SYNTHESIS OF HUPERZINE-A AND ITS ANALOGS AND THEIR ANTICHOLINESTERASE ACTIVITY

被引:121
作者
KOZIKOWSKI, AP
XIA, Y
REDDY, ER
TUCKMANTEL, W
HANIN, I
TANG, XC
机构
[1] UNIV PITTSBURGH,DEPT CHEM,PITTSBURGH,PA 15260
[2] LOYOLA UNIV,STRITCH SCH MED,DEPT PHARMACOL & EXPTL THERAPEUT,MAYWOOD,IL 60153
[3] UNIV PITTSBURGH,DEPT BEHAV NEUROSCI,PITTSBURGH,PA 15260
关键词
D O I
10.1021/jo00015a014
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Huperzine A is a new alkaloid isolated from the club moss Huperzia serrata (Thunb.) Trev., a Chinese folk medicine. This alkaloid exhibits potent activity as an inhibitor of acetylcholinesterase. Consequently, the compound is presently being investigated in China for the treatment of individuals suffering from various forms of memory impairment including Alzheimer's dementia. Details of the total synthesis of (+/-)-huperzine A are described as well as the preparation of a variety of huperzine analogues including its presumed pharmacophore. The extent of these new compounds to inhibit acetylcholinesterase is presented along with a discussion of the effects of the structural changes on biological activity.
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页码:4636 / 4645
页数:10
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