State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, PR China; TCM and Ethnomedicine Innovation & Development International Laboratory, Innovative Materia Medica Research Institute, School of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, PR China.
State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, PR China.
Phytochemistry. 2019 Jun;162:216-223. doi: 10.1016/j.phytochem.2019.03.022. Epub 2019 Apr 3.
Ten previously undescribed bibenzyl derivatives (bletistrins A-J), including 5 that have hydroxyl-substituted chiral centres on the aliphatic bibenzyl bridge, along with twelve known bibenzyl derivatives, were isolated from the rhizomes of Bletilla striata. The structures of bletistrins A-J were primarily elucidated on the basis of their 1D and 2D NMR spectroscopic data. The absolute configurations of bletistrins A, D, F, H and I were determined by electronic circular dichroism (ECD) spectroscopic analysis and optical rotation value. Most of the isolated compounds were evaluated for their antibacterial activities against 3 g-positive bacterial strains and 1 g-negative bacterial strain. Bletistrins F, G, and J, bulbocol, shanciguol and shancigusin B showed inhibitory activities, with MICs of (3-28 μg/mL) against S. aureus ATCC 6538.
从白及的根茎中分离得到了 10 种以前未描述的联苄基衍生物(bletistrins A-J),包括 5 种在脂肪族联苄基桥上具有羟基取代的手性中心的化合物,以及 12 种已知的联苄基衍生物。bletistrins A-J 的结构主要根据它们的 1D 和 2D NMR 光谱数据来阐明。通过电子圆二色性(ECD)光谱分析和旋光度值确定了 bletistrins A、D、F、H 和 I 的绝对构型。对分离得到的大部分化合物进行了抗菌活性评价,测定了它们对 3 种革兰氏阳性菌和 1 种革兰氏阴性菌的抑制活性。bletistrins F、G 和 J、 bulbocol、shanciguol 和 shancigusin B 表现出抑制活性,对金黄色葡萄球菌 ATCC 6538 的 MIC 值为(3-28μg/mL)。