KR101438851B1 - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR101438851B1 KR101438851B1 KR1020097004995A KR20097004995A KR101438851B1 KR 101438851 B1 KR101438851 B1 KR 101438851B1 KR 1020097004995 A KR1020097004995 A KR 1020097004995A KR 20097004995 A KR20097004995 A KR 20097004995A KR 101438851 B1 KR101438851 B1 KR 101438851B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- imidazol
- aryl
- heterocyclyl
- carbonyl
- 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 CC(C)(C)OC([C@@](*)N(*)C(*)=O)=O Chemical compound CC(C)(C)OC([C@@](*)N(*)C(*)=O)=O 0.000 description 13
- UHSMSJIGOANPKB-AWEZNQCLSA-N CC(C)(C)OC(N(CCC1)[C@@H]1C(NCC(c1cccc(Br)c1)=O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1C(NCC(c1cccc(Br)c1)=O)=O)=O UHSMSJIGOANPKB-AWEZNQCLSA-N 0.000 description 1
- TUWBUUKNTUQSTN-AWEZNQCLSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1nc(C(NC)=O)c(-c(cc2)ccc2Br)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1nc(C(NC)=O)c(-c(cc2)ccc2Br)[nH]1)=O TUWBUUKNTUQSTN-AWEZNQCLSA-N 0.000 description 1
- VVUABVJPAULPES-INIZCTEOSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cc(C)c2Br)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cc(C)c2Br)[nH]1)=O VVUABVJPAULPES-INIZCTEOSA-N 0.000 description 1
- PZDUMRRRPMDUBC-ZDUSSCGKSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cnc2Br)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)cnc2Br)[nH]1)=O PZDUMRRRPMDUBC-ZDUSSCGKSA-N 0.000 description 1
- JBSGOHFOTPZGBY-KRWDZBQOSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cn2)cnc2Cl)[n]1COCC[Si](C)(C)C)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cn2)cnc2Cl)[n]1COCC[Si](C)(C)C)=O JBSGOHFOTPZGBY-KRWDZBQOSA-N 0.000 description 1
- VRDPDAJHHVOZQT-FQEVSTJZSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c2cc(C)c(B3OC(C)(C)C(C)(C)O3)cc2)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c2cc(C)c(B3OC(C)(C)C(C)(C)O3)cc2)[nH]1)=O VRDPDAJHHVOZQT-FQEVSTJZSA-N 0.000 description 1
- SGQMAQQIIDVEFL-VQHVLOKHSA-N CCC(C=CC=C1)/C1=C/C(O)=O Chemical compound CCC(C=CC=C1)/C1=C/C(O)=O SGQMAQQIIDVEFL-VQHVLOKHSA-N 0.000 description 1
- ZUCSUKWYYWJTHM-LLVKDONJSA-N CCN(CC)[C@@H](C(O)=O)c1ccccc1 Chemical compound CCN(CC)[C@@H](C(O)=O)c1ccccc1 ZUCSUKWYYWJTHM-LLVKDONJSA-N 0.000 description 1
- HPLKZZNEIGEKQV-UHFFFAOYSA-N CCOC(C(c1ccncc1)N(C)C)=O Chemical compound CCOC(C(c1ccncc1)N(C)C)=O HPLKZZNEIGEKQV-UHFFFAOYSA-N 0.000 description 1
- IARSHNWRCPTAHF-UHFFFAOYSA-N CN(C)C(C(O)=O)c1ccncc1 Chemical compound CN(C)C(C(O)=O)c1ccncc1 IARSHNWRCPTAHF-UHFFFAOYSA-N 0.000 description 1
- XUXLCKDCNOQMOC-ATUXXYJQSA-N CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(c(C(F)(F)F)c2)ccc2-c2cnc([C@H](CCC3)N3C([C@@H](c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 Chemical compound CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(c(C(F)(F)F)c2)ccc2-c2cnc([C@H](CCC3)N3C([C@@H](c3ccccc3)N(C)C)=O)[nH]2)[nH]1)=O)c1ccccc1 XUXLCKDCNOQMOC-ATUXXYJQSA-N 0.000 description 1
- WWTABXAXNXQPOH-CNZKWPKMSA-N CN(C[C@@H](C1)F)C1C(O)=O Chemical compound CN(C[C@@H](C1)F)C1C(O)=O WWTABXAXNXQPOH-CNZKWPKMSA-N 0.000 description 1
- OGTOIFIZXISZKS-MRVPVSSYSA-N CNC(N[C@@H](C(O)=O)c1ccccc1)=O Chemical compound CNC(N[C@@H](C(O)=O)c1ccccc1)=O OGTOIFIZXISZKS-MRVPVSSYSA-N 0.000 description 1
- KTKKSRKCCYISPK-PUPDPRJKSA-N COC(N[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ccc2-c2cnc([C@H](CCC3)N3C(N3CCOCC3)=O)[nH]2)[nH]1)=O)c1ccccc1)=O Chemical compound COC(N[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ccc2-c2cnc([C@H](CCC3)N3C(N3CCOCC3)=O)[nH]2)[nH]1)=O)c1ccccc1)=O KTKKSRKCCYISPK-PUPDPRJKSA-N 0.000 description 1
- CJDYTWDZWVAESP-OWPQXHQJSA-N COC(N[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ncc2-c2cnc([C@H]3NCCC3)[nH]2)[nH]1)=O)c1ccccc1)=O Chemical compound COC(N[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(nc2)ncc2-c2cnc([C@H]3NCCC3)[nH]2)[nH]1)=O)c1ccccc1)=O CJDYTWDZWVAESP-OWPQXHQJSA-N 0.000 description 1
- QEIFWXUIJHFGPI-IMJSIDKUSA-N C[C@@H]([C@@H](C(O)=O)NC(OC)=O)O Chemical compound C[C@@H]([C@@H](C(O)=O)NC(OC)=O)O QEIFWXUIJHFGPI-IMJSIDKUSA-N 0.000 description 1
- KFXVSKIKSXJAJS-UHFFFAOYSA-N Cc(cc(cc1)C(CBr)=O)c1Br Chemical compound Cc(cc(cc1)C(CBr)=O)c1Br KFXVSKIKSXJAJS-UHFFFAOYSA-N 0.000 description 1
- PEOCDMIGOUXRKB-ZDUSSCGKSA-N Cc1cc(C(COC([C@H]2N(C)CCC2)=O)=O)ccc1Br Chemical compound Cc1cc(C(COC([C@H]2N(C)CCC2)=O)=O)ccc1Br PEOCDMIGOUXRKB-ZDUSSCGKSA-N 0.000 description 1
- ZGUNAGUHMKGQNY-SSDOTTSWSA-N N[C@@H](C(O)=O)c1ccccc1 Chemical compound N[C@@H](C(O)=O)c1ccccc1 ZGUNAGUHMKGQNY-SSDOTTSWSA-N 0.000 description 1
- RTSLQVZQORGDQQ-UHFFFAOYSA-N O=C(CBr)c(cc1)ccc1-c(cc1)ccc1C(CBr)=O Chemical compound O=C(CBr)c(cc1)ccc1-c(cc1)ccc1C(CBr)=O RTSLQVZQORGDQQ-UHFFFAOYSA-N 0.000 description 1
- ZLAKPURGNBLUCC-VUWPPUDQSA-N OC(C(c1ccccc1)N(CC1)C[C@H]1F)=O Chemical compound OC(C(c1ccccc1)N(CC1)C[C@H]1F)=O ZLAKPURGNBLUCC-VUWPPUDQSA-N 0.000 description 1
- GOSVNXMOCBVLPW-UHFFFAOYSA-N OC(Cc1c(CN2CCOCC2)cccc1)=O Chemical compound OC(Cc1c(CN2CCOCC2)cccc1)=O GOSVNXMOCBVLPW-UHFFFAOYSA-N 0.000 description 1
- OZJNQHRPTQSJDF-LLVKDONJSA-N OC([C@@H](c1ccccc1)N1CCOCC1)=O Chemical compound OC([C@@H](c1ccccc1)N1CCOCC1)=O OZJNQHRPTQSJDF-LLVKDONJSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P31/20—Antivirals for DNA 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Biotechnology (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83699906P | 2006-08-11 | 2006-08-11 | |
| US60/836,999 | 2006-08-11 | ||
| PCT/US2007/075545 WO2008021928A2 (en) | 2006-08-11 | 2007-08-09 | Hepatitis c virus inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20090040910A KR20090040910A (ko) | 2009-04-27 |
| KR101438851B1 true KR101438851B1 (ko) | 2014-09-11 |
Family
ID=38895921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097004995A Expired - Fee Related KR101438851B1 (ko) | 2006-08-11 | 2007-08-09 | C형 간염 바이러스 억제제 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7659270B2 (enExample) |
| EP (1) | EP2049116B1 (enExample) |
| JP (1) | JP5306203B2 (enExample) |
| KR (1) | KR101438851B1 (enExample) |
| CN (1) | CN101528232B (enExample) |
| AT (1) | ATE547103T1 (enExample) |
| AU (1) | AU2007286223B2 (enExample) |
| CA (1) | CA2660628C (enExample) |
| EA (1) | EA017348B1 (enExample) |
| ES (1) | ES2382005T3 (enExample) |
| IL (1) | IL196815A (enExample) |
| MX (1) | MX2009001436A (enExample) |
| NO (1) | NO20090453L (enExample) |
| NZ (1) | NZ574769A (enExample) |
| WO (1) | WO2008021928A2 (enExample) |
| ZA (1) | ZA200900935B (enExample) |
Families Citing this family (167)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7745636B2 (en) | 2006-08-11 | 2010-06-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8303944B2 (en) * | 2006-08-11 | 2012-11-06 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7759495B2 (en) | 2006-08-11 | 2010-07-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8329159B2 (en) * | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN101815533A (zh) | 2007-05-04 | 2010-08-25 | 弗特克斯药品有限公司 | 用于治疗hcv感染的组合治疗 |
| US7741347B2 (en) * | 2007-05-17 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2520561B1 (en) | 2007-06-08 | 2016-02-10 | MannKind Corporation | IRE-1A Inhibitors |
| WO2009006567A2 (en) * | 2007-07-05 | 2009-01-08 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| US8629171B2 (en) | 2007-08-08 | 2014-01-14 | Bristol-Myers Squibb Company | Crystalline form of methyl ((1S)-1-((25)-2-(5-(4'-(2-((25)-1((2S)-2-((methoxycarbonyl)amino)-3-methylbutanoyl)-2-pyrrolidinyl)-1H-imidazol-2-yl)-1-pyrrolidinyl)carbonyl)-2-methylpropyl)carbamate dihydrochloride salt |
| US7728027B2 (en) * | 2007-08-08 | 2010-06-01 | Bristol-Myers Squibb Company | Process for synthesizing compounds useful for treating hepatitis C |
| CA2715400A1 (en) | 2008-02-12 | 2009-08-20 | Bristol-Myers Squibb Company | Heterocyclic derivatives as hepatitis c virus inhibitors |
| KR101468765B1 (ko) * | 2008-02-12 | 2014-12-04 | 브리스톨-마이어스 스큅 컴퍼니 | C형 간염 바이러스 억제제 |
| ES2391600T3 (es) * | 2008-02-13 | 2012-11-28 | Bristol-Myers Squibb Company | Imidazoli bifenil imidazoles como inhibidores del virus de la hepatitis C |
| US8147818B2 (en) * | 2008-02-13 | 2012-04-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7704992B2 (en) | 2008-02-13 | 2010-04-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7906655B2 (en) | 2008-08-07 | 2011-03-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| AP3272A (en) * | 2008-09-22 | 2015-05-31 | Cayman Chem Co | Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases |
| US8383094B2 (en) | 2008-10-01 | 2013-02-26 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2010062821A1 (en) * | 2008-11-28 | 2010-06-03 | Glaxosmithkline Llc | Anti-viral compounds, compositions, and methods of use |
| SG171890A1 (en) * | 2008-12-03 | 2011-07-28 | Presidio Pharmaceuticals Inc | Inhibitors of hcv ns5a |
| BRPI0922366B8 (pt) * | 2008-12-03 | 2021-05-25 | Presidio Pharmaceuticals Inc | composto, composição farmacêutica e uso de um composto |
| EP2367823A1 (en) | 2008-12-23 | 2011-09-28 | Abbott Laboratories | Anti-viral compounds |
| ES2567047T3 (es) | 2008-12-23 | 2016-04-19 | Abbvie Inc. | Derivados de pirimidina anti-virales |
| US8637561B2 (en) | 2009-02-17 | 2014-01-28 | Enanta Pharmaceuticals, Inc. | Linked diimidazole derivatives |
| US8394968B2 (en) | 2009-02-17 | 2013-03-12 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8242156B2 (en) | 2009-02-17 | 2012-08-14 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole derivatives |
| TWI438200B (zh) * | 2009-02-17 | 2014-05-21 | 必治妥美雅史谷比公司 | C型肝炎病毒抑制劑 |
| US8188132B2 (en) | 2009-02-17 | 2012-05-29 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole derivatives |
| US8420686B2 (en) | 2009-02-17 | 2013-04-16 | Enanta Pharmaceuticals, Inc. | Linked diimidazole antivirals |
| WO2010096777A1 (en) * | 2009-02-23 | 2010-08-26 | Presidio Pharmaceuticals, Inc. | Inhibitors of hcv ns5a |
| US10752611B2 (en) | 2009-02-27 | 2020-08-25 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8101643B2 (en) * | 2009-02-27 | 2012-01-24 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US9765087B2 (en) | 2009-02-27 | 2017-09-19 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| MX2011008982A (es) * | 2009-02-27 | 2011-09-15 | Enata Pharmaceuticals Inc | Inhibidores del virus de la hepatitis c. |
| US8426458B2 (en) | 2009-02-27 | 2013-04-23 | Enanta Pharmaceuticals, Inc. | Hepatitis C Virus inhibitors |
| US8673954B2 (en) | 2009-02-27 | 2014-03-18 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8507522B2 (en) | 2009-03-06 | 2013-08-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8975247B2 (en) | 2009-03-18 | 2015-03-10 | The Board Of Trustees Of The Leland Stanford Junion University | Methods and compositions of treating a flaviviridae family viral infection |
| EP2410841A4 (en) | 2009-03-27 | 2012-10-24 | Presidio Pharmaceuticals Inc | SUBSTITUTED BICYCLIC HCV INHIBITORS |
| EP2410843A4 (en) * | 2009-03-27 | 2012-08-08 | Presidio Pharmaceuticals Inc | FUSIONED CORE INHIBITORS OF HEPATITIS C |
| US8796466B2 (en) * | 2009-03-30 | 2014-08-05 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI476190B (zh) * | 2009-03-30 | 2015-03-11 | 必治妥美雅史谷比公司 | C型肝炎病毒抑制劑 |
| TW201038559A (en) | 2009-04-09 | 2010-11-01 | Bristol Myers Squibb Co | Hepatitis C virus inhibitors |
| US8143414B2 (en) | 2009-04-13 | 2012-03-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| JP5734956B2 (ja) * | 2009-04-15 | 2015-06-17 | アッヴィ・インコーポレイテッド | 抗ウィルス化合物 |
| JP2012526834A (ja) * | 2009-05-12 | 2012-11-01 | シェーリング コーポレイション | ウイルス疾患治療に有用な縮合型三環式アリール化合物 |
| MX363732B (es) | 2009-05-13 | 2019-04-01 | Gilead Pharmasset Llc Star | Compuestos antivirales. |
| US8980920B2 (en) | 2009-05-29 | 2015-03-17 | Merck Sharp & Dohme Corp. | Antiviral compounds of three linked aryl moieties to treat diseases such as hepatitis C |
| US8138215B2 (en) | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| AU2010253790A1 (en) | 2009-05-29 | 2011-12-15 | Merck Sharp & Dohme Corp. | Antiviral compounds composed of three aligned aryl moieties to treat diseases such as Hepatitis C |
| US8211928B2 (en) * | 2009-05-29 | 2012-07-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | Abbvie Inc. | Anti-viral compounds |
| AR077060A1 (es) * | 2009-06-11 | 2011-07-27 | Abbott Lab | Compuestos antivirales |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| US8716454B2 (en) | 2009-06-11 | 2014-05-06 | Abbvie Inc. | Solid compositions |
| US8221737B2 (en) | 2009-06-16 | 2012-07-17 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8609648B2 (en) | 2009-07-02 | 2013-12-17 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| WO2011004276A1 (en) * | 2009-07-06 | 2011-01-13 | Pfizer Limited | Hepatitis c virus inhibitors |
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