发明名称 AZA-BICYCLOALKYL ETHER AND THEIR USE AS alpha7-NACHR AGONIST
摘要 <p><P>PROBLEM TO BE SOLVED: To provide a new 1-aza-bicycloalkyl derivative. <P>SOLUTION: There are provided 1-aza-bicycloalkyl derivatives which areα7-nicotinic acetylcholine receptor (nAChR) agonists, represented by formula (I) [wherein X is CH<SB>2</SB>or a single bond; Y is a group of formula (A); R is a substituted or unsubstituted 5-10C aryl or (un)substituted hetero-5-10C aryl, N(R<SP>1</SP>)(R<SP>4</SP>) or N(R<SP>2</SP>)(CHR<SP>3</SP>R<SP>4</SP>) (wherein R<SP>1</SP>, R<SP>2</SP>and R<SP>3</SP>are each independently H, 1-4C alkyl or CF<SB>3</SB>; and R<SP>4</SP>is a substituted or unsubstituted 5-10C aryl or (un)substituted hetero-5-10C aryl)]. The method for production of these derivatives, their use as pharmaceuticals and pharmaceutical compositions comprising them are also disclosed. <P>COPYRIGHT: (C)2009,JPO&INPIT</p>
申请公布号 JP2009143956(A) 申请公布日期 2009.07.02
申请号 JP20090036918 申请日期 2009.02.19
申请人 NOVARTIS AG 发明人 FEUERBACH DOMINIK;HURTH KONSTANZE;RITCHIE TIMOTHY JOHN
分类号 C07D453/02;A61K31/444;A61K31/501;A61K31/506;A61P21/00;A61P21/04;A61P25/00;A61P25/04;A61P25/08;A61P25/14;A61P25/16;A61P25/18;A61P25/20;A61P25/22;A61P25/24;A61P25/28;A61P25/34;A61P29/00;A61P31/18;A61P43/00;C07D487/08 主分类号 C07D453/02
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