Therapeutic prospects of thiazolo[3,2-b][1,2,4]triazole derivatives: a comprehensive review of biological activities and structure-activity relationship insights.

IF 3.3 4区 医学 Q3 CHEMISTRY, MEDICINAL
Priya Jajoriya, Sangeeta Sharma, Annu Jangra, Gulshan Singh, Virender Kumar, Prince Kumar, Ranjana Aggarwal, Mona Hooda
{"title":"Therapeutic prospects of thiazolo[3,2-<i>b</i>][1,2,4]triazole derivatives: a comprehensive review of biological activities and structure-activity relationship insights.","authors":"Priya Jajoriya, Sangeeta Sharma, Annu Jangra, Gulshan Singh, Virender Kumar, Prince Kumar, Ranjana Aggarwal, Mona Hooda","doi":"10.1080/17568919.2026.2748648","DOIUrl":null,"url":null,"abstract":"<p><p>Thiazolo[3,2-<i>b</i>][1,2,4]triazole derivatives have emerged as a promising class of fused heterocyclic scaffolds in medicinal chemistry. Over the past decade, this class of compounds has attracted considerable attention as potential leads for developing therapeutically relevant agents. Owing to the remarkable therapeutic profile of this scaffold, in the present review, we aim to provide a comprehensive overview of the biological significance of thiazolo[3,2-<i>b</i>][1,2,4]triazole derivatives reported between 2015 and 2026, emphasizing anticancer, antimicrobial, antiviral, analgesic, anti-inflammatory, and enzyme-inhibitory activities. To get insights into the structural features and modifications essential for the activity, detailed structure-activity relationship (SAR) studies are carried out. Additionally, to better understand the binding mechanism and to support the <i>in vitro</i> results, molecular docking studies are discussed. The present review may help researchers working in the field of medicinal chemistry for designing highly potent, novel, multifunctional derivatives that exhibit excellent target selectivity and drug-like characteristics.</p>","PeriodicalId":12475,"journal":{"name":"Future medicinal chemistry","volume":" ","pages":"1-13"},"PeriodicalIF":3.3000,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17568919.2026.2748648","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Thiazolo[3,2-b][1,2,4]triazole derivatives have emerged as a promising class of fused heterocyclic scaffolds in medicinal chemistry. Over the past decade, this class of compounds has attracted considerable attention as potential leads for developing therapeutically relevant agents. Owing to the remarkable therapeutic profile of this scaffold, in the present review, we aim to provide a comprehensive overview of the biological significance of thiazolo[3,2-b][1,2,4]triazole derivatives reported between 2015 and 2026, emphasizing anticancer, antimicrobial, antiviral, analgesic, anti-inflammatory, and enzyme-inhibitory activities. To get insights into the structural features and modifications essential for the activity, detailed structure-activity relationship (SAR) studies are carried out. Additionally, to better understand the binding mechanism and to support the in vitro results, molecular docking studies are discussed. The present review may help researchers working in the field of medicinal chemistry for designing highly potent, novel, multifunctional derivatives that exhibit excellent target selectivity and drug-like characteristics.

噻唑[3,2-b][1,2,4]三唑衍生物的治疗前景:生物活性和构效关系的综合综述。
噻唑[3,2-b][1,2,4]三唑衍生物是一类很有前途的融合杂环支架。在过去的十年中,这类化合物作为开发治疗相关药物的潜在线索引起了相当大的关注。由于该支架具有显著的治疗效果,在本综述中,我们旨在全面概述2015年至2026年间报道的噻唑[3,2-b][1,2,4]三唑衍生物的生物学意义,重点介绍抗癌、抗菌、抗病毒、镇痛、抗炎和酶抑制活性。为了深入了解活动的结构特征和必要的修饰,进行了详细的构效关系(SAR)研究。此外,为了更好地了解结合机制并支持体外实验结果,本文还讨论了分子对接研究。本文综述可能有助于药物化学领域的研究人员设计出高效、新颖、多功能的衍生物,这些衍生物具有优异的靶向选择性和药物样特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书