摘要
２┐（２┐噻吩基）丙酸的合成ＳＹＮＴＨＥＳＩＳＯＦ２┐（２┐ＴＨＩＥＮＹＬ）ＰＲＯＰＩＯＮＩＣＡＣＩＤ赵桂森＊袁玉梅段效勇△（山东医科大学药化教研室，济南２５００１２）ＺＨＡＯＧｕｉ－Ｓｅｎ＊，ＹＵＡＮＹｕ－Ｍｅｉ，ＤＵＡＮＸｉａｏ－Ｙｏｎｇ（Ｄｅｐ...
Three guanidino substituted 1,2 diphenylethylenes as calmodulin antagonist were synthesized.It was found that they were more potent in their inhibitory activity than trifluoperazine.
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
1997年第6期273-274,共2页
Chinese Journal of Pharmaceuticals
关键词
噻吩基
丙酸
中间体
合成
噻洛芬酸
calmodulin antagonists,6 guanidino 1,2 diphenylhex 1 ene,SN 2 reaction
