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新型 4-噻唑烷酮衍生物作为有潜力的抗真菌和抗菌药物。

Novel 4-thiazolidinone derivatives as potential antifungal and antibacterial drugs.

机构信息

Department of Pharmaceutical Chemistry of Aristotle, School of Pharmacy, University of Thessaloniki, Thessaloniki, Greece.

出版信息

Bioorg Med Chem. 2010 Jan 1;18(1):426-32. doi: 10.1016/j.bmc.2009.10.041. Epub 2009 Oct 27.

Abstract

As part of ongoing studies in developing new antimicrobials, a class of structurally novel 4-thiazolidinone derivatives incorporating three known bioactive nuclei such as thiazole, thiazolidinone and adamantane was synthesized by the multi-step reaction protocol, already reported in the literature. NMR and Molecular Modeling techniques were employed for structure elucidation and Z/E potential isomerism configuration of the analogues. Evaluation of antibacterial and antifungal activity showed that almost all compounds exhibited better results than reference drugs thus they could be promising candidates for novel drugs.

摘要

作为开发新型抗菌药物研究的一部分,通过多步反应方案合成了一类结构新颖的 4-噻唑烷酮衍生物,其中包含噻唑、噻唑烷酮和金刚烷等三个已知的生物活性核。已经在文献中报道了该方法。NMR 和分子建模技术用于结构阐明和类似物的 Z/E 立体异构构型。抗菌和抗真菌活性评估表明,几乎所有化合物都表现出比参考药物更好的结果,因此它们可能是新型药物的有前途的候选药物。

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