α-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae)

被引:81
作者
Mbaze, Luc Meva'a
Poumale, Herve Martial P.
Wansi, Jean Duplex
Lado, Jean Alexandre
Khan, Shamsun Nahar
Iqbal, Muhammad Choudhary
Ngadjui, Bonaventure Tchaleu
Laatsch, Hartmut
机构
[1] Univ Douala, Fac Sci, Dept Chem, Douala, Cameroon
[2] Univ Gottingen, Dept Organ & Biomol Chem, D-37077 Gottingen, Germany
[3] Univ Yaounde, Fac Sci, Dept Organ Chem, Yaounde, Cameroon
[4] Univ Karachi, HEJ Res Inst Chem, Karachi 75270, Pakistan
关键词
Fagara tessmannii; Rutaceae; pentacyclic triterpene; antifungal; antibacterial; alpha-glucosidase inhibition;
D O I
10.1016/j.phytochem.2006.12.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
in addition to fatty acids, a mixture of sterols (beta-sitosterol, stigmasterol, campesterol and stigmastanol), lupeol, arctigenin methylether, sesamin, vanillic acid (1), 2,6-dimethoxy-1,4-benzoquinone (2), betulinic acid and two pentacyclic triterpene acetates were isolated from Fagara tessmannii Engl. They were identified as 30-acetoxy-16 beta-hydroxybetulinic acid (3a) and 3 beta,16 beta-diacetoxybetulinic acid (3b), and their structures were established using 1 and 2D NMR spectra and by comparison with published data. Two derivatives of the compounds were prepared. Some isolated compounds were evaluated for their antifungal and antibacterial activities. Compounds 1 and 3a showed significant inhibition of alpha-glucosidase. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:591 / 595
页数:5
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