乙酰胆碱酯酶
生物碱
阿扑啡
化学
阿切
丁酰胆碱酯酶
立体化学
IC50型
胆碱酯酶
塔克林
酶
药理学
生物化学
体外
生物
作者
Xiaodan Zhang,Mihyue Oh,Seulgi Kim,Jimin Kim,Hye‐Yeon Kim,Sungun Kim,Peter J. Houghton,Wan Kyunn Whang
标识
DOI:10.1080/14786419.2012.708660
摘要
A novel aporphine alkaloid was isolated from the leaves of Epimedium koreanum Nakai during activity-guided fractionation in search of compounds with an anticholinesterase activity. The structure of the new compound was assigned as 1,10-methoxy-7-hydroxy-aporphine (1), which we have named epimediphine. Unambiguous 1H-NMR and 13C-NMR data for epimediphine are described. Epimediphine inhibited an acetylcholinesterase (AchE) activity in a dose-dependent manner with an IC50 value of 3.1 µM. Meanwhile, tacrine, dehydroevodiamine and physostigmine, which are therapeutic drugs or candidates for AD, exhibited an anti-AchE activity with IC50 values of 0.4, 37.9 and 0.12 µM, respectively.
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