亚精胺
腐胺
化学
分离(微生物学)
传统医学
植物
生物
生物化学
酶
医学
微生物学
作者
Dagmar Jankovská,Nikol Jurčová,Renata Kubínová,Jiří Václavík,Emil Švajdlenka,Anna Mascellani,Petr Maršík,Kateřina Bouzková,Milan Malaník
出处
期刊:Plants
[Multidisciplinary Digital Publishing Institute]
日期:2024-04-24
卷期号:13 (9): 1181-1181
被引量:2
标识
DOI:10.3390/plants13091181
摘要
Five putrescine and spermidine derivatives (1–5) together with five rotenoids (6–10) were isolated from a methanolic extract of the flowers of A fruticosa that displayed promising inhibition of 76.0 ± 1.9% for AChE and 90.0 ± 4.0% for BuChE at a concentration of 1 mg/mL. Although the anticholinesterase activities of the isolated compounds did not reach that of galantamine, molecular docking revealed that all-trans-tri-p-coumaroylspermidine and trans-trans-cis-tri-p-coumaroylspermidine showed binding poses mimicking the known inhibitor galantamine and thus could serve as model molecules in future searches for new AChE and BuChE inhibitors.
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