Department of Pharmaceutical Sciences, Faculty of Pharmacy, University of Jordan, Amman 11942, Jordan.
Z Naturforsch C J Biosci. 2010 May-Jun;65(5-6):322-6. doi: 10.1515/znc-2010-5-603.
A new trimeric proanthocyanidin, epigallocatechin-3-O-gallat-(4beta-->8)-epigallocatechin-(4beta-->8)-catechin (1), was isolated together with three known flavan-3-ols, catechin (2), epicatechin (3), and epigallocatechin (4), and three dimeric proanthocyanidins, 5-7, from the air-dried leaves of Mangifera indica. Their chemical structures were determined on the basis of 1D- and 2D-NMR spectra (HSQC, HMBC) of their peracetylated derivatives, MALDI-TOF-mass spectra, and by acid-catalyzed degradation with phloroglucinol. The isolated compounds 1-7 were in vitro tested for their inhibitory activities against COX-1 and COX-2. Compound 1 was found to have a potent inhibitory effect on COX-2, while compounds 1 and 5-7 exhibited moderate inhibition against COX-1.
从芒果干叶中分离得到了一种新的三聚原花青素,表没食子儿茶素-3-O-没食子酸酯-(4β→8)-表儿茶素-(4β→8)-儿茶素(1),以及三种已知的黄烷-3-醇,儿茶素(2)、表儿茶素(3)和表没食子儿茶素(4),以及三种二聚原花青素 5-7。其化学结构是基于它们的全乙酰化衍生物的 1D 和 2D-NMR 光谱(HSQC、HMBC)、MALDI-TOF 质谱和间苯三酚酸催化降解来确定的。分离得到的化合物 1-7 进行了体外 COX-1 和 COX-2 抑制活性测试。发现化合物 1 对 COX-2 具有很强的抑制作用,而化合物 1 和 5-7 对 COX-1 表现出中等抑制作用。