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噻唑衍生物的抗癌潜力:回顾性评价。

Anticancer Potential of Thiazole Derivatives: A Retrospective Review.

机构信息

Department of Pharmacy, Dr. H.S. Gour University, Sagar (M.P.) 470003, India.

Pharmacy College, Uttar Pradesh University of Medical Sciences, Saifai, Etawah (U.P.) 206130, India.

出版信息

Mini Rev Med Chem. 2018;18(8):640-655. doi: 10.2174/1389557517666171123211321.

Abstract

This review brings forth the potential of thiazole derivatives for their anticancer activities. The emphasis is placed on the structural diversity of thiazole derivatives, responsible for their specific anticancer activity. Multiple classes of thiazole derivatives such as Schiff base, mono-, di-, tri-, and heterocyclic substituents that possess anticancer activity have been exemplified. Molecular modelling of compounds that predicts enhanced anticancer activity of the modified structures has also been elaborated in the review. Significant advancements in synthetic chemistry related to cytotoxicity can now better position the drug discovery team to undertake thiazoles as valuable leads. The beneficial thiazole derivatives possessing anticancer activity will reignite the interest of medicinal chemists in thiazole and their derivatives.

摘要

本文综述了噻唑衍生物在抗癌活性方面的潜力。重点介绍了噻唑衍生物的结构多样性,这是其具有特定抗癌活性的原因。本文举例说明了多种噻唑衍生物,如席夫碱、单、二、三、杂环取代基,它们都具有抗癌活性。本文还详细阐述了化合物的分子建模,该模型预测了修饰结构的抗癌活性增强。与细胞毒性相关的合成化学的重大进展现在可以使药物发现团队更好地将噻唑作为有价值的先导化合物。具有抗癌活性的有益噻唑衍生物将重新激发药物化学家对噻唑及其衍生物的兴趣。

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