STUDIES ON INHIBITORY ACTIVITY AGAINST ACETYLCHOLINESTERASE OF NEW BISBENZYLISOQUINOLINE ALKALOID AND ITS RELATED-COMPOUNDS

Citation
T. Ogino et al., STUDIES ON INHIBITORY ACTIVITY AGAINST ACETYLCHOLINESTERASE OF NEW BISBENZYLISOQUINOLINE ALKALOID AND ITS RELATED-COMPOUNDS, Heterocycles, 45(11), 1997, pp. 2253-2260
Citations number
7
Journal title
ISSN journal
03855414
Volume
45
Issue
11
Year of publication
1997
Pages
2253 - 2260
Database
ISI
SICI code
0385-5414(1997)45:11<2253:SOIAAA>2.0.ZU;2-8
Abstract
A new phenolic bisbenzylisoquinoline (BBI) alkaloid named 2'-N-norfang chinoline was isolated from the root of Stephania tetrandra S. MOORE a long withfangchinoline (2) and atherospermoline (3). The chemical stru cture of 2'-N-norfangchinoline was proved to be 4 by spectral analyses and chemical methods. Moreover three phenolic BBI alkaloidal compound s, 2,2'-N,N-dinorfangchinoline (8), 2'-N-noratherospermoline (9), 2-N- norfangchinoline (10) were derived from tetrandrine (1). And 12-O-acet yl atherospermoline (11) was obtained by partial acetylation of athero spermoline (3). Seven phenolic BBI compounds (2, 3, 4, 8, 9, 10, and 1 1) also have the inhibitory effect on acetylcholinesterase.