发明名称 DERIVATIVE HAVING PPAR AGONISTIC ACTIVITY
摘要 PROBLEM TO BE SOLVED: To provide a compound useful as a PPAR (peroxisome proliferator-activated receptor) agonist. SOLUTION: There is provided a compound represented by formula (I), a pharmaceutically acceptable salt or solvate thereof (wherein ring Q is an optionally substituted monocyclic or fused aryl or heteroaryl; Y<SP>1</SP>is a single bond, -NR<SP>6</SP>- or the like; ring A is an optionally substituted nonaromatic heterocyclic-diyl; the formula, -Y<SP>2</SP>Z<SP>1</SP>- is a specific binding group having N, S and O atoms; Z<SP>1</SP>is a single bond, O, S or NR<SP>9</SP>; ring B is an optionally substituted aromatic carbocyclic- or heterocyclic-diyl; Y<SP>3</SP>is a single bond, an optionally substituted lower alkylene optionally interposed by -O-, an optionally substituted lower alkenylene or the like; and Z<SP>2</SP>is COOR<SP>3</SP>or the like). COPYRIGHT: (C)2008,JPO&INPIT
申请公布号 JP2008208129(A) 申请公布日期 2008.09.11
申请号 JP20080061970 申请日期 2008.03.12
申请人 IYAKU BUNSHI SEKKEI KENKYUSHO:KK;SHIONOGI & CO LTD 发明人 ITAI AKIKO;MUTO SUSUMU;TOKUYAMA TATSUMITSU;FUKAZAWA HIROSHI;OHARA TAKAFUMI;KATO TERUKAZU
分类号 C07D211/16;A61K31/439;A61K31/445;A61K31/454;A61K31/495;A61K31/496;A61K31/498;A61K31/501;A61K31/506;A61K31/5377;A61K31/551;A61P1/04;A61P1/18;A61P3/04;A61P3/06;A61P3/10;A61P5/14;A61P5/50;A61P9/10;A61P9/12;A61P13/12;A61P15/08;A61P17/06;A61P19/02;A61P19/10;A61P25/00;A61P25/16;A61P25/28;A61P29/00;A61P35/00;A61P37/08;A61P43/00;C07D215/38;C07D241/04;C07D241/44;C07D277/20;C07D277/42;C07D277/82;C07D401/04;C07D403/04;C07D405/04;C07D405/14;C07D413/04;C07D417/04;C07D417/12;C07D417/14;C07D487/08;C07D513/04 主分类号 C07D211/16
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