硝基呋喃
抗菌剂
前药
硝基咪唑
化学
组合化学
咪唑
药品
药理学
医学
立体化学
有机化学
生物
生物化学
遗传学
作者
Stanislav Kalinin,Tatiana Vedekhina,Polina Paramonova,Mikhail Krasavin
标识
DOI:10.2174/0929867328666210216114838
摘要
The last decade has been characterized by the development and approval of pretomanid and delamanid, which are nitroimidazole based drugs for multidrug -resistant tuberculosis. This attracted renewed attention to the nitroheterocyclic scaffolds as a source of safe and efficient antimicrobial agents. While the primary focus is still on nitrofurans and nitroimidazoles, well known as bioreducible prodrugs, a number of studies have been published on other 5-membered nitroheteroaromatic compounds. The latter not only show promising antimicrobial activity but also demonstrate modes of action different from the conventional reductive activation of the nitro group. Considering the potential of these efforts to impact the continuing race against drug-resistant pathogens, herein we review non-furan/imidazole-based 5-membered nitroheteroaromatics investigated as antimicrobial agents in 2010-2020.
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