抗细菌
硝基
化学
硝基还原酶
细胞毒性
毒性
硝基化合物
结构-活动关系
硝基呋喃
立体化学
药理学
生物活性
体外
组合化学
生物化学
酶
肺结核
结核分枝杆菌
有机化学
生物
医学
烷基
病理
遗传学
作者
Galina Karabanovich,Viktória Fabianová,Anthony Vocat,Ján Dušek,Lenka Valášková,Jiřina Stolaříková,Russell R. A. Kitson,Petr Pávek,Kateřina Vávrová,Kamel Djaout,Katarı́na Mikušová,Alain R. Baulard,Stewart T. Cole,Jana Korduláková,Jaroslav Roh
标识
DOI:10.1021/acs.jmedchem.3c00925
摘要
3,5-Dinitrobenzylsulfanyl tetrazoles and 1,3,4-oxadiazoles, previously identified as having high in vitro activities against both replicating and nonreplicating mycobacteria and favorable cytotoxicity and genotoxicity profiles were investigated. First we demonstrated that these compounds act in a deazaflavin-dependent nitroreduction pathway and thus require a nitro group for their activity. Second, we confirmed the necessity of both nitro groups for antimycobacterial activity through extensive structure-activity relationship studies using 32 structural types of analogues, each in a five-membered series. Only the analogues with shifted nitro groups, namely, 2,5-dinitrobenzylsulfanyl oxadiazoles and tetrazoles, maintained high antimycobacterial activity but in this case mainly as a result of DprE1 inhibition. However, these analogues also showed increased toxicity to the mammalian cell line. Thus, both nitro groups in 3,5-dinitrobenzylsulfanyl-containing antimycobacterial agents remain essential for their high efficacy, and further efforts should be directed at finding ways to address the possible toxicity and solubility issues, for example, by targeted delivery.
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