JP2012513410A - 抗ウイルス化合物 - Google Patents
抗ウイルス化合物 Download PDFInfo
- Publication number
- JP2012513410A JP2012513410A JP2011542571A JP2011542571A JP2012513410A JP 2012513410 A JP2012513410 A JP 2012513410A JP 2011542571 A JP2011542571 A JP 2011542571A JP 2011542571 A JP2011542571 A JP 2011542571A JP 2012513410 A JP2012513410 A JP 2012513410A
- Authority
- JP
- Japan
- Prior art keywords
- independently
- carbocyclyl
- optionally
- substituted
- alkyl
- 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 Cc1c(C)[n](*)nc1** Chemical compound Cc1c(C)[n](*)nc1** 0.000 description 32
- QHPXWANZCGLXDU-UHFFFAOYSA-N CC(C)(C)c1cc2nccc(NC)c2cc1 Chemical compound CC(C)(C)c1cc2nccc(NC)c2cc1 QHPXWANZCGLXDU-UHFFFAOYSA-N 0.000 description 1
- CDHNVHUCZGPVBO-UHFFFAOYSA-N CC(C)(C)c1nc2nccc(C)c2cc1 Chemical compound CC(C)(C)c1nc2nccc(C)c2cc1 CDHNVHUCZGPVBO-UHFFFAOYSA-N 0.000 description 1
- NFWFQBSKLXUWTI-UHFFFAOYSA-N CC(C)(C)c1nc2ncnc(NC)c2cc1 Chemical compound CC(C)(C)c1nc2ncnc(NC)c2cc1 NFWFQBSKLXUWTI-UHFFFAOYSA-N 0.000 description 1
- PLTZWKQRPKTANB-UHFFFAOYSA-N CC(C)(C)c1nc2ncnc(NC)c2cn1 Chemical compound CC(C)(C)c1nc2ncnc(NC)c2cn1 PLTZWKQRPKTANB-UHFFFAOYSA-N 0.000 description 1
- DJCOVAGGOSVPJN-UHFFFAOYSA-N CC(C)(c1nc2ncnc(NC)c2cc1)O Chemical compound CC(C)(c1nc2ncnc(NC)c2cc1)O DJCOVAGGOSVPJN-UHFFFAOYSA-N 0.000 description 1
- QDLFUTKJZIQPSG-RMKNXTFCSA-N CC(C)C(N/C(/NC)=C/C(/NC)=N\C)=O Chemical compound CC(C)C(N/C(/NC)=C/C(/NC)=N\C)=O QDLFUTKJZIQPSG-RMKNXTFCSA-N 0.000 description 1
- OBNCYYSRQWEGJV-UHFFFAOYSA-N CC(C)CC(c1cc(NC)ccn1)O Chemical compound CC(C)CC(c1cc(NC)ccn1)O OBNCYYSRQWEGJV-UHFFFAOYSA-N 0.000 description 1
- YUPNCQQBTVHPGC-UHFFFAOYSA-N CC(C)CC(c1cc(NC)ccn1)OC Chemical compound CC(C)CC(c1cc(NC)ccn1)OC YUPNCQQBTVHPGC-UHFFFAOYSA-N 0.000 description 1
- WLQLIAZPFDTONL-UHFFFAOYSA-N CC(C)CC(c1cc(NC)ncn1)N(C)C Chemical compound CC(C)CC(c1cc(NC)ncn1)N(C)C WLQLIAZPFDTONL-UHFFFAOYSA-N 0.000 description 1
- QDWXYILXZJPRLB-UHFFFAOYSA-N CC(C)CC(c1cc(NC)ncn1)O Chemical compound CC(C)CC(c1cc(NC)ncn1)O QDWXYILXZJPRLB-UHFFFAOYSA-N 0.000 description 1
- ZZPUTVJMXAKIMS-UHFFFAOYSA-N CC(C)c(cc1)nc2c1c(Nc(cc(cc1)C(NCCNC(c(cc3)cc(Nc4c(ccc(C(C)C)n5)c5ncn4)c3Sc(cc3)ccc3N)=O)=O)c1Sc(cc1)ccc1N)ncn2 Chemical compound CC(C)c(cc1)nc2c1c(Nc(cc(cc1)C(NCCNC(c(cc3)cc(Nc4c(ccc(C(C)C)n5)c5ncn4)c3Sc(cc3)ccc3N)=O)=O)c1Sc(cc1)ccc1N)ncn2 ZZPUTVJMXAKIMS-UHFFFAOYSA-N 0.000 description 1
- ANRJALPWXQIIRQ-UHFFFAOYSA-N CC(C)c(cc1)nc2c1c(Nc1cc(C(O)=O)ccc1)ncn2 Chemical compound CC(C)c(cc1)nc2c1c(Nc1cc(C(O)=O)ccc1)ncn2 ANRJALPWXQIIRQ-UHFFFAOYSA-N 0.000 description 1
- SCVMPMMTUDBWRM-UHFFFAOYSA-N CC(C)c1nc2ncnc(Nc3cc(-c(cc4)ccc4-c(cc4)cc(Nc5ncnc6c5ccc(C(C)C)n6)c4Sc(cc4)ccc4N)ccc3Sc(cc3)ccc3N)c2cc1 Chemical compound CC(C)c1nc2ncnc(Nc3cc(-c(cc4)ccc4-c(cc4)cc(Nc5ncnc6c5ccc(C(C)C)n6)c4Sc(cc4)ccc4N)ccc3Sc(cc3)ccc3N)c2cc1 SCVMPMMTUDBWRM-UHFFFAOYSA-N 0.000 description 1
- AQYVANGEPZMAAM-UHFFFAOYSA-N CC(c1nc2ncnc(NC)c2cc1)OC Chemical compound CC(c1nc2ncnc(NC)c2cc1)OC AQYVANGEPZMAAM-UHFFFAOYSA-N 0.000 description 1
- QBGXVJOEJVDPDR-UHFFFAOYSA-N CCc(cc1)cc2c1c(NC)ccn2 Chemical compound CCc(cc1)cc2c1c(NC)ccn2 QBGXVJOEJVDPDR-UHFFFAOYSA-N 0.000 description 1
- HBEOOHNYVPFGGU-UHFFFAOYSA-N CCc1nc2nccc([NH-])c2cc1 Chemical compound CCc1nc2nccc([NH-])c2cc1 HBEOOHNYVPFGGU-UHFFFAOYSA-N 0.000 description 1
- LBSNCVUWSRRLDH-UHFFFAOYSA-N CCc1nc2ncnc(C)c2cc1 Chemical compound CCc1nc2ncnc(C)c2cc1 LBSNCVUWSRRLDH-UHFFFAOYSA-N 0.000 description 1
- ASBQFCFHZYTYLC-UHFFFAOYSA-N CCc1nc2ncnc(NC)c2cn1 Chemical compound CCc1nc2ncnc(NC)c2cn1 ASBQFCFHZYTYLC-UHFFFAOYSA-N 0.000 description 1
- RXYPXQSKLGGKOL-UHFFFAOYSA-N CN1CCN(C)CC1 Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 1
- JLKXIRVGILUMEX-UHFFFAOYSA-N CNc1c(ccc(-c2ccc[o]2)c2)c2ncc1 Chemical compound CNc1c(ccc(-c2ccc[o]2)c2)c2ncc1 JLKXIRVGILUMEX-UHFFFAOYSA-N 0.000 description 1
- POEVSVZFPWRRHJ-UHFFFAOYSA-N CNc1c(ccc(COC)n2)c2ncc1 Chemical compound CNc1c(ccc(COC)n2)c2ncc1 POEVSVZFPWRRHJ-UHFFFAOYSA-N 0.000 description 1
- VSKARIKWTFETIN-UHFFFAOYSA-N CNc1c(cnc(-c2ccc[o]2)n2)c2ncn1 Chemical compound CNc1c(cnc(-c2ccc[o]2)n2)c2ncn1 VSKARIKWTFETIN-UHFFFAOYSA-N 0.000 description 1
- JFVUQKOTPOLWAZ-UHFFFAOYSA-N CNc1c(cncn2)c2ncn1 Chemical compound CNc1c(cncn2)c2ncn1 JFVUQKOTPOLWAZ-UHFFFAOYSA-N 0.000 description 1
- BDKKLUHVIRLKHO-UHFFFAOYSA-N CNc1ccnc2c1cccn2 Chemical compound CNc1ccnc2c1cccn2 BDKKLUHVIRLKHO-UHFFFAOYSA-N 0.000 description 1
- BZKSAWDBBGWYNF-UHFFFAOYSA-N CNc1ccnc2ccccc12 Chemical compound CNc1ccnc2ccccc12 BZKSAWDBBGWYNF-UHFFFAOYSA-N 0.000 description 1
- UDERBCRIPZAQNT-UHFFFAOYSA-N CNc1ncnc2ncccc12 Chemical compound CNc1ncnc2ncccc12 UDERBCRIPZAQNT-UHFFFAOYSA-N 0.000 description 1
- LOMBYWOEYMBBGZ-UHFFFAOYSA-N Cc(cc1)cc2c1c(C)ccn2 Chemical compound Cc(cc1)cc2c1c(C)ccn2 LOMBYWOEYMBBGZ-UHFFFAOYSA-N 0.000 description 1
- DAAZAERHRIADTM-UHFFFAOYSA-N Cc(cc1)nc2c1c(NC)ccn2 Chemical compound Cc(cc1)nc2c1c(NC)ccn2 DAAZAERHRIADTM-UHFFFAOYSA-N 0.000 description 1
- QMFZFVXMMRVHKA-UHFFFAOYSA-N Cc1ccc(c(NC)ncn2)c2n1 Chemical compound Cc1ccc(c(NC)ncn2)c2n1 QMFZFVXMMRVHKA-UHFFFAOYSA-N 0.000 description 1
- LCBFCYZASVKFAQ-UHFFFAOYSA-N Cc1ccc2c(NC)nccc2n1 Chemical compound Cc1ccc2c(NC)nccc2n1 LCBFCYZASVKFAQ-UHFFFAOYSA-N 0.000 description 1
- YHLYUNYJHHPISM-UHFFFAOYSA-N Cc1ncc(c(NC)ncn2)c2n1 Chemical compound Cc1ncc(c(NC)ncn2)c2n1 YHLYUNYJHHPISM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14031808P | 2008-12-23 | 2008-12-23 | |
| US61/140,318 | 2008-12-23 | ||
| PCT/US2009/069188 WO2010075380A1 (en) | 2008-12-23 | 2009-12-22 | Anti-viral compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012513410A true JP2012513410A (ja) | 2012-06-14 |
| JP2012513410A5 JP2012513410A5 (https=) | 2013-02-14 |
Family
ID=42167446
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011542571A Pending JP2012513410A (ja) | 2008-12-23 | 2009-12-22 | 抗ウイルス化合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8546405B2 (https=) |
| EP (1) | EP2367823A1 (https=) |
| JP (1) | JP2012513410A (https=) |
| CN (1) | CN102245604A (https=) |
| CA (1) | CA2740195A1 (https=) |
| MX (1) | MX2011006333A (https=) |
| RU (1) | RU2505539C2 (https=) |
| SG (1) | SG172353A1 (https=) |
| WO (1) | WO2010075380A1 (https=) |
| ZA (1) | ZA201105356B (https=) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2367823A1 (en) | 2008-12-23 | 2011-09-28 | Abbott Laboratories | Anti-viral compounds |
| CA2740193A1 (en) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Anti-viral compounds |
| CN102459165B (zh) * | 2009-04-15 | 2015-09-02 | Abbvie公司 | 抗病毒化合物 |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| 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 |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | Abbvie Inc. | Anti-viral compounds |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| MX2013004655A (es) | 2010-10-26 | 2013-08-27 | Presidio Pharmaceuticals Inc | Inhibidores del virus de la hepatitis c. |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| CN103917536B (zh) | 2011-10-03 | 2016-07-06 | 瑞斯比维特有限公司 | 1-吡唑基-3-(4-((2-(苯氨基)嘧啶-4-基)氧基)萘-1-基)脲用作p38 MAP激酶抑制剂 |
| EP2578582A1 (en) | 2011-10-03 | 2013-04-10 | Respivert Limited | 1-Pyrazolyl-3-(4-((2-anilinopyrimidin-4-yl)oxy)napththalen-1-yl)ureas as p38 MAP kinase inhibitors |
| US9034832B2 (en) | 2011-12-29 | 2015-05-19 | Abbvie Inc. | Solid compositions |
| GB201214750D0 (en) | 2012-08-17 | 2012-10-03 | Respivert Ltd | Compounds |
| GB201215357D0 (en) | 2012-08-29 | 2012-10-10 | Respivert Ltd | Compounds |
| US11484534B2 (en) | 2013-03-14 | 2022-11-01 | Abbvie Inc. | Methods for treating HCV |
| EP2970190A1 (en) | 2013-03-14 | 2016-01-20 | Respivert Limited | Kinase inhibitors |
| JP6223563B2 (ja) | 2013-10-14 | 2017-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 選択的に置換されたキノリン化合物 |
| CN105636945B (zh) | 2013-10-14 | 2017-11-17 | 卫材R&D管理有限公司 | 选择性取代的喹啉化合物 |
| EP3076968B1 (en) | 2013-12-02 | 2019-04-17 | ChemoCentryx, Inc. | Ccr6 compounds |
| EP3089757A1 (en) | 2014-01-03 | 2016-11-09 | AbbVie Inc. | Solid antiviral dosage forms |
| JO3589B1 (ar) | 2014-08-06 | 2020-07-05 | Novartis Ag | مثبطات كيناز البروتين c وطرق استخداماتها |
| KR20200087273A (ko) | 2014-10-24 | 2020-07-20 | 란도스 바이오파마, 인크. | 란티오닌 합성효소 c-유사 2-계 치료제 |
| CN110494432B (zh) | 2016-12-28 | 2022-08-12 | 米尼奥尔克斯治疗有限公司 | 异喹啉化合物,其制备方法及其在与β-半乳糖苷酶活性改变相关的病症中的治疗用途 |
| BR122023024273A2 (pt) | 2018-02-27 | 2024-02-20 | Incyte Corporation | Compostos imidazopirimidinas e triazolopirimidinas, seus usos, método para inibir uma atividade de um receptor de adenosina e composição farmacêutica dos mesmos |
| WO2019222677A1 (en) | 2018-05-18 | 2019-11-21 | Incyte Corporation | Fused pyrimidine derivatives as a2a / a2b inhibitors |
| GEP20237548B (en) | 2018-07-05 | 2023-10-10 | Incyte Corp | Fused pyrazine derivatives as a2a /a2b inhibitors |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶 |
| BR112022002387A2 (pt) | 2019-12-20 | 2022-09-06 | Landos Biopharma Inc | Composto da fórmula z-y-q-y' ou um sal ou éster farmaceuticamente aceitável do mesmo |
| US12234578B2 (en) | 2020-01-29 | 2025-02-25 | Wisconsin Alumni Research Foundation | Tannin composite fibers |
| WO2021257863A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Pyrrolotriazine compounds as jak2 v617f inhibitors |
| WO2021257857A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Naphthyridinone compounds as jak2 v617f inhibitors |
| SMT202500271T1 (it) | 2020-07-02 | 2025-09-12 | Incyte Corp | Composti di urea triciclici come inibitori di v617f di jak2 |
| US11767323B2 (en) | 2020-07-02 | 2023-09-26 | Incyte Corporation | Tricyclic pyridone compounds as JAK2 V617F inhibitors |
| US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| WO2022140231A1 (en) | 2020-12-21 | 2022-06-30 | Incyte Corporation | Deazaguaine compounds as jak2 v617f inhibitors |
| AR125273A1 (es) | 2021-02-25 | 2023-07-05 | Incyte Corp | Lactamas espirocíclicas como inhibidores de jak2 v617f |
| CN119173514A (zh) | 2022-03-17 | 2024-12-20 | 因赛特公司 | 作为jak2 v617f抑制剂的三环脲化合物 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005531638A (ja) * | 2002-07-01 | 2005-10-20 | ファルマシア・アンド・アップジョン・カンパニー・エルエルシー | Hcvns5bポリメラーゼ阻害剤 |
| WO2007076034A2 (en) * | 2005-12-21 | 2007-07-05 | Abbott Laboratories | Anti-viral compounds |
| WO2007076035A2 (en) * | 2005-12-21 | 2007-07-05 | Abbott Laboratories | Anti-viral compounds |
| WO2007081517A2 (en) * | 2005-12-21 | 2007-07-19 | Abbott Laboratories | Anti-viral compounds |
| JP2008508296A (ja) * | 2004-07-27 | 2008-03-21 | ギリアード サイエンシーズ, インコーポレイテッド | イミダゾ[4,5−d]ピリミジン、それらの使用および調製方法 |
| WO2008064218A2 (en) * | 2006-11-21 | 2008-05-29 | Smithkline Beecham Corporation | Amido anti-viral compounds |
| JP2008528564A (ja) * | 2005-01-31 | 2008-07-31 | アロウ セラピューティクス リミテッド | 抗ウイルス剤としてのキナゾリン誘導体 |
| WO2008133753A2 (en) * | 2006-12-20 | 2008-11-06 | Abbott Laboratories | Anti-viral compounds |
| WO2008144463A1 (en) * | 2007-05-18 | 2008-11-27 | Smithkline Beecham Corporation | Quinoline derivatives as pi3 kinase inhibitors |
Family Cites Families (171)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE75755C (de) * | 1894-06-14 | DAHL & COMP, in Barmen | Verfahren zur Darstellung von aromatisch substituirten Amidodinaphtylmethanen. | |
| WO1994027627A1 (en) | 1993-05-24 | 1994-12-08 | Smithkline Beecham Corporation | Hemoregulatory peptides |
| US6037157A (en) | 1995-06-29 | 2000-03-14 | Abbott Laboratories | Method for improving pharmacokinetics |
| US5935982A (en) * | 1997-02-28 | 1999-08-10 | The University Of North Carolina At Chapel Hill | Methods of treating retroviral infection and compounds useful therefor |
| US6235493B1 (en) * | 1997-08-06 | 2001-05-22 | The Regents Of The University Of California | Amino acid substituted-cresyl violet, synthetic fluorogenic substrates for the analysis of agents in individual in vivo cells or tissue |
| CZ289425B6 (cs) | 1998-05-20 | 2002-01-16 | Eli Lilly And Company | Imidazo[1,2-a] pyridinové sloučeniny, jejich pouľití a farmaceutický přípravek s jejich obsahem |
| US6911462B2 (en) | 1998-05-22 | 2005-06-28 | Avanir Pharmaceuticals | Benzimidazole compounds for regulating IgE |
| US6369091B1 (en) * | 1998-05-22 | 2002-04-09 | Avanir Pharmaceuticals | Benzimidazole analogs as down-regulators of IgE |
| US6919366B2 (en) | 1998-05-22 | 2005-07-19 | Avanir Pharmaceuticals | Benzimidazole derivatives as modulators of IgE |
| RU2236220C2 (ru) | 1998-05-22 | 2004-09-20 | Аванир Фармасьютикэлз | Аналоги бензимидазола в качестве понижающих регуляторов ige |
| US6387885B1 (en) | 1998-08-26 | 2002-05-14 | Abbott Laboratories | 3′,3′-N-bis-desmethyl-3′-N-cycloalkyl erythromycin derivatives as LHRH antagonists |
| WO2001046196A1 (en) | 1999-12-21 | 2001-06-28 | Sugen, Inc. | 4-substituted 7-aza-indolin-2-ones and their use as protein kinase inhibitors |
| HK1052509B (en) | 2000-08-14 | 2007-09-07 | Ortho-Mcneil Pharmaceutical, Inc. | Substituted pyrazole |
| EP1341788B1 (en) * | 2000-12-15 | 2005-08-10 | Glaxo Group Limited | Pyrazolopyridines |
| JP4169246B2 (ja) * | 2001-03-16 | 2008-10-22 | 富士フイルム株式会社 | ヘテロ環化合物及びそれを用いた発光素子 |
| CN101624391A (zh) * | 2001-06-11 | 2010-01-13 | 病毒化学医药公司 | 用作黄病毒感染抗病毒剂的噻吩衍生物 |
| EP2335700A1 (en) * | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Hepatitis C virus polymerase inhibitors with a heterobicylic structure |
| RU2286343C2 (ru) | 2001-08-10 | 2006-10-27 | Орто-Макнейл Фармасьютикал, Инк. | Замещенные пиразолы |
| MY151199A (en) | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
| TW200304820A (en) | 2002-03-25 | 2003-10-16 | Avanir Pharmaceuticals | Use of benzimidazole analogs in the treatment of cell proliferation |
| JP3925265B2 (ja) | 2002-03-25 | 2007-06-06 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子及びそれを用いた表示装置 |
| MXPA04012642A (es) | 2002-06-14 | 2005-03-23 | Merck & Co Inc | Inhibidores de la cinesina mitotica. |
| CA2491895C (en) | 2002-07-09 | 2011-01-18 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
| WO2004014852A2 (en) | 2002-08-12 | 2004-02-19 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of hcv replication |
| US7208490B2 (en) * | 2002-10-07 | 2007-04-24 | Pharmacia & Upjohn Company Llc | Tricyclic tetrahydroquinoline antibacterial agents |
| GB0229518D0 (en) | 2002-12-19 | 2003-01-22 | Astrazeneca Ab | Chemical compounds |
| TW200508224A (en) * | 2003-02-12 | 2005-03-01 | Bristol Myers Squibb Co | Cyclic derivatives as modulators of chemokine receptor activity |
| US7132426B2 (en) | 2003-07-14 | 2006-11-07 | Arena Pharmaceuticals, Inc. | Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
| CA2534649A1 (en) | 2003-08-01 | 2005-02-10 | Genelabs Technologies, Inc. | Bicyclic imidazol derivatives against flaviviridae |
| WO2005026129A1 (en) | 2003-09-15 | 2005-03-24 | Gpc Biotech Ag | Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases |
| CA2543696A1 (en) | 2003-10-27 | 2005-05-12 | Vertex Pharmaceuticals Incorporated | Combinations for hcv treatment |
| CA2545422C (en) | 2003-12-03 | 2015-06-02 | Cytopia Research Pty Ltd | Tubulin inhibitors |
| EP1765332A2 (en) | 2004-06-17 | 2007-03-28 | Cengent Therapeutics, Inc. | Trisubstituted nitrogen modulators of tyrosine phosphatases |
| US7772271B2 (en) | 2004-07-14 | 2010-08-10 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| MX2007001661A (es) | 2004-08-13 | 2007-04-23 | Praecis Pharm Inc | Metodos y composiciones para modular la actividad del receptor de esfingosina -1 fosfato (sip). |
| CN101146793A (zh) * | 2005-02-16 | 2008-03-19 | 先灵公司 | 具有cxcr3拮抗剂活性的新的杂环取代了的吡啶或苯基化合物 |
| WO2006093867A1 (en) | 2005-02-28 | 2006-09-08 | The Rockefeller University | Structure of the hepatitits c virus ns5a protein |
| US20060235036A1 (en) | 2005-04-15 | 2006-10-19 | Doherty Elizabeth M | Vanilloid receptor ligands and their use in treatments |
| US8143288B2 (en) | 2005-06-06 | 2012-03-27 | Bristol-Myers Squibb Company | Inhibitors of HCV replication |
| PE20070099A1 (es) | 2005-06-30 | 2007-02-06 | Janssen Pharmaceutica Nv | N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso |
| JP2009501217A (ja) | 2005-07-15 | 2009-01-15 | アストラゼネカ アクチボラグ | 治療薬 |
| BRPI0619733A2 (pt) | 2005-12-12 | 2011-10-11 | Genelabs Tech Inc | compostos antivirais de n-(anel aromático de 6 membros)-amido |
| BRPI0619730A2 (pt) | 2005-12-12 | 2011-10-11 | Genelabs Tech Inc | compostos antivirais de n-(anel aromático de 5 membros)-amido |
| CA2634699A1 (en) | 2005-12-21 | 2007-06-28 | Decode Genetics Ehf | N-linked aryl heteroaryl inhibitors of lta4h for treating inflammation |
| WO2007082554A1 (en) | 2006-01-23 | 2007-07-26 | Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa | Modulators of hcv replication |
| AU2007250443B2 (en) | 2006-05-16 | 2013-06-13 | Pharmascience Inc. | IAP BIR domain binding compounds |
| MX2008015662A (es) | 2006-06-08 | 2009-01-12 | Lilly Co Eli | Nuevos receptores antagonistas de la hormona concentradora de melanina (mch). |
| ES2392104T3 (es) | 2006-06-16 | 2012-12-04 | Syngenta Participations Ag | Derivados de carboxamida etenílica útiles como microbiocidas |
| US20100056495A1 (en) | 2006-07-24 | 2010-03-04 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
| WO2008014238A2 (en) | 2006-07-24 | 2008-01-31 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
| US8303944B2 (en) | 2006-08-11 | 2012-11-06 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8329159B2 (en) | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7659270B2 (en) * | 2006-08-11 | 2010-02-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7759495B2 (en) * | 2006-08-11 | 2010-07-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US20100158862A1 (en) | 2006-08-11 | 2010-06-24 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US7745636B2 (en) * | 2006-08-11 | 2010-06-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| PE20080906A1 (es) | 2006-08-17 | 2008-07-05 | Kemia Inc | Derivados heteroarilo como inhibidores de citocina |
| US20100055071A1 (en) * | 2006-11-21 | 2010-03-04 | Martin Robert Leivers | Anti-Viral Compounds |
| WO2008074450A2 (en) | 2006-12-20 | 2008-06-26 | Nicox S.A. | Non-peptidic renin inhibitors nitroderivatives |
| JP5454943B2 (ja) | 2007-04-12 | 2014-03-26 | ジョイアント ファーマスーティカルズ、インク. | 抗癌剤として有用なsmac模倣二量体及び三量体 |
| US7741347B2 (en) | 2007-05-17 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| CL2008001631A1 (es) | 2007-06-06 | 2009-01-02 | Smithkline Beecham Corp | Compuestos derivados de heterociclos sustituidos, con la presencia de un grupo fenoxi, inhibidores de transcriptasa inversa; composicion farmaceutica; y uso en el tratamiento de infecciones virales por vih. |
| WO2009003009A1 (en) | 2007-06-26 | 2008-12-31 | Enanta Pharmaceuticals, Inc. | Substituted pyrrolidine as anti-infectives |
| EP2185154A2 (en) | 2007-08-03 | 2010-05-19 | Schering Corporation | Method of treating cxcr3 mediated diseases using heterocyclic substituted piperazines |
| 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 |
| US20090047247A1 (en) | 2007-08-13 | 2009-02-19 | Yao-Ling Qiu | Pyrrolidine Derivatives |
| GB0801199D0 (en) | 2008-01-23 | 2008-02-27 | Acal Energy Ltd | Fuel cells |
| JP5581219B2 (ja) | 2008-01-25 | 2014-08-27 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | チオフェンおよびホスファチジルイノシトール3−キナーゼ(pi3k)阻害薬としてのその使用 |
| JP2011511841A (ja) | 2008-02-12 | 2011-04-14 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎ウイルス阻害剤 |
| ATE551337T1 (de) | 2008-02-12 | 2012-04-15 | Bristol Myers Squibb Co | Inhibitoren des hepatitis-c-virus |
| US8147818B2 (en) | 2008-02-13 | 2012-04-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7704992B2 (en) | 2008-02-13 | 2010-04-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| HRP20120706T1 (hr) | 2008-02-13 | 2012-09-30 | Bristol-Myers Squibb Company | Imidazolil bifenil imidazoli kao inhibitori virusa hepatitisa c |
| US8034966B1 (en) * | 2008-02-20 | 2011-10-11 | Cell Viable Corporation | Phenoxyisobutyric acid compounds and methods for synthesis |
| WO2009136290A1 (en) | 2008-05-05 | 2009-11-12 | Aegera Therapeutics, Inc. | Functionalized pyrrolidines and use thereof as iap inhibitors |
| WO2009143361A1 (en) | 2008-05-22 | 2009-11-26 | Smithkline Beecham Corporation | Amido anti-viral compounds |
| WO2009155709A1 (en) | 2008-06-27 | 2009-12-30 | Aegera Therapeutics Inc. | Bridged secondary amines and use thereof as iap bir domain binding compounds |
| US20100068197A1 (en) * | 2008-07-11 | 2010-03-18 | Myriad Pharmaceuticals, Inc. | Pharmaceutical compounds as inhibitors of cell proliferation and the use thereof |
| US7906655B2 (en) | 2008-08-07 | 2011-03-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2010015090A1 (en) | 2008-08-07 | 2010-02-11 | Aegera Therapeutics Inc. | Functionalized pyrrolidines and use thereof as iap inhibitors |
| US8383094B2 (en) | 2008-10-01 | 2013-02-26 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8946289B2 (en) | 2008-11-19 | 2015-02-03 | Duke University | Manassatin compounds and methods of making and using the same |
| JP2010126571A (ja) | 2008-11-26 | 2010-06-10 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子材料および有機エレクトロルミネッセンス素子 |
| US8729077B2 (en) | 2008-11-28 | 2014-05-20 | Glaxosmithkline Llc | Anti-viral compounds, compositions, and methods of use |
| WO2010065668A1 (en) | 2008-12-03 | 2010-06-10 | Presidio Pharmaceuticals, Inc. | Inhibitors of hcv ns5a |
| SI2373172T1 (sl) | 2008-12-03 | 2013-12-31 | Presidio Pharmaceuticals, Inc. | Inhibitorji HCV NS5A |
| EP2367823A1 (en) | 2008-12-23 | 2011-09-28 | Abbott Laboratories | Anti-viral compounds |
| CA2740193A1 (en) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Anti-viral compounds |
| US8314135B2 (en) | 2009-02-09 | 2012-11-20 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole antivirals |
| EP2393359A4 (en) | 2009-02-09 | 2012-10-03 | Enanta Pharm Inc | COMPOUND DIBENZIMIDAZOLE DERIVATIVES |
| US8420686B2 (en) | 2009-02-17 | 2013-04-16 | Enanta Pharmaceuticals, Inc. | Linked diimidazole antivirals |
| US8394968B2 (en) | 2009-02-17 | 2013-03-12 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8188132B2 (en) | 2009-02-17 | 2012-05-29 | Enanta Pharmaceuticals, Inc. | Linked dibenzimidazole derivatives |
| WO2010096462A1 (en) | 2009-02-17 | 2010-08-26 | Enanta Pharmaceuticals, Inc | Linked diimidazole derivatives |
| US8242156B2 (en) | 2009-02-17 | 2012-08-14 | 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 |
| US8637561B2 (en) | 2009-02-17 | 2014-01-28 | Enanta Pharmaceuticals, Inc. | Linked diimidazole derivatives |
| WO2010094977A1 (en) | 2009-02-23 | 2010-08-26 | Arrow Therapeutics Limited | Novel biphenyl compounds useful for the treatment of hepatitis c |
| WO2010096777A1 (en) | 2009-02-23 | 2010-08-26 | Presidio Pharmaceuticals, Inc. | Inhibitors of hcv ns5a |
| US8426458B2 (en) | 2009-02-27 | 2013-04-23 | Enanta Pharmaceuticals, Inc. | Hepatitis C Virus inhibitors |
| KR101411889B1 (ko) | 2009-02-27 | 2014-06-27 | 이난타 파마슈티칼스, 인코포레이티드 | C형 간염 바이러스 억제제 |
| US8101643B2 (en) | 2009-02-27 | 2012-01-24 | Enanta Pharmaceuticals, Inc. | Benzimidazole derivatives |
| US8507522B2 (en) | 2009-03-06 | 2013-08-13 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| SG174929A1 (en) | 2009-03-27 | 2011-11-28 | Merck Sharp & Dohme | Inhibitors of hepatitis c virus replication |
| WO2010111673A1 (en) | 2009-03-27 | 2010-09-30 | Presidio Pharmaceuticals, Inc. | Substituted bicyclic hcv inhibitors |
| SG174883A1 (en) | 2009-03-27 | 2011-11-28 | Presidio Pharmaceuticals Inc | Fused ring inhibitors of hepatitis c |
| US20110237636A1 (en) | 2009-03-30 | 2011-09-29 | Bristol-Myers Squibb Company | Hepatitis C Virus Inhibitors |
| US8796466B2 (en) | 2009-03-30 | 2014-08-05 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| TWI476190B (zh) | 2009-03-30 | 2015-03-11 | 必治妥美雅史谷比公司 | C型肝炎病毒抑制劑 |
| WO2010115767A1 (en) | 2009-04-08 | 2010-10-14 | Basf Se | Pyrrolopyrrole derivatives, their manufacture and use as semiconductors |
| 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 |
| RU2528231C2 (ru) | 2009-04-24 | 2014-09-10 | Тиботек Фармасьютикалз | Диариловые эфиры |
| 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 |
| US8211928B2 (en) | 2009-05-29 | 2012-07-03 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8138215B2 (en) | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| 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 |
| 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 |
| US9394279B2 (en) | 2009-06-11 | 2016-07-19 | Abbvie Inc. | Anti-viral compounds |
| UA118080C2 (uk) | 2009-06-11 | 2018-11-26 | Еббві Айрленд Анлімітед Компані | Противірусні сполуки |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| WO2010148006A1 (en) | 2009-06-16 | 2010-12-23 | Enanta Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| 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 |
| WO2011004276A1 (en) | 2009-07-06 | 2011-01-13 | Pfizer Limited | Hepatitis c virus inhibitors |
| IN2012DN00999A (https=) | 2009-07-16 | 2015-04-10 | Vertex Pharma | |
| CN102471324B (zh) | 2009-08-07 | 2014-12-17 | 泰博特克药品公司 | 作为丙型肝炎病毒抑制剂的双苯并咪唑衍生物 |
| CN102482260A (zh) | 2009-09-03 | 2012-05-30 | 泰博特克药品公司 | 双-苯并咪唑衍生物 |
| EA201290089A1 (ru) | 2009-09-04 | 2012-09-28 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Химические соединения |
| WO2011031904A1 (en) | 2009-09-11 | 2011-03-17 | Enanta Pharmaceuticals, Inc | Hepatitis c virus inhibitors |
| US8927709B2 (en) | 2009-09-11 | 2015-01-06 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| US8759332B2 (en) | 2009-09-11 | 2014-06-24 | Enanta Pharmaceuticals, Inc. | Hepatitis C virus inhibitors |
| EP2475254A4 (en) | 2009-09-11 | 2013-05-22 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| US8815928B2 (en) | 2009-09-11 | 2014-08-26 | 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 |
| WO2011050146A1 (en) | 2009-10-23 | 2011-04-28 | Glaxosmithkline Llc | Chemical compounds |
| UA108211C2 (uk) | 2009-11-04 | 2015-04-10 | Янссен Рід Айрленд | Бензімідазолімідазольні похідні |
| 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 |
| 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 |
| EP2507232B1 (en) | 2009-12-04 | 2019-03-20 | National Health Research Institutes | Proline derivatives |
| 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 |
| 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 |
| KR20120118008A (ko) | 2009-12-18 | 2012-10-25 | 아이데닉스 파마슈티칼스, 인코포레이티드 | 5,5-융합 아릴렌 또는 헤테로아릴렌 간염 c 바이러스 억제제 |
| 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 |
| WO2011079327A1 (en) | 2009-12-24 | 2011-06-30 | Vertex Pharmaceuticals Incorporated | Analogues for the treatment or prevention of flavivirus infections |
| US8362020B2 (en) | 2009-12-30 | 2013-01-29 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2011091446A1 (en) | 2010-01-22 | 2011-07-28 | Glaxosmithkline Llc | Chemical compounds |
| MA34013B1 (fr) | 2010-01-25 | 2013-02-01 | Enanta Pharm Inc | Inhibiteurs du virus de l'hépatite c |
| WO2011091532A1 (en) | 2010-01-28 | 2011-08-04 | Boehringer Ingelheim International Gmbh | Hepatitis c inhibitor compounds |
| 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 |
| WO2011119858A1 (en) | 2010-03-24 | 2011-09-29 | Vertex Pharmaceuticals Incorporated | Analogues for the treatment or prevention of flavivirus infections |
| CN103038237A (zh) | 2010-03-24 | 2013-04-10 | 沃泰克斯药物股份有限公司 | 用于黄病毒感染治疗或预防的类似物 |
| TW201141857A (en) | 2010-03-24 | 2011-12-01 | Vertex Pharma | Analogues for the treatment or prevention of flavivirus infections |
| EP2555622A4 (en) | 2010-04-09 | 2013-09-18 | Enanta Pharm Inc | HEPATITIS C-VIRUS HEMMER |
| US20110312996A1 (en) | 2010-05-17 | 2011-12-22 | Intermune, Inc. | Novel inhibitors of hepatitis c virus replication |
| WO2011150243A1 (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 |
| EP2580209A4 (en) | 2010-06-09 | 2013-11-06 | Presidio Pharmaceuticals Inc | INHIBITORS OF HCV NS5A PROTEIN |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| MX2013006828A (es) | 2010-12-16 | 2014-10-14 | Abbvie Inc | Compuestos antivirales. |
| MX2013006951A (es) | 2010-12-16 | 2013-10-03 | Abbvie Inc | Compuestos antivirales. |
-
2009
- 2009-12-22 EP EP09795662A patent/EP2367823A1/en not_active Withdrawn
- 2009-12-22 MX MX2011006333A patent/MX2011006333A/es active IP Right Grant
- 2009-12-22 CA CA2740195A patent/CA2740195A1/en not_active Abandoned
- 2009-12-22 SG SG2011046257A patent/SG172353A1/en unknown
- 2009-12-22 JP JP2011542571A patent/JP2012513410A/ja active Pending
- 2009-12-22 US US12/644,432 patent/US8546405B2/en active Active
- 2009-12-22 CN CN2009801499565A patent/CN102245604A/zh active Pending
- 2009-12-22 RU RU2011130831/04A patent/RU2505539C2/ru not_active IP Right Cessation
- 2009-12-22 WO PCT/US2009/069188 patent/WO2010075380A1/en not_active Ceased
-
2011
- 2011-07-20 ZA ZA2011/05356A patent/ZA201105356B/en unknown
-
2013
- 2013-09-04 US US14/017,901 patent/US9249138B2/en active Active
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005531638A (ja) * | 2002-07-01 | 2005-10-20 | ファルマシア・アンド・アップジョン・カンパニー・エルエルシー | Hcvns5bポリメラーゼ阻害剤 |
| JP2008508296A (ja) * | 2004-07-27 | 2008-03-21 | ギリアード サイエンシーズ, インコーポレイテッド | イミダゾ[4,5−d]ピリミジン、それらの使用および調製方法 |
| JP2008528564A (ja) * | 2005-01-31 | 2008-07-31 | アロウ セラピューティクス リミテッド | 抗ウイルス剤としてのキナゾリン誘導体 |
| WO2007076034A2 (en) * | 2005-12-21 | 2007-07-05 | Abbott Laboratories | Anti-viral compounds |
| WO2007076035A2 (en) * | 2005-12-21 | 2007-07-05 | Abbott Laboratories | Anti-viral compounds |
| WO2007081517A2 (en) * | 2005-12-21 | 2007-07-19 | Abbott Laboratories | Anti-viral compounds |
| WO2008064218A2 (en) * | 2006-11-21 | 2008-05-29 | Smithkline Beecham Corporation | Amido anti-viral compounds |
| WO2008133753A2 (en) * | 2006-12-20 | 2008-11-06 | Abbott Laboratories | Anti-viral compounds |
| WO2008144463A1 (en) * | 2007-05-18 | 2008-11-27 | Smithkline Beecham Corporation | Quinoline derivatives as pi3 kinase inhibitors |
Non-Patent Citations (4)
| Title |
|---|
| JPN6014010288; Takagi,S. et al.: 'Antimicrobial agents from Bletilla striata' Phytochemistry Vol.22, Issue 4, 1983, p.1011-1015 * |
| JPN6014010290; Sawyer,J.S. et al.: 'Synthetic and Structure/Activity Studies on Acid-Substituted 2-Arylphenols: Discovery of 2-[2-Propyl' Journal of Medicinal Chemistry Vol.38, Issue 22, 1995, p.4411-4432 * |
| JPN6014010291; Smith,D.C. et al.: 'Reissert compound chemistry. XXVI. The syntheses of bis-benzylisoquinolines' Journal of Heterocyclic Chemistry Vol.13, Issue 3, 1976, p.573-576 * |
| JPN6014010293; Liu, Y. et al.: 'Discovery of a Novel CCR5 Antagonist Lead Compound Through Fragment Assembly' Molecules Vol.13, Issue 10, 2008, p.2426-2441 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2740195A1 (en) | 2010-07-01 |
| RU2505539C2 (ru) | 2014-01-27 |
| US9249138B2 (en) | 2016-02-02 |
| US20140213595A1 (en) | 2014-07-31 |
| MX2011006333A (es) | 2011-06-27 |
| WO2010075380A1 (en) | 2010-07-01 |
| EP2367823A1 (en) | 2011-09-28 |
| CN102245604A (zh) | 2011-11-16 |
| ZA201105356B (en) | 2012-03-28 |
| RU2011130831A (ru) | 2013-01-27 |
| SG172353A1 (en) | 2011-07-28 |
| US20100160355A1 (en) | 2010-06-24 |
| US8546405B2 (en) | 2013-10-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2505539C2 (ru) | Антивирусные соединения | |
| EP2367824B1 (en) | Anti-viral derivatives of pyrimidine | |
| JP5906253B2 (ja) | 抗ウイルス性化合物 | |
| US9394279B2 (en) | Anti-viral compounds | |
| US8232246B2 (en) | Anti-viral compounds | |
| US20120115918A1 (en) | Anti-Viral Compounds | |
| US20100267634A1 (en) | Anti-Viral Compounds | |
| MX2011005673A (es) | Compuestos anti-virales para tratar infeccion por vhc. | |
| US20140364616A1 (en) | Anti-viral compounds | |
| US20150105548A1 (en) | Anti-viral compounds | |
| HK1159619B (en) | Anti-viral derivatives of pyrimidine | |
| JP6038179B2 (ja) | Hcvプロテアーゼ阻害剤の製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121221 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20121221 |
|
| A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20130701 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130822 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140306 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140311 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140605 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140612 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140911 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150224 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150518 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20151027 |