JP2010509359A - C型肝炎ウイルス阻害剤 - Google Patents
C型肝炎ウイルス阻害剤 Download PDFInfo
- Publication number
- JP2010509359A JP2010509359A JP2009536467A JP2009536467A JP2010509359A JP 2010509359 A JP2010509359 A JP 2010509359A JP 2009536467 A JP2009536467 A JP 2009536467A JP 2009536467 A JP2009536467 A JP 2009536467A JP 2010509359 A JP2010509359 A JP 2010509359A
- Authority
- JP
- Japan
- Prior art keywords
- methoxy
- carbamoyl
- prolinamide
- oxy
- isoquinolinyl
- 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.)
- Pending
Links
- 0 CC1*(C2)C1C2(C(*)=O)NC([C@](C[C@](C1)Oc2c(c(*)c(*)c(*)c3*)c3c(*)c(*)n2)N1C(C(*)N*)=O)=O Chemical compound CC1*(C2)C1C2(C(*)=O)NC([C@](C[C@](C1)Oc2c(c(*)c(*)c(*)c3*)c3c(*)c(*)n2)N1C(C(*)N*)=O)=O 0.000 description 14
- SPGDRXRIVPMUCK-UHFFFAOYSA-N CC(C)(C)NS(CCCCl)(=O)=O Chemical compound CC(C)(C)NS(CCCCl)(=O)=O SPGDRXRIVPMUCK-UHFFFAOYSA-N 0.000 description 2
- WMSPXQIQBQAWLL-UHFFFAOYSA-N NS(C1CC1)(=O)=O Chemical compound NS(C1CC1)(=O)=O WMSPXQIQBQAWLL-UHFFFAOYSA-N 0.000 description 2
- GPKDGVXBXQTHRY-UHFFFAOYSA-N O=S(CCCCl)(Cl)=O Chemical compound O=S(CCCCl)(Cl)=O GPKDGVXBXQTHRY-UHFFFAOYSA-N 0.000 description 2
- QHTNRCHCBYXOJP-LRNSAUPQSA-N CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N)=O)=O)Nc(cn1)ccc1OC Chemical compound CC(C)(C)C(C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N)=O)=O)Nc(cn1)ccc1OC QHTNRCHCBYXOJP-LRNSAUPQSA-N 0.000 description 1
- MWDFYACQVMHOMV-ZZNRJTPNSA-N CC(C)(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(N)=O)=O)Nc1ccccc1 Chemical compound CC(C)(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(OC)n2)[C@@H]1C(N)=O)=O)Nc1ccccc1 MWDFYACQVMHOMV-ZZNRJTPNSA-N 0.000 description 1
- JTZIZFSBVOHJQD-UHFFFAOYSA-N CC(C)(C)NS(C1CC1)(=O)=O Chemical compound CC(C)(C)NS(C1CC1)(=O)=O JTZIZFSBVOHJQD-UHFFFAOYSA-N 0.000 description 1
- IUSCDEKGYWTWPX-VYIIXAMBSA-N CC(C)(C)OC(N(CC(C1)Oc2nccc3c2cccc3C)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CC(C1)Oc2nccc3c2cccc3C)[C@@H]1C(O)=O)=O IUSCDEKGYWTWPX-VYIIXAMBSA-N 0.000 description 1
- LFKDJXLFVYVEFG-UHFFFAOYSA-N CC(C)(C)OC(N)=O Chemical compound CC(C)(C)OC(N)=O LFKDJXLFVYVEFG-UHFFFAOYSA-N 0.000 description 1
- DSKCOVBHIFAJRI-UHFFFAOYSA-N CC(C)(C)OC(NC1(CC1)C(O)=O)=O Chemical compound CC(C)(C)OC(NC1(CC1)C(O)=O)=O DSKCOVBHIFAJRI-UHFFFAOYSA-N 0.000 description 1
- NLJRSHWRIQKGLB-WBVHZDCISA-N CC(C)(C)OC(NCC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(N)=O)=O)=O Chemical compound CC(C)(C)OC(NCC(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3ccn2)[C@@H]1C(N)=O)=O)=O NLJRSHWRIQKGLB-WBVHZDCISA-N 0.000 description 1
- ZKCDJWKMAYLLLJ-YHHKDRGWSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N)=O)=O)Nc1cc(C(NC(C)(C)c2ccccc2)=O)ccc1 Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C(N)=O)=O)Nc1cc(C(NC(C)(C)c2ccccc2)=O)ccc1 ZKCDJWKMAYLLLJ-YHHKDRGWSA-N 0.000 description 1
- WTLHJEYPFGNROT-NAEWKNJDSA-N CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(-c(cc3)ccc3OC(F)(F)F)cc3c2CCC(OC)=C3)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)NC1=NCCCS1 Chemical compound CC(C)(C)[C@@H](C(N(C[C@@H](C1)Oc2nc(-c(cc3)ccc3OC(F)(F)F)cc3c2CCC(OC)=C3)[C@@H]1C(N[C@](C1)([C@@H]1C=C)C(NS(C1CC1)(=O)=O)=O)=O)=O)NC1=NCCCS1 WTLHJEYPFGNROT-NAEWKNJDSA-N 0.000 description 1
- QMVJPJXMIUGGSK-XKQFRSSLSA-N CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(N(C)C)n2)[C@@H]1C=O)=O)Nc1ccccc1 Chemical compound CC(C)C(C(N(C[C@@H](C1)Oc2c(ccc(OC)c3)c3cc(N(C)C)n2)[C@@H]1C=O)=O)Nc1ccccc1 QMVJPJXMIUGGSK-XKQFRSSLSA-N 0.000 description 1
- KHEZKDIWDCVMTL-UHFFFAOYSA-N CCCNC(C1(CC1)S(N)(=O)=O)=O Chemical compound CCCNC(C1(CC1)S(N)(=O)=O)=O KHEZKDIWDCVMTL-UHFFFAOYSA-N 0.000 description 1
- JUKMPAPPOVLPIG-IEDSLXKASA-N CCNS(c(cc1)ccc1NC(C(C)(C)C)C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C=O)=O)(=O)=O Chemical compound CCNS(c(cc1)ccc1NC(C(C)(C)C)C(N(C[C@@H](C1)Oc(nc2)c(cc(cc3)Cl)c3c2OC)[C@@H]1C=O)=O)(=O)=O JUKMPAPPOVLPIG-IEDSLXKASA-N 0.000 description 1
- IVTWLMSFYBSYLA-UHFFFAOYSA-N CN(C)c(cc1)ccc1-c1nc(Cl)c(ccc(OC)c2)c2c1 Chemical compound CN(C)c(cc1)ccc1-c1nc(Cl)c(ccc(OC)c2)c2c1 IVTWLMSFYBSYLA-UHFFFAOYSA-N 0.000 description 1
- XHQZPXMBPFBQIK-UHFFFAOYSA-N COc(cc1)cc(CBr)c1C#N Chemical compound COc(cc1)cc(CBr)c1C#N XHQZPXMBPFBQIK-UHFFFAOYSA-N 0.000 description 1
- INEGVASWXOSBGG-UHFFFAOYSA-N COc(cc1CC#N)ccc1C#N Chemical compound COc(cc1CC#N)ccc1C#N INEGVASWXOSBGG-UHFFFAOYSA-N 0.000 description 1
- OEVYXCYYDZXFMV-UHFFFAOYSA-N COc(cn1)c(ccc(Cl)c2)c2c1[O]=C Chemical compound COc(cn1)c(ccc(Cl)c2)c2c1[O]=C OEVYXCYYDZXFMV-UHFFFAOYSA-N 0.000 description 1
- YWINCAALNYCNRW-UHFFFAOYSA-N COc1cc2cc(-c3ccncc3)nc(Cl)c2cc1 Chemical compound COc1cc2cc(-c3ccncc3)nc(Cl)c2cc1 YWINCAALNYCNRW-UHFFFAOYSA-N 0.000 description 1
- FYYNPQAXKRSYCY-UHFFFAOYSA-N COc1cc2cc(F)nc(Br)c2cc1 Chemical compound COc1cc2cc(F)nc(Br)c2cc1 FYYNPQAXKRSYCY-UHFFFAOYSA-N 0.000 description 1
- UTZJYSXOFHCSGZ-UHFFFAOYSA-N COc1ccc2c(Cl)nccc2c1 Chemical compound COc1ccc2c(Cl)nccc2c1 UTZJYSXOFHCSGZ-UHFFFAOYSA-N 0.000 description 1
- LZPNXAULYJPXEH-AATRIKPKSA-N COc1cccc(/C=C/C(O)=O)c1 Chemical compound COc1cccc(/C=C/C(O)=O)c1 LZPNXAULYJPXEH-AATRIKPKSA-N 0.000 description 1
- GPIQOFWTZXXOOV-UHFFFAOYSA-N COc1nc(Cl)nc(OC)n1 Chemical compound COc1nc(Cl)nc(OC)n1 GPIQOFWTZXXOOV-UHFFFAOYSA-N 0.000 description 1
- XPTACUKJASSGKX-UHFFFAOYSA-N NC(NS(C1CC1)(=O)=O)=O Chemical compound NC(NS(C1CC1)(=O)=O)=O XPTACUKJASSGKX-UHFFFAOYSA-N 0.000 description 1
- AAYHAFZXFMIUSN-UHFFFAOYSA-N NS(C1CCCCC1)(=O)=O Chemical compound NS(C1CCCCC1)(=O)=O AAYHAFZXFMIUSN-UHFFFAOYSA-N 0.000 description 1
- PQENWYCGXBURQN-RCOVLWMOSA-N O=C([C@@]1(C2)[C@H]2CC1)NS(C1CC1)(=O)=O Chemical compound O=C([C@@]1(C2)[C@H]2CC1)NS(C1CC1)(=O)=O PQENWYCGXBURQN-RCOVLWMOSA-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
- C07D401/14—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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86503406P | 2006-11-09 | 2006-11-09 | |
| US11/934,840 US7772180B2 (en) | 2006-11-09 | 2007-11-05 | Hepatitis C virus inhibitors |
| PCT/US2007/084012 WO2008060927A2 (en) | 2006-11-09 | 2007-11-08 | Hepatitis c virus inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010509359A true JP2010509359A (ja) | 2010-03-25 |
| JP2010509359A5 JP2010509359A5 (https=) | 2010-12-24 |
Family
ID=39304590
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009536467A Pending JP2010509359A (ja) | 2006-11-09 | 2007-11-08 | C型肝炎ウイルス阻害剤 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7772180B2 (https=) |
| EP (1) | EP2086963B1 (https=) |
| JP (1) | JP2010509359A (https=) |
| KR (1) | KR20090082467A (https=) |
| CN (1) | CN101541784B (https=) |
| AR (1) | AR063653A1 (https=) |
| AU (1) | AU2007319435A1 (https=) |
| BR (1) | BRPI0718625A2 (https=) |
| CA (1) | CA2669310A1 (https=) |
| CL (1) | CL2007003250A1 (https=) |
| EA (1) | EA200900676A1 (https=) |
| IL (1) | IL198248A0 (https=) |
| MX (1) | MX2009004888A (https=) |
| NO (1) | NO20091591L (https=) |
| NZ (1) | NZ576817A (https=) |
| PE (1) | PE20081344A1 (https=) |
| TW (1) | TW200826938A (https=) |
| WO (1) | WO2008060927A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013539763A (ja) * | 2010-10-08 | 2013-10-28 | ノバルティス アーゲー | スルファミドns3阻害剤のビタミンe製剤 |
| JP2015524450A (ja) * | 2012-08-08 | 2015-08-24 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | (アザ−)イソキノリノン誘導体 |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US9512125B2 (en) | 2004-11-19 | 2016-12-06 | The Regents Of The University Of California | Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents |
| WO2007114926A2 (en) | 2006-04-04 | 2007-10-11 | The Regents Of The University Of California | Kinase antagonists |
| SG174809A1 (en) * | 2007-05-03 | 2011-10-28 | Intermune Inc | Macrocyclic compounds useful as inhibitors of hepatitis c virus |
| JP2010526834A (ja) * | 2007-05-10 | 2010-08-05 | インターミューン・インコーポレーテッド | C型肝炎ウイルス複製の新規ペプチド阻害剤 |
| WO2009005690A2 (en) * | 2007-06-29 | 2009-01-08 | Gilead Sciences, Inc. | Antiviral compounds |
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
| TWI487522B (zh) | 2007-12-21 | 2015-06-11 | 賽基艾維洛米斯研究股份有限公司 | Hcv蛋白酶抑制劑及其用途(一) |
| RU2515318C2 (ru) | 2007-12-21 | 2014-05-10 | Авила Терапьютикс, Инк. | Ингибиторы протеазы вируса гепатита с и их применение |
| US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
| EP3613743B1 (en) | 2008-01-04 | 2022-03-16 | Intellikine, LLC | Processes for the preparation of 1h-pyrazolo[3,4-d]pyrimidin-4-amine derivatives |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| ES2437147T3 (es) * | 2008-02-04 | 2014-01-09 | Idenix Pharmaceuticals, Inc. | Inhibidores de serina proteasa macrocíclicos |
| US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
| US8637542B2 (en) * | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
| WO2009142842A2 (en) * | 2008-04-15 | 2009-11-26 | Intermune, Inc. | Novel macrocyclic inhibitors of hepatitis c virus replication |
| US20090285774A1 (en) * | 2008-05-15 | 2009-11-19 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US20110224223A1 (en) | 2008-07-08 | 2011-09-15 | The Regents Of The University Of California, A California Corporation | MTOR Modulators and Uses Thereof |
| JP5788316B2 (ja) * | 2008-07-08 | 2015-09-30 | インテリカイン, エルエルシー | キナーゼインヒビターおよび使用方法 |
| US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
| KR20110075019A (ko) * | 2008-10-15 | 2011-07-05 | 인터뮨, 인크. | 치료용 항바이러스성 펩티드 |
| WO2010045542A2 (en) | 2008-10-16 | 2010-04-22 | The Regents Of The University Of California | Fused ring heteroaryl kinase inhibitors |
| US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
| 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. |
| TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
| KR101018330B1 (ko) | 2009-04-30 | 2011-03-04 | 한국외국어대학교 연구산학협력단 | 3,4-디히드로이소퀴놀리늄 유도체 및 이를 포함하는 약학 조성물 |
| EP2427195B1 (en) | 2009-05-07 | 2019-05-01 | Intellikine, LLC | Heterocyclic compounds and uses thereof |
| US8936781B2 (en) | 2009-05-13 | 2015-01-20 | Enanta Pharmaceuticals, Inc. | Macrocyclic compounds as hepatitis C virus inhibitors |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| EP2461811B1 (en) | 2009-08-05 | 2016-04-20 | Idenix Pharmaceuticals LLC. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
| CN102741270B (zh) * | 2009-09-28 | 2015-07-22 | 英特穆恩公司 | C型肝炎病毒复制的环肽抑制剂 |
| US20110082182A1 (en) * | 2009-10-01 | 2011-04-07 | Intermune, Inc. | Therapeutic antiviral peptides |
| US8980899B2 (en) | 2009-10-16 | 2015-03-17 | The Regents Of The University Of California | Methods of inhibiting Ire1 |
| US9193740B2 (en) * | 2009-10-19 | 2015-11-24 | Enanta Pharmaceuticals, Inc. | Bismacrocyclic compounds as hepatitis C virus inhibitors |
| CA2799579A1 (en) | 2010-05-21 | 2011-11-24 | Intellikine, Inc. | Chemical compounds, compositions and methods for kinase modulation |
| CN102134240A (zh) * | 2010-06-29 | 2011-07-27 | 嘉兴宜博生物医药科技有限公司 | 一种6-氟-7-氮杂吲哚的合成方法 |
| JP2013545749A (ja) | 2010-11-10 | 2013-12-26 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | 複素環化合物及びその使用 |
| CA2822357A1 (en) | 2010-12-22 | 2012-06-28 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
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| US20080119461A1 (en) | 2008-05-22 |
| MX2009004888A (es) | 2009-05-19 |
| WO2008060927A2 (en) | 2008-05-22 |
| US7772180B2 (en) | 2010-08-10 |
| CA2669310A1 (en) | 2008-05-22 |
| NZ576817A (en) | 2011-08-26 |
| BRPI0718625A2 (pt) | 2014-04-01 |
| CL2007003250A1 (es) | 2008-05-23 |
| NO20091591L (no) | 2009-07-28 |
| EP2086963A2 (en) | 2009-08-12 |
| WO2008060927A3 (en) | 2008-07-03 |
| AR063653A1 (es) | 2009-02-04 |
| CN101541784A (zh) | 2009-09-23 |
| KR20090082467A (ko) | 2009-07-30 |
| AU2007319435A1 (en) | 2008-05-22 |
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