A Review on Synthetic Thiazole Derivatives as an Antimalarial Agent.

Tutumoni Kalita, Ankita Choudhury, Anshul Shakya, Surajit Kumar Ghosh, Udaya Pratap Singh, Hans Raj Bhat
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Abstract

Background: Thiazole is a widely studied core structure in heterocyclic chemistry and has proven to be a valuable scaffold in medicinal chemistry. The presence of thiazole in both naturally occurring and synthetic pharmacologically active compounds demonstrates the adaptability of these derivatives.

Methods: The current study attempted to review and compile the contributions of numerous researchers over the last 20 years to the medicinal importance of these scaffolds, with a primary focus on antimalarial activity. The review is based on an extensive search of PubMed, Google Scholar, Elsevier, and other renowned journal sites for a thorough literature survey involving various research and review articles.

Results: A comprehensive review of the antimalarial activity of the thiazole scaffold revealed potential therapeutic targets in Plasmodium species. Furthermore, the correlation of structure-activity-relationship (SAR) studies from various articles suggests that the thiazole ring has therapeutic potential.

Conclusion: This article intends to point researchers in the right direction for developing potential thiazole-based compounds as antimalarial agents in the future.

关于合成噻唑衍生物作为抗疟药物的综述。
背景:噻唑是杂环化学中一种被广泛研究的核心结构,已被证明是药物化学中一种有价值的支架。噻唑在天然存在和合成的具有药理活性的化合物中的存在表明了这些衍生物的适应性:本研究试图回顾和汇编过去 20 年来众多研究人员对这些支架的药用重要性所做的贡献,主要侧重于抗疟活性。该综述基于对 PubMed、Google Scholar、Elsevier 和其他知名期刊网站的广泛搜索,进行了全面的文献调查,涉及各种研究和综述文章:结果:对噻唑支架抗疟活性的全面综述揭示了疟原虫的潜在治疗目标。此外,不同文章中结构-活性-关系(SAR)研究的相关性表明,噻唑环具有治疗潜力:本文旨在为研究人员指明正确的方向,以便在未来开发出潜在的噻唑基化合物作为抗疟药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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