JP2009538358A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2009538358A5 JP2009538358A5 JP2009513231A JP2009513231A JP2009538358A5 JP 2009538358 A5 JP2009538358 A5 JP 2009538358A5 JP 2009513231 A JP2009513231 A JP 2009513231A JP 2009513231 A JP2009513231 A JP 2009513231A JP 2009538358 A5 JP2009538358 A5 JP 2009538358A5
- Authority
- JP
- Japan
- Prior art keywords
- oxazol
- piperidin
- methanone
- benzyl
- ylmethyl
- 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- Withdrawn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
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80872306P | 2006-05-26 | 2006-05-26 | |
| PCT/US2007/012631 WO2007140005A2 (en) | 2006-05-26 | 2007-05-25 | Oxazolyl piperidine modulators of fatty acid amide hydrolase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009538358A JP2009538358A (ja) | 2009-11-05 |
| JP2009538358A5 true JP2009538358A5 (https=) | 2010-07-01 |
Family
ID=38779275
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009513231A Withdrawn JP2009538358A (ja) | 2006-05-26 | 2007-05-25 | 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20100292266A1 (https=) |
| EP (1) | EP2023728A4 (https=) |
| JP (1) | JP2009538358A (https=) |
| WO (1) | WO2007140005A2 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2254415B1 (en) | 2008-02-19 | 2013-01-23 | Janssen Pharmaceutica, N.V. | Aryl-hydroxyethylamino-pyrimidines and triazines as modulators of fatty acid amide hydrolase |
| AU2009257795A1 (en) * | 2008-06-11 | 2009-12-17 | Merck Sharp & Dohme Corp. | Pyrazole derivatives useful as inhibitors of FAAH |
| US8906914B2 (en) | 2009-08-18 | 2014-12-09 | Janssen Pharmaceutica Nv | Ethylene diamine modulators of fatty acid hydrolase |
| WO2011085216A2 (en) | 2010-01-08 | 2011-07-14 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating parkinson's disease and restless legs syndrome |
| US20130224151A1 (en) | 2010-03-31 | 2013-08-29 | United States Of America | Use of FAAH Inhibitors for Treating Abdominal, Visceral and Pelvic Pain |
| BR112012023974A2 (pt) * | 2010-04-08 | 2017-09-26 | Merck Sharp & Dohme | composto, composição farmacêutica, método de tratar uma doença mediada com faah, e, uso de um composto. |
| EP2670245B1 (en) * | 2011-02-04 | 2015-09-09 | The Scripps Research Institute | Alpha-ketoheterocycles and methods of making and using |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| JP2017529401A (ja) * | 2014-09-26 | 2017-10-05 | チャーンジョウ インシュヨン ファーマシューティカル カンパニー,リミティド | Ns4b阻害剤としてのベンゾフラン類似体 |
| CN108084130B (zh) * | 2017-12-15 | 2019-09-10 | 东南大学 | 一种降糖药达格列净的制备方法 |
| WO2020179859A1 (ja) | 2019-03-06 | 2020-09-10 | 第一三共株式会社 | ピロロピラゾール誘導体 |
| CN110804048A (zh) * | 2019-11-08 | 2020-02-18 | 暨南大学 | 恶唑酮类化合物及其应用、faah的正电子药物 |
| EP4329881A4 (en) * | 2021-04-30 | 2025-06-11 | Vanqua Bio, Inc. | Small molecule modulators of glucocerebrosidase activity and uses thereof |
| CN115850241B (zh) * | 2021-09-24 | 2025-01-14 | 中国药科大学 | 一种含α-酮骨架的取代杂环类化合物及其用途 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5856537A (en) * | 1996-06-26 | 1999-01-05 | The Scripps Research Institute | Inhibitors of oleamide hydrolase |
| US6462054B1 (en) * | 2000-03-27 | 2002-10-08 | The Scripps Research Institute | Inhibitors of fatty acid amide hydrolase |
| EA010267B1 (ru) * | 2002-10-07 | 2008-06-30 | Те Риджентс Оф Те Юниверсити Оф Калифорния | Модуляция тревоги через блокаду гидролиза анандамида |
| AU2004289303A1 (en) * | 2003-11-10 | 2005-05-26 | Synta Pharmaceuticals, Corp. | Fused heterocyclic compounds |
| WO2006044617A1 (en) * | 2004-10-15 | 2006-04-27 | The Scripps Research Institute | Oxadiazole ketone inhibitors of fatty acid amide hydrolase |
| NZ590148A (en) * | 2004-12-30 | 2012-04-27 | Janssen Pharmaceutica Nv | Piperazinyl and piperidinyl ureas as modulators of fatty acid amide hydrolase |
-
2007
- 2007-05-25 WO PCT/US2007/012631 patent/WO2007140005A2/en not_active Ceased
- 2007-05-25 EP EP07795432A patent/EP2023728A4/en not_active Withdrawn
- 2007-05-25 US US12/227,756 patent/US20100292266A1/en not_active Abandoned
- 2007-05-25 JP JP2009513231A patent/JP2009538358A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2009538358A5 (https=) | ||
| CN103214482B (zh) | 作为受体酪氨酸激酶抑制剂的咪唑并[1,2-a]吡啶化合物 | |
| KR100955967B1 (ko) | 바닐로이드 수용체 길항제 활성이 있는 통증 치료용 우레아-화합물 | |
| CN1034502C (zh) | N-(3-羟基-4-哌啶基)苯并含氧杂环甲酰胺衍生物的制法 | |
| JP4754068B2 (ja) | δ−オピオイドレセプターに結合する4−[アリール(ピペリジン−4−イル)]アミノベンズアミド類 | |
| TWI567068B (zh) | Trk抑制化合物 | |
| CN103974950B (zh) | 作为ccr(4)拮抗剂的取代的苯并咪唑类和苯并吡唑类 | |
| JP2008509982A5 (https=) | ||
| JP2009538358A (ja) | 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター | |
| CN108349936A (zh) | 作为毒蕈碱性受体4(m4)拮抗剂用于治疗神经学疾病的n-[2-(1-苄基哌啶-4-基)乙基]-4-(吡嗪-2-基)-哌嗪-1-甲酰胺衍生物及相关化合物 | |
| JP2006521343A5 (https=) | ||
| JP2005516969A (ja) | メタボトロピックグルタミン酸受容体−5のヘテロアリール置換ピロールモジュレーター | |
| KR20000022214A (ko) | 플루오르화 1,4-이치환 피페리딘 유도체 | |
| HRP20140593T1 (hr) | Derivati 1,3-disupstituiranih imidazolidin-2-ona kao cyp 17-inhibitori | |
| JP2011506480A5 (https=) | ||
| JP2005516986A5 (https=) | ||
| JP2008508352A5 (https=) | ||
| CA2586179A1 (en) | Sulfonyl benzimidazole derivatives | |
| CA2569654A1 (en) | Benzimidazolone carboxylic acid derivatives | |
| WO2004078723A1 (ja) | 4-ピリジルアルキルチオ基を置換基として有する新規化合物 | |
| JP2010511628A5 (https=) | ||
| CZ186698A3 (cs) | Substituované piperidiny, jako antagonisté tachykininu | |
| JP5612080B2 (ja) | 新規なオキサゾリジノン誘導体 | |
| KR20230026418A (ko) | 아릴설포닐 유도체 및 무스카린성 아세틸콜린 수용체 m5 억제제로서의 이의 용도 | |
| WO2010090009A1 (ja) | インドリン誘導体 |