Discovery of 1,3-Disubstituted Pyrazole derivatives as Mycobacterium tuberculosis inhibitors

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL
Guoquan Wan , Chao Gao , Xiaorui Zhang , Huapei Qiu , Qifan Tang , Jumei Zeng , Luoting Yu
{"title":"Discovery of 1,3-Disubstituted Pyrazole derivatives as Mycobacterium tuberculosis inhibitors","authors":"Guoquan Wan ,&nbsp;Chao Gao ,&nbsp;Xiaorui Zhang ,&nbsp;Huapei Qiu ,&nbsp;Qifan Tang ,&nbsp;Jumei Zeng ,&nbsp;Luoting Yu","doi":"10.1016/j.bmcl.2025.130156","DOIUrl":null,"url":null,"abstract":"<div><div>Tuberculosis is a global epidemic caused by <em>Mycobacterium tuberculosis</em>, predominantly impacting underprivileged regions worldwide. Here, we identified a novel 1,3-disubstituted pyrazole derivative, compound <strong>A</strong>, that exhibits antitubercular activity through <em>in vitro</em> screening. Further SAR studies resulted in the identification of compounds <strong>4c</strong> and <strong>6b</strong>, which exhibited improved antitubercular activity, with MIC values of 5.34 and 5.04 μg/mL against H37Ra, respectively. Additionally, compounds <strong>4c</strong> and <strong>6b</strong> exhibited favorable safety profiles, showing no obvious toxicity to Vero, A549, and HepG2 cell lines. Our docking studies suggest that PptT may serve as one of the potential targets for these compounds. These encouraging results provide valuable insights for the development of novel structured antitubercular agents.</div></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"121 ","pages":"Article 130156"},"PeriodicalIF":2.5000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X25000654","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

Tuberculosis is a global epidemic caused by Mycobacterium tuberculosis, predominantly impacting underprivileged regions worldwide. Here, we identified a novel 1,3-disubstituted pyrazole derivative, compound A, that exhibits antitubercular activity through in vitro screening. Further SAR studies resulted in the identification of compounds 4c and 6b, which exhibited improved antitubercular activity, with MIC values of 5.34 and 5.04 μg/mL against H37Ra, respectively. Additionally, compounds 4c and 6b exhibited favorable safety profiles, showing no obvious toxicity to Vero, A549, and HepG2 cell lines. Our docking studies suggest that PptT may serve as one of the potential targets for these compounds. These encouraging results provide valuable insights for the development of novel structured antitubercular agents.

Abstract Image

1,3-二取代吡唑衍生物结核分枝杆菌抑制剂的发现。
结核病是由结核分枝杆菌引起的全球性流行病,主要影响世界各地的贫困地区。在这里,我们通过体外筛选发现了一种新型 1,3-二取代吡唑衍生物--化合物 A,它具有抗结核活性。进一步的 SAR 研究发现了化合物 4c 和 6b,它们的抗结核活性有所提高,对 H37Ra 的 MIC 值分别为 5.34 和 5.04 μg/mL。此外,化合物 4c 和 6b 还具有良好的安全性,对 Vero、A549 和 HepG2 细胞系没有明显毒性。我们的对接研究表明,PptT 可能是这些化合物的潜在靶点之一。这些令人鼓舞的结果为开发新型结构抗结核药物提供了宝贵的启示。
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
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
×
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:481959085
Book学术官方微信