JP2004529161A5 - - Google Patents

Download PDF

Info

Publication number
JP2004529161A5
JP2004529161A5 JP2002586869A JP2002586869A JP2004529161A5 JP 2004529161 A5 JP2004529161 A5 JP 2004529161A5 JP 2002586869 A JP2002586869 A JP 2002586869A JP 2002586869 A JP2002586869 A JP 2002586869A JP 2004529161 A5 JP2004529161 A5 JP 2004529161A5
Authority
JP
Japan
Prior art keywords
alkyl
aryl
hydrogen
group
independently
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
Application number
JP2002586869A
Other languages
English (en)
Japanese (ja)
Other versions
JP2004529161A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2002/013856 external-priority patent/WO2002089729A2/en
Publication of JP2004529161A publication Critical patent/JP2004529161A/ja
Publication of JP2004529161A5 publication Critical patent/JP2004529161A5/ja
Pending legal-status Critical Current

Links

JP2002586869A 2001-05-04 2002-05-03 縮合複素環式化合物 Pending JP2004529161A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28866501P 2001-05-04 2001-05-04
PCT/US2002/013856 WO2002089729A2 (en) 2001-05-04 2002-05-03 Fused heterocyclic compounds

Publications (2)

Publication Number Publication Date
JP2004529161A JP2004529161A (ja) 2004-09-24
JP2004529161A5 true JP2004529161A5 (enExample) 2005-12-22

Family

ID=23108101

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002586869A Pending JP2004529161A (ja) 2001-05-04 2002-05-03 縮合複素環式化合物

Country Status (9)

Country Link
US (1) US6858619B2 (enExample)
EP (1) EP1392298B1 (enExample)
JP (1) JP2004529161A (enExample)
AT (1) ATE422887T1 (enExample)
AU (1) AU2002305323A1 (enExample)
CA (1) CA2446351A1 (enExample)
DE (1) DE60231202D1 (enExample)
ES (1) ES2319619T3 (enExample)
WO (1) WO2002089729A2 (enExample)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070135425A1 (en) * 2001-05-04 2007-06-14 Amgen Inc. Fused heterocyclic compounds
US6809104B2 (en) * 2001-05-04 2004-10-26 Tularik Inc. Fused heterocyclic compounds
EP1392298B1 (en) 2001-05-04 2009-02-18 Amgen Inc. Fused heterocyclic compounds
EP1451156A4 (en) * 2001-11-27 2005-05-25 Merck & Co Inc 4-AMINOCHINOLINVERBINDUNGEN
AU2002352878B2 (en) * 2001-11-27 2007-11-22 Merck Sharp & Dohme Corp. 2-Aminoquinoline compounds
US6906075B2 (en) 2002-01-10 2005-06-14 Neurogen Corp. Melanin concentrating hormone receptor ligands: substituted benzoimidazole analogues
JP2005532991A (ja) 2002-01-10 2005-11-04 ニューロジェン・コーポレーション メラニン凝集ホルモン受容体リガンド:置換2−(4−ベンジル−ピペラジン−1−イルメチル)−及び2−(4−ベンジル−ジアゼパン−1−イルメチル)−1h−ベンゾイミダゾールアナログ
MXPA05004739A (es) * 2002-11-06 2005-08-02 Tularik Inc Compuestos heterociclicos fusionados.
US7727998B2 (en) * 2003-02-10 2010-06-01 Banyu Pharmaceutical Co., Ltd. Melanin-concentrating hormone receptor antagonists containing piperidine derivatives as the active ingredient
US7241787B2 (en) 2004-01-25 2007-07-10 Sanofi-Aventis Deutschland Gmbh Substituted N-cycloexylimidazolinones, process for their preparation and their use as medicaments
US7319108B2 (en) 2004-01-25 2008-01-15 Sanofi-Aventis Deutschland Gmbh Aryl-substituted heterocycles, process for their preparation and their use as medicaments
DE102004039789A1 (de) 2004-08-16 2006-03-02 Sanofi-Aventis Deutschland Gmbh Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
CA2623722A1 (en) 2005-09-30 2007-04-12 F. Hoffmann-La Roche Ag Indane derivatives as mch receptor antagonists
TW200800907A (en) 2006-02-15 2008-01-01 Sanofi Aventis Novel aminoalcohol-substituted aryldihydroisoquinolinones, process for their preparation and their use as medicaments
AU2007283113A1 (en) 2006-08-08 2008-02-14 Sanofi-Aventis Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
UY31968A (es) 2008-07-09 2010-01-29 Sanofi Aventis Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
TW201040153A (en) 2009-02-13 2010-11-16 Sanofi Aventis Novel substituted tetrahydronaphthalenes, process for preparation thereof and use thereof as medicaments
AR075401A1 (es) 2009-02-13 2011-03-30 Sanofi Aventis Indanos sustituidos, procesos para su preparacion y uso de los mismos como un medicamento
BR112012003973A2 (pt) 2009-08-26 2015-09-08 Sanofi Sa hidratos de fluoroglicosídeo heteroaromático cristalinos, produtos farmacêuticos compreendendo estes compostos e seu uso
US8575186B2 (en) * 2009-10-05 2013-11-05 Albany Molecular Research, Inc. Epiminocycloalkyl[b] indole derivatives as serotonin sub-type 6 (5-HT6) modulators and uses thereof
WO2012099952A2 (en) 2011-01-19 2012-07-26 Albany Molecular Research, Inc. Benzofuro[3,2-c] pyridines and related analogs as serotonin sub-type 6 (5-ht6) modulators for the treatment of obesity, metabolic syndrome, cognition and schizophrenia
US8710050B2 (en) 2011-03-08 2014-04-29 Sanofi Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8895547B2 (en) 2011-03-08 2014-11-25 Sanofi Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof
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
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
US8809325B2 (en) 2011-03-08 2014-08-19 Sanofi Benzyl-oxathiazine derivatives substituted with adamantane and noradamantane, medicaments containing said compounds and use thereof
EP2683701B1 (de) 2011-03-08 2014-12-24 Sanofi Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120050A1 (de) 2011-03-08 2012-09-13 Sanofi Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung
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
WO2012120053A1 (de) 2011-03-08 2012-09-13 Sanofi Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
JP2015509969A (ja) * 2012-03-16 2015-04-02 グルソックス・バイオテック・アーベー Nox4阻害活性を示すチオフェン−ベースの化合物および療法におけるその使用
JP6274384B2 (ja) * 2012-04-27 2018-02-07 Nok株式会社 メタルガスケット及びその製造方法
WO2020087031A1 (en) 2018-10-26 2020-04-30 The Research Foundation For The State University Of New York Combination serotonin specific reuptake inhibitor and serotonin 1a receptor partial agonist for reducing l-dopa-induced dyskinesia

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2906654B2 (ja) 1989-11-28 1999-06-21 東レ株式会社 免疫抑制剤及びその製造方法
JP3253077B2 (ja) * 1991-07-05 2002-02-04 スミスクライン・ビーチャム・ファーマシューティチ・ソシエタ・ペル・アチオニ ヒドロイソキノリン誘導体
CA2124455C (en) 1992-09-29 2004-09-14 Hiroshi Nagase Indole derivatives, process for producing the same and medicinal uses of the same
US5464841A (en) 1993-11-08 1995-11-07 Univ Minnesota Use of delta opioid receptor antagonists to treat immunoregulatory disorders
US5578725A (en) 1995-01-30 1996-11-26 Regents Of The University Of Minnesota Delta opioid receptor antagonists
AU739367B2 (en) 1997-01-16 2001-10-11 Toray Industries, Inc. Indolomorphinan derivative and agent for curing and preventing cerebral disorder
JP3886030B2 (ja) 1998-10-07 2007-02-28 シャープ株式会社 半導体レーザ素子
GB9822158D0 (en) 1998-10-09 1998-12-02 Nycomed Imaging As Compositions
EP1153932A1 (en) 1999-02-19 2001-11-14 Takeda Chemical Industries, Ltd. Novel g protein-coupled receptor protein and dna thereof
EP1196572A1 (en) 1999-07-27 2002-04-17 Smithkline Beecham Plc Axor21, a g-protein coupled receptor
JP2001226269A (ja) 2000-02-18 2001-08-21 Takeda Chem Ind Ltd メラニン凝集ホルモン拮抗剤
CA2408913A1 (en) 2000-05-16 2001-11-22 Takeda Chemical Industries, Ltd. Melanin-concentrating hormone antagonist
ATE489626T1 (de) 2000-07-05 2010-12-15 Takeda Pharmaceutical Verfahren zum screenen von mhc- rezeptorantagonisten oder -agonisten
WO2002002744A2 (en) 2000-07-05 2002-01-10 Synaptic Pharmaceutical Corporation Dna encoding a human melanin concentrating hormone receptor (mch1) and uses thereof
AU783403B2 (en) 2000-07-05 2005-10-20 H. Lundbeck A/S Selective melanin concentrating hormone-1 (MCH1) receptor antagonists and uses thereof
AU2001279294A1 (en) 2000-07-06 2002-01-21 Neurogen Corporation Melanin concentrating hormone receptor ligands
HUP0301382A2 (hu) 2000-10-20 2003-11-28 Pfizer Products Inc. Alfa-aril-etanol-amin-származékok és e vegyületeket tartalmazó béta-3 adrenergiás receptor agonista hatású gyógyászati készítmények
US20030022891A1 (en) 2000-12-01 2003-01-30 Anandan Palani MCH antagonists and their use in the treatment of obesity
IL155772A0 (en) 2000-12-22 2003-12-23 Schering Corp Piperidine mch antagonists and their use in the treatment of obesity
US6900329B2 (en) 2001-03-21 2005-05-31 Schering Corporation MCH antagonists and their use in the treatment of obesity
NZ527680A (en) 2001-03-21 2005-07-29 Pharmacopeia Drug Discovery Aryl and biaryl compounds having MCH modulatory activity
CA2443672C (en) 2001-04-12 2011-03-29 Pharmacopeia, Inc. Aryl and biaryl piperidines used as mch antagonists
EP1392298B1 (en) 2001-05-04 2009-02-18 Amgen Inc. Fused heterocyclic compounds
EP1389189A2 (en) 2001-05-22 2004-02-18 Neurogen Corporation Melanin concentrating hormone receptor ligands: substituted 1-benzyl-4-aryl piperazine analogues

Similar Documents

Publication Publication Date Title
JP2004529161A5 (enExample)
JP4345230B2 (ja) カルボン酸誘導体およびその誘導体を有効成分として含有する薬剤
JP5697163B2 (ja) 置換された3−ヒドロキシ−4−ピリドン誘導体
CN1534023A (zh) 作为多巴胺-d3配位体的杂环化合物
CN1124269C (zh) 取代的嘧啶化合物和其用途
JP2005508318A5 (enExample)
TW201625536A (zh) 抑制組蛋白去甲基酶之化合物及方法
JP2002520309A5 (enExample)
JP2005508967A5 (enExample)
CN103717593B (zh) 调节激酶的组合物和方法
JP2012236838A5 (enExample)
JP2009524611A5 (ja) S1p1受容体アゴニスト、免疫抑制剤および抗炎症剤としての3,5ージ(アリールまたはヘテロアリール)イソキサゾールおよび1,2,4−オキサジアゾール
TW201024287A (en) New compounds
JP2016505063A (ja) ソルチリン阻害剤としてのn置換された5置換フタルアミド酸
JP2004517813A5 (enExample)
JP2014513131A (ja) 炎症および免疫関連用途のための化合物
CN105143188B (zh) 新型磺酰胺trpa1受体拮抗剂
JP2004517847A5 (enExample)
JP2005536519A5 (enExample)
JPH10287651A5 (enExample)
JP2022539126A (ja) ベンゾジアゼピン系化合物及びその製造方法並びに医薬における作用
JP2009502921A5 (enExample)
RU2004117595A (ru) Производные пиридина в качестве лигандов рецептора nmda
JP2004525178A5 (enExample)
WO2008058448A1 (en) Pyrroline derivatives against cell releasing tumor necrosis factor, preparation methods and uses thereof