JP5089402B2 - C型肝炎ウイルスインヒビター - Google Patents
C型肝炎ウイルスインヒビター Download PDFInfo
- Publication number
- JP5089402B2 JP5089402B2 JP2007555172A JP2007555172A JP5089402B2 JP 5089402 B2 JP5089402 B2 JP 5089402B2 JP 2007555172 A JP2007555172 A JP 2007555172A JP 2007555172 A JP2007555172 A JP 2007555172A JP 5089402 B2 JP5089402 B2 JP 5089402B2
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- JP
- Japan
- Prior art keywords
- compound
- mmol
- nmr
- solution
- 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.)
- Expired - Fee Related
Links
- 0 CCC(C1)C1(*)NC(OCC*)=O Chemical compound CCC(C1)C1(*)NC(OCC*)=O 0.000 description 10
- ZQEBQGAAWMOMAI-ZETCQYMHSA-N CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O ZQEBQGAAWMOMAI-ZETCQYMHSA-N 0.000 description 4
- FWJMQXZDGRCGEJ-UHFFFAOYSA-N COc1cc2ccnc([O]=C)c2cc1 Chemical compound COc1cc2ccnc([O]=C)c2cc1 FWJMQXZDGRCGEJ-UHFFFAOYSA-N 0.000 description 2
- XTEPWMXNXVHQEV-UHFFFAOYSA-N C=[O]C(N(C1)Cc2c1cccc2F)=O Chemical compound C=[O]C(N(C1)Cc2c1cccc2F)=O XTEPWMXNXVHQEV-UHFFFAOYSA-N 0.000 description 1
- VQXWDAAONGOPPT-UHFFFAOYSA-N CC(C)(C)CS(N)(=O)=O Chemical compound CC(C)(C)CS(N)(=O)=O VQXWDAAONGOPPT-UHFFFAOYSA-N 0.000 description 1
- BWYQYLMHOVIAON-UHFFFAOYSA-N CC(C)(C)NC(OCC(NCCCC1(CC1)C(N)=O)=O)=O Chemical compound CC(C)(C)NC(OCC(NCCCC1(CC1)C(N)=O)=O)=O BWYQYLMHOVIAON-UHFFFAOYSA-N 0.000 description 1
- LAVNXJXCPNOUGI-UHFFFAOYSA-N CC(C)(C)NCOCC[O](O)#C Chemical compound CC(C)(C)NCOCC[O](O)#C LAVNXJXCPNOUGI-UHFFFAOYSA-N 0.000 description 1
- VUESGWZNWAOMNS-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)C1C(NC1(CC1)C(O)=O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)C1C(NC1(CC1)C(O)=O)=O)=O VUESGWZNWAOMNS-UHFFFAOYSA-N 0.000 description 1
- OAHSKBSASLHPIK-VIFPVBQESA-N CC(C)[C@@H](C(NCCCC1(CC1)C(N)=O)=O)O Chemical compound CC(C)[C@@H](C(NCCCC1(CC1)C(N)=O)=O)O OAHSKBSASLHPIK-VIFPVBQESA-N 0.000 description 1
- XDXMJRIZSBCDGA-UHFFFAOYSA-N CCC1(CC1)S(N)(=O)=O Chemical compound CCC1(CC1)S(N)(=O)=O XDXMJRIZSBCDGA-UHFFFAOYSA-N 0.000 description 1
- AXIIEOPSQHRYCU-UHFFFAOYSA-N CN(C1)Cc2c1cccc2 Chemical compound CN(C1)Cc2c1cccc2 AXIIEOPSQHRYCU-UHFFFAOYSA-N 0.000 description 1
- WXUCBUGUUVYAAN-YNODCEANSA-N COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O Chemical compound COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O WXUCBUGUUVYAAN-YNODCEANSA-N 0.000 description 1
- NPNZHBLHGARCRC-AVSAUPPFSA-N COc(cc1)cc2c1c(O[C@H](C1)CN[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)cc(-c1ccccc1)n2 Chemical compound COc(cc1)cc2c1c(O[C@H](C1)CN[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)cc(-c1ccccc1)n2 NPNZHBLHGARCRC-AVSAUPPFSA-N 0.000 description 1
- SJLNTKAREUAQFX-UHFFFAOYSA-N COc(cc1)cc2c1c([O]=C)cc(-c1ccccc1)n2 Chemical compound COc(cc1)cc2c1c([O]=C)cc(-c1ccccc1)n2 SJLNTKAREUAQFX-UHFFFAOYSA-N 0.000 description 1
- PKGOAHVKZIEDOX-UHFFFAOYSA-N COc1cc2ccnc(Cl)c2cc1F Chemical compound COc1cc2ccnc(Cl)c2cc1F PKGOAHVKZIEDOX-UHFFFAOYSA-N 0.000 description 1
- NAPKFJWPMSUWBB-UHFFFAOYSA-N Cc(c1nc(-c2cc(OC)ccc2)c2)n[o]c1c2O Chemical compound Cc(c1nc(-c2cc(OC)ccc2)c2)n[o]c1c2O NAPKFJWPMSUWBB-UHFFFAOYSA-N 0.000 description 1
- VFPFMOXMHVQFNR-UHFFFAOYSA-N Clc1c(cc[s]2)c2ccn1 Chemical compound Clc1c(cc[s]2)c2ccn1 VFPFMOXMHVQFNR-UHFFFAOYSA-N 0.000 description 1
- MBSACDZZSVRCER-UHFFFAOYSA-N Clc1cc(-c2ccc[s]2)cc(-c2ccccc2)n1 Chemical compound Clc1cc(-c2ccc[s]2)cc(-c2ccccc2)n1 MBSACDZZSVRCER-UHFFFAOYSA-N 0.000 description 1
- AAZYJKNISGEWEV-UHFFFAOYSA-N Clc1nc(-c2ccccc2)ccn1 Chemical compound Clc1nc(-c2ccccc2)ccn1 AAZYJKNISGEWEV-UHFFFAOYSA-N 0.000 description 1
- PLJRNLOBHYWBKZ-UHFFFAOYSA-N NCCCC1(CC1)C(N)=O Chemical compound NCCCC1(CC1)C(N)=O PLJRNLOBHYWBKZ-UHFFFAOYSA-N 0.000 description 1
- BTEDODVKNAUJNJ-UHFFFAOYSA-N O=C(C1(CC1)NCCCC1NCCC1)NS(C1CC1)=O Chemical compound O=C(C1(CC1)NCCCC1NCCC1)NS(C1CC1)=O BTEDODVKNAUJNJ-UHFFFAOYSA-N 0.000 description 1
- KONIJUGGJSBXQD-UHFFFAOYSA-N O=C1NC(c2ccccc2)=CC(c2ccc[s]2)=C1 Chemical compound O=C1NC(c2ccccc2)=CC(c2ccc[s]2)=C1 KONIJUGGJSBXQD-UHFFFAOYSA-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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K38/20—Interleukins [IL]
- A61K38/2013—IL-2
-
- 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
- A61K38/20—Interleukins [IL]
- A61K38/204—IL-6
-
- 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
- A61K38/20—Interleukins [IL]
- A61K38/208—IL-12
-
- 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]
- A61K38/212—IFN-alpha
-
- 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
- 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
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Virology (AREA)
- Biochemistry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65079805P | 2005-02-08 | 2005-02-08 | |
| US60/650,798 | 2005-02-08 | ||
| PCT/US2006/004278 WO2006086381A2 (en) | 2005-02-08 | 2006-02-07 | Hepatitis c virus inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008530096A JP2008530096A (ja) | 2008-08-07 |
| JP2008530096A5 JP2008530096A5 (OSRAM) | 2009-04-09 |
| JP5089402B2 true JP5089402B2 (ja) | 2012-12-05 |
Family
ID=36793637
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007555172A Expired - Fee Related JP5089402B2 (ja) | 2005-02-08 | 2006-02-07 | C型肝炎ウイルスインヒビター |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7323447B2 (OSRAM) |
| EP (1) | EP1863793B1 (OSRAM) |
| JP (1) | JP5089402B2 (OSRAM) |
| CN (1) | CN101189223A (OSRAM) |
| ES (1) | ES2389054T3 (OSRAM) |
| NO (1) | NO20073706L (OSRAM) |
| WO (1) | WO2006086381A2 (OSRAM) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US7176208B2 (en) * | 2003-04-18 | 2007-02-13 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl macrocyclic hepatitis C serine protease inhibitors |
| WO2004103189A1 (en) * | 2003-05-16 | 2004-12-02 | C.R. Bard, Inc. | Single intubation, multi-stitch endoscopic suturing system |
| US7491794B2 (en) * | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| US7592336B2 (en) | 2005-05-10 | 2009-09-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7601686B2 (en) | 2005-07-11 | 2009-10-13 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| GEP20105124B (en) | 2005-07-25 | 2010-11-25 | Array Biopharma Inc | Novel macrocyclic inhibitors of hepatitis c virus replication |
| BRPI0617274A2 (pt) | 2005-10-11 | 2011-07-19 | Intermune Inc | compostos e métodos para a inibição de replicação viral de hepatite c |
| US7772183B2 (en) | 2005-10-12 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7741281B2 (en) | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| RU2008152171A (ru) * | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
| WO2008008776A2 (en) * | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| EP2041156B1 (en) | 2006-07-13 | 2013-11-20 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| KR20090049600A (ko) * | 2006-09-13 | 2009-05-18 | 노파르티스 아게 | 마크로시클릭 hcv 억제제 및 그의 용도 |
| US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2008070358A2 (en) * | 2006-11-16 | 2008-06-12 | Phenomix Corporation | N-cyclopropyl-hydroxyproline-based tripeptidic hepatitis c serine protease inhibitors containing an isoindole, pyrrolopyridine, pyrrolopyrimidine or pyrrolopyrazine heterocycle in the side chain |
| US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20100120716A1 (en) * | 2006-12-06 | 2010-05-13 | Phenomix Corporation | Macrocyclic hepatitis c serine protease inhibitors and uses therefor |
| JP2010519339A (ja) | 2007-02-26 | 2010-06-03 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Hcv複製阻害剤として有用な三級アミン置換ペプチド |
| MX2009012093A (es) | 2007-05-10 | 2010-01-25 | Intermune Inc | Nuevos peptidos inhibidores de la replicacion del virus de la hepatitis c. |
| KR101596524B1 (ko) | 2007-06-29 | 2016-02-22 | 길리애드 사이언시즈, 인코포레이티드 | 항바이러스 화합물 |
| MX2009013830A (es) | 2007-06-29 | 2010-03-01 | Gilead Sciences Inc | Compuestos antivirales. |
| WO2009042668A2 (en) | 2007-09-24 | 2009-04-02 | Achillion Pharmaceuticals, Inc. | Urea-containing peptides as inhibitors of viral replication |
| US8419332B2 (en) * | 2007-10-19 | 2013-04-16 | Atlas Bolt & Screw Company Llc | Non-dimpling fastener |
| US8383583B2 (en) | 2007-10-26 | 2013-02-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic, pyridazinone-containing hepatitis C serine protease inhibitors |
| US8304385B2 (en) | 2007-11-14 | 2012-11-06 | Enanta Pharmaceuticals, Inc. | Macrocyclic tetrazolyl hepatitis C serine protease inhibitors |
| CA2708150A1 (en) | 2007-12-05 | 2009-06-18 | Enanta Pharmaceuticals, Inc. | Fluorinated tripeptide hcv serine protease inhibitors |
| US8273709B2 (en) | 2007-12-14 | 2012-09-25 | Enanta Pharmaceuticals, Inc. | Triazole-containing macrocyclic HCV serine protease inhibitors |
| CN101951769B (zh) * | 2007-12-21 | 2014-12-31 | 阿维拉制药公司 | Hcv蛋白酶抑制剂和其用途 |
| US8202996B2 (en) | 2007-12-21 | 2012-06-19 | Bristol-Myers Squibb Company | Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide |
| JP5755449B2 (ja) | 2007-12-21 | 2015-07-29 | セルジーン アビロミクス リサーチ, インコーポレイテッド | Hcvプロテアーゼ阻害剤およびその使用 |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| US8309685B2 (en) * | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| TW200936131A (en) * | 2008-02-04 | 2009-09-01 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
| MX2010010276A (es) | 2008-03-20 | 2011-03-25 | Enanta Pharm Inc | Compuestos macrociclicos fluorinados como inhibidores del virus de hepatitis c. |
| CN102046622A (zh) | 2008-04-15 | 2011-05-04 | 因特蒙公司 | 丙型肝炎病毒复制的新颖大环抑制剂 |
| US8163921B2 (en) * | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8044023B2 (en) | 2008-05-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
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| US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
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| AU2009324643B2 (en) | 2008-12-10 | 2014-08-28 | Achillion Pharmaceuticals, Inc. | New 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
| US8283310B2 (en) | 2008-12-15 | 2012-10-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| AR075584A1 (es) | 2009-02-27 | 2011-04-20 | Intermune Inc | COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO. |
| WO2010118078A1 (en) | 2009-04-08 | 2010-10-14 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| MX363732B (es) * | 2009-05-13 | 2019-04-01 | Gilead Pharmasset Llc Star | Compuestos antivirales. |
| CA2769652A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
| US8933227B2 (en) * | 2009-08-14 | 2015-01-13 | Boehringer Ingelheim International Gmbh | Selective synthesis of functionalized pyrimidines |
| JP5539518B2 (ja) * | 2009-08-14 | 2014-07-02 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 2−アミノ−5−トリフルオロメチルピリミジン誘導体の位置選択的調製 |
| WO2012061248A2 (en) | 2010-11-01 | 2012-05-10 | Rfs Pharma, Llc | Novel specific hcv ns3 protease inhibitors |
| WO2012092411A2 (en) | 2010-12-30 | 2012-07-05 | Enanta Pharmaceuticals, Inc. | Phenanthridine macrocyclic hepatitis c serine protease inhibitors |
| JP2014502620A (ja) | 2010-12-30 | 2014-02-03 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状c型肝炎セリンプロテアーゼ阻害剤 |
| TW201309690A (zh) | 2011-02-10 | 2013-03-01 | Idenix Pharmaceuticals Inc | 巨環絲胺酸蛋白酶抑制劑,其醫藥組合物及其於治療hcv感染之用途 |
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
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