JP2007525514A5 - - Google Patents
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- Publication number
- JP2007525514A5 JP2007525514A5 JP2007500955A JP2007500955A JP2007525514A5 JP 2007525514 A5 JP2007525514 A5 JP 2007525514A5 JP 2007500955 A JP2007500955 A JP 2007500955A JP 2007500955 A JP2007500955 A JP 2007500955A JP 2007525514 A5 JP2007525514 A5 JP 2007525514A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- pharmaceutically acceptable
- group
- rotamer
- tautomer
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 118
- 241000711549 Hepacivirus C Species 0.000 claims 28
- 108091005804 Peptidases Proteins 0.000 claims 20
- 239000004365 Protease Substances 0.000 claims 20
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims 20
- 150000002148 esters Chemical class 0.000 claims 18
- 150000003839 salts Chemical class 0.000 claims 18
- 239000012453 solvate Substances 0.000 claims 18
- 230000001747 exhibiting effect Effects 0.000 claims 16
- 230000002401 inhibitory effect Effects 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 13
- 239000000203 mixture Substances 0.000 claims 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- 125000003118 aryl group Chemical group 0.000 claims 10
- 125000001072 heteroaryl group Chemical group 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- -1 heteroalkenyl Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 229940079322 interferon Drugs 0.000 claims 7
- 102000014150 Interferons Human genes 0.000 claims 6
- 108010050904 Interferons Proteins 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 125000003342 alkenyl group Chemical group 0.000 claims 5
- 125000000304 alkynyl group Chemical group 0.000 claims 5
- 125000004404 heteroalkyl group Chemical group 0.000 claims 5
- 239000003443 antiviral agent Substances 0.000 claims 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 2
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical group N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004422 alkyl sulphonamide group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000005281 alkyl ureido group Chemical group 0.000 claims 2
- 125000001769 aryl amino group Chemical group 0.000 claims 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 2
- 125000004421 aryl sulphonamide group Chemical group 0.000 claims 2
- 125000005110 aryl thio group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 150000003857 carboxamides Chemical class 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229960000329 ribavirin Drugs 0.000 claims 2
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- RGICCULPCWNRAB-UHFFFAOYSA-N 2-[2-(2-hexoxyethoxy)ethoxy]ethanol Chemical compound CCCCCCOCCOCCOCCO RGICCULPCWNRAB-UHFFFAOYSA-N 0.000 claims 1
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 1
- 208000005176 Hepatitis C Diseases 0.000 claims 1
- 229930194542 Keto Natural products 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 125000000468 ketone group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229920001184 polypeptide Polymers 0.000 claims 1
- 102000004196 processed proteins & peptides Human genes 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- 238000007920 subcutaneous administration Methods 0.000 claims 1
- 229940124530 sulfonamide Drugs 0.000 claims 1
- 150000003456 sulfonamides Chemical class 0.000 claims 1
- 150000003457 sulfones Chemical class 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 0 CC(C)(C)OC(C[C@]1C(NC(CC2CCC2)C(C(N)=O)=O)=O)CN1C([C@](C1CCCCC1)NC(NC1(C*)CCCCC1)=O)=O Chemical compound CC(C)(C)OC(C[C@]1C(NC(CC2CCC2)C(C(N)=O)=O)=O)CN1C([C@](C1CCCCC1)NC(NC1(C*)CCCCC1)=O)=O 0.000 description 6
- FBTCAECCGIRNCW-MLFWNAKGSA-N CC(C)(C)/S(/CC1(CCCCC1)NC(N[C@@H](C1(C)CCCC1)C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CC1)C(C(NCC=C)=O)=O)=O)=O)=O)=C\C Chemical compound CC(C)(C)/S(/CC1(CCCCC1)NC(N[C@@H](C1(C)CCCC1)C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CC1)C(C(NCC=C)=O)=O)=O)=O)=O)=C\C FBTCAECCGIRNCW-MLFWNAKGSA-N 0.000 description 1
- ZGWAWMZWQXNJAO-VGCMAJOSSA-N CC(C)(C)[C@@H](C(N(CC(C1)OCc2ccccc2)[C@@H]1C(NC(CC1CCC1)C(C(N)=O)=O)=O)=O)NC(NC1(C/S(/C(C)(C)C)=C/C)CCCCC1)=O Chemical compound CC(C)(C)[C@@H](C(N(CC(C1)OCc2ccccc2)[C@@H]1C(NC(CC1CCC1)C(C(N)=O)=O)=O)=O)NC(NC1(C/S(/C(C)(C)C)=C/C)CCCCC1)=O ZGWAWMZWQXNJAO-VGCMAJOSSA-N 0.000 description 1
- LKGRKMBRSSOYDN-WGMSXAEXSA-N CC(C)(C)[C@@H](C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CCC1)C(C(NCCC=C)=O)=O)=O)=O)NC(NC1(C/S=[O]/C)CCCCC1)=O Chemical compound CC(C)(C)[C@@H](C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CCC1)C(C(NCCC=C)=O)=O)=O)=O)NC(NC1(C/S=[O]/C)CCCCC1)=O LKGRKMBRSSOYDN-WGMSXAEXSA-N 0.000 description 1
- QZUHEBVEOWOTHR-AMRHDSLHSA-N CC(C)(C)[C@@H](C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CCC#C)C(C(NCCC#C)=O)=O)=O)=O)NC(NC1(CS(c2ccccc2)(=O)=O)CCCCC1)=O Chemical compound CC(C)(C)[C@@H](C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CCC#C)C(C(NCCC#C)=O)=O)=O)=O)NC(NC1(CS(c2ccccc2)(=O)=O)CCCCC1)=O QZUHEBVEOWOTHR-AMRHDSLHSA-N 0.000 description 1
- XPWMILXSXBEPNU-MWESMXAXSA-N CC(C)(C)[C@@H](C(N(CC1C(C)(C)C1C12)[C@@H]1C2C(NC(CC1CC1)C(C(NCC=C)=O)=O)=O)=O)NC(NC1(CS(C)(=O)=O)CCCCC1)=O Chemical compound CC(C)(C)[C@@H](C(N(CC1C(C)(C)C1C12)[C@@H]1C2C(NC(CC1CC1)C(C(NCC=C)=O)=O)=O)=O)NC(NC1(CS(C)(=O)=O)CCCCC1)=O XPWMILXSXBEPNU-MWESMXAXSA-N 0.000 description 1
- DBNVQVFEYNCUMD-YCWZNOKWSA-N CCCC(C(C(NCC=C)=O)=O)NC([C@H](C1C(C)(C)[C@@H]1C1)N1C([C@H](C1(C)CCCC1)NC(NC1(CS(C(C)(C)C)(=O)=O)CCCCC1)=O)=O)=O Chemical compound CCCC(C(C(NCC=C)=O)=O)NC([C@H](C1C(C)(C)[C@@H]1C1)N1C([C@H](C1(C)CCCC1)NC(NC1(CS(C(C)(C)C)(=O)=O)CCCCC1)=O)=O)=O DBNVQVFEYNCUMD-YCWZNOKWSA-N 0.000 description 1
- RRYBDHATVTVEJW-VZEHBEODSA-N CCCCC(C(C(N)=O)=O)NC([C@H](C1C(C)(C)C1C1)N1C([C@H](C(C)(C)C)NC(NC1(CS(C(C)(C)C)(=O)=O)CCCCC1)=O)=O)=O Chemical compound CCCCC(C(C(N)=O)=O)NC([C@H](C1C(C)(C)C1C1)N1C([C@H](C(C)(C)C)NC(NC1(CS(C(C)(C)C)(=O)=O)CCCCC1)=O)=O)=O RRYBDHATVTVEJW-VZEHBEODSA-N 0.000 description 1
- BPVHJIIIBCGHBH-TZCGXBFMSA-N CCS(CC1(CCCCC1)NC(N[C@@H](C(C)(C)C)C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CC1)C(C(N)=O)=O)=O)=O)=O)(=O)=O Chemical compound CCS(CC1(CCCCC1)NC(N[C@@H](C(C)(C)C)C(N(CC1C(C)(C)C11)[C@@H]1C(NC(CC1CC1)C(C(N)=O)=O)=O)=O)=O)(=O)=O BPVHJIIIBCGHBH-TZCGXBFMSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54867004P | 2004-02-27 | 2004-02-27 | |
| US60/548,670 | 2004-02-27 | ||
| PCT/US2005/005795 WO2005087731A1 (en) | 2004-02-27 | 2005-02-24 | Sulfur compounds as inhibitors of hepatitis c virus ns3 serine protease |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007525514A JP2007525514A (ja) | 2007-09-06 |
| JP2007525514A5 true JP2007525514A5 (enExample) | 2008-03-27 |
| JP4714732B2 JP4714732B2 (ja) | 2011-06-29 |
Family
ID=34961556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007500955A Expired - Fee Related JP4714732B2 (ja) | 2004-02-27 | 2005-02-24 | Ｃ型肝炎ウイルスｎｓ３セリンプロテアーゼのインヒビターとしての硫黄化合物 |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US8067379B2 (enExample) |
| EP (1) | EP1730110B9 (enExample) |
| JP (1) | JP4714732B2 (enExample) |
| KR (2) | KR101316137B1 (enExample) |
| CN (2) | CN101076516A (enExample) |
| AR (1) | AR048241A1 (enExample) |
| AT (1) | ATE470660T1 (enExample) |
| AU (1) | AU2005222060A1 (enExample) |
| BR (1) | BRPI0508085A (enExample) |
| CA (1) | CA2557495C (enExample) |
| CY (1) | CY1111212T1 (enExample) |
| DE (1) | DE602005021760D1 (enExample) |
| DK (1) | DK1730110T3 (enExample) |
| EC (1) | ECSP066791A (enExample) |
| ES (1) | ES2346233T3 (enExample) |
| HR (1) | HRP20100416T1 (enExample) |
| IL (1) | IL177544A (enExample) |
| MY (1) | MY145081A (enExample) |
| NO (1) | NO20064358L (enExample) |
| NZ (1) | NZ549223A (enExample) |
| PE (1) | PE20051150A1 (enExample) |
| PL (1) | PL1730110T3 (enExample) |
| PT (1) | PT1730110E (enExample) |
| RS (1) | RS51394B (enExample) |
| RU (1) | RU2428428C9 (enExample) |
| SG (1) | SG186041A1 (enExample) |
| SI (1) | SI1730110T1 (enExample) |
| TW (2) | TWI314927B (enExample) |
| WO (1) | WO2005087731A1 (enExample) |
| ZA (1) | ZA200607096B (enExample) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN183120B (enExample) | 1996-10-18 | 1999-09-11 | Vertex Pharma | |
| ATE470660T1 (de) * | 2004-02-27 | 2010-06-15 | Schering Corp | Schwefelverbindungen als inhibitoren der ns3- serinprotease des hepatitis-c-virus |
| US7816326B2 (en) * | 2004-02-27 | 2010-10-19 | Schering Corporation | Sulfur compounds as inhibitors of hepatitis C virus NS3 serine protease |
| GB0426661D0 (en) * | 2004-12-06 | 2005-01-05 | Isis Innovation | Pyrrolidine compounds |
| US20060276406A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| US20070237818A1 (en) * | 2005-06-02 | 2007-10-11 | Malcolm Bruce A | Controlled-release formulation of HCV protease inhibitor and methods using the same |
| US20060276407A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Methods of treating hepatitis C virus |
| AU2006252623A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation useful for treating disorders associated with hepatitis C virus |
| EP1919478B1 (en) * | 2005-06-02 | 2016-03-23 | Merck Sharp & Dohme Corp. | Combination of hcv protease inhibitors with a surfactant |
| WO2006130626A2 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Method for modulating activity of hcv protease through use of a novel hcv protease inhibitor to reduce duration of treatment period |
| US20060276404A1 (en) * | 2005-06-02 | 2006-12-07 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
| NZ563361A (en) | 2005-06-02 | 2011-02-25 | Schering Corp | HCV protease inhibitors in combination with food |
| US20070021351A1 (en) * | 2005-06-02 | 2007-01-25 | Schering Corporation | Liver/plasma concentration ratio for dosing hepatitis C virus protease inhibitor |
| US20060275366A1 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Controlled-release formulation |
| AR055395A1 (es) | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
| US7816348B2 (en) | 2006-02-03 | 2010-10-19 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| WO2007106317A2 (en) * | 2006-03-03 | 2007-09-20 | Schering Corporation | Pharmaceutical combinations of hcv-protease and -ires inhibitors |
| KR101398259B1 (ko) | 2006-03-16 | 2014-05-26 | 버텍스 파마슈티칼스 인코포레이티드 | 입체 화합물의 제조 방법 및 이를 위한 중간체 |
| CA2647158C (en) * | 2006-03-23 | 2012-07-31 | Schering Corporation | Combinations of hcv protease inhibitor(s) and cyp3a4 inhibitor(s), and methods of treatment related thereto |
| US7825152B2 (en) | 2006-04-11 | 2010-11-02 | Novartis Ag | Organic compounds and their uses |
| DE102006059317A1 (de) | 2006-07-04 | 2008-01-10 | Evonik Degussa Gmbh | Verfahren zur Herstellung von β-Amino-α-hydroxy-carbonsäureamiden |
| MX2009000882A (es) | 2006-08-17 | 2009-02-04 | Boehringer Ingelheim Int | Inhibidores de la polimerasa virica. |
| US20100081672A1 (en) * | 2006-12-07 | 2010-04-01 | Schering Corporation | Ph sensitive matrix formulation |
| MX2009006878A (es) | 2006-12-22 | 2009-07-07 | Schering Corp | Derivados indolicos con anillo unido en las posiciones 4,5 para tratar o prevenir infecciones virales por virus de la hepatitis c e infecciones virales relacionadas. |
| US8268803B2 (en) | 2006-12-22 | 2012-09-18 | Merck Sharp & Dohme Corp. | 5, 6-ring annulated indole derivatives and use thereof |
| KR20090094154A (ko) | 2006-12-22 | 2009-09-03 | 쉐링 코포레이션 | Ｈｃｖ 및 관련 바이러스 감염을 치료 또는 예방하기 위한 4,5-환 환상 인돌 유도체 |
| WO2008078563A1 (ja) * | 2006-12-22 | 2008-07-03 | Sumitomo Seika Chemicals Co., Ltd. | ３－ベンジルオキシベンゼンチオールの製造方法 |
| EP2188274A4 (en) | 2007-08-03 | 2011-05-25 | Boehringer Ingelheim Int | VIRAL POLYMERASE HEMMER |
| TW200924751A (en) | 2007-08-29 | 2009-06-16 | Schering Corp | 2,3-substituted indole derivatives and methods of use thereof |
| CN101821252A (zh) | 2007-08-29 | 2010-09-01 | 先灵公司 | 取代的吲哚衍生物及其使用方法 |
| KR20100065167A (ko) | 2007-08-29 | 2010-06-15 | 쉐링 코포레이션 | 바이러스 감염 치료용 2,3-치환된 아자인돌 유도체 |
| NZ583825A (en) * | 2007-09-14 | 2012-06-29 | Schering Corp | Method of treating hepatitis C patients comprising an HCV protease inhibitor, an antiviral compound and an interferon |
| CN101868452B (zh) | 2007-10-10 | 2014-08-06 | 诺华股份有限公司 | 螺环吡咯烷类与其对抗hcv和hiv感染的应用 |
| US8765757B2 (en) | 2007-11-16 | 2014-07-01 | Merck Sharp & Dohme Corp. | 3-heterocyclic substituted indole derivatives and methods of use thereof |
| MX2010005355A (es) | 2007-11-16 | 2010-06-02 | Schering Corp | Derivados de indol sustituidos con 3-aminosulfonilo y metodos de uso de los mismos. |
| US8476257B2 (en) | 2007-12-19 | 2013-07-02 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| US7964560B2 (en) * | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MX2010013630A (es) | 2008-06-13 | 2010-12-21 | Schering Corp | Derivados triciclicos de indol y metodos de uso de los mismos. |
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| BR112012022125A2 (pt) | 2010-03-09 | 2016-11-01 | Merck Sharp & Dhme Corp | composto, sal de dicloridrato, composição farmacêutica, uso do composto, e, método para tratar um paciente |
| JP2013541499A (ja) | 2010-07-26 | 2013-11-14 | メルク・シャープ・エンド・ドーム・コーポレイション | 置換されたビフェニレン化合物およびウイルス性疾患の治療のためのその使用方法 |
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| US10167298B2 (en) | 2013-10-30 | 2019-01-01 | Merck Sharp & Dohme Corp. | Pseudopolymorphs of an HCV NS5A inhibitor and uses thereof |
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| US12435088B2 (en) | 2018-12-21 | 2025-10-07 | Memorial Sloan-Kettering Cancer Center | Salicyl-adenosinemonosulfamate analogs and uses thereof |
| WO2021209563A1 (en) | 2020-04-16 | 2021-10-21 | Som Innovation Biotech, S.A. | Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus |
| US11351149B2 (en) | 2020-09-03 | 2022-06-07 | Pfizer Inc. | Nitrile-containing antiviral compounds |
| US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
| EP4653420A1 (en) | 2023-01-17 | 2025-11-26 | Shenyang Haisco Pharmaceutical Co., Ltd. | Method for preparing chiral amino alcohol pharmaceutical intermediates |
Family Cites Families (22)
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|---|---|---|---|---|
| DE69133617D1 (de) | 1990-04-04 | 2009-07-23 | Novartis Vaccines & Diagnostic | Protease von Hepatitis C Virus |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| IN183120B (enExample) | 1996-10-18 | 1999-09-11 | Vertex Pharma | |
| GB9623908D0 (en) | 1996-11-18 | 1997-01-08 | Hoffmann La Roche | Amino acid derivatives |
| PT1012180E (pt) | 1997-08-11 | 2005-04-29 | Boehringer Ingelheim Ca Ltd | Analogos de peptidos inibidores da hepatite c |
| AR022061A1 (es) | 1998-08-10 | 2002-09-04 | Boehringer Ingelheim Ca Ltd | Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos. |
| US6323180B1 (en) * | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
| US6608027B1 (en) | 1999-04-06 | 2003-08-19 | Boehringer Ingelheim (Canada) Ltd | Macrocyclic peptides active against the hepatitis C virus |
| JP4806154B2 (ja) | 2000-04-03 | 2011-11-02 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼ、特にｃ型肝炎ウイルスｎｓ３プロテアーゼのインヒビター |
| NZ521455A (en) | 2000-04-05 | 2004-06-25 | Schering Corp | Macrocyclic NS3-Serine protease inhibitors of hepatitis C virus comprising N-Cyclic P2 Moieties |
| BR0110104A (pt) | 2000-04-19 | 2003-01-07 | Schering Corp | Inibidores de ns-3 serina rotease macrocìclica do vìrus da hepatite c compreendendo porções de alquil e aril alanina p2 |
| AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
| WO2002008251A2 (en) | 2000-07-21 | 2002-01-31 | Corvas International, Inc. | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
| MY139078A (en) | 2000-07-21 | 2009-08-28 | Schering Corp | Peptides as ns3-serine protease inhibitors of hepatitis c virus |
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| US7244721B2 (en) * | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
| SV2003000617A (es) * | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| EP1343807B1 (en) | 2000-12-12 | 2009-04-29 | Schering Corporation | Diaryl peptides as ns3-serine protease inhibitors of hepatits c virus |
| WO2003035060A1 (en) * | 2001-10-24 | 2003-05-01 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine protease, particularly hepatitis c virus ns3-ns4a protease, incorporating a fused ring system |
| US7816326B2 (en) | 2004-02-27 | 2010-10-19 | Schering Corporation | Sulfur compounds as inhibitors of hepatitis C virus NS3 serine protease |
| ATE470660T1 (de) * | 2004-02-27 | 2010-06-15 | Schering Corp | Schwefelverbindungen als inhibitoren der ns3- serinprotease des hepatitis-c-virus |
| EP1919478B1 (en) | 2005-06-02 | 2016-03-23 | Merck Sharp & Dohme Corp. | Combination of hcv protease inhibitors with a surfactant |
-
2005
- 2005-02-24 AT AT05723607T patent/ATE470660T1/de active
- 2005-02-24 PE PE2005000220A patent/PE20051150A1/es not_active Application Discontinuation
- 2005-02-24 SI SI200531086T patent/SI1730110T1/sl unknown
- 2005-02-24 AU AU2005222060A patent/AU2005222060A1/en not_active Abandoned
- 2005-02-24 MY MYPI20050737A patent/MY145081A/en unknown
- 2005-02-24 SG SG2012087664A patent/SG186041A1/en unknown
- 2005-02-24 JP JP2007500955A patent/JP4714732B2/ja not_active Expired - Fee Related
- 2005-02-24 TW TW094105518A patent/TWI314927B/zh not_active IP Right Cessation
- 2005-02-24 HR HR20100416T patent/HRP20100416T1/hr unknown
- 2005-02-24 ES ES05723607T patent/ES2346233T3/es not_active Expired - Lifetime
- 2005-02-24 CA CA2557495A patent/CA2557495C/en not_active Expired - Fee Related
- 2005-02-24 AR ARP050100679A patent/AR048241A1/es not_active Application Discontinuation
- 2005-02-24 DE DE602005021760T patent/DE602005021760D1/de not_active Expired - Lifetime
- 2005-02-24 PT PT05723607T patent/PT1730110E/pt unknown
- 2005-02-24 WO PCT/US2005/005795 patent/WO2005087731A1/en not_active Ceased
- 2005-02-24 CN CNA2005800128593A patent/CN101076516A/zh active Pending
- 2005-02-24 PL PL05723607T patent/PL1730110T3/pl unknown
- 2005-02-24 KR KR1020067017257A patent/KR101316137B1/ko not_active Expired - Fee Related
- 2005-02-24 RS RSP-2010/0360A patent/RS51394B/sr unknown
- 2005-02-24 RU RU2006134003/04A patent/RU2428428C9/ru active
- 2005-02-24 EP EP05723607A patent/EP1730110B9/en not_active Expired - Lifetime
- 2005-02-24 NZ NZ549223A patent/NZ549223A/en not_active IP Right Cessation
- 2005-02-24 BR BRPI0508085-1A patent/BRPI0508085A/pt not_active IP Right Cessation
- 2005-02-24 DK DK05723607.7T patent/DK1730110T3/da active
- 2005-02-24 CN CN2012103533032A patent/CN103102389A/zh active Pending
- 2005-02-24 TW TW098107879A patent/TWI393704B/zh not_active IP Right Cessation
- 2005-02-24 US US11/064,673 patent/US8067379B2/en active Active
- 2005-02-24 KR KR1020127034290A patent/KR20130018418A/ko not_active Withdrawn
-
2006
- 2006-08-17 IL IL177544A patent/IL177544A/en not_active IP Right Cessation
- 2006-08-24 ZA ZA200607096A patent/ZA200607096B/xx unknown
- 2006-08-25 EC EC2006006791A patent/ECSP066791A/es unknown
- 2006-09-26 NO NO20064358A patent/NO20064358L/no not_active Application Discontinuation
-
2010
- 2010-09-01 CY CY20101100796T patent/CY1111212T1/el unknown
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