JP2009538358A5 - - Google Patents

Download PDF

Info

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Withdrawn
Application number
JP2009513231A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009538358A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/012631 external-priority patent/WO2007140005A2/en
Publication of JP2009538358A publication Critical patent/JP2009538358A/ja
Publication of JP2009538358A5 publication Critical patent/JP2009538358A5/ja
Withdrawn legal-status Critical Current

Links

JP2009513231A 2006-05-26 2007-05-25 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター Withdrawn JP2009538358A (ja)

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JP2009513231A Withdrawn JP2009538358A (ja) 2006-05-26 2007-05-25 脂肪酸アミド加水分解酵素のオキサゾリルピペリジン・モジュレーター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)

* Cited by examiner, † Cited by third party
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
CA2714743C (en) 2008-02-19 2017-01-17 Janssen Pharmaceutica N.V. Aryl-hydroxyethylamino-pyrimidines and triazines as modulators of fatty acid amide hydrolase
EP2299824B1 (en) * 2008-06-11 2013-06-19 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
WO2011123719A2 (en) 2010-03-31 2011-10-06 Ironwood Pharmaceuticals, Inc. Use of faah inhibitors for treating abdominal, visceral and pelvic pain
JP2013523814A (ja) * 2010-04-08 2013-06-17 メルク・シャープ・エンド・ドーム・コーポレイション Faahの調節薬として有用なオキサゾール誘導体
EP2670245B1 (en) * 2011-02-04 2015-09-09 The Scripps Research Institute Alpha-ketoheterocycles and methods of making and using
US8828995B2 (en) 2011-03-08 2014-09-09 Sanofi Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
EP2683705B1 (de) 2011-03-08 2015-04-22 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8871758B2 (en) 2011-03-08 2014-10-28 Sanofi Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
WO2012120052A1 (de) 2011-03-08 2012-09-13 Sanofi Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung
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
WO2016045587A1 (zh) * 2014-09-26 2016-03-31 常州寅盛药业有限公司 作为ns4b抑制剂的苯并呋喃类似物
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)

* Cited by examiner, † Cited by third party
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
EP1558591B1 (en) * 2002-10-07 2014-05-07 The Regents of The University of California Modulation of anxiety through blockade of anandamide hydrolysis
AU2004289303A1 (en) * 2003-11-10 2005-05-26 Synta Pharmaceuticals, Corp. Fused heterocyclic compounds
US7351724B2 (en) * 2004-10-15 2008-04-01 The Scripps Research Institute Oxadiazole ketone inhibitors of fatty acid amide hydrolase
AR055831A1 (es) * 2004-12-30 2007-09-12 Janssen Pharmaceutica Nv Pepirazinilureas y piperidinilureas como moduladores de hidrolasa de amida de acidos grasos

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
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=)
JP2008503585A5 (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