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假尿嘧啶核苷:首个选择性抑制细菌 RNA 聚合酶的核苷类似物。

Pseudouridimycin: The First Nucleoside Analogue That Selectively Inhibits Bacterial RNA Polymerase.

机构信息

Institute of Chemistry and Biotechnology, Center for Organic and Medicinal Chemistry, Zurich University of Applied Sciences (ZHAW), Einsiedlerstrasse 31, 8820, Wädenswil, Switzerland.

出版信息

Angew Chem Int Ed Engl. 2017 Oct 16;56(43):13184-13186. doi: 10.1002/anie.201708133. Epub 2017 Sep 12.

DOI:10.1002/anie.201708133
PMID:28895263
Abstract

Seek, and ye shall find: After years of focusing research on synthetic antibiotics out of fear that all the useful natural ones had already been found, a novel antibacterial compound has been discovered through conventional microbial extract screening. The broad-spectrum nucleoside-analogue inhibitor pseudouridimycin is selective for bacterial RNA polymerase and elicits very low resistance rates.

摘要

寻找,便会发现:多年来,由于担心所有有用的天然抗生素都已被发现,人们一直专注于合成抗生素的研究,而通过常规微生物提取物筛选,一种新型抗菌化合物已被发现。广谱核苷类似物抑制剂 pseudouridimycin 对细菌 RNA 聚合酶具有选择性,并产生非常低的耐药率。

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