Suppr超能文献

从白及块茎中分离得到的具有抗菌作用的联苄类衍生物。

Antibacterial bibenzyl derivatives from the tubers of Bletilla striata.

机构信息

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.

出版信息

Phytochemistry. 2019 Jun;162:216-223. doi: 10.1016/j.phytochem.2019.03.022. Epub 2019 Apr 3.

Abstract

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.

摘要

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)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验