JP4271148B2 - 置換シクロアルキルp1’c型肝炎ウイルスインヒビター - Google Patents
置換シクロアルキルp1’c型肝炎ウイルスインヒビター Download PDFInfo
- Publication number
- JP4271148B2 JP4271148B2 JP2004551405A JP2004551405A JP4271148B2 JP 4271148 B2 JP4271148 B2 JP 4271148B2 JP 2004551405 A JP2004551405 A JP 2004551405A JP 2004551405 A JP2004551405 A JP 2004551405A JP 4271148 B2 JP4271148 B2 JP 4271148B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- compound
- cycloalkyl
- aryloxy
- alkylaryl
- 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.)
- Expired - Fee Related
Links
- 0 C[C@](CC1(CC1)CC1)*1C([C@@](*C(NC(C)(C)C)=O)C(C)(C)C)=O Chemical compound C[C@](CC1(CC1)CC1)*1C([C@@](*C(NC(C)(C)C)=O)C(C)(C)C)=O 0.000 description 26
- VEYPDQPVVPIYOC-UHFFFAOYSA-N C/C(/O)=S(\C1(Cc2c(-c3ccccc3)[o]cn2)CC1)/N Chemical compound C/C(/O)=S(\C1(Cc2c(-c3ccccc3)[o]cn2)CC1)/N VEYPDQPVVPIYOC-UHFFFAOYSA-N 0.000 description 1
- OVCOAJLTWSNCPL-RPLWNJQUSA-N C/C(/c1ccccc1)=C\C(\O)=C(\C=CC([U]C)=C1)/C1=C Chemical compound C/C(/c1ccccc1)=C\C(\O)=C(\C=CC([U]C)=C1)/C1=C OVCOAJLTWSNCPL-RPLWNJQUSA-N 0.000 description 1
- UFALAUZAIDONSZ-RFZPGFLSSA-N C=C[C@H](C1)[C@@H]1N Chemical compound C=C[C@H](C1)[C@@H]1N UFALAUZAIDONSZ-RFZPGFLSSA-N 0.000 description 1
- YUMQBLSWIPRSGU-LSSONSMQSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(O)=O)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(O)=O)=O)=O)NC(OC(C)(C)C)=O YUMQBLSWIPRSGU-LSSONSMQSA-N 0.000 description 1
- GMIUPWHJUOSTHR-LSSONSMQSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(N)=O)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(N)=O)=O)=O)NC(OC(C)(C)C)=O GMIUPWHJUOSTHR-LSSONSMQSA-N 0.000 description 1
- ALNMRSKSHFLWHN-LSSONSMQSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(O)=O)=O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(O)=O)=O)=O)NC(OC(C)(C)C)=O ALNMRSKSHFLWHN-LSSONSMQSA-N 0.000 description 1
- SZXBQTSZISFIAO-ZETCQYMHSA-N CC(C)[C@@H](C(O)=O)NC(OC(C)(C)C)=O Chemical compound CC(C)[C@@H](C(O)=O)NC(OC(C)(C)C)=O SZXBQTSZISFIAO-ZETCQYMHSA-N 0.000 description 1
- DWRVAPQPTBGMOE-UHFFFAOYSA-N CC1C(c2ccccc2)=CC([U+])=C(C=CC(OC)=C2)C2=C1 Chemical compound CC1C(c2ccccc2)=CC([U+])=C(C=CC(OC)=C2)C2=C1 DWRVAPQPTBGMOE-UHFFFAOYSA-N 0.000 description 1
- NQVPOLJUWKKJRG-SRLMCJKZSA-N CCC#CCC1(CC1)S(NC([C@@](C1)([C@@H]1C=C)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)N1C(CNC(OC(C)(C)C)=O)=O)=O)=O)(=O)=O Chemical compound CCC#CCC1(CC1)S(NC([C@@](C1)([C@@H]1C=C)NC([C@H](C[C@H](C1)Oc2c(ccc(OC)c3)c3nc(C3=CCCC=C3)c2)N1C(CNC(OC(C)(C)C)=O)=O)=O)=O)(=O)=O NQVPOLJUWKKJRG-SRLMCJKZSA-N 0.000 description 1
- HMJBGZOKWXLUQS-ULIBGMESSA-N CCOC(N[C@@H](C(C)(C)C)C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C([N]#C[C@](C1)(C1C=C)C(O)=O)=O)=O)O Chemical compound CCOC(N[C@@H](C(C)(C)C)C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3nc(-c3ccccc3)c2)[C@@H]1C([N]#C[C@](C1)(C1C=C)C(O)=O)=O)=O)O HMJBGZOKWXLUQS-ULIBGMESSA-N 0.000 description 1
- PBQVUKQRDDQULW-DWLKFMQCSA-N CC[C@H](C1)[C@]1(C(NS(C1(Cc2ccccc2)CC1)(=O)=O)=O)NC(C(C[C@H](C1)Oc2c(ccc(OC)c3)c3nc(C3C=CC=CC3)c2)N1C([C@H](C(C)(C)C)NC(OC1(CC1)C(OCC)=O)=O)=O)=O Chemical compound CC[C@H](C1)[C@]1(C(NS(C1(Cc2ccccc2)CC1)(=O)=O)=O)NC(C(C[C@H](C1)Oc2c(ccc(OC)c3)c3nc(C3C=CC=CC3)c2)N1C([C@H](C(C)(C)C)NC(OC1(CC1)C(OCC)=O)=O)=O)=O PBQVUKQRDDQULW-DWLKFMQCSA-N 0.000 description 1
- JBDCSYPSAMOEKX-UHFFFAOYSA-N COC(C(C1)(C11CCCC1)N)=O Chemical compound COC(C(C1)(C11CCCC1)N)=O JBDCSYPSAMOEKX-UHFFFAOYSA-N 0.000 description 1
- OWNCDMARPWNRJZ-UHFFFAOYSA-N COC(C1(CCC1)NCl)=O Chemical compound COC(C1(CCC1)NCl)=O OWNCDMARPWNRJZ-UHFFFAOYSA-N 0.000 description 1
- JDIJMRKNULSEHI-UHFFFAOYSA-N Cc1n[o]c(C)c1NC(C1(CC1)S(N)(=O)=O)=O Chemical compound Cc1n[o]c(C)c1NC(C1(CC1)S(N)(=O)=O)=O JDIJMRKNULSEHI-UHFFFAOYSA-N 0.000 description 1
- QPOCDFSJBNGOLR-UHFFFAOYSA-N NS(C1(CC2CC2)CC1)(=O)=O Chemical compound NS(C1(CC2CC2)CC1)(=O)=O QPOCDFSJBNGOLR-UHFFFAOYSA-N 0.000 description 1
- HDHTTYUKRGFFMG-UHFFFAOYSA-M NS(C1(Cc2ncccc2)CC1)([O-])=O Chemical compound NS(C1(Cc2ncccc2)CC1)([O-])=O HDHTTYUKRGFFMG-UHFFFAOYSA-M 0.000 description 1
- DALKOEVEKVKJQX-UHFFFAOYSA-N Nc1ccc(CC(F)(F)F)cc1 Chemical compound Nc1ccc(CC(F)(F)F)cc1 DALKOEVEKVKJQX-UHFFFAOYSA-N 0.000 description 1
- JUNSJTPSENXKBD-UHFFFAOYSA-N O=C(C1C[IH]C1)OC1CCCC1 Chemical compound O=C(C1C[IH]C1)OC1CCCC1 JUNSJTPSENXKBD-UHFFFAOYSA-N 0.000 description 1
- VVPYMDXMQNSHHS-UHFFFAOYSA-P [NH3+]S(C1(Cc2cc[nH+]cc2)CC1)(O)=O Chemical compound [NH3+]S(C1(Cc2cc[nH+]cc2)CC1)(O)=O VVPYMDXMQNSHHS-UHFFFAOYSA-P 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
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
-
- 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
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Virology (AREA)
- Zoology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38214902P | 2002-05-20 | 2002-05-20 | |
| PCT/US2003/015780 WO2004043339A2 (en) | 2002-05-20 | 2003-05-20 | Substituted cycloalkyl p1' hepatitis c virus inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006501307A JP2006501307A (ja) | 2006-01-12 |
| JP2006501307A5 JP2006501307A5 (enExample) | 2006-05-18 |
| JP4271148B2 true JP4271148B2 (ja) | 2009-06-03 |
Family
ID=32312406
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004551405A Expired - Fee Related JP4271148B2 (ja) | 2002-05-20 | 2003-05-20 | 置換シクロアルキルp1’c型肝炎ウイルスインヒビター |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6878722B2 (enExample) |
| EP (1) | EP1505945B1 (enExample) |
| JP (1) | JP4271148B2 (enExample) |
| AT (1) | ATE413411T1 (enExample) |
| AU (1) | AU2003301959A1 (enExample) |
| DE (1) | DE60324552D1 (enExample) |
| ES (1) | ES2315568T3 (enExample) |
| IS (1) | IS7531A (enExample) |
| NO (1) | NO20044895L (enExample) |
| PL (1) | PL213029B1 (enExample) |
| WO (1) | WO2004043339A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007535491A (ja) * | 2003-11-20 | 2007-12-06 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルスインヒビター |
Families Citing this family (148)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001000843A2 (en) * | 1999-06-25 | 2001-01-04 | Basf Aktiengesellschaft | Corynebacterium glutamicum genes encoding metabolic pathway proteins |
| MY140680A (en) * | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| CA2516018C (en) * | 2003-03-05 | 2011-08-23 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor peptide analogs |
| WO2004101605A1 (en) * | 2003-03-05 | 2004-11-25 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibiting compounds |
| 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 |
| US7642235B2 (en) * | 2003-09-22 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis C virus |
| 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 |
| US7309708B2 (en) | 2003-11-20 | 2007-12-18 | Birstol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CA2549851C (en) * | 2004-01-21 | 2012-09-11 | Boehringer Ingelheim International Gmbh | Macrocyclic peptides active against the hepatitis c virus |
| UA84050C2 (en) | 2004-01-30 | 2008-09-10 | Медивир Аб | Hcv ns-3-serine protease inhibitors |
| RS52931B (sr) | 2004-02-20 | 2014-02-28 | Boehringer Ingelheim International Gmbh | Inhibitori virusne polimeraze |
| US7514557B2 (en) * | 2004-05-25 | 2009-04-07 | Boehringer Ingelheim International Gmbh | Process for preparing acyclic HCV protease inhibitors |
| WO2006000085A1 (en) * | 2004-06-28 | 2006-01-05 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor peptide analogs |
| UY29016A1 (es) * | 2004-07-20 | 2006-02-24 | Boehringer Ingelheim Int | Analogos de dipeptidos inhibidores de la hepatitis c |
| JP4914355B2 (ja) * | 2004-07-20 | 2012-04-11 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | C型肝炎インヒビターペプチド類似体 |
| GB0500784D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| US7323447B2 (en) | 2005-02-08 | 2008-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GB0505969D0 (en) * | 2005-03-23 | 2005-04-27 | Novartis Ag | Organic compounds |
| US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GB0514203D0 (en) * | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI389908B (zh) * | 2005-07-14 | 2013-03-21 | Gilead Sciences Inc | 抗病毒化合物類 |
| US20080200497A1 (en) * | 2005-07-20 | 2008-08-21 | Bailey Murray D | Hepatitis C Inhibitor Peptide Analogs |
| BRPI0613962A2 (pt) * | 2005-07-25 | 2009-03-24 | Intermune Inc | inibidores macrocìclicos inovadores de replicação de vìrus da hepatite c |
| PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
| CA2618682C (en) | 2005-08-12 | 2011-06-21 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| DK1999129T3 (da) | 2005-10-11 | 2011-02-07 | Intermune Inc | Forbindelser og fremgangsmåder til inhibering af replikationen af hepatitis C-virus |
| US7772183B2 (en) | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7741281B2 (en) | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PT2420491E (pt) * | 2005-12-30 | 2013-10-14 | Novartis Ag | Compostos de piperidina 3,5-substituída como inibidores de renina |
| US7816348B2 (en) | 2006-02-03 | 2010-10-19 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
| GB0612809D0 (en) * | 2006-06-28 | 2006-08-09 | Univ Sunderland | Formulation |
| KR20090024834A (ko) * | 2006-07-05 | 2009-03-09 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 억제제 |
| WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| EP2041156B1 (en) | 2006-07-13 | 2013-11-20 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| EP1886685A1 (en) | 2006-08-11 | 2008-02-13 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods, uses and compositions for modulating replication of hcv through the farnesoid x receptor (fxr) activation or inhibition |
| MX2009000882A (es) | 2006-08-17 | 2009-02-04 | Boehringer Ingelheim Int | Inhibidores de la polimerasa virica. |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| TW200827364A (en) * | 2006-11-02 | 2008-07-01 | Taigen Biotechnology Co Ltd | HCV protease inhibitors |
| US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2008095058A1 (en) * | 2007-02-01 | 2008-08-07 | Taigen Biotechnology Co. Ltd. | Hcv protease inhibitors |
| EP2495249A1 (en) | 2007-02-26 | 2012-09-05 | Achillion Pharmaceuticals, Inc. | Tertiary amine substituted peptides useful as inhibitors of HCV replication |
| EP2160392A2 (en) * | 2007-05-03 | 2010-03-10 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| BRPI0811447A2 (pt) * | 2007-05-10 | 2014-10-29 | Intermune Inc | Compostos, composição farmacêutica e métodos de inibição da atividade da protease ns3/ns4, de tratamento da fibrose hepática e de intensificação da função hepática num indivíduo tendo infecção de vírus da hepatite c. |
| WO2009000811A1 (en) | 2007-06-25 | 2008-12-31 | Novartis Ag | N5-(2-ethoxyethyl)-n3-(2-pyridinyl)-3,5-piperidinedicarboxamide derivatives for use as renin inhibitors |
| US20090047252A1 (en) * | 2007-06-29 | 2009-02-19 | Gilead Sciences, Inc. | Antiviral compounds |
| TW200914013A (en) * | 2007-06-29 | 2009-04-01 | Gilead Sciences Inc | Antiviral compounds |
| KR101596524B1 (ko) | 2007-06-29 | 2016-02-22 | 길리애드 사이언시즈, 인코포레이티드 | 항바이러스 화합물 |
| EP2188274A4 (en) | 2007-08-03 | 2011-05-25 | Boehringer Ingelheim Int | VIRAL POLYMERASE HEMMER |
| EP2190858A4 (en) | 2007-09-24 | 2013-02-13 | Achillion Pharmaceuticals Inc | PEPTIDES CONTAINING UREA AS INHIBITORS OF VIRAL REPLICATION |
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| JP2007535491A (ja) * | 2003-11-20 | 2007-12-06 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルスインヒビター |
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| EP1505945A2 (en) | 2005-02-16 |
| ATE413411T1 (de) | 2008-11-15 |
| ES2315568T3 (es) | 2009-04-01 |
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| IS7531A (is) | 2004-11-16 |
| PL213029B1 (pl) | 2012-12-31 |
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| AU2003301959A1 (en) | 2004-06-03 |
| NO20044895L (no) | 2004-12-28 |
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| PL373374A1 (en) | 2005-08-22 |
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| EP1505945A4 (en) | 2006-11-22 |
| US6878722B2 (en) | 2005-04-12 |
| JP2006501307A (ja) | 2006-01-12 |
| WO2004043339A3 (en) | 2004-07-22 |
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