KR20120107991A - C형 간염 바이러스 억제제 - Google Patents
C형 간염 바이러스 억제제 Download PDFInfo
- Publication number
- KR20120107991A KR20120107991A KR1020127018317A KR20127018317A KR20120107991A KR 20120107991 A KR20120107991 A KR 20120107991A KR 1020127018317 A KR1020127018317 A KR 1020127018317A KR 20127018317 A KR20127018317 A KR 20127018317A KR 20120107991 A KR20120107991 A KR 20120107991A
- Authority
- KR
- South Korea
- Prior art keywords
- cap
- mmol
- mixture
- hcv
- added
- 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.)
- Withdrawn
Links
- 0 *[C@@](C[n]1nccc1)C(O)=O Chemical compound *[C@@](C[n]1nccc1)C(O)=O 0.000 description 3
- ORUKAYIXMZDYIZ-CONSDPRKSA-N CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2c(C3CC3)nc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)[nH]1)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2c(C3CC3)nc([C@H](CCC3)N3C(OC(C)(C)C)=O)[nH]2)[nH]1)=O ORUKAYIXMZDYIZ-CONSDPRKSA-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
- FKRSSPOQAMALKA-CUPIEXAXSA-N CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H](C(C)C)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O Chemical compound CC(C)[C@@H](C(N(CCC1)[C@@H]1c1ncc(-c(cc2)ccc2-c(cc2)ccc2-c2cnc([C@H](CCC3)N3C([C@H](C(C)C)NC(OC)=O)=O)[nH]2)[nH]1)=O)NC(OC)=O FKRSSPOQAMALKA-CUPIEXAXSA-N 0.000 description 1
- VTAWWVOYSQUFLT-VIFPVBQESA-N CC(C)[C@@H](C(O)=O)Nc1cccnc1 Chemical compound CC(C)[C@@H](C(O)=O)Nc1cccnc1 VTAWWVOYSQUFLT-VIFPVBQESA-N 0.000 description 1
- LUPBXSFJQGMBOL-VVNDHPTOSA-N CC(C1)(C2)[C@@H]1N[C@@H]2c([nH]1)nc(-c(cc2)ccc2-c(cc2)cc(cc3)c2c2c3[nH]c([C@H](CC3)N[C@@H]3C#C)n2)c1Cl Chemical compound CC(C1)(C2)[C@@H]1N[C@@H]2c([nH]1)nc(-c(cc2)ccc2-c(cc2)cc(cc3)c2c2c3[nH]c([C@H](CC3)N[C@@H]3C#C)n2)c1Cl LUPBXSFJQGMBOL-VVNDHPTOSA-N 0.000 description 1
- LWZSTDVWNKMIFQ-UHFFFAOYSA-N CC1(CCOCC1)C(OC)=O Chemical compound CC1(CCOCC1)C(OC)=O LWZSTDVWNKMIFQ-UHFFFAOYSA-N 0.000 description 1
- CZPYIONABGXNGD-UHFFFAOYSA-N CCC(CC)C(C1)(C1NC(OC)=O)C(O)=O Chemical compound CCC(CC)C(C1)(C1NC(OC)=O)C(O)=O CZPYIONABGXNGD-UHFFFAOYSA-N 0.000 description 1
- GKJACXUIWWDMBO-UHFFFAOYSA-N CN(C)c(c1c2)cccc1c(C(O)=O)nc2Cl Chemical compound CN(C)c(c1c2)cccc1c(C(O)=O)nc2Cl GKJACXUIWWDMBO-UHFFFAOYSA-N 0.000 description 1
- DZUQNZQVLXKOHX-UHFFFAOYSA-N CN(C1)C(C(O)=O)c2c1cccc2 Chemical compound CN(C1)C(C(O)=O)c2c1cccc2 DZUQNZQVLXKOHX-UHFFFAOYSA-N 0.000 description 1
- CVGOEYPEMCHQPY-ZETCQYMHSA-N COC(N[C@@H](C(CC1)CCC1(F)F)C(O)=O)=O Chemical compound COC(N[C@@H](C(CC1)CCC1(F)F)C(O)=O)=O CVGOEYPEMCHQPY-ZETCQYMHSA-N 0.000 description 1
- FNGKZNPMMOWQPF-YFKPBYRVSA-N COCC[C@@H](C(O)=O)NC(OC)=O Chemical compound COCC[C@@H](C(O)=O)NC(OC)=O FNGKZNPMMOWQPF-YFKPBYRVSA-N 0.000 description 1
- VHDAAWICDHYPDZ-UDRQUUIHSA-N C[C@@H](C[C@H]1c2ncc(-c(cc3)ccc3-c(cc3)ccc3-c3cnc([C@H](C[C@H](C)C4)N4C(OC(C)(C)C)=O)[nH]3)[nH]2)CN1C(OC(C)(C)C)=O Chemical compound C[C@@H](C[C@H]1c2ncc(-c(cc3)ccc3-c(cc3)ccc3-c3cnc([C@H](C[C@H](C)C4)N4C(OC(C)(C)C)=O)[nH]3)[nH]2)CN1C(OC(C)(C)C)=O VHDAAWICDHYPDZ-UDRQUUIHSA-N 0.000 description 1
- PZNMMKDKVFGHBB-UZYDLOFFSA-N C[C@@H]([C@H](C1)N(C)C2)C2N1C(C(O)=O)c1ccccc1 Chemical compound C[C@@H]([C@H](C1)N(C)C2)C2N1C(C(O)=O)c1ccccc1 PZNMMKDKVFGHBB-UZYDLOFFSA-N 0.000 description 1
- BHFMWPOZZNNSRV-KVSKUHBBSA-N C[C@H](C1)O[C@@H](C)C[C@@H]1O Chemical compound C[C@H](C1)O[C@@H](C)C[C@@H]1O BHFMWPOZZNNSRV-KVSKUHBBSA-N 0.000 description 1
- JHXKGCLHEYMKHG-UHFFFAOYSA-N NC(C1CC(CC2)OC2C1)C(OCc1ccccc1)=O Chemical compound NC(C1CC(CC2)OC2C1)C(OCc1ccccc1)=O JHXKGCLHEYMKHG-UHFFFAOYSA-N 0.000 description 1
- XWUJGUIPMCLRBE-UHFFFAOYSA-N O=C1CC(CC2)OC2C1 Chemical compound O=C1CC(CC2)OC2C1 XWUJGUIPMCLRBE-UHFFFAOYSA-N 0.000 description 1
- VTWIAFKDMLQFFE-UHFFFAOYSA-N OC(c1c(cccc2)c2cc(N2CCOCC2)n1)=O Chemical compound OC(c1c(cccc2)c2cc(N2CCOCC2)n1)=O VTWIAFKDMLQFFE-UHFFFAOYSA-N 0.000 description 1
- WJHVISCCHZWZNV-UHFFFAOYSA-N OCC(CCC1CO)C11OCCO1 Chemical compound OCC(CCC1CO)C11OCCO1 WJHVISCCHZWZNV-UHFFFAOYSA-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
- 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
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28694209P | 2009-12-16 | 2009-12-16 | |
| US61/286,942 | 2009-12-16 | ||
| US12/957,512 US8377980B2 (en) | 2009-12-16 | 2010-12-01 | Hepatitis C virus inhibitors |
| US12/957,512 | 2010-12-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20120107991A true KR20120107991A (ko) | 2012-10-04 |
Family
ID=43479603
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127018317A Withdrawn KR20120107991A (ko) | 2009-12-16 | 2010-12-13 | C형 간염 바이러스 억제제 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8377980B2 (enExample) |
| EP (1) | EP2513091B1 (enExample) |
| JP (1) | JP5785189B2 (enExample) |
| KR (1) | KR20120107991A (enExample) |
| CN (1) | CN102741242B (enExample) |
| AR (1) | AR079634A1 (enExample) |
| AU (1) | AU2010332034B2 (enExample) |
| BR (1) | BR112012014677A2 (enExample) |
| CA (1) | CA2784662A1 (enExample) |
| CL (1) | CL2012001637A1 (enExample) |
| CO (1) | CO6561788A2 (enExample) |
| EA (1) | EA020815B1 (enExample) |
| MA (1) | MA33806B1 (enExample) |
| MX (1) | MX2012006635A (enExample) |
| NZ (1) | NZ601220A (enExample) |
| PE (1) | PE20121479A1 (enExample) |
| PH (1) | PH12012500979A1 (enExample) |
| SG (1) | SG181700A1 (enExample) |
| TN (1) | TN2012000264A1 (enExample) |
| TW (1) | TWI487702B (enExample) |
| WO (1) | WO2011075439A1 (enExample) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8329159B2 (en) | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8303944B2 (en) | 2006-08-11 | 2012-11-06 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CN102264737A (zh) * | 2008-12-23 | 2011-11-30 | 雅培制药有限公司 | 抗病毒化合物 |
| RU2505539C2 (ru) | 2008-12-23 | 2014-01-27 | Эбботт Лэборетриз | Антивирусные соединения |
| US8394968B2 (en) | 2009-02-17 | 2013-03-12 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PE20120834A1 (es) | 2009-03-23 | 2012-07-25 | Glenmark Pharmaceuticals Sa | Derivados de furopirimidindiona como moduladores de trpa1 |
| US20190127365A1 (en) | 2017-11-01 | 2019-05-02 | Merck Sharp & Dohme Corp. | Inhibitors of hepatitis c virus replication |
| HUE027755T2 (en) | 2009-03-27 | 2016-11-28 | Merck Sharp & Dohme | Inhibitors of hepatitis C virus replication |
| 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 |
| WO2010120935A1 (en) * | 2009-04-15 | 2010-10-21 | Abbott Laboratories | Anti-viral compounds |
| AU2010249080A1 (en) | 2009-05-12 | 2012-01-12 | Merck Sharp & Dohme Corp. | Fused tricyclic aryl compounds useful for the treatment of viral diseases |
| SG176015A1 (en) | 2009-05-13 | 2011-12-29 | Gilead Sciences Inc | Antiviral compounds |
| US8138215B2 (en) | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| JP2012528195A (ja) | 2009-05-29 | 2012-11-12 | メルク・シャープ・アンド・ドーム・コーポレーション | C型肝炎などの疾患を処置するための3つの結合アリール部分で構成された抗菌性化合物 |
| EP2435421A1 (en) | 2009-05-29 | 2012-04-04 | 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 |
| EP2853531A3 (en) | 2009-06-11 | 2015-08-12 | AbbVie Bahamas Ltd. | Antiviral 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 |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | Abbvie Inc. | Anti-viral compounds |
| US8354419B2 (en) | 2009-07-16 | 2013-01-15 | Vertex Pharmaceuticals Incorporated | Benzimidazole analogues for the treatment or prevention of flavivirus infections |
| 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 |
| WO2011087740A1 (en) | 2009-12-22 | 2011-07-21 | Schering Corporation | Fused tricyclic compounds and methods of use thereof for the treatment of viral diseases |
| CN102883718A (zh) * | 2009-12-24 | 2013-01-16 | 顶点制药公司 | 用于治疗或预防黄病毒感染的类似物 |
| US8362020B2 (en) | 2009-12-30 | 2013-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| MA34147B1 (fr) | 2010-03-09 | 2013-04-03 | Merck Sharp & Dohme | Composes tricycliques fusionnes de silyle et leurs methodes d'utilisation dans le cadre du traitement de maladies virales |
| WO2011119853A1 (en) | 2010-03-24 | 2011-09-29 | Vertex Pharmaceuticals Incorporated | Analogues for the treatment or prevention of flavivirus infections |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| BR112013004520A2 (pt) | 2010-08-26 | 2016-06-07 | Univ Emory | inibidores potentes e seletivos do virus da hepatite c |
| EP2621279B1 (en) | 2010-09-29 | 2018-04-04 | Merck Sharp & Dohme Corp. | Fused tetracycle derivatives and methods of use thereof for the treatment of viral diseases |
| WO2012048421A1 (en) * | 2010-10-14 | 2012-04-19 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor compounds |
| CA2814534A1 (en) | 2010-11-04 | 2012-05-10 | Theravance, Inc. | Novel inhibitors of hepatitis c virus |
| KR101835474B1 (ko) * | 2010-11-17 | 2018-03-08 | 길리애드 파마셋 엘엘씨 | 항바이러스 화합물 |
| US8552047B2 (en) | 2011-02-07 | 2013-10-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2012122716A1 (en) | 2011-03-17 | 2012-09-20 | Merck Sharp & Dohme Corp. | Tetracyclic xanthene derivatives and methods of use thereof for treatment of viral diseases |
| 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 |
| EA201490254A1 (ru) * | 2011-08-24 | 2014-07-30 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Комбинированное лечение гепатита с |
| WO2013030750A1 (en) | 2011-09-01 | 2013-03-07 | Lupin Limited | Antiviral compounds |
| WO2013039878A1 (en) * | 2011-09-14 | 2013-03-21 | Merck Sharp & Dohme Corp. | Silyl-containing heterocyclic compounds and methods of use thereof for the treatment of viral diseases |
| HRP20180237T4 (hr) | 2011-09-16 | 2020-12-11 | Gilead Pharmasset Llc | Metode za liječenje hcv-a |
| AR088630A1 (es) | 2011-11-03 | 2014-06-25 | Theravance Inc | Inhibidores del virus de la hepatitis c |
| US20130164260A1 (en) | 2011-11-16 | 2013-06-27 | Gilead Sciences, Inc. | Antiviral compounds |
| 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 |
| US9073943B2 (en) | 2012-02-10 | 2015-07-07 | Lupin Limited | Antiviral compounds with a dibenzooxaheterocycle moiety |
| LT2850075T (lt) | 2012-04-25 | 2017-05-10 | Theravance Biopharma R&D Ip, Llc | Piperazino-piperidino junginiai, kaip hepatito c viruso inhibitoriai |
| CA2869908C (en) | 2012-04-25 | 2018-02-20 | Theravance Biopharma R&D Ip, Llc | Hepatitis c virus inhibitors |
| US9079887B2 (en) * | 2012-05-16 | 2015-07-14 | Gilead Sciences, Inc. | Antiviral compounds |
| US20130309196A1 (en) | 2012-05-16 | 2013-11-21 | Gilead Sciences, Inc. | Antiviral compounds |
| JP6196678B2 (ja) * | 2012-10-24 | 2017-09-13 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎ウイルス阻害剤 |
| WO2014110687A1 (en) | 2013-01-16 | 2014-07-24 | Merck Sharp & Dohme Corp. | Thiazolyl-substitued tetracyclic compounds and methods of use thereof for treatment of viral diseases |
| EP2950786B1 (en) | 2013-01-31 | 2019-11-27 | Gilead Pharmasset LLC | Combination formulation of two antiviral compounds |
| 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 |
| EP3019196B1 (en) | 2013-07-09 | 2018-06-06 | Bristol-Myers Squibb Company | Combinations of hepatitis c virus inhibitors |
| JP2016527232A (ja) | 2013-07-17 | 2016-09-08 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Hcvの治療に使用するためのビフェニル誘導体を含む組み合わせ |
| EA201690473A1 (ru) | 2013-08-27 | 2017-03-31 | ГАЙЛИД ФАРМАССЕТ ЭлЭлСи | Комбинированный состав двух противовирусных соединений |
| CN103450071A (zh) * | 2013-09-05 | 2013-12-18 | 南京工业大学 | 一种医药中间体2-氮杂双环[3.1.0]己烷-2,3-二碳酸叔丁酯的不对称合成方法 |
| US20160311806A1 (en) * | 2013-12-11 | 2016-10-27 | Bristol-Myers Squibb Company | 4,4'-biphenyldiyl-bis-(1 h-imidazolyl) derivatives as hepatitis hcv inhibitors |
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| CN102741242B (zh) | 2015-07-01 |
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