结核病研究中的合成奇迹:作为抗结核药物的 1,3,4-恶二唑衍生物深度综述

Isha Kapila , Ankita Bharwal , Poonam Sharma , Neeraj Choudhary , Vikrant Abbot
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引用次数: 0

摘要

鉴于结核病耐药性和非活动性病例的增加,开发新型强效化学品来治疗这种致命疾病势在必行。含有噁二唑的化合物就是一类可以考虑用来满足这一要求的化学品。结构中含有 1,3,4-恶二唑环的化合物具有多种生物作用。五元杂环的众多功能激发了从事新型分子设计的医药化学家和有机合成化学家的兴趣。小而简单的 1,3,4-恶二唑核存在于多种化合物中,具有显著的药理作用,如抗结核和用于评估新型商品,因此其开发潜力巨大。这篇综述文章重点介绍了生成 1,3,4-恶二唑核的各种方法、1,3,4-恶二唑衍生物的靶向活性及其结构活性关系,以生产潜在的抗结核药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthetic marvels in tuberculosis research: An in-depth review of 1,3,4-oxadiazole derivatives as antitubercular agents

Given the growth in drug-resistant and inactive cases of tuberculosis, it is imperative to develop novel, potent chemicals to treat this deadly illness. Compounds containing oxadiazole are one such class of chemicals that could be taken into consideration to meet this requirement. The biological action of compounds with a 1,3,4-oxadiazole ring in their structure is diverse. The numerous functions of a five-member heterocyclic ring have sparked interest of medicinal and synthetic organic chemists involved in the design of novel molecules. The development of the small and straightforward 1,3,4-oxadiazole nucleus, which is found in a variety of compounds with significant pharmacological capabilities like antitubercular and is intended to assess novel goods, has a lot of potential. This review article highlights the various approaches used to generate the 1,3,4-oxadiazole nucleus, the targeted activity of 1,3,4-oxadiazole derivatives and their structure activity relationship to produce potential antitubercular drugs.

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