Department of Organic Chemistry, Faculty of Pharmacy, Medical University of Lublin, 4a Chodzki Str., 20-093, Lublin, Poland.
Eur J Med Chem. 2021 Apr 5;215:113266. doi: 10.1016/j.ejmech.2021.113266. Epub 2021 Feb 6.
Thiazolidin-4-one scaffold has great potential for medicinal chemistry and is of interest to scientists in view of wide spectrum of biological activity. This scaffold is often used for designing of small molecules with various biological activity including antituberculosis activity. The presented review is an attempt to gather, analyze and systemize data about antitubercular properties of thiazolidine-4-ones from two last decades. Some of them have promising antitubercular activity which is significantly higher than that of the reference drugs. Among them compounds 82c, 82d and 84 that were active against M. tuberculosis H37Rv strain with MICs in the range of 0.05-0.2 μg/mL and compound 108 exhibited activity with MIC = 0.36 μM. Compounds 115a-115c and 116a-116c were very effective against M. tuberculosis H37Ra with MIC values in the range of 0.031-0.125 μg/mL. Acidomycin was showed activity against seven MDR M. tuberculosis strains with MICs in the range of 0.6-0.62 μM and against two XDR M. tuberculosis strains with MICs 0.096 and 1.2 μM. The structure-activity relationship (SAR) of some groups of compounds, as well as some potential molecular targets were also discussed.
噻唑烷-4-酮骨架在药物化学方面具有巨大的潜力,鉴于其广泛的生物活性,引起了科学家们的关注。该骨架常用于设计具有各种生物活性的小分子,包括抗结核活性。本综述旨在收集、分析和系统化过去二十年中关于噻唑烷-4-酮类化合物的抗结核特性的数据。其中一些具有很有前途的抗结核活性,明显高于参考药物。其中化合物 82c、82d 和 84 对结核分枝杆菌 H37Rv 株具有活性,MIC 值在 0.05-0.2μg/mL 范围内,化合物 108 的 MIC 值为 0.36μM。化合物 115a-115c 和 116a-116c 对结核分枝杆菌 H37Ra 具有非常有效的活性,MIC 值在 0.031-0.125μg/mL 范围内。阿霉素对 7 株耐多药结核分枝杆菌株和 2 株广泛耐药结核分枝杆菌株具有活性,MIC 值在 0.6-0.62μM 和 0.096-1.2μM 范围内。还讨论了一些化合物组的构效关系(SAR)以及一些潜在的分子靶标。