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
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (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)
- Peptides Or Proteins (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (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 (https=) |
| EP (1) | EP2245027B1 (https=) |
| JP (1) | JP5455933B2 (https=) |
| KR (1) | KR101624365B1 (https=) |
| CN (1) | CN102143959B (https=) |
| AR (1) | AR070366A1 (https=) |
| AT (1) | ATE555109T1 (https=) |
| AU (1) | AU2009214997B2 (https=) |
| BR (1) | BRPI0908240A2 (https=) |
| CA (1) | CA2715559A1 (https=) |
| CL (1) | CL2009000324A1 (https=) |
| CO (1) | CO6290682A2 (https=) |
| CY (1) | CY1112999T1 (https=) |
| DK (1) | DK2245027T3 (https=) |
| EA (1) | EA018313B1 (https=) |
| ES (1) | ES2384911T3 (https=) |
| HR (1) | HRP20120523T1 (https=) |
| IL (1) | IL207459A (https=) |
| MX (1) | MX2010008749A (https=) |
| NZ (1) | NZ587322A (https=) |
| PE (1) | PE20091381A1 (https=) |
| PL (1) | PL2245027T3 (https=) |
| PT (1) | PT2245027E (https=) |
| SI (1) | SI2245027T1 (https=) |
| TW (1) | TWI458482B (https=) |
| WO (1) | WO2009102633A1 (https=) |
| ZA (1) | ZA201005484B (https=) |
Families Citing this family (112)
| 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 |
| CA2740193A1 (en) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Anti-viral compounds |
| EP2367823A1 (en) | 2008-12-23 | 2011-09-28 | Abbott Laboratories | Anti-viral compounds |
| 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 |
| US8188132B2 (en) | 2009-02-17 | 2012-05-29 | 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 |
| WO2010094977A1 (en) * | 2009-02-23 | 2010-08-26 | Arrow Therapeutics Limited | Novel biphenyl compounds useful for the treatment of hepatitis c |
| US9765087B2 (en) | 2009-02-27 | 2017-09-19 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8673954B2 (en) | 2009-02-27 | 2014-03-18 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8101643B2 (en) * | 2009-02-27 | 2012-01-24 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| KR101411889B1 (ko) | 2009-02-27 | 2014-06-27 | 이난타 파마슈티칼스, 인코포레이티드 | C형 간염 바이러스 억제제 |
| 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 |
| CN102459165B (zh) * | 2009-04-15 | 2015-09-02 | Abbvie公司 | 抗病毒化合物 |
| WO2010132538A1 (en) | 2009-05-12 | 2010-11-18 | Schering Corporation | Fused tricyclic aryl compounds useful for the treatment of viral diseases |
| PT3309157T (pt) | 2009-05-13 | 2019-12-02 | Gilead Pharmasset Llc | Compostos antivirais |
| US8772505B2 (en) | 2009-05-29 | 2014-07-08 | 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 |
| 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 |
| US8138215B2 (en) | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| UA118080C2 (uk) * | 2009-06-11 | 2018-11-26 | Еббві Айрленд Анлімітед Компані | Противірусні сполуки |
| 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 |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | 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 |
| IN2012DN00999A (https=) | 2009-07-16 | 2015-04-10 | Vertex Pharma | |
| EA201290089A1 (ru) | 2009-09-04 | 2012-09-28 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Химические соединения |
| EP2475254A4 (en) * | 2009-09-11 | 2013-05-22 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| WO2011031904A1 (en) * | 2009-09-11 | 2011-03-17 | Enanta Pharmaceuticals, Inc | Hepatitis c virus inhibitors |
| US8759332B2 (en) * | 2009-09-11 | 2014-06-24 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8927709B2 (en) * | 2009-09-11 | 2015-01-06 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8822700B2 (en) * | 2009-09-11 | 2014-09-02 | 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 |
| US20110274648A1 (en) | 2009-11-11 | 2011-11-10 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20110269956A1 (en) | 2009-11-11 | 2011-11-03 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20110281910A1 (en) | 2009-11-12 | 2011-11-17 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| JP2013512246A (ja) * | 2009-11-25 | 2013-04-11 | メルク・シャープ・アンド・ドーム・コーポレーション | ウイルス疾患治療に有用な縮合型三環式化合物およびその誘導体 |
| US20110137633A1 (en) * | 2009-12-03 | 2011-06-09 | Abbott Laboratories | Anti-viral compounds and methods of identifying the same |
| US8653070B2 (en) * | 2009-12-14 | 2014-02-18 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8377980B2 (en) | 2009-12-16 | 2013-02-19 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| KR20120118008A (ko) * | 2009-12-18 | 2012-10-25 | 아이데닉스 파마슈티칼스, 인코포레이티드 | 5,5-융합 아릴렌 또는 헤테로아릴렌 간염 c 바이러스 억제제 |
| CN104530079B (zh) * | 2009-12-18 | 2017-10-20 | 北京凯因科技股份有限公司 | C型肝炎病毒复制的新型抑制剂 |
| US20130156731A1 (en) | 2009-12-22 | 2013-06-20 | Kevin X. Chen | Fused tricyclic compounds and methods of use thereof for the treatment of viral diseas |
| US8362020B2 (en) | 2009-12-30 | 2013-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MA34013B1 (fr) | 2010-01-25 | 2013-02-01 | Enanta Pharm Inc | Inhibiteurs du virus de l'hépatite c |
| US8933110B2 (en) | 2010-01-25 | 2015-01-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8623814B2 (en) * | 2010-02-23 | 2014-01-07 | Enanta Pharmaceuticals, Inc. | Antiviral agents |
| US8178531B2 (en) * | 2010-02-23 | 2012-05-15 | Enanta Pharmaceuticals, Inc. | Antiviral agents |
| KR20120124495A (ko) * | 2010-03-04 | 2012-11-13 | 이난타 파마슈티칼스, 인코포레이티드 | Hcv 복제의 억제제로서의 조합 제약 작용제 |
| EA201290882A1 (ru) * | 2010-03-09 | 2013-04-30 | Мерк Шарп Энд Домэ Корп. | Конденсированные трициклические силильные соединения и способы их применения для лечения вирусных заболеваний |
| CA2794145A1 (en) | 2010-03-24 | 2011-09-29 | Vertex Pharmaceuticals Incorporated | Analogues for the treatment or prevention of flavivirus infections |
| EP2555622A4 (en) | 2010-04-09 | 2013-09-18 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| EP2575819A4 (en) | 2010-06-04 | 2013-11-27 | Enanta Pharm Inc | INHIBITORS OF HEPATITIS C VIRUS |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| EP2585448A1 (en) | 2010-06-28 | 2013-05-01 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of flavivirus infections |
| AU2011276526A1 (en) | 2010-06-28 | 2013-01-10 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of Flavivirus infections |
| CA2807305A1 (en) * | 2010-08-04 | 2012-02-09 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| US20120195857A1 (en) | 2010-08-12 | 2012-08-02 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| EP2603080A4 (en) | 2010-08-12 | 2014-01-22 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| AU2011292040A1 (en) | 2010-08-17 | 2013-03-07 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of Flaviviridae viral infections |
| BR112013004520A2 (pt) | 2010-08-26 | 2016-06-07 | Univ Emory | inibidores potentes e seletivos do virus da hepatite c |
| MX2013004655A (es) | 2010-10-26 | 2013-08-27 | Presidio Pharmaceuticals Inc | Inhibidores del virus de la hepatitis c. |
| SI2640719T1 (sl) * | 2010-11-17 | 2017-07-31 | Gilead Pharmasset Llc | Antivirusne spojine |
| CA2822357A1 (en) | 2010-12-22 | 2012-06-28 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
| US8552047B2 (en) | 2011-02-07 | 2013-10-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20120252721A1 (en) | 2011-03-31 | 2012-10-04 | Idenix Pharmaceuticals, Inc. | Methods for treating drug-resistant hepatitis c virus infection with a 5,5-fused arylene or heteroarylene hepatitis c virus inhibitor |
| US9546160B2 (en) | 2011-05-12 | 2017-01-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| WO2012158861A2 (en) | 2011-05-18 | 2012-11-22 | Enanta Pharmaceuticals, Inc. | Processes for the preparation of 5-azaspiro[2.4]heptane-6-carboxylic acid and its derivatives |
| WO2012175581A1 (en) | 2011-06-24 | 2012-12-27 | F. Hoffmann-La Roche Ag | Antiviral compounds |
| WO2013016492A1 (en) | 2011-07-26 | 2013-01-31 | Vertex Pharmaceuticals Incorporated | Thiophene compounds |
| WO2013016499A1 (en) | 2011-07-26 | 2013-01-31 | Vertex Pharmaceuticals Incorporated | Methods for preparation of thiophene compounds |
| WO2013021344A1 (en) | 2011-08-08 | 2013-02-14 | Lupin Limited | Imidazole derivatives as antiviral agents |
| PH12014500311A1 (en) | 2011-08-08 | 2014-03-31 | Lupin Ltd | Antiviral compounds with a fused tricyclic ring |
| WO2013030750A1 (en) | 2011-09-01 | 2013-03-07 | Lupin Limited | Antiviral compounds |
| PL2709613T5 (pl) | 2011-09-16 | 2020-12-14 | Gilead Pharmasset Llc | Metody leczenia hcv |
| JP6082749B2 (ja) | 2011-11-16 | 2017-02-15 | ギリアド ファーマセット エルエルシー | 抗ウイルス化合物としての縮合イミダゾリルイミダゾール |
| US9034832B2 (en) | 2011-12-29 | 2015-05-19 | Abbvie Inc. | Solid compositions |
| US9326973B2 (en) | 2012-01-13 | 2016-05-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CA2862755A1 (en) | 2012-02-10 | 2013-08-15 | Lupin Limited | Antiviral compounds with a dibenzooxaheterocycle moiety |
| US9012427B2 (en) | 2012-03-22 | 2015-04-21 | Alios Biopharma, Inc. | Pharmaceutical combinations comprising a thionucleotide analog |
| EP2850072B1 (en) | 2012-04-25 | 2016-08-31 | Theravance Biopharma R&D IP, LLC | Hepatitis c virus inhibitors |
| HUE032173T2 (en) | 2012-04-25 | 2017-09-28 | Theravance Biopharma R&D Ip Llc | Piperazine piperidine compounds as inhibitors of hepatitis C virus |
| US20130309196A1 (en) * | 2012-05-16 | 2013-11-21 | Gilead Sciences, Inc. | Antiviral compounds |
| PT2950786T (pt) | 2013-01-31 | 2020-03-03 | Gilead Pharmasset Llc | Formulação de combinação de dois compostos antivirais |
| US20150065439A1 (en) | 2013-02-28 | 2015-03-05 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions |
| US11484534B2 (en) | 2013-03-14 | 2022-11-01 | Abbvie Inc. | Methods for treating HCV |
| US9717712B2 (en) | 2013-07-02 | 2017-08-01 | Bristol-Myers Squibb Company | Combinations comprising tricyclohexadecahexaene derivatives for use in the treatment of hepatitis C virus |
| US20150023913A1 (en) | 2013-07-02 | 2015-01-22 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US9775831B2 (en) | 2013-07-17 | 2017-10-03 | Bristol-Myers Squibb Company | Combinations comprising biphenyl derivatives for use in the treatment of HCV |
| EA201690473A1 (ru) | 2013-08-27 | 2017-03-31 | ГАЙЛИД ФАРМАССЕТ ЭлЭлСи | Комбинированный состав двух противовирусных соединений |
| EP3046924A1 (en) | 2013-09-20 | 2016-07-27 | IDENIX Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
| WO2015184644A1 (zh) * | 2014-06-06 | 2015-12-10 | 爱博新药研发(上海)有限公司 | 抑制丙肝病毒的化合物、药物组合物及其应用 |
| TWI721947B (zh) | 2014-06-11 | 2021-03-21 | 美商基利法瑪席特有限責任公司 | 抗病毒化合物的固態形式 |
| CN105968101B (zh) * | 2015-03-12 | 2019-03-01 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的化合物及其在药物中的应用 |
| US10617675B2 (en) | 2015-08-06 | 2020-04-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| BR102018007822A2 (pt) | 2017-04-20 | 2018-11-06 | Gilead Sciences, Inc. | composto, métodos para inibir pd-1, pd-l1 e/ou interação de pd-1/pd-l1 e para tratamento de câncer, composição farmacêutica, e, kit para tratamento de ou prevenção de câncer ou uma doença ou condição |
| TWI707849B (zh) | 2018-02-13 | 2020-10-21 | 美商基利科學股份有限公司 | Pd‐1/pd‐l1抑制劑 |
| KR102591947B1 (ko) | 2018-04-19 | 2023-10-25 | 길리애드 사이언시즈, 인코포레이티드 | Pd-1/pd-l1 억제제 |
| EP3820572B1 (en) | 2018-07-13 | 2023-08-16 | Gilead Sciences, Inc. | Pd-1/pd-l1 inhibitors |
| US11236085B2 (en) | 2018-10-24 | 2022-02-01 | Gilead Sciences, Inc. | PD-1/PD-L1 inhibitors |
| JP7584418B2 (ja) | 2018-12-04 | 2024-11-15 | ブリストル-マイヤーズ スクイブ カンパニー | 多重反応同位体分子種反応モニタリングによる、サンプル内検量線を用いた分析方法 |
| CA3219397A1 (en) | 2021-05-21 | 2022-11-24 | Gilead Sciences, Inc. | Tetracyclic compounds for the treatment of zika virus infection |
| CA3220903A1 (en) | 2021-05-21 | 2022-11-24 | Gilead Sciences, Inc. | Pentacyclic derivatives as zika virus inhibitors |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006020082A1 (en) | 2004-08-09 | 2006-02-23 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
| WO2006133326A1 (en) | 2005-06-06 | 2006-12-14 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5654451B1 (en) * | 1993-01-14 | 2000-02-22 | Magainin Pharma | Amino acids and peptides having modified c-terminals and modified n-terminals |
| CA2153987A1 (en) | 1993-01-14 | 1994-07-21 | U. Prasad Kari | Amino acids and peptides having modified terminals |
| WO2006093867A1 (en) | 2005-02-28 | 2006-09-08 | The Rockefeller University | Structure of the hepatitits c virus ns5a protein |
| WO2007031791A1 (en) | 2005-09-16 | 2007-03-22 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
| WO2007058384A1 (en) | 2005-11-17 | 2007-05-24 | Osaka University | Method of suppressing replication of hepatitis c virus, inhibitor of replication of the virus and method of screening for the same |
| SG133452A1 (en) | 2005-12-30 | 2007-07-30 | Novartis Ag | Peptide deformylase inhibitors for treatment of mycobacterial and other parasitic diseases |
| WO2007138242A1 (en) | 2006-05-30 | 2007-12-06 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
| US8329159B2 (en) | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7759495B2 (en) * | 2006-08-11 | 2010-07-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| 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 |
| US7659270B2 (en) * | 2006-08-11 | 2010-02-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8236950B2 (en) | 2006-12-20 | 2012-08-07 | Abbott Laboratories | Anti-viral compounds |
| US7741347B2 (en) | 2007-05-17 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus 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 |
-
2009
- 2009-01-23 US US12/358,587 patent/US8147818B2/en active Active
- 2009-02-06 SI SI200930300T patent/SI2245027T1/sl unknown
- 2009-02-06 PT PT09709849T patent/PT2245027E/pt unknown
- 2009-02-06 WO PCT/US2009/033380 patent/WO2009102633A1/en not_active Ceased
- 2009-02-06 DK DK09709849.5T patent/DK2245027T3/da active
- 2009-02-06 ES ES09709849T patent/ES2384911T3/es active Active
- 2009-02-06 CA CA2715559A patent/CA2715559A1/en not_active Abandoned
- 2009-02-06 AU AU2009214997A patent/AU2009214997B2/en not_active Ceased
- 2009-02-06 KR KR1020107020306A patent/KR101624365B1/ko not_active Expired - Fee Related
- 2009-02-06 HR HRP20120523AT patent/HRP20120523T1/hr unknown
- 2009-02-06 CN CN200980112993.9A patent/CN102143959B/zh not_active Expired - Fee Related
- 2009-02-06 MX MX2010008749A patent/MX2010008749A/es active IP Right Grant
- 2009-02-06 BR BRPI0908240A patent/BRPI0908240A2/pt not_active IP Right Cessation
- 2009-02-06 PL PL09709849T patent/PL2245027T3/pl unknown
- 2009-02-06 NZ NZ587322A patent/NZ587322A/en not_active IP Right Cessation
- 2009-02-06 JP JP2010546841A patent/JP5455933B2/ja not_active Expired - Fee Related
- 2009-02-06 AT AT09709849T patent/ATE555109T1/de active
- 2009-02-06 EP EP09709849A patent/EP2245027B1/en active Active
- 2009-02-06 EA EA201001273A patent/EA018313B1/ru not_active IP Right Cessation
- 2009-02-11 PE PE2009000200A patent/PE20091381A1/es not_active Application Discontinuation
- 2009-02-12 CL CL2009000324A patent/CL2009000324A1/es unknown
- 2009-02-12 AR ARP090100503A patent/AR070366A1/es unknown
- 2009-02-13 TW TW098104731A patent/TWI458482B/zh not_active IP Right Cessation
-
2010
- 2010-07-30 ZA ZA2010/05484A patent/ZA201005484B/en unknown
- 2010-08-08 IL IL207459A patent/IL207459A/en not_active IP Right Cessation
- 2010-08-11 CO CO10098657A patent/CO6290682A2/es active IP Right Grant
-
2012
- 2012-07-20 CY CY20121100642T patent/CY1112999T1/el unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006020082A1 (en) | 2004-08-09 | 2006-02-23 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
| WO2006133326A1 (en) | 2005-06-06 | 2006-12-14 | Bristol-Myers Squibb Company | Inhibitors of hcv replication |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101624365B1 (ko) | C형 간염 바이러스 억제제 | |
| KR101614964B1 (ko) | C형 간염 바이러스 억제제로서 사용하기 위한 형태적으로 제한된 바이페닐 유도체 | |
| JP5611959B2 (ja) | C型肝炎ウイルス阻害剤 | |
| JP5558556B2 (ja) | C型肝炎ウイルス阻害剤 | |
| KR101468765B1 (ko) | C형 간염 바이러스 억제제 | |
| KR101492672B1 (ko) | C형 간염 바이러스 억제제로서의 이미다졸릴 바이페닐 이미다졸 | |
| JP5599792B2 (ja) | C型肝炎ウイルス阻害剤としてのbi−1h−ベンズアミダゾール | |
| JP5612661B2 (ja) | C型肝炎ウイルス阻害剤 | |
| JP5558557B2 (ja) | C型肝炎ウイルス阻害剤 | |
| KR20100123717A (ko) | C형 간염 바이러스 억제제로서의 헤테로시클릭 유도체 | |
| KR20120107991A (ko) | C형 간염 바이러스 억제제 | |
| KR20110124774A (ko) | C형 간염 바이러스 억제제 | |
| JP2010527373A (ja) | C型肝炎ウイルス阻害剤 | |
| KR20140045903A (ko) | C형 간염 바이러스 억제제 | |
| WO2010138368A1 (en) | Hepatitis c virus inhibitors | |
| KR20120034603A (ko) | C형 간염 바이러스 억제제 | |
| JP2012528166A (ja) | C型肝炎ウイルス阻害剤 | |
| HK1143812B (en) | Hepatitis c virus inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| A201 | Request for examination | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
St.27 status event code: A-1-2-D10-D22-exm-PE0701 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
St.27 status event code: A-2-4-F10-F11-exm-PR0701 |
|
| PR1002 | Payment of registration fee |
St.27 status event code: A-2-2-U10-U12-oth-PR1002 Fee payment year number: 1 |
|
| PG1601 | Publication of registration |
St.27 status event code: A-4-4-Q10-Q13-nap-PG1601 |
|
| R18-X000 | Changes to party contact information recorded |
St.27 status event code: A-5-5-R10-R18-oth-X000 |
|
| LAPS | Lapse due to unpaid annual fee | ||
| PC1903 | Unpaid annual fee |
St.27 status event code: A-4-4-U10-U13-oth-PC1903 Not in force date: 20190520 Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: N-4-6-H10-H13-oth-PC1903 Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE Not in force date: 20190520 |
|
| R18-X000 | Changes to party contact information recorded |
St.27 status event code: A-5-5-R10-R18-oth-X000 |