发明名称 SULFUR-CONTAINING HETEROCYCLIC DERIVATIVE HAVING BETA SECRETASE INHIBITORY ACTIVITY
摘要 The following compound is provided as an agent for treating a disease induced by production, secretion and/or deposition of amyloid β protein, for example, a compound represented by the formula (I):;wherein ring A is an optionally substituted carbocyclic group or an optionally substituted heterocyclic group,R1 is optionally substituted lower alkyl or the like,R2a and R2b are each independently hydrogen, optionally substituted lower alkyl or the like,R3a and R3c are each independently hydrogen, halogen, hydroxy, optionally substituted lower alkyl or the like,or a pharmaceutically acceptable salt thereof, or a solvate thereof.
申请公布号 US2016108052(A1) 申请公布日期 2016.04.21
申请号 US201514981343 申请日期 2015.12.28
申请人 Shionogi & Co., Ltd. 发明人 Hori Akihiro;Yonezawa Shuji;Fujikoshi Chiaki;Matsumoto Sae;Kooriyama Yuuji;Ueno Tatsuhiko;Kato Terukazu
分类号 C07D487/04;C07D279/06;C07D417/10;C07D417/12;C07D417/14 主分类号 C07D487/04
代理机构 代理人
主权项 1. A compound represented by the formula (I): wherein ring A is an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; R1 is optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, cyano, an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; R2a and R2b are each independently hydrogen, optionally substituted lower alkyl or optionally substituted acyl; R3a and R3c are each independently hydrogen, halogen, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted acyl, optionally substituted lower alkoxy, optionally substituted aryl lower alkyl, optionally substituted heteroaryl lower alkyl, optionally substituted aryl lower alkoxy, optionally substituted heteroaryl lower alkoxy, optionally substituted lower alkylthio, carboxy, cyano, optionally substituted lower alkoxycarbonyl, optionally substituted amino, optionally substituted carbamoyl, an optionally substituted carbocyclic group or an optionally substituted heterocyclic group, or R3a and R3c may be taken together to form a ring, or its pharmaceutically acceptable salt, or a solvate thereof.
地址 Osaka JP
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