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具有PPAR激動劑活性之衍生物
专利权人:
INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC.;SHIONOGI & CO., LTD.; INC.;INSTITUTE OF MEDICINAL MOLECULAR DESIGN
发明人:
ITAI, AKIKO,板井昭子,MUTO, SUSUMU,武藤进,武藤進,TOKUYAMA, RYUKO,德山龙光,德山龍光,FUKASAWA, HIROSHI,深泽弘志,深澤弘志,OHARA, TAKAFUMI,大原孝文,KATO, TERUKAZU,加藤辉和,加藤輝和
申请号:
TW095131233
公开号:
TWI395743B
申请日:
2006.08.25
申请国别(地区):
TW
年份:
2013
代理人:
摘要:
The present invention provides a compound of the following formula (I):ring Q represents an optionally substituted monocyclic aryl group、an optionally substituted monocyclic heteroaryl group、an optionally substituted condensed aryl groupring or an optionally substituted condensed heteroaryl group、Y1represents a single bond or -NR6-, etc., ring A represents an optionally substituted non-aromatic heterocyclic diyl group, formula-Y2Z1- represents a group of the following formula:each of the R7represents a hydrogen atom or an optionally substituted lower alkyl group, etc., each of the R8and R9represent a hydrogen atom or an optionally substituted lower alkyl group, n is an integer of 0~3, Z1represents a single bond, O, S or NR9, ring B represents an optionally substituted aromatic carbon cyclo diyl group, or an optionally substituted aromatic heterocyclo diyl group, Y3represents a single bond, a lower alkylene group that optionally substituted and may mediated with -O-, or an optionally substituted lower alkenylene group, etc., Z2represent COOR3, etc.), or the pharmaceutical acceptable salt thereof or the solvate thereof.本發明為提供如下式(I):環Q為可被取代之單環芳基、可被取代之單環雜芳基、可被取代之稠合芳基或可被取代之稠合雜芳基,Y1為單鍵或-NR6-等,環A為可被取代之非芳香族雜環二基,式:-Y2Z1-為之基,R7各為氫或可被取代之低烷基等,R8及R9各為氫或可被取代之低烷基,n為0~3之整數,Z1為單鍵、O、S或NR9,環B為可被取代之芳香族碳環二基或可被取代之芳香族雜環二基,Y3為單鍵、可被取代而可有-O-介入之低伸烷基或可被取代之低伸烯基等,Z2為COOR3等)之化合物、其製藥容許鹽或其溶劑合物。
来源网站:
中国工程科技知识中心
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