Amorpha fruticosa 花甲醇提取物的抗胆碱酯酶活性以及轮烯类化合物和 Putrescine 与 Spermidine 衍生物的分离

Plants Pub Date : 2024-04-24 DOI:10.3390/plants13091181
D. Jankovská, Nikol Jurčová, Renata Kubínová, Jiří Václavík, Emil Švajdlenka, A. Mascellani, Petr Maršík, Kateřina Bouzková, Milan Malaník
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引用次数: 0

摘要

从A. fruticosa花的甲醇提取物中分离出了五种腐胺和亚精胺衍生物(1-5)以及五种鱼藤酮类化合物(6-10),在浓度为1毫克/毫升时,它们对AChE的抑制率为76.0 ± 1.9%,对BuChE的抑制率为90.0 ± 4.0%。虽然分离出的化合物的抗胆碱酯酶活性没有达到加兰他敏的水平,但分子对接显示,全反式-三对香豆酰过氧吡啶和反式-反式-顺式-三对香豆酰过氧吡啶显示出与已知抑制剂加兰他敏相似的结合位置,因此可以作为未来寻找新的 AChE 和 BuChE 抑制剂的模型分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticholinesterase Activity of Methanolic Extract of Amorpha fruticosa Flowers and Isolation of Rotenoids and Putrescine and Spermidine Derivatives
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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