THE SYNTHESIS AND INVITRO ACETYLCHOLINESTERASE AND BUTYRYLCHOLINESTERASE INHIBITORY ACTIVITY OF TACRINE (COGNEX(R)) DERIVATIVES

被引:68
|
作者
GREGOR, VE
EMMERLING, MR
LEE, C
MOORE, CJ
机构
[1] Parke-Davis Pharmaceutical Research, Warner-Lambert Co., Ann Arbor
关键词
D O I
10.1016/S0960-894X(00)80545-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Chlorosubstituted derivatives of tacrine (1), 1,4-methylenetacrine (2), and their in vitro acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities are described. The most potent analogues are 6-chlorotacrine (1b) in AChE and 7-chlorotacrine (1c) in BChE inhibition.
引用
收藏
页码:861 / 864
页数:4
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