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稠合雜環衍生物
专利权人:
LIMITED;DAIICHI SANKYO COMPANY
发明人:
UTO, YOSHIKAZU,宇都芳一,UENO, YUKO,上野悠子,SUZUKI, KEIKO,铃木敬子,鈴木敬子,MORI, YUTAKA,森裕
申请号:
TW101133419
公开号:
TW201317229A
申请日:
2012.09.13
申请国别(地区):
TW
年份:
2013
代理人:
摘要:
The subject of present invention is related to a compound or the pharmaceutically acceptable salt thereof having excellent inhibition to DGAT and ingestion inhibition. The solution of present invention is to provide a compound represented by the general formula (I) or the pharmaceutically acceptable salt thereof: [in formula, R1 is hydrogen atom or carboxy group; R2 and R3 each independently represents C1-C6 alkyl group, or R2 and R3 are together with the carbon atom to which they bind to form C3-C6 cycloalkane optionally substituted by one carboxy group or carboxymethyl group; U is nitrogen atom and the like; V is nitrogen atom and the like; W is nitrogen atom and the like; Z is nitrogen atom and the like; R4’s each independently represents halogen atom or C1-C6 alkyl group; A is oxygen atom and the like; E is nitrogen atom and the like; J is nitrogen atom and the like; L is nitrogen atom and the like; M is nitrogen atom and the like; m is 0 or 1; n is an integer of 0-2].本發明之課題係關於具有優異的DGAT阻礙作用及攝食抑制作用的化合物或其藥理上可容許的鹽。本發明之解決手段係提供一種通式(I)所表示之化合物或其藥理上可容許的鹽:[式中,R1為氫原子或羧基;R2及R3獨立表示為C1-C6烷基,或R2及R3與結合的碳原子一起形成可經1個羧基或羧甲基取代的C3-C6環烷;U為氮原子等;V為氮原子等;W為氮原子等;Z為氮原子等;R4獨立為鹵素原子或C1-C6烷基;A為氧原子等;E為氮原子等;J為氮原子等;L為氮原子等;M為氮原子等;m為0或1;n為0至2之整數]。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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