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来自裸茎榕的三异戊烯基黄酮类化合物及其α-葡萄糖苷酶抑制特性。

Triprenylated flavonoids from Dorstenia psilurus and their alpha-glucosidase inhibition properties.

作者信息

Tabopda Turibio K, Ngoupayo Joseph, Awoussong Patrice K, Mitaine-Offer Anne-Claire, Ali Muhammad S, Ngadjui Bonaventure T, Lacaille-Dubois Marie-Aleth

机构信息

Organic Chemistry Department, University of Yaoundé I, P.O. Box 8664, Yaoundé, Cameroon.

出版信息

J Nat Prod. 2008 Dec;71(12):2068-72. doi: 10.1021/np800509u.

Abstract

Six new unusual C-4'-prenylated flavonols, dorsilurins F-K (1-6), together with six known compounds were isolated from the roots of Dorstenia psilurus, and their structures were elucidated on the basis of spectroscopic evidence. The isolated compounds exhibited moderate to low alpha-glucosidase inhibitory activity. Dorsilurin F (1), with three unmodified prenyl groups, was the most active, while dorsilurin K (6), with only one unmodified prenyl group, was the least active compound. Furthermore, NMR data of dorsilurin C (7), isolated some years ago from the same plant, have been revised.

摘要

从裸茎Dorstenia psilurus的根部分离出6个新的罕见C-4'-异戊烯基黄酮醇,即背叶菊素F-K(1-6),以及6个已知化合物,并根据光谱数据阐明了它们的结构。分离得到的化合物表现出中度至低度的α-葡萄糖苷酶抑制活性。具有3个未修饰异戊烯基的背叶菊素F(1)活性最高,而仅具有1个未修饰异戊烯基的背叶菊素K(6)活性最低。此外,几年前从同一植物中分离得到的背叶菊素C(7)的核磁共振数据也已得到修正。

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