JP2012533630A5 - - Google Patents
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- JP2012533630A5 JP2012533630A5 JP2012521700A JP2012521700A JP2012533630A5 JP 2012533630 A5 JP2012533630 A5 JP 2012533630A5 JP 2012521700 A JP2012521700 A JP 2012521700A JP 2012521700 A JP2012521700 A JP 2012521700A JP 2012533630 A5 JP2012533630 A5 JP 2012533630A5
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- JP
- Japan
- Prior art keywords
- optionally substituted
- pharmaceutically acceptable
- substituted
- acceptable salt
- membered
- Prior art date
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- HZXBVTUZHCBOSI-UHFFFAOYSA-N C(COC1)C1OC1CCCCC1 Chemical compound C(COC1)C1OC1CCCCC1 HZXBVTUZHCBOSI-UHFFFAOYSA-N 0.000 description 2
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- COACHVJQVZURCG-IFSQOONMSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc(nn1)ccc1O)c1c(C(O)=O)[s]c(C#CC2(CCC2)C(F)(F)F)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc(nn1)ccc1O)c1c(C(O)=O)[s]c(C#CC2(CCC2)C(F)(F)F)c1)=O COACHVJQVZURCG-IFSQOONMSA-N 0.000 description 1
- HUEMGDNXEQTFAN-PBCKQTSCSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1c(CN(CC2)CC2N(C)C)ccnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1c(CN(CC2)CC2N(C)C)ccnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O HUEMGDNXEQTFAN-PBCKQTSCSA-N 0.000 description 1
- CDPLEDLRPNRMEH-QWZLJSJVSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1cc(CN(C)C)ccn1)c1c(C(O)=O)[s]c(C#CC2(CC2)C(F)(F)F)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1cc(CN(C)C)ccn1)c1c(C(O)=O)[s]c(C#CC2(CC2)C(F)(F)F)c1)=O CDPLEDLRPNRMEH-QWZLJSJVSA-N 0.000 description 1
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- DWVPQAZEQIOEDS-MUGGOUMZSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1nc(CN2CCOCC2)ccc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1nc(CN2CCOCC2)ccc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O DWVPQAZEQIOEDS-MUGGOUMZSA-N 0.000 description 1
- UUCQLJNFHZYTON-MVBYDDMTSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1nccc(CN(C)C)c1)c1c(C(O)=O)[s]c(C#CC2(CCC2)C(F)(F)F)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1nccc(CN(C)C)c1)c1c(C(O)=O)[s]c(C#CC2(CCC2)C(F)(F)F)c1)=O UUCQLJNFHZYTON-MVBYDDMTSA-N 0.000 description 1
- SXKJFTGLURDMII-CHDDOINTSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1ncncc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Oc1ncncc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O SXKJFTGLURDMII-CHDDOINTSA-N 0.000 description 1
- HWFPVIWQOUDLIC-REODPECZSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1S/C(/NN)=C/N)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1S/C(/NN)=C/N)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O HWFPVIWQOUDLIC-REODPECZSA-N 0.000 description 1
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- OYMKPOCENOJCMQ-KBQPQWKXSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Sc1ccccn1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Sc1ccccn1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O OYMKPOCENOJCMQ-KBQPQWKXSA-N 0.000 description 1
- JCGVRQXBRNGKFH-YSXIEMCBSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Sc1nnc(C)[o]1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@@H]1Sc1nnc(C)[o]1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O JCGVRQXBRNGKFH-YSXIEMCBSA-N 0.000 description 1
- GSRQLELLPZXJEL-AGJYPBCPSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Oc1cccnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Oc1cccnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O GSRQLELLPZXJEL-AGJYPBCPSA-N 0.000 description 1
- HUDMIVJEYSDLFN-SVRSMAFJSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Oc1cncnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Oc1cncnc1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O HUDMIVJEYSDLFN-SVRSMAFJSA-N 0.000 description 1
- HSSVKHZTWZIETE-PVPVSOICSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Sc1ncc[s]1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CC1)CC[C@H]1Sc1ncc[s]1)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O HSSVKHZTWZIETE-PVPVSOICSA-N 0.000 description 1
- HYGZCHJAYASXHA-YDHSSHFGSA-N C[C@H](CC1)CC[C@@H]1C(N([C@H](CCOc1ccccn1)OC1=O)c2c1[s]c(C#CC(C)(C)C)c2)=O Chemical compound C[C@H](CC1)CC[C@@H]1C(N([C@H](CCOc1ccccn1)OC1=O)c2c1[s]c(C#CC(C)(C)C)c2)=O HYGZCHJAYASXHA-YDHSSHFGSA-N 0.000 description 1
- ICVBBGCKGONZJH-HDJSIYSDSA-N C[C@H](CC1)CC[C@@H]1[IH](N(C)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O Chemical compound C[C@H](CC1)CC[C@@H]1[IH](N(C)c1c(C(O)=O)[s]c(C#CC(C)(C)C)c1)=O ICVBBGCKGONZJH-HDJSIYSDSA-N 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22736709P | 2009-07-21 | 2009-07-21 | |
| US61/227,367 | 2009-07-21 | ||
| US24091109P | 2009-09-09 | 2009-09-09 | |
| US61/240,911 | 2009-09-09 | ||
| US35946610P | 2010-06-29 | 2010-06-29 | |
| US61/359,466 | 2010-06-29 | ||
| PCT/US2010/042394 WO2011011303A1 (en) | 2009-07-21 | 2010-07-19 | Inhibitors of flaviviridae viruses |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015160807A Division JP2015205940A (ja) | 2009-07-21 | 2015-08-18 | フラビウイルス科ウイルスの阻害剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012533630A JP2012533630A (ja) | 2012-12-27 |
| JP2012533630A5 true JP2012533630A5 (enExample) | 2015-02-26 |
| JP5841531B2 JP5841531B2 (ja) | 2016-01-13 |
Family
ID=42711860
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012521700A Expired - Fee Related JP5841531B2 (ja) | 2009-07-21 | 2010-07-19 | フラビウイルス科ウイルスの阻害剤 |
| JP2015160807A Withdrawn JP2015205940A (ja) | 2009-07-21 | 2015-08-18 | フラビウイルス科ウイルスの阻害剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015160807A Withdrawn JP2015205940A (ja) | 2009-07-21 | 2015-08-18 | フラビウイルス科ウイルスの阻害剤 |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US8569302B2 (enExample) |
| EP (1) | EP2475657B1 (enExample) |
| JP (2) | JP5841531B2 (enExample) |
| KR (1) | KR20120051022A (enExample) |
| CN (1) | CN102471327A (enExample) |
| AP (1) | AP3409A (enExample) |
| AR (1) | AR077765A1 (enExample) |
| AU (1) | AU2010276441B2 (enExample) |
| CA (1) | CA2767088C (enExample) |
| CL (1) | CL2012000147A1 (enExample) |
| CO (1) | CO6491049A2 (enExample) |
| CR (1) | CR20120081A (enExample) |
| DK (1) | DK2475657T3 (enExample) |
| EA (1) | EA020816B1 (enExample) |
| EC (1) | ECSP12011684A (enExample) |
| ES (1) | ES2427342T3 (enExample) |
| IL (1) | IL217243A (enExample) |
| MX (1) | MX2012000959A (enExample) |
| NZ (1) | NZ597528A (enExample) |
| PE (1) | PE20120666A1 (enExample) |
| SG (1) | SG177709A1 (enExample) |
| TW (1) | TW201116525A (enExample) |
| UY (1) | UY32793A (enExample) |
| WO (1) | WO2011011303A1 (enExample) |
| ZA (1) | ZA201200940B (enExample) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20120666A1 (es) * | 2009-07-21 | 2012-06-01 | Gilead Sciences Inc | Inhibidores de los virus flaviviridae |
| US8501714B2 (en) | 2009-09-09 | 2013-08-06 | Gilead Sciences, Inc. | Inhibitors of Flaviviridae viruses |
| DK2480559T3 (da) | 2009-09-21 | 2013-08-05 | Gilead Sciences Inc | Fremgangsmåder og mellemprodukter til fremstillingen af 1'-cyano-carbanukleosid-analoger |
| WO2011088303A1 (en) * | 2010-01-15 | 2011-07-21 | Gilead Sciences , Inc. | Inhibitors of flaviviridae viruses |
| JP5868872B2 (ja) | 2010-01-15 | 2016-02-24 | ギリアード サイエンシーズ， インコーポレイテッド | フラビウイルス科ウイルスのインヒビター |
| AU2011276526A1 (en) * | 2010-06-28 | 2013-01-10 | Vertex Pharmaceuticals Incorporated | Compounds and methods for the treatment or prevention of Flavivirus infections |
| EA201300160A1 (ru) | 2010-07-22 | 2013-06-28 | Новартис Аг | 2,3,5-тризамещенные тиофены и их применение |
| MA34470B1 (fr) | 2010-07-22 | 2013-08-01 | Gilead Sciences Inc | Procédés et composés pour traiter des infections à virus paramyxoviridae |
| US8741946B2 (en) | 2011-07-13 | 2014-06-03 | Gilead Sciences, Inc. | Inhibitors of flaviviridae viruses |
| PL2864291T3 (pl) | 2012-06-26 | 2017-07-31 | Bayer Pharma Aktiengesellschaft | N-[4-(chinolin-4-yloksy)cykloheksylo(metylo)](hetero)arylokarboksyamidy jako antagoniści receptora androgenowego, ich wytwarzanie i zastosowanie jako produktów medycznych |
| US8927741B2 (en) | 2012-08-17 | 2015-01-06 | Gilead Sciences, Inc. | Synthesis of an antiviral compound |
| US8841340B2 (en) | 2012-08-17 | 2014-09-23 | Gilead Sciences, Inc. | Solid forms of an antiviral compound |
| US8759544B2 (en) | 2012-08-17 | 2014-06-24 | Gilead Sciences, Inc. | Synthesis of an antiviral compound |
| CN102964295B (zh) * | 2012-12-17 | 2014-08-20 | 寿光富康制药有限公司 | 一种2-取代-4-（哌啶基甲基）吡啶的制备方法 |
| EP2762124A1 (en) * | 2013-01-31 | 2014-08-06 | IP Gesellschaft für Management mbH | Packaging comprising administration units of polymorphs, amorphous forms or solvates |
| US9492438B2 (en) * | 2014-07-25 | 2016-11-15 | Bette Pollard | Amphiphilic pyridinum compounds to treat epilepsy and other disorders of the nervous system |
| TWI767201B (zh) | 2014-10-29 | 2022-06-11 | 美商基利科學股份有限公司 | 絲狀病毒科病毒感染之治療 |
| CN118286245A (zh) | 2014-12-26 | 2024-07-05 | 埃莫里大学 | N4-羟基胞苷和衍生物及与其相关的抗病毒用途 |
| MX394858B (es) | 2015-09-16 | 2025-03-24 | Gilead Sciences Inc | Compuestos de formula i para usarse en el tratamiento de infecciones por virus arenaviridae y coronaviridae |
| EP4483875A3 (en) | 2016-05-10 | 2025-04-02 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
| EP4491236A3 (en) | 2016-05-10 | 2025-04-02 | C4 Therapeutics, Inc. | Heterocyclic degronimers for target protein degradation |
| WO2017197046A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | C3-carbon linked glutarimide degronimers for target protein degradation |
| CN109790143A (zh) | 2016-05-10 | 2019-05-21 | C4医药公司 | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 |
| HRP20220479T1 (hr) | 2016-06-01 | 2022-05-27 | Athira Pharma, Inc. | Spojevi |
| CA3056072C (en) | 2017-03-14 | 2022-08-23 | Gilead Sciences, Inc. | Methods of treating feline coronavirus infections |
| KR20190141747A (ko) | 2017-05-01 | 2019-12-24 | 길리애드 사이언시즈, 인코포레이티드 | (S)-2-에틸부틸 2-(((S)-(((2R,3S,4R,5R)-5-(4-아미노피롤로[2,1-f] [1,2,4]트리아진-7-일)-5-시아노-3,4-디히드록시테트라히드로푸란-2-일)메톡시)(페녹시) 포스포릴)아미노)프로파노에이트의 결정질 형태 |
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