JP2008525513A5 - - Google Patents

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Publication number
JP2008525513A5
JP2008525513A5 JP2007548747A JP2007548747A JP2008525513A5 JP 2008525513 A5 JP2008525513 A5 JP 2008525513A5 JP 2007548747 A JP2007548747 A JP 2007548747A JP 2007548747 A JP2007548747 A JP 2007548747A JP 2008525513 A5 JP2008525513 A5 JP 2008525513A5
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JP
Japan
Prior art keywords
substituted
unsubstituted
compound
formula
pharmaceutical composition
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
JP2007548747A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008525513A (ja
Filing date
Publication date
Priority claimed from EP04380279A external-priority patent/EP1676844A1/en
Application filed filed Critical
Publication of JP2008525513A publication Critical patent/JP2008525513A/ja
Publication of JP2008525513A5 publication Critical patent/JP2008525513A5/ja
Pending legal-status Critical Current

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JP2007548747A 2004-12-28 2005-12-27 5−ht7受容体拮抗薬 Pending JP2008525513A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04380279A EP1676844A1 (en) 2004-12-28 2004-12-28 5-HT7 receptor antagonists
US11/048,992 US7345057B2 (en) 2004-12-28 2005-02-02 5-HT7 receptor antagonists
PCT/EP2005/014046 WO2006069776A1 (en) 2004-12-28 2005-12-27 5-ht7 receptor antagonists

Publications (2)

Publication Number Publication Date
JP2008525513A JP2008525513A (ja) 2008-07-17
JP2008525513A5 true JP2008525513A5 (enExample) 2009-02-12

Family

ID=34931894

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007548747A Pending JP2008525513A (ja) 2004-12-28 2005-12-27 5−ht7受容体拮抗薬

Country Status (11)

Country Link
US (1) US7345057B2 (enExample)
EP (2) EP1676844A1 (enExample)
JP (1) JP2008525513A (enExample)
KR (1) KR20070091040A (enExample)
CN (1) CN101090898A (enExample)
AU (1) AU2005321463A1 (enExample)
BR (1) BRPI0519792A2 (enExample)
CA (1) CA2590666A1 (enExample)
MX (1) MX2007007894A (enExample)
RU (1) RU2007128926A (enExample)
WO (1) WO2006069776A1 (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060063766A1 (en) 2004-07-15 2006-03-23 Molino Bruce F Use of aryl- and heteroaryl-substituted tetrahydroisoquinolines to block reuptake of norepinephrine, dopamine, and serotonin
WO2008064329A1 (en) * 2006-11-21 2008-05-29 University Of Tennessee Research Foundation Therapeutic tetrahydroisoquinoline-based compositions for cancer therapy
WO2008141020A1 (en) * 2007-05-11 2008-11-20 Eli Lilly And Company 2-[4-(pyrazol-4-ylalkyl)piperazin-1-yl]-3-phenyl pyrazines and pyridines and 3-[4-(pyrazol-4-ylalkyl)piperazin-1-yl]-2-phenyl pyridines as 5-ht7 receptor antagonists
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
US8809538B2 (en) 2009-01-12 2014-08-19 Array Biopharma Inc. Piperidine-containing compounds and use thereof
US8815894B2 (en) * 2009-05-12 2014-08-26 Bristol-Myers Squibb Company Crystalline forms of (S)-7-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline and use thereof
PE20120373A1 (es) * 2009-05-12 2012-05-17 Albany Molecular Res Inc 7-([1,2,4]triazolo[1,5-a]piridin-6-il)-4-(3,4-diclorofenil)-1,2,3,4-tetrahidroisoquinolina
JP2012526823A (ja) * 2009-05-12 2012-11-01 アルバニー モレキュラー リサーチ, インコーポレイテッド アリール、ヘテロアリール、および複素環置換テトラヒドロイソキノリンならびにそれらの使用
GB201209587D0 (en) * 2012-05-30 2012-07-11 Takeda Pharmaceutical Therapeutic compounds
EA029430B1 (ru) * 2013-06-21 2018-03-30 Такеда Фармасьютикл Компани Лимитед Производные 1-сульфонилпиперидина в качестве модуляторов рецепторов прокинетицина
GB201420095D0 (en) * 2014-11-12 2014-12-24 Takeda Pharmaceutical New use
EP3589626B1 (en) * 2017-03-03 2024-06-12 National Taiwan University 8-phenyl-isoquinolines and pharmaceutical composition thereof used in the treatment of irritable bowel syndrome
WO2018165520A1 (en) 2017-03-10 2018-09-13 Vps-3, Inc. Metalloenzyme inhibitor compounds
CN112083107B (zh) * 2020-09-28 2022-07-05 中国计量科学研究院 检测蜂蜜基质中磺胺类药物葡萄糖醛酸结合物的方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ193654A (en) 1979-05-16 1984-08-24 Wuelfing Johann A Naphthalene sulphonamido-alkyl-piperidines,pyrrolidines or piperazines and pharmaceutical compositions
DE3276313D1 (en) 1981-09-24 1987-06-19 Beecham Wuelfing Gmbh & Co Kg Sulphonamides
JP2000504677A (ja) 1996-02-09 2000-04-18 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー 5ht7レセプター・アンタゴニスト用のスルホンアミド誘導体
GB9612884D0 (en) 1996-06-20 1996-08-21 Smithkline Beecham Plc Novel compounds
EP0912550A1 (en) * 1996-06-25 1999-05-06 Smithkline Beecham Plc Sulfonamide derivatives as 5ht7 receptor antagonists
AU1558899A (en) 1997-11-10 1999-05-31 F. Hoffmann-La Roche Ag Isoquinoline derivatives for use against cns disorders
AU4698299A (en) * 1998-06-30 2000-01-17 Du Pont Pharmaceuticals Company 5-HT7 receptor antagonists
GB0128885D0 (en) 2001-12-03 2002-01-23 Merck Sharp & Dohme Therapeutic agents

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