KR101624365B1 - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR101624365B1 KR101624365B1 KR1020107020306A KR20107020306A KR101624365B1 KR 101624365 B1 KR101624365 B1 KR 101624365B1 KR 1020107020306 A KR1020107020306 A KR 1020107020306A KR 20107020306 A KR20107020306 A KR 20107020306A KR 101624365 B1 KR101624365 B1 KR 101624365B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- mmol
- aryl
- heterocyclyl
- halo
- 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(C1*CC1)C1*CCC1 Chemical compound C(C1*CC1)C1*CCC1 0.000 description 11
- JVWZSHDIPVXYQE-UHFFFAOYSA-N CC(C(O)=O)(c1ccccc1)N(C)C Chemical compound CC(C(O)=O)(c1ccccc1)N(C)C JVWZSHDIPVXYQE-UHFFFAOYSA-N 0.000 description 1
- VXIIZQXOIDYWBS-QUFPSDLASA-N CC(C)(C)OC(N(C(C1)[C@H]1C1)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(C(C1)[C@H]1C1)[C@@H]1C(O)=O)=O VXIIZQXOIDYWBS-QUFPSDLASA-N 0.000 description 1
- PDCUJLHHLCAIAN-DNKZHYAASA-N CC(C)(C)OC(N(CCC1)C1c1ncc(-c(cc2)ccc2-c2ccc(-c(nc3[C@H](CCCC4)N4C(OC(C)(C)C)=O)c(CCCC4)[n]3O)c4c2)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)C1c1ncc(-c(cc2)ccc2-c2ccc(-c(nc3[C@H](CCCC4)N4C(OC(C)(C)C)=O)c(CCCC4)[n]3O)c4c2)[nH]1)=O PDCUJLHHLCAIAN-DNKZHYAASA-N 0.000 description 1
- WWYQPVXUIRJIMN-HEVIKAOCSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c2ccc(-c3c(CCCC4)[nH]c([C@H](CCCC5)N5C(OC(C)(C)C)=O)n3)c4c2)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c2ccc(-c3c(CCCC4)[nH]c([C@H](CCCC5)N5C(OC(C)(C)C)=O)n3)c4c2)[nH]1)=O WWYQPVXUIRJIMN-HEVIKAOCSA-N 0.000 description 1
- SIGJBDNBLCTRPL-SCSAIBSYSA-N CC(C)([C@@H](C(O)=O)NC(OC)=O)O Chemical compound CC(C)([C@@H](C(O)=O)NC(OC)=O)O SIGJBDNBLCTRPL-SCSAIBSYSA-N 0.000 description 1
- VNWSHSMCDQYRJL-LEKBNUHKSA-N CC(C)[C@@H](C(N(C(C1C2)C1N=C)[C@@H]2c1ncc(-c(c(F)c2)ccc2-c2cc3ccc4[nH]c([C@H](CC5C6C5)N6OC(c5ccccc5)=O)nc4c3cc2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(C(C1C2)C1N=C)[C@@H]2c1ncc(-c(c(F)c2)ccc2-c2cc3ccc4[nH]c([C@H](CC5C6C5)N6OC(c5ccccc5)=O)nc4c3cc2)[nH]1)=O)NC(OC)=O VNWSHSMCDQYRJL-LEKBNUHKSA-N 0.000 description 1
- SPTVPPUZZFHDTO-CPCREDONSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1c1nc2ccc(cc(cc3)-c4cc5ccc6[nH]c([C@H]7NCCCC7)nc6c5cc4)c3c2[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1c1nc2ccc(cc(cc3)-c4cc5ccc6[nH]c([C@H]7NCCCC7)nc6c5cc4)c3c2[nH]1)=O)NC(OC)=O SPTVPPUZZFHDTO-CPCREDONSA-N 0.000 description 1
- HQQGFVVRYLEWDY-MTHGYUFKSA-N CC(C)[C@@H](C(N([C@@H](CC1C2)c3nc4ccc(cc(cc5)-c6cc7ccc8[nH]c([C@H](CC[C@@H]9C%10C9)N%10OC(c9ccccc9)=O)nc8c7cc6)c5c4[nH]3)C12C=C)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N([C@@H](CC1C2)c3nc4ccc(cc(cc5)-c6cc7ccc8[nH]c([C@H](CC[C@@H]9C%10C9)N%10OC(c9ccccc9)=O)nc8c7cc6)c5c4[nH]3)C12C=C)=O)NC(OC)=O HQQGFVVRYLEWDY-MTHGYUFKSA-N 0.000 description 1
- LQCMMXGKEGWUIM-UHFFFAOYSA-N CC(c(c(O)c1)ccc1Br)=O Chemical compound CC(c(c(O)c1)ccc1Br)=O LQCMMXGKEGWUIM-UHFFFAOYSA-N 0.000 description 1
- ZFJVQDOOKDWBQX-UHFFFAOYSA-N CCCCCC[ClH+] Chemical compound CCCCCC[ClH+] ZFJVQDOOKDWBQX-UHFFFAOYSA-N 0.000 description 1
- YQYOETRYLLWJMC-NNAABLSCSA-N CCN(CC)[C@@H](C(N(C(C1)C1C1)[C@@H]1c1ncc(-c(c(F)c2)ccc2-c2cc3ccc4[nH]c([C@H](C[C@@H]5C6CC5)N6C([C@@H](c5ccccc5)N(CC)CC)=O)nc4c3cc2)[nH]1)=O)c1ccccc1 Chemical compound CCN(CC)[C@@H](C(N(C(C1)C1C1)[C@@H]1c1ncc(-c(c(F)c2)ccc2-c2cc3ccc4[nH]c([C@H](C[C@@H]5C6CC5)N6C([C@@H](c5ccccc5)N(CC)CC)=O)nc4c3cc2)[nH]1)=O)c1ccccc1 YQYOETRYLLWJMC-NNAABLSCSA-N 0.000 description 1
- ZKXOJPCWOHKOQR-UHFFFAOYSA-N CCOc1c(cc(nc2C#N)Cl)c2ccc1 Chemical compound CCOc1c(cc(nc2C#N)Cl)c2ccc1 ZKXOJPCWOHKOQR-UHFFFAOYSA-N 0.000 description 1
- ANQBUBVGJORSTE-UHFFFAOYSA-N CN(C)C1(C(O)=O)c2ccccc2CC1 Chemical compound CN(C)C1(C(O)=O)c2ccccc2CC1 ANQBUBVGJORSTE-UHFFFAOYSA-N 0.000 description 1
- SKCUMFJFAWFXDL-UHFFFAOYSA-N CN(C)C1(Cc2ccccc2C1)C(O)=O Chemical compound CN(C)C1(Cc2ccccc2C1)C(O)=O SKCUMFJFAWFXDL-UHFFFAOYSA-N 0.000 description 1
- MLOBRLOZPSSKKO-SECBINFHSA-N CN(C)[C@@H](C(O)=O)c1ccccc1 Chemical compound CN(C)[C@@H](C(O)=O)c1ccccc1 MLOBRLOZPSSKKO-SECBINFHSA-N 0.000 description 1
- NLVXWIBDIWBXLM-UHFFFAOYSA-N CN(CCC#N)Cc1cccc(Br)c1 Chemical compound CN(CCC#N)Cc1cccc(Br)c1 NLVXWIBDIWBXLM-UHFFFAOYSA-N 0.000 description 1
- WGUNWFNMFQNCGQ-UHFFFAOYSA-N COC(NC(C1)C1(C1CCOCC1)C(O)=O)=O Chemical compound COC(NC(C1)C1(C1CCOCC1)C(O)=O)=O WGUNWFNMFQNCGQ-UHFFFAOYSA-N 0.000 description 1
- XQEHBQMNCVYKKI-ZBZPLXCBSA-N COC(N[C@@H](C(N(C(C1)C1C1)[C@@H]1c1nc2ccc(cc(cc3)-c4cc5ccc6[nH]c([C@H](CC[C@@H]7C8C7)N8C([C@@H](c7ccccc7)NC(OC)=O)=O)nc6c5cc4)c3c2[nH]1)=O)c1ccccc1)=O Chemical compound COC(N[C@@H](C(N(C(C1)C1C1)[C@@H]1c1nc2ccc(cc(cc3)-c4cc5ccc6[nH]c([C@H](CC[C@@H]7C8C7)N8C([C@@H](c7ccccc7)NC(OC)=O)=O)nc6c5cc4)c3c2[nH]1)=O)c1ccccc1)=O XQEHBQMNCVYKKI-ZBZPLXCBSA-N 0.000 description 1
- QCYOIFVBYZNUNW-BYPYZUCNSA-N C[C@@H](C(O)=O)N(C)C Chemical compound C[C@@H](C(O)=O)N(C)C QCYOIFVBYZNUNW-BYPYZUCNSA-N 0.000 description 1
- OOIJOKDKOOJZJS-BYPYZUCNSA-N C[C@@H](C(O)=O)NC(N(C)C)=O Chemical compound C[C@@H](C(O)=O)NC(N(C)C)=O OOIJOKDKOOJZJS-BYPYZUCNSA-N 0.000 description 1
- YGYLYUIRSJSFJS-QMMMGPOBSA-N C[C@@H](C(OCc1ccccc1)=O)N Chemical compound C[C@@H](C(OCc1ccccc1)=O)N YGYLYUIRSJSFJS-QMMMGPOBSA-N 0.000 description 1
- VOGHVBZAMPRNEG-IBGZPJMESA-N O=C(c1ccccc1)ON(CCC1)[C@@H]1c1nc(CCc2cc(Br)ccc2-2)c-2[nH]1 Chemical compound O=C(c1ccccc1)ON(CCC1)[C@@H]1c1nc(CCc2cc(Br)ccc2-2)c-2[nH]1 VOGHVBZAMPRNEG-IBGZPJMESA-N 0.000 description 1
Classifications
-
- 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
-
- 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
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2827708P | 2008-02-13 | 2008-02-13 | |
| US61/028,277 | 2008-02-13 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100124290A KR20100124290A (ko) | 2010-11-26 |
| KR101624365B1 true KR101624365B1 (ko) | 2016-05-25 |
Family
ID=40581591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107020306A Expired - Fee Related KR101624365B1 (ko) | 2008-02-13 | 2009-02-06 | C형 간염 바이러스 억제제 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8147818B2 (enExample) |
| EP (1) | EP2245027B1 (enExample) |
| JP (1) | JP5455933B2 (enExample) |
| KR (1) | KR101624365B1 (enExample) |
| CN (1) | CN102143959B (enExample) |
| AR (1) | AR070366A1 (enExample) |
| AT (1) | ATE555109T1 (enExample) |
| AU (1) | AU2009214997B2 (enExample) |
| BR (1) | BRPI0908240A2 (enExample) |
| CA (1) | CA2715559A1 (enExample) |
| CL (1) | CL2009000324A1 (enExample) |
| CO (1) | CO6290682A2 (enExample) |
| CY (1) | CY1112999T1 (enExample) |
| DK (1) | DK2245027T3 (enExample) |
| EA (1) | EA018313B1 (enExample) |
| ES (1) | ES2384911T3 (enExample) |
| HR (1) | HRP20120523T1 (enExample) |
| IL (1) | IL207459A (enExample) |
| MX (1) | MX2010008749A (enExample) |
| NZ (1) | NZ587322A (enExample) |
| PE (1) | PE20091381A1 (enExample) |
| PL (1) | PL2245027T3 (enExample) |
| PT (1) | PT2245027E (enExample) |
| SI (1) | SI2245027T1 (enExample) |
| TW (1) | TWI458482B (enExample) |
| WO (1) | WO2009102633A1 (enExample) |
| ZA (1) | ZA201005484B (enExample) |
Families Citing this family (111)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8303944B2 (en) * | 2006-08-11 | 2012-11-06 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7906655B2 (en) * | 2008-08-07 | 2011-03-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8383094B2 (en) | 2008-10-01 | 2013-02-26 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| EP2367823A1 (en) | 2008-12-23 | 2011-09-28 | Abbott Laboratories | Anti-viral compounds |
| MX2011006332A (es) | 2008-12-23 | 2011-06-27 | Abbott Lab | Compuestos antivirales. |
| 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 |
| US8394968B2 (en) | 2009-02-17 | 2013-03-12 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8188132B2 (en) | 2009-02-17 | 2012-05-29 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole derivatives |
| US8242156B2 (en) * | 2009-02-17 | 2012-08-14 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole derivatives |
| WO2010094977A1 (en) * | 2009-02-23 | 2010-08-26 | Arrow Therapeutics Limited | Novel biphenyl compounds useful for the treatment of hepatitis c |
| CA2753382C (en) | 2009-02-27 | 2014-12-23 | Enanta Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| US8673954B2 (en) | 2009-02-27 | 2014-03-18 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US9765087B2 (en) | 2009-02-27 | 2017-09-19 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8101643B2 (en) * | 2009-02-27 | 2012-01-24 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8507522B2 (en) | 2009-03-06 | 2013-08-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8796466B2 (en) | 2009-03-30 | 2014-08-05 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| 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 |
| SG175144A1 (en) * | 2009-04-15 | 2011-11-28 | Abbott Lab | Anti-viral compounds |
| EP2430015B1 (en) | 2009-05-12 | 2015-06-17 | Merck Sharp & Dohme Corp. | Fused tricyclic compounds useful for the treatment of viral diseases |
| BRPI1010795B1 (pt) | 2009-05-13 | 2018-12-11 | Gilead Pharmasset Llc | compostos antivirais, seu uso e composição farmacêutica compreendendo os mesmos |
| US8138215B2 (en) | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2010138790A1 (en) | 2009-05-29 | 2010-12-02 | Schering Corporation | 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 |
| CA2763140A1 (en) | 2009-05-29 | 2010-12-02 | Schering Corporation | Antiviral compounds composed of three linked aryl moieties to treat diseases such as hepatitis c |
| PE20110679A1 (es) * | 2009-06-11 | 2011-10-20 | Abbvie Bahamas Ltd | Derivados de (4-tert-butilfenil)pirrolidin-2,5-difenil como inhibidores del hcv |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | Abbvie Inc. | Anti-viral compounds |
| US8716454B2 (en) | 2009-06-11 | 2014-05-06 | Abbvie Inc. | Solid compositions |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| 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 |
| CN102656160A (zh) | 2009-07-16 | 2012-09-05 | 顶点制药公司 | 用于治疗或预防黄病毒感染的苯并咪唑类似物 |
| CN102480971B (zh) | 2009-09-04 | 2014-11-26 | 杨森制药公司 | 化合物 |
| US8759332B2 (en) * | 2009-09-11 | 2014-06-24 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US9156818B2 (en) * | 2009-09-11 | 2015-10-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8703938B2 (en) * | 2009-09-11 | 2014-04-22 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8815928B2 (en) | 2009-09-11 | 2014-08-26 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8822700B2 (en) * | 2009-09-11 | 2014-09-02 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8927709B2 (en) * | 2009-09-11 | 2015-01-06 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| WO2011031934A1 (en) * | 2009-09-11 | 2011-03-17 | Enanta Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| US20110269956A1 (en) | 2009-11-11 | 2011-11-03 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20110274648A1 (en) | 2009-11-11 | 2011-11-10 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20110281910A1 (en) | 2009-11-12 | 2011-11-17 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| EP2503881B1 (en) * | 2009-11-25 | 2015-05-13 | Merck Sharp & Dohme Corp. | Fused tricyclic compounds and derivatives thereof useful for the treatment of viral diseases |
| US20110137633A1 (en) * | 2009-12-03 | 2011-06-09 | Abbott Laboratories | Anti-viral compounds and methods of identifying the same |
| EP2512480A4 (en) * | 2009-12-14 | 2013-05-15 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| US8377980B2 (en) | 2009-12-16 | 2013-02-19 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| RU2554087C2 (ru) | 2009-12-18 | 2015-06-27 | Айденикс Фармасьютикалз, Инк. | 5,5-конденсированные ариленовые или гетероариленовые ингибиторы вируса гепатита с |
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