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作为分枝杆菌生长抑制剂的嘧啶核苷类似物。

Analogues of Pyrimidine Nucleosides as Mycobacteria Growth Inhibitors.

作者信息

Alexandrova Liudmila A, Khandazhinskaya Anastasia L, Matyugina Elena S, Makarov Dmitriy A, Kochetkov Sergey N

机构信息

Engelhardt Institute of Molecular Biology RAS, 32 Vavilov Str., 119991 Moscow, Russia.

出版信息

Microorganisms. 2022 Jun 27;10(7):1299. doi: 10.3390/microorganisms10071299.

Abstract

Tuberculosis (TB) is the oldest human infection disease. Mortality from TB significantly decreased in the 20th century, because of vaccination and the widespread use of antibiotics. However, about a third of the world's population is currently infected with () and the death rate from TB is about 1.4-2 million people per year. In the second half of the 20th century, new extensively multidrug-resistant strains of were identified, which are steadily increasing among TB patients. Therefore, there is an urgent need to develop new anti-TB drugs, which remains one of the priorities of pharmacology and medicinal chemistry. The antimycobacterial activity of nucleoside derivatives and analogues was revealed not so long ago, and a lot of studies on their antibacterial properties have been published. Despite the fact that there are no clinically used drugs based on nucleoside analogues, some progress has been made in this area. This review summarizes current research in the field of the design and study of inhibitors of mycobacteria, primarily .

摘要

结核病(TB)是最古老的人类传染病。由于疫苗接种和抗生素的广泛使用,20世纪结核病死亡率显著下降。然而,目前全球约三分之一的人口感染了(此处原文括号内容缺失),结核病死亡率约为每年140万至200万人。在20世纪下半叶,发现了新型广泛耐多药结核菌株,且在结核病患者中不断增加。因此,迫切需要开发新的抗结核药物,这仍然是药理学和药物化学的优先事项之一。核苷衍生物和类似物的抗分枝杆菌活性是不久前才被发现的,并且已经发表了许多关于它们抗菌特性的研究。尽管目前还没有基于核苷类似物的临床用药,但该领域已取得了一些进展。本综述总结了分枝杆菌抑制剂设计和研究领域的当前研究,主要是(此处原文表述不完整)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ea2/9322969/428c26128079/microorganisms-10-01299-g001.jpg

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