JP2008501649A5 - - Google Patents

Download PDF

Info

Publication number
JP2008501649A5
JP2008501649A5 JP2007513783A JP2007513783A JP2008501649A5 JP 2008501649 A5 JP2008501649 A5 JP 2008501649A5 JP 2007513783 A JP2007513783 A JP 2007513783A JP 2007513783 A JP2007513783 A JP 2007513783A JP 2008501649 A5 JP2008501649 A5 JP 2008501649A5
Authority
JP
Japan
Prior art keywords
group
compound
formula
lower alkyl
alkyl group
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.)
Granted
Application number
JP2007513783A
Other languages
English (en)
Japanese (ja)
Other versions
JP4594386B2 (ja
JP2008501649A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2005/005594 external-priority patent/WO2005117865A1/en
Publication of JP2008501649A publication Critical patent/JP2008501649A/ja
Publication of JP2008501649A5 publication Critical patent/JP2008501649A5/ja
Application granted granted Critical
Publication of JP4594386B2 publication Critical patent/JP4594386B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2007513783A 2004-06-02 2005-05-24 ヒスタミン3受容体のリガンドとして有用なナフタレン誘導体 Expired - Fee Related JP4594386B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04102460 2004-06-02
PCT/EP2005/005594 WO2005117865A1 (en) 2004-06-02 2005-05-24 Naphthaline derivatives useful as histamine-3-receptor ligands

Publications (3)

Publication Number Publication Date
JP2008501649A JP2008501649A (ja) 2008-01-24
JP2008501649A5 true JP2008501649A5 (enExample) 2010-09-24
JP4594386B2 JP4594386B2 (ja) 2010-12-08

Family

ID=34982058

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007513783A Expired - Fee Related JP4594386B2 (ja) 2004-06-02 2005-05-24 ヒスタミン3受容体のリガンドとして有用なナフタレン誘導体

Country Status (24)

Country Link
US (2) US7259158B2 (enExample)
EP (1) EP1755593B1 (enExample)
JP (1) JP4594386B2 (enExample)
KR (1) KR100854212B1 (enExample)
CN (1) CN1960727B (enExample)
AR (1) AR049433A1 (enExample)
AT (1) ATE383857T1 (enExample)
AU (1) AU2005249196B2 (enExample)
BR (1) BRPI0511778A (enExample)
CA (1) CA2566526C (enExample)
DE (1) DE602005004404T2 (enExample)
DK (1) DK1755593T3 (enExample)
ES (1) ES2299074T3 (enExample)
IL (1) IL179370A (enExample)
MX (1) MXPA06014017A (enExample)
MY (1) MY139704A (enExample)
NO (1) NO20065733L (enExample)
NZ (1) NZ550764A (enExample)
PL (1) PL1755593T3 (enExample)
PT (1) PT1755593E (enExample)
RU (1) RU2387638C2 (enExample)
TW (1) TWI299992B (enExample)
WO (1) WO2005117865A1 (enExample)
ZA (1) ZA200609678B (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007097149A1 (ja) 2006-02-20 2007-08-30 Konica Minolta Holdings, Inc. 有機エレクトロルミネッセンス素子、白色発光素子、表示装置、及び照明装置
EP2079694B1 (en) 2006-12-28 2017-03-01 Rigel Pharmaceuticals, Inc. N-substituted-heterocycloalkyloxybenzamide compounds and methods of use
JP5698887B2 (ja) 2007-05-03 2015-04-08 セファロン、インク. (r)−2−メチルピロリジンおよび(s)−2−メチルピロリジンならびにその酒石酸塩を調製するための方法
KR101573091B1 (ko) 2007-11-16 2015-11-30 리겔 파마슈티칼스, 인크. 대사성 장애를 위한 카르복스아미드, 술폰아미드 및 아민 화합물
CA2707047C (en) 2007-12-12 2017-11-28 Rigel Pharmaceuticals, Inc. Carboxamide, sulfonamide and amine compounds for metabolic disorders
CA2722139C (en) 2008-04-23 2017-04-11 Rigel Pharmaceuticals, Inc. Carboxamide compounds for the treatment of metabolic disorders
EP2569280B1 (en) 2010-05-11 2015-02-25 Sanofi Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof
WO2011143145A1 (en) 2010-05-11 2011-11-17 Sanofi Substituted n-alkyl and n-acyl tetrahydro-isoquinoline derivatives, preparation and therapeutic use thereof
EP2569294B1 (en) 2010-05-11 2015-03-11 Sanofi Substituted n-heteroaryl bipyrrolidine carboxamides, preparation and therapeutic use thereof
TW201206444A (en) 2010-05-11 2012-02-16 Sanofi Aventis Substituted N-heteroaryl tetrahydro-isoquinoline derivatives, preparation and therapeutic use thereof
TW201202251A (en) 2010-05-11 2012-01-16 Sanofi Aventis Substituted N-heteroaryl spirolactam bipyrrolidines, preparation and therapeutic use thereof
JP2013529198A (ja) 2010-05-11 2013-07-18 サノフイ 置換されたn−ヘテロシクロアルキルビピロリジニルフェニルアミド誘導体、その製造及び治療上の使用
KR101408699B1 (ko) 2012-02-29 2014-06-19 중앙대학교 산학협력단 지르코늄 선택적 형광 프루브
TWI631097B (zh) * 2012-07-27 2018-08-01 百健Ma公司 作爲s1p調節劑及/或atx調節劑之化合物
ES2684995T3 (es) 2012-07-27 2018-10-05 Biogen Ma Inc. Derivados del ácido 2-(1-(1-(6-((ciclohexil)oxi)-5-(trifluorometil)naftalen-2-il)etil)piperidin-3-il)acético como moduladores de la autotaxina (atx) para el tratamiento de inflamaciones y trastornos autoinmunes
PL2888243T3 (pl) * 2012-08-23 2017-01-31 Suven Life Sciences Limited Związki akryloamidowe jako ligandy receptora histaminowego H3
CN117229207B (zh) * 2023-09-01 2024-09-03 浙江工业大学 一种苯基萘类化合物及其制备与应用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19621483A1 (de) * 1996-05-29 1997-12-04 Hoechst Ag Substituierte 2-Naphthoylguanidine, Verfahren zur ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
CN1159292C (zh) * 1996-05-31 2004-07-28 法玛西雅厄普约翰美国公司 用作选择性多巴胺d3配体的芳基取代的环胺类化合物
AU2002254114A1 (en) * 2001-03-23 2002-10-08 Eli Lilly And Company Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic uses
GB0224557D0 (en) * 2002-10-22 2002-11-27 Glaxo Group Ltd Novel compounds
EP1569637A1 (en) * 2002-11-12 2005-09-07 Abbott Laboratories Bicyclic-substituted amines as histamine-3 receptor ligands
ATE517882T1 (de) * 2004-10-19 2011-08-15 Hoffmann La Roche Chinolinderivate

Similar Documents

Publication Publication Date Title
JP2008501649A5 (enExample)
JP2007500753A5 (enExample)
RU2011129383A (ru) Производное амина, обладающее антагостической активностью в отношении рецептора npy y5
WO2008006043A3 (en) 1,3-oxazole derivatives useful as anti-atherosclerotic, anti-dyslipidemic, anti-diabetic and anti-obesity agents
JP2005514410A5 (enExample)
JP2005523310A5 (enExample)
JP2009541415A5 (enExample)
EA201000395A1 (ru) Фунгицидные производные 2-алкилтио-2-хинолинилоксиацетамида
EP2085388A4 (en) NEW 1,2-DIHYDROCHINOLINE DERIVATIVE WITH SUBSTITUTED PHENYLAMINOENE ALKYL GROUP AND PHENYL GROUP INTRODUCED BY AN ESTER AS SUBSTITUENTS
HUS1500006I1 (hu) Benzotiazol-származék vegyületek, kompozíciók és alkalmazások
JP2010520851A5 (enExample)
JP2008519084A5 (enExample)
HRP20080529T3 (en) Amide prodrug of gemcitabine, compositions and use thereof
JP2004535380A5 (enExample)
NO20061317L (no) Imidazopyridinderivater som induserbare NO-syntaseinhibatorer
JP2009075520A5 (enExample)
SG151306A1 (en) Novel benzothiazoles and the use thereof as medicaments
HRP20080447T3 (en) 7-(2-(4-(3-trifluoromethyl-phenyl)-1,2,3,6-tetrahydro-pyrid-1-yl)ethyl) isoquinoline besylate salt, preparation and therapeutic use thereof
JP2008501844A5 (enExample)
JP2003504349A5 (enExample)
WO2008072079A3 (en) Processes for the preparation of 3-(4-(2,4-difluorobenzyloxy)-3-bromo-6-methyl-2-oxopyridin-1(2h)-yl)-n,4-dimethylbenzamide
DK1613594T3 (da) 4-(2-Phenylsulfanyl-phenyl)-1,2,3,6-tetrahydropyridin derivater som serotonin-genoptagelseshæmmere
JP2011057638A5 (enExample)
WO2008099076A3 (fr) Derives de n-(4-cyano-l h-p yrazol-3 -yl)methylamine substitues, leur preparation et leur application en therapeutique
NO20061316L (no) Imidazopyndinderivater som induserbare NO-syntaseinhibitorer