT03700743T patent/ATE414098T1/de active
- 2003-01-24 PL PL03371007A patent/PL371007A1/xx not_active Application Discontinuation
- 2003-01-24 CN CNA038054841A patent/CN1639187A/zh active Pending
- 2003-01-24 ES ES03700743T patent/ES2316718T3/es not_active Expired - Lifetime
- 2003-01-24 EP EP03700743A patent/EP1472278B1/en not_active Expired - Lifetime
- 2003-01-24 WO PCT/CA2003/000089 patent/WO2003064455A2/en not_active Ceased
- 2003-01-24 KR KR10-2004-7011682A patent/KR20040077899A/ko not_active Ceased
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- 2003-01-28 TW TW092101813A patent/TW200307692A/zh unknown
- 2003-01-29 AR ARP030100252A patent/AR038330A1/es unknown
- 2003-01-29 PE PE2003000095A patent/PE20030818A1/es not_active Application Discontinuation
- 2003-01-29 UY UY27630A patent/UY27630A1/es not_active Application Discontinuation
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| JP2005524632A (ja) | 2005-08-18 |
| ATE414098T1 (de) | 2008-11-15 |
| SA03230569B1 (ar) | 2007-03-05 |
| TW200307692A (en) | 2003-12-16 |
| RS67004A (sr) | 2006-10-27 |
| ES2316718T3 (es) | 2009-04-16 |
| HRP20040689A2 (en) | 2005-06-30 |
| NZ534929A (en) | 2006-08-31 |
| PL371007A1 (en) | 2005-06-13 |
| JP4040578B2 (ja) | 2008-01-30 |
| WO2003064455A2 (en) | 2003-08-07 |
| CN1639187A (zh) | 2005-07-13 |
| EA200400886A1 (ru) | 2005-02-24 |
| AR038330A1 (es) | 2005-01-12 |
| EA007738B1 (ru) | 2006-12-29 |
| BR0307297A (pt) | 2004-12-21 |
| EP1472278A2 (en) | 2004-11-03 |
| DE60324660D1 (de) | 2008-12-24 |
| PE20030818A1 (es) | 2003-10-30 |
| NO20043591L (no) | 2004-08-27 |
| EP1472278B1 (en) | 2008-11-12 |
| KR20040077899A (ko) | 2004-09-07 |
| MXPA04007462A (es) | 2005-07-13 |
| ECSP045243A (es) | 2004-09-28 |
| US20030181363A1 (en) | 2003-09-25 |
| WO2003064455A3 (en) | 2004-02-05 |
| UY27630A1 (es) | 2003-08-29 |
| ZA200405639B (en) | 2005-07-01 |
| UA78014C2 (en) | 2007-02-15 |
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