发明名称 TRIAZOLE DERIVATIVE
摘要 <p>An object of the present invention is to provide a compound having an action of inhibiting binding between S1P and its receptor, Edg-1 (S1P 1 ), and is useful as a pharmaceutical compound. A compound or a pharmaceutically acceptable salt thereof, which compound is represented by the formula below (where A represents an oxygen atom, a sulfur atom, a group represented by Formula -SO-, a group represented by Formula -SO 2 -, or the like, R 1 represents a hydrogen atom, an alkyl group having 1-6 carbon atoms, or the like, R 1A represents a hydrogen atom or the like, R 2 represents an alkyl group having 1-6 carbon atoms, a cycloalkyl group having 3-6 carbon atoms, or the like, R 3 represents an aryl group, R 4 represents a hydrogen atom or an alkyl group having 1-6 carbon atoms and optionally substituted with a carboxyl group, and R 5 represents an alkyl group having 1-10 carbon atoms, a cycloalkyl group having 3-8 carbon atoms, an aryl group which is optionally substituted, or the like).</p>
申请公布号 EP1988083(A1) 申请公布日期 2008.11.05
申请号 EP20070708069 申请日期 2007.02.05
申请人 TAISHO PHARMACEUTICAL CO. LTD. 发明人 ONO, NAOYA;TAKAYAMA, TETSUO;SHIOZAWA, FUMIYASU;KATAKAI, HIRONORI;YABUUCHI, TETSUYA;OTA, TOMOMI;YAGI, MAKOTO;SATO, MASAKAZU
分类号 C07D249/08;A61K31/4196;A61K31/422;A61K31/4245;A61K31/427;A61K31/428;A61K31/433;A61K31/438;A61K31/4439;A61K31/454;A61K31/4709;A61K31/4725;A61K31/496;A61K31/506;A61K31/519;A61K31/5377;A61P1/04;A61P11/06;A61P17/00;A61P17/06 主分类号 C07D249/08
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