首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antimicrobial activities of 3-O-alkyl analogues of (+)-catechin: improvement of stability and proposed action mechanism.
【24h】

Synthesis and antimicrobial activities of 3-O-alkyl analogues of (+)-catechin: improvement of stability and proposed action mechanism.

机译:(+)-儿茶素的3-O-烷基类似物的合成和抗菌活性:稳定性的改善和建议的作用机理。

获取原文
获取原文并翻译 | 示例
           

摘要

We report here the synthesis and biological properties of 3-O-alkyl analogues of (+)-catechin (5), which itself is one of the major natural polyphenols found in green tea and has several physiological activities. Starting from 5, a series of 3-O-alkyl-(+)-catechin derivatives were investigated as potent antimicrobial agents. The presence of an alkyl chain rather than acyl on 3-O- showed an increase in antimicrobial activity which may be due to stability in standard culture condition. The most promising compound is 8e, 3-O-decyl analogue, with the MIC of 0.5-2, 32-128 and 2-4 microg/mL against Gram-positive bacteria, Gram-negative bacteria and human pathogenic fungi, respectively. Regarding action mechanism, the antimicrobial activity is possibly due to the lipophilicity and disrupting ability of the analogues to the liposome membrane.
机译:我们在这里报告(+)-儿茶素(5)的3-O-烷基类似物的合成和生物学特性,其本身是绿茶中发现的主要天然多酚之一,具有多种生理活性。从5开始,研究了一系列3-O-烷基-(+)-儿茶素衍生物作为有效的抗菌剂。 3-O-上烷基链而不是酰基的存在表明抗菌活性增加,这可能是由于标准培养条件下的稳定性所致。最有前途的化合物是8e,3-O-癸基类似物,对革兰氏阳性菌,革兰氏阴性菌和人类病原真菌的MIC分别为0.5-2、32-128和2-4 microg / mL。关于作用机理,抗微生物活性可能是由于类似物对脂质体膜的亲脂性和破坏能力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号