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Advances in the Development of Antituberculotics Acting on Multidrug-Resistant Strains

机译:作用于多药耐药菌株的抗结核药物的研究进展

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The aim of this review is to outline the recent advances in the development of new drugs against multidrug-resistant tuberculosis (MDR-TB). The occurrence of resistance to anti-tuberculosis drugs, particularly of MDR-TB, has become a major public health problem. The emergence of MDR-TB has made many currently available anti-TB drugs ineffective. Due to a many reasons, there is an urgent need to identify new drug targets and to find novel chemical structures. The research of novel anti-MDR-TB potential drugs follows structure modification of known antituberculotics, new lead structures with novel mechanism of the action (linezolid, TMC207, PA-824, OPC-67683, SQ109, FAS20013, LL-3858, BM212) and novel drug targets, i.e. cell wall biosynthesis (mycolic acid synthesis, protein synthesis, arabinogalactan and peptidoglycan biosynthesis inhibitors) or other novel targets.
机译:这篇综述的目的是概述针对耐多药结核病(MDR-TB)的新药开发的最新进展。对抗结核药物,特别是耐多药结核病的抗药性的出现,已经成为主要的公共卫生问题。耐多药结核病的出现使许多目前可用的抗结核药无效。由于许多原因,迫切需要鉴定新的药物靶标并寻找新的化学结构。新型抗MDR-TB潜在药物的研究遵循已知抗结核药的结构修饰,具有新作用机制的新先导结构(利奈唑胺,TMC207,PA-824,OPC-67683,SQ109,FAS20013,LL-3858,BM212)和新型药物靶标,即细胞壁生物合成(霉菌酸合成,蛋白质合成,阿拉伯半乳聚糖和肽聚糖生物合成抑制剂)或其他新型靶标。

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