JP2008504267A5 - - Google Patents

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Publication number
JP2008504267A5
JP2008504267A5 JP2007518190A JP2007518190A JP2008504267A5 JP 2008504267 A5 JP2008504267 A5 JP 2008504267A5 JP 2007518190 A JP2007518190 A JP 2007518190A JP 2007518190 A JP2007518190 A JP 2007518190A JP 2008504267 A5 JP2008504267 A5 JP 2008504267A5
Authority
JP
Japan
Prior art keywords
compound
indol
alkyl
sulfonyl
optionally substituted
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Withdrawn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
JP2007518190A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008504267A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/021852 external-priority patent/WO2006002125A1/en
Publication of JP2008504267A publication Critical patent/JP2008504267A/ja
Publication of JP2008504267A5 publication Critical patent/JP2008504267A5/ja
Withdrawn legal-status Critical Current

Links

JP2007518190A 2004-06-23 2005-06-21 5−ヒドロキシトリプタミン−6配位子としてのインドリルアルキルアミン代謝物 Withdrawn JP2008504267A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58229004P 2004-06-23 2004-06-23
PCT/US2005/021852 WO2006002125A1 (en) 2004-06-23 2005-06-21 Indolylalkylamine metabolites as 5-hydroxytrytamine-6 ligands

Publications (2)

Publication Number Publication Date
JP2008504267A JP2008504267A (ja) 2008-02-14
JP2008504267A5 true JP2008504267A5 (enExample) 2008-07-24

Family

ID=35033547

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007518190A Withdrawn JP2008504267A (ja) 2004-06-23 2005-06-21 5−ヒドロキシトリプタミン−6配位子としてのインドリルアルキルアミン代謝物

Country Status (19)

Country Link
US (1) US7498327B2 (enExample)
EP (1) EP1758898A1 (enExample)
JP (1) JP2008504267A (enExample)
KR (1) KR20070041514A (enExample)
CN (1) CN1976928A (enExample)
AR (1) AR049449A1 (enExample)
AU (1) AU2005258025A1 (enExample)
BR (1) BRPI0512540A (enExample)
CA (1) CA2570818A1 (enExample)
CR (1) CR8825A (enExample)
EC (1) ECSP067096A (enExample)
IL (1) IL180198A0 (enExample)
MX (1) MX2007000182A (enExample)
NO (1) NO20070065L (enExample)
PA (1) PA8637801A1 (enExample)
PE (1) PE20060303A1 (enExample)
RU (1) RU2006146923A (enExample)
TW (1) TW200606148A (enExample)
WO (1) WO2006002125A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7635710B2 (en) 2006-02-15 2009-12-22 Neurim Pharmaceuticals (1991) Ltd. Pyrone-indole derivatives and process for their preparation
US9101613B2 (en) 2006-02-15 2015-08-11 Neurim Pharmaceuticals (1991) Ltd. Methods for treating neurological disease
EP1953153A1 (en) * 2007-01-31 2008-08-06 Laboratorios del Dr. Esteve S.A. Heterocyclyl-substituted sulfonamides for the treatment of cognitive or food ingestion related disorders
EP2053052A1 (en) 2007-10-23 2009-04-29 Laboratorios del Dr. Esteve S.A. Process for the preparation of 6-substituted imidazo[2,1-b]thiazole-5-sulfonyl halide
WO2015090233A1 (en) 2013-12-20 2015-06-25 Sunshine Lake Pharma Co., Ltd. Aromatic heterocyclic compounds and their application in pharmaceuticals

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3489767A (en) * 1966-01-12 1970-01-13 Sumitomo Chemical Co 1-(phenylsulfonyl)-3-indolyl aliphatic acid derivatives
GB9820113D0 (en) * 1998-09-15 1998-11-11 Merck Sharp & Dohme Therapeutic agents
US6380166B1 (en) * 1999-09-13 2002-04-30 American Home Products Corporation Glucopyranosides conjugates of 2-(4-hydroxy-phenyl)-3-methyl-1-[4-(2-amin-1-yl-ethoxy)-benzyl]-1H-indol-5-ols
KR100985140B1 (ko) * 2001-12-20 2010-10-05 와이어쓰 엘엘씨 5-하이드록시트립타민-6 리간드로서의 인돌릴알킬아민 유도체
JPWO2004078719A1 (ja) * 2003-03-06 2006-06-08 小野薬品工業株式会社 インドール誘導体化合物およびその化合物を有効成分とする薬剤
KR101415503B1 (ko) * 2003-07-17 2014-07-04 플렉시콘, 인코퍼레이티드 Ppar 활성 화합물
WO2005040112A1 (en) * 2003-10-14 2005-05-06 Oxagen Limited Compounds with pgd2 antagonist activity

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