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新型林可霉素衍生物的合成及其抗菌活性。I. 通过引入取代氮杂环丁烷增强抗菌活性。

Synthesis and antibacterial activity of novel lincomycin derivatives. I. Enhancement of antibacterial activities by introduction of substituted azetidines.

作者信息

Kumura Ko, Wakiyama Yoshinari, Ueda Kazutaka, Umemura Eijiro, Watanabe Takashi, Shitara Eiki, Fushimi Hideki, Yoshida Takuji, Ajito Keiichi

机构信息

Pharmaceutical Research Center, Meiji Seika Pharma Co., Ltd., Yokohama, Japan.

出版信息

J Antibiot (Tokyo). 2016 Jun;69(6):440-5. doi: 10.1038/ja.2015.134. Epub 2016 Jan 13.

Abstract

The synthesis and antibacterial activity of (7S)-7-sulfur-azetidin-3-yl lincomycin derivatives are described. Modification was achieved by a simple reaction of (7R)-7-O-methanesulfonyllincomycin and the corresponding substituted azetidine-2-thiol. Several compounds first showed moderate antibacterial activity against Streptococcus pneumoniae and Streptococcus pyogenes with erm gene as lincomycin derivatives.

摘要

描述了(7S)-7-硫代氮杂环丁烷-3-基林可霉素衍生物的合成及其抗菌活性。通过(7R)-7-O-甲磺酰基林可霉素与相应的取代氮杂环丁烷-2-硫醇的简单反应实现修饰。几种化合物首先表现出对肺炎链球菌和化脓性链球菌具有中等抗菌活性,与林可霉素衍生物一样携带erm基因。

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