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从益母草中分离得到的新二萜类化合物及其乙酰胆碱酯酶抑制活性。

New diterpenoids isolated from Leonurus japonicus and their acetylcholinesterase inhibitory activity.

机构信息

College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.

出版信息

Chin J Nat Med. 2017 Nov;15(11):860-864. doi: 10.1016/S1875-5364(18)30020-7.

Abstract

Three new labdane diterpenoids, leojaponicone A (1), isoleojaponicone A (2) and methylisoleojaponicone A (3), were isolated from the herb of Leonurus japonicus. The chemical structures of these secondary metabolites were elucidated on the basis of 1D and 2D NMR, including HMQC, and HMBC spectroscopic techniques. All the new compounds were tested in vitro for their acetylcholinesterase and α-glucosidase inhibitory activity. Compounds 1-3 exhibited low inhibitory effects on α-glucosidase with respect to acarbose and exhibited high inhibitory effects on acetylcholinesterase with respect to huperzine A.

摘要

从益母草中分离得到三个新的角鲨烷二萜类化合物,即莱奥蓬酮 A(1)、异莱奥蓬酮 A(2)和甲基异莱奥蓬酮 A(3)。基于 1D 和 2D NMR,包括 HMQC 和 HMBC 光谱技术,阐明了这些次生代谢物的化学结构。所有新化合物均在体外进行了乙酰胆碱酯酶和α-葡萄糖苷酶抑制活性测试。与阿卡波糖相比,化合物 1-3 对α-葡萄糖苷酶的抑制作用较弱,而与石杉碱甲相比,对乙酰胆碱酯酶的抑制作用较强。

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