CN102448956B - 丙型肝炎病毒抑制剂 - Google Patents
丙型肝炎病毒抑制剂 Download PDFInfo
- Publication number
- CN102448956B CN102448956B CN201080024916.0A CN201080024916A CN102448956B CN 102448956 B CN102448956 B CN 102448956B CN 201080024916 A CN201080024916 A CN 201080024916A CN 102448956 B CN102448956 B CN 102448956B
- Authority
- CN
- China
- Prior art keywords
- base
- phenyl
- imidazoles
- pyrrolidyl
- urethylane
- 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 CN=*C1*(*)C(*)C(*)C1 Chemical compound CN=*C1*(*)C(*)C(*)C1 0.000 description 7
- XGLLZRBZMUKLJG-ZEQRLZLVSA-N C(c(cc1)ccc1-c1c[nH]c([C@H]2NCCC2)n1)OCc(cc1)ccc1-c1c[nH]c([C@H]2NCCC2)n1 Chemical compound C(c(cc1)ccc1-c1c[nH]c([C@H]2NCCC2)n1)OCc(cc1)ccc1-c1c[nH]c([C@H]2NCCC2)n1 XGLLZRBZMUKLJG-ZEQRLZLVSA-N 0.000 description 1
- BJPCXZMEJRLORA-QMMMGPOBSA-N CC(C)(C)OC(N([C@@H](CC1(C)C)C(OC)=O)C1=O)=O Chemical compound CC(C)(C)OC(N([C@@H](CC1(C)C)C(OC)=O)C1=O)=O BJPCXZMEJRLORA-QMMMGPOBSA-N 0.000 description 1
- USSZTWWIRXXOPO-XYPHTWIQSA-N CC(C)(C)OC(N([C@H](C1)[C@H]1C1)[C@@H]1c1ncc(-c2cccc([Br]=C)c2)[nH]1)=O Chemical compound CC(C)(C)OC(N([C@H](C1)[C@H]1C1)[C@@H]1c1ncc(-c2cccc([Br]=C)c2)[nH]1)=O USSZTWWIRXXOPO-XYPHTWIQSA-N 0.000 description 1
- IOZIIBVXXMCAQH-YQROCVEUSA-N CC(C)C(C(N([C@H](C1)[C@H]1C1)[C@@H]1c1ncc(-c2cccc(C#Cc3cccc(-c4cnc([C@H](C[C@@H]5[C@H]6C5)N6C(C(C(C)C)NC(OC)=O)=O)[nH]4)c3)c2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)C(C(N([C@H](C1)[C@H]1C1)[C@@H]1c1ncc(-c2cccc(C#Cc3cccc(-c4cnc([C@H](C[C@@H]5[C@H]6C5)N6C(C(C(C)C)NC(OC)=O)=O)[nH]4)c3)c2)[nH]1)=O)NC(OC)=O IOZIIBVXXMCAQH-YQROCVEUSA-N 0.000 description 1
- CEFVHPDFGLDQKU-UHFFFAOYSA-N CC(C)C(C(O)=O)NC(OC)=O Chemical compound CC(C)C(C(O)=O)NC(OC)=O CEFVHPDFGLDQKU-UHFFFAOYSA-N 0.000 description 1
- MQOIVKUPEBCUIJ-UHFFFAOYSA-N CC(C)COC(C(C(C)C)NC(OC)=O)=O Chemical compound CC(C)COC(C(C(C)C)NC(OC)=O)=O MQOIVKUPEBCUIJ-UHFFFAOYSA-N 0.000 description 1
- VKZJIXGTLJUZSN-QMMMGPOBSA-N CC(C)COC([C@H](C(C)C)N)=O Chemical compound CC(C)COC([C@H](C(C)C)N)=O VKZJIXGTLJUZSN-QMMMGPOBSA-N 0.000 description 1
- VJHWUEWJEIGNSC-QMMMGPOBSA-N CC(C)[C@@H](C(O)=O)Nc1cncnc1 Chemical compound CC(C)[C@@H](C(O)=O)Nc1cncnc1 VJHWUEWJEIGNSC-QMMMGPOBSA-N 0.000 description 1
- YQZBFMJOASEONC-UHFFFAOYSA-N CCCc1ccccc1C Chemical compound CCCc1ccccc1C YQZBFMJOASEONC-UHFFFAOYSA-N 0.000 description 1
- ORKWOWVNPONBOR-CYBMUJFWSA-N CCN(CC)[C@H](CO)C(OCc1ccccc1)=O Chemical compound CCN(CC)[C@H](CO)C(OCc1ccccc1)=O ORKWOWVNPONBOR-CYBMUJFWSA-N 0.000 description 1
- WWLGVUMNEWUZMN-IYTFMMMVSA-N CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c2ccc(COCc(cc3)ccc3-c3cnc([C@H](CCC4)N4C([C@@H](c4ccccc4)N(C)C)=O)[nH]3)cc2)[nH]1)=O)c1ccccc1 Chemical compound CN(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c2ccc(COCc(cc3)ccc3-c3cnc([C@H](CCC4)N4C([C@@H](c4ccccc4)N(C)C)=O)[nH]3)cc2)[nH]1)=O)c1ccccc1 WWLGVUMNEWUZMN-IYTFMMMVSA-N 0.000 description 1
- XCRUAPMUQWKDIE-BLFWJTLLSA-N COC(NC(C1CCOCC1)C(N(CCC1)[C@@H]1c1ncc(-c2cccc(C#Cc3cccc(-c4cnc(C(C=CC5)N5C([C@H](C5CCOCC5)NC(OC)=O)=O)[nH]4)c3)c2)[nH]1)=O)=O Chemical compound COC(NC(C1CCOCC1)C(N(CCC1)[C@@H]1c1ncc(-c2cccc(C#Cc3cccc(-c4cnc(C(C=CC5)N5C([C@H](C5CCOCC5)NC(OC)=O)=O)[nH]4)c3)c2)[nH]1)=O)=O XCRUAPMUQWKDIE-BLFWJTLLSA-N 0.000 description 1
- PCRRPOJDJXDSHT-ZETCQYMHSA-N COC(N[C@@H](C1CCOCC1)C(O)=O)=O Chemical compound COC(N[C@@H](C1CCOCC1)C(O)=O)=O PCRRPOJDJXDSHT-ZETCQYMHSA-N 0.000 description 1
- GTTMQWUCWHABAS-UHFFFAOYSA-N COC(c1ccc(COCc(cc2)ccc2C(OC)=O)cc1)=O Chemical compound COC(c1ccc(COCc(cc2)ccc2C(OC)=O)cc1)=O GTTMQWUCWHABAS-UHFFFAOYSA-N 0.000 description 1
- JAFZODJINWJNPZ-VKHMYHEASA-N C[C@@H](C(O)=O)NC(OC)=O Chemical compound C[C@@H](C(O)=O)NC(OC)=O JAFZODJINWJNPZ-VKHMYHEASA-N 0.000 description 1
- YTLCHNBFNGFDSD-YUMQZZPRSA-N C[C@@H](C[C@@H](C(OC)=O)N1C(OC(C)(C)C)=O)C1=O Chemical compound C[C@@H](C[C@@H](C(OC)=O)N1C(OC(C)(C)C)=O)C1=O YTLCHNBFNGFDSD-YUMQZZPRSA-N 0.000 description 1
- YTLCHNBFNGFDSD-SFYZADRCSA-N C[C@H](C[C@@H](C(OC)=O)N1C(OC(C)(C)C)=O)C1=O Chemical compound C[C@H](C[C@@H](C(OC)=O)N1C(OC(C)(C)C)=O)C1=O YTLCHNBFNGFDSD-SFYZADRCSA-N 0.000 description 1
- QEIFWXUIJHFGPI-DMTCNVIQSA-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-DMTCNVIQSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Cc1ccccc1 Chemical compound Cc1ccccc1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- WERRAEHFUCLWKK-UHFFFAOYSA-N O=C(CCl)c(cc1)ccc1Oc1cccc(C(CCl)=O)c1 Chemical compound O=C(CCl)c(cc1)ccc1Oc1cccc(C(CCl)=O)c1 WERRAEHFUCLWKK-UHFFFAOYSA-N 0.000 description 1
- ZPZQHSNTACFFLT-UHFFFAOYSA-N OC(C(c1ccccc1)N1C2CCC1CC2)=O Chemical compound OC(C(c1ccccc1)N1C2CCC1CC2)=O ZPZQHSNTACFFLT-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
- 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
- C07D403/02—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 two hetero rings
- C07D403/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16453109P | 2009-03-30 | 2009-03-30 | |
| US61/164531 | 2009-03-30 | ||
| US12/729940 | 2010-03-23 | ||
| US12/729,940 US8796466B2 (en) | 2009-03-30 | 2010-03-23 | Hepatitis C virus inhibitors |
| PCT/US2010/028456 WO2010117635A1 (en) | 2009-03-30 | 2010-03-24 | Hepatitis c virus inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102448956A CN102448956A (zh) | 2012-05-09 |
| CN102448956B true CN102448956B (zh) | 2015-05-06 |
Family
ID=42320079
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201080024916.0A Expired - Fee Related CN102448956B (zh) | 2009-03-30 | 2010-03-24 | 丙型肝炎病毒抑制剂 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US8796466B2 (enExample) |
| EP (1) | EP2414350B1 (enExample) |
| JP (1) | JP5612660B2 (enExample) |
| KR (1) | KR20120034603A (enExample) |
| CN (1) | CN102448956B (enExample) |
| AR (1) | AR076002A1 (enExample) |
| AU (1) | AU2010234970A1 (enExample) |
| BR (1) | BRPI1013393A2 (enExample) |
| CA (1) | CA2757269A1 (enExample) |
| CL (1) | CL2011002426A1 (enExample) |
| CO (1) | CO6430431A2 (enExample) |
| EA (1) | EA022384B1 (enExample) |
| IL (1) | IL215055A0 (enExample) |
| MX (1) | MX2011009948A (enExample) |
| NZ (1) | NZ595168A (enExample) |
| PE (1) | PE20120546A1 (enExample) |
| SG (1) | SG174521A1 (enExample) |
| WO (1) | WO2010117635A1 (enExample) |
| ZA (1) | ZA201106795B (enExample) |
Families Citing this family (91)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5762971B2 (ja) | 2008-12-03 | 2015-08-12 | プレシディオ ファーマシューティカルズ インコーポレイテッド | Hcvns5aの阻害剤 |
| 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. |
| US8314135B2 (en) | 2009-02-09 | 2012-11-20 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole antivirals |
| US8188132B2 (en) | 2009-02-17 | 2012-05-29 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole 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 |
| 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 |
| 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 |
| BRPI1016172A2 (pt) * | 2009-04-24 | 2016-04-19 | Tibotec Pharm Ltd | éteres diarílicos |
| 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 |
| US8211928B2 (en) | 2009-05-29 | 2012-07-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PE20110679A1 (es) * | 2009-06-11 | 2011-10-20 | Abbvie Bahamas Ltd | Derivados de (4-tert-butilfenil)pirrolidin-2,5-difenil como inhibidores del hcv |
| 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 |
| 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 |
| US8815928B2 (en) | 2009-09-11 | 2014-08-26 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8759332B2 (en) | 2009-09-11 | 2014-06-24 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8703938B2 (en) | 2009-09-11 | 2014-04-22 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US9156818B2 (en) | 2009-09-11 | 2015-10-13 | 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 |
| 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 |
| 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 |
| US8362020B2 (en) | 2009-12-30 | 2013-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PE20130244A1 (es) | 2010-01-25 | 2013-03-10 | Enanta Pharm Inc | Inhibidores del virus de la hepatitis c |
| US8933110B2 (en) | 2010-01-25 | 2015-01-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8178531B2 (en) | 2010-02-23 | 2012-05-15 | Enanta Pharmaceuticals, Inc. | Antiviral agents |
| US8623814B2 (en) | 2010-02-23 | 2014-01-07 | Enanta Pharmaceuticals, Inc. | Antiviral agents |
| BR112012022311A2 (pt) | 2010-03-04 | 2016-08-23 | Enanta Pharm Inc | agentes farmacêuticos de combinação como inibidores da replicação de hcv. |
| MX2012010918A (es) * | 2010-03-24 | 2013-01-18 | Vertex Pharma | Analogos para el tratamiento o prevencion de infecciones por flavivirus. |
| EP2555622A4 (en) | 2010-04-09 | 2013-09-18 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| CA2800530A1 (en) * | 2010-05-28 | 2011-12-01 | Presidio Pharmaceuticals, Inc. | Inhibitors of hcv ns5a |
| 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 |
| AU2011276526A1 (en) | 2010-06-28 | 2013-01-10 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of Flavivirus infections |
| WO2012006060A1 (en) | 2010-06-28 | 2012-01-12 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of flavivirus infections |
| WO2012006070A1 (en) | 2010-06-28 | 2012-01-12 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of flavivirus infections |
| US8697704B2 (en) | 2010-08-12 | 2014-04-15 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| AU2011292040A1 (en) | 2010-08-17 | 2013-03-07 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of Flaviviridae viral infections |
| EP2619195A1 (en) * | 2010-09-24 | 2013-07-31 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| AU2014203655B2 (en) * | 2010-10-13 | 2016-07-07 | Abbvie Ireland Unlimited Company | Anti-viral compounds |
| RU2452735C1 (ru) | 2010-11-30 | 2012-06-10 | Александр Васильевич Иващенко | Замещенные азолы, противовирусный активный компонент, фармацевтическая композиция, способ получения и применения |
| CN103354808B (zh) * | 2010-12-16 | 2016-08-10 | Abbvie公司 | 抗病毒化合物 |
| CN103384664A (zh) * | 2010-12-16 | 2013-11-06 | Abbvie公司 | 抗病毒化合物 |
| US8552047B2 (en) | 2011-02-07 | 2013-10-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| 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 |
| CN103687489A (zh) | 2011-05-18 | 2014-03-26 | 埃南塔制药公司 | 制备5-氮杂螺[2.4]庚烷-6-甲酸及其衍生物的方法 |
| CA2841095A1 (en) * | 2011-07-09 | 2013-01-17 | Sunshine Lake Pharma Co., Ltd. | Spiro compounds as hepatitis c virus inhibitors |
| WO2013016499A1 (en) | 2011-07-26 | 2013-01-31 | Vertex Pharmaceuticals Incorporated | Methods for preparation of thiophene compounds |
| EP2736893A1 (en) | 2011-07-26 | 2014-06-04 | Vertex Pharmaceuticals Incorporated | Thiophene compounds |
| WO2013021344A1 (en) | 2011-08-08 | 2013-02-14 | Lupin Limited | Imidazole derivatives as antiviral agents |
| AP2014007575A0 (en) | 2011-09-16 | 2012-04-30 | Gilead Pharmasset Llc | Methods for treating HCV |
| CA2852700A1 (en) | 2011-11-03 | 2013-05-10 | Theravance, Inc. | Rod-like hepatitis c virus inhibitors containing the fragment {2-[4-(biphenyl-4-yl)-1h-imidazo-2-yl]pyrrolidine-1-carbonlymethyl}amine |
| JP6170944B2 (ja) | 2011-12-28 | 2017-07-26 | ヤンセン・サイエンシズ・アイルランド・ユーシー | Hcv阻害剤としてのヘテロ−二環式誘導体 |
| 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 |
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| AU2010234970A1 (en) | 2011-10-06 |
| KR20120034603A (ko) | 2012-04-12 |
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| EA022384B1 (ru) | 2015-12-30 |
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| US8796466B2 (en) | 2014-08-05 |
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| NZ595168A (en) | 2013-05-31 |
| JP2012522053A (ja) | 2012-09-20 |
| ZA201106795B (en) | 2013-02-27 |
| CN102448956A (zh) | 2012-05-09 |
| AR076002A1 (es) | 2011-05-11 |
| EP2414350A1 (en) | 2012-02-08 |
| SG174521A1 (en) | 2011-10-28 |
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