噻唑烷衍生物:合成和生物活性的最新综述。

IF 3.3 4区 医学 Q3 CHEMISTRY, MEDICINAL
Chaimaa Hatim, Abdelghani Boussetta, Marieme Kacem, Mustapha Dib, Khadija Ouchetto, Abderrafia Hafid, Mostafa Khouili, Hajiba Ouchetto
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引用次数: 0

摘要

引言:近十年来,噻唑烷类衍生物因其具有丰富的生物活性、治疗潜力和杂环类环状结构而成为药物化学中很有前途的杂环类化合物。一些研究表明,与标准药物相比,某些噻唑烷衍生物表现出优越的活性,并具有未来制药应用的潜力。本文综述了噻唑烷衍生物的主要合成策略,并重点介绍了它们的生物活性。方法:本研究基于2015年至2024年在有机合成和生物活性领域最新和最广泛的噻唑烷结构研究,以及近年来应用最广泛的方法。结果:本文介绍的三种合成噻唑烷衍生物的方法是近几十年来最常用的,并引起了有趣的生物活性和具有化学和生物学意义的化合物的促进。讨论:噻唑烷骨架化合物的合成在有机化学中扮演着重要而有趣的角色,其方法变得越来越复杂和易于使用,使得获得具有生物学和药理学重要性的衍生物成为可能,并为未来的研究奠定了基础。结论:噻唑烷支架为构建具有重要生物活性的复杂分子结构提供了一条高效的合成途径。它们的多用途反应性使它们在有机化学、生物化学和药理学中特别有趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiazolidine Derivatives: An Up-to-Date Review of Synthesis and Biological Activity.

Introduction: Over the past decade, thiazolidine derivatives have become promising heterocyclic compounds in medicinal chemistry, and much research work has been devoted to this ring due to their diverse biological activities, therapeutic potential, and heterocyclic ring-like structure. Several studies have shown that certain thiazolidine derivatives exhibit superior activity compared to standard drugs and hold potential for future pharmaceutical applications. This review comprehensively summarizes the key synthetic strategies for thiazolidine derivatives and highlights their biological activities.

Methods: The present study is based on the most recent and extensive research on the Thiazolidine structure in the fields of organic synthesis and biological activities from 2015 to 2024, as well as the most widely used methodologies in recent years.

Results: The three methods described in this review for the synthesis of thioazolidine derivatives are the most commonly used in recent decades and have given rise to interesting biological activities and the promotion of compounds with chemical and biological significance.

Discussions: The synthesis of compounds with a thiazolidine skeleton plays a vital and interesting role in organic chemistry, with methods that are becoming increasingly sophisticated and easy to use, making it possible to obtain derivatives of biological and pharmacological importance, and a basis for future research.

Conclusion: The thiazolidine scaffold provides an efficient synthetic route for constructing complex molecular structures with significant biological activities. Their versatile reactivity makes them particularly interesting in organic chemistry, as well as biochemistry and pharmacology.

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来源期刊
CiteScore
6.40
自引率
2.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Current Topics in Medicinal Chemistry is a forum for the review of areas of keen and topical interest to medicinal chemists and others in the allied disciplines. Each issue is solely devoted to a specific topic, containing six to nine reviews, which provide the reader a comprehensive survey of that area. A Guest Editor who is an expert in the topic under review, will assemble each issue. The scope of Current Topics in Medicinal Chemistry will cover all areas of medicinal chemistry, including current developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, compound diversity measurements, drug absorption, drug distribution, metabolism, new and emerging drug targets, natural products, pharmacogenomics, and structure-activity relationships. Medicinal chemistry is a rapidly maturing discipline. The study of how structure and function are related is absolutely essential to understanding the molecular basis of life. Current Topics in Medicinal Chemistry aims to contribute to the growth of scientific knowledge and insight, and facilitate the discovery and development of new therapeutic agents to treat debilitating human disorders. The journal is essential for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important advances.
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