A Pharmacological Update of Oxadiazole Derivatives: A Review.

IF 3.3 4区 医学 Q3 CHEMISTRY, MEDICINAL Current topics in medicinal chemistry Pub Date : 2025-01-01 DOI:10.2174/0115680266349715250122001314
Magesh Mohan, Gandhimathi Rathinasamy, Bharathi Devarajan, Gowramma Byran, Kaviarasan Lakshmanan
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Abstract

Background: Recent advancements in the synthesis of novel heterocyclic compounds, particularly oxadiazole derivatives, have garnered significant interest due to their broad pharmacological activities. Despite the oxadiazole ring being a relatively small structure, its derivatives have shown considerable therapeutic potential across a range of diseases. These compounds have been explored for a variety of biological effects, including anti-inflammatory, anticonvulsant, hypoglycemic, antitubercular, anxiolytic, antimicrobial, antitumor, and anticancer properties. The growing issue of drug resistance has further fueled research into the therapeutic promise of oxadiazolebased compounds, particularly for their ability to target resistant diseases.

Objective: This review aims to highlight the pharmacological profiles of oxadiazole derivatives, with a focus on how structural modifications can enhance their activity against specific therapeutic targets. Additionally, the review seeks to explore strategies for overcoming resistance mechanisms associated with these compounds, underscoring their potential in addressing emerging drug-resistant diseases.

Conclusion: Oxadiazole derivatives represent a promising class of compounds with significant therapeutic potential, particularly in the face of increasing drug resistance. Their diverse pharmacological activities and ability to be structurally optimized for specific therapeutic targets position them as valuable candidates for further research. Continued exploration of oxadiazole derivatives, with an emphasis on overcoming resistance, may lead to the development of novel treatments for a variety of challenging diseases.

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恶二唑衍生物药理研究进展综述。
背景:近年来,新型杂环化合物,特别是恶二唑衍生物的合成取得了重大进展,因为它们具有广泛的药理活性。尽管恶二唑环是一个相对较小的结构,但其衍生物在一系列疾病中显示出相当大的治疗潜力。这些化合物具有多种生物效应,包括抗炎、抗惊厥、降血糖、抗结核、抗焦虑、抗菌、抗肿瘤和抗癌特性。日益严重的耐药性问题进一步推动了对以恶二唑为基础的化合物的治疗前景的研究,特别是它们针对耐药疾病的能力。目的:本综述旨在重点介绍恶二唑衍生物的药理学概况,重点介绍结构修饰如何增强其对特定治疗靶点的活性。此外,本综述旨在探索克服与这些化合物相关的耐药机制的策略,强调它们在解决新出现的耐药疾病方面的潜力。结论:恶二唑衍生物是一类很有前途的化合物,具有显著的治疗潜力,特别是面对日益增加的耐药性。它们多样的药理活性和针对特定治疗靶点进行结构优化的能力使它们成为进一步研究的有价值的候选者。继续探索恶二唑衍生物,重点是克服耐药性,可能会导致各种具有挑战性的疾病的新治疗方法的发展。
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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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