Insights into the Antiparasitic Activity of Pyrazole-benzimidazole against Trypanosoma cruzi.

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Vitoria Barbosa Paes, Leonardo da Silva Lara, Lorraine Martins Rocha Orlando, Guilherme Curty Lechuga, Thamyris Pérez de Souza, Byanca Silva Ferreira, Mariana de Oliveira Zago, Maurício Silva Dos Santos, Mirian Claudia de Souza Pereira
{"title":"Insights into the Antiparasitic Activity of Pyrazole-benzimidazole against Trypanosoma cruzi.","authors":"Vitoria Barbosa Paes, Leonardo da Silva Lara, Lorraine Martins Rocha Orlando, Guilherme Curty Lechuga, Thamyris Pérez de Souza, Byanca Silva Ferreira, Mariana de Oliveira Zago, Maurício Silva Dos Santos, Mirian Claudia de Souza Pereira","doi":"10.2174/0109298673342932241016032905","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Chagas disease (CD), a life-threatening disease caused by Trypanosoma cruzi, remains a significant global public health concern. The limited efficacy of the available drugs (nifurtimox and benznidazole), their severe adverse events, and the unsatisfactory outcomes of clinical trials drive the search for new, effective, and safe drugs.</p><p><strong>Objective: </strong>This study describes the synthesis, structural characterization, and in vitro antiparasitic activity of novel pyrazole-benzimidazole derivatives against mammalian developmental stages of T. cruzi.</p><p><strong>Methods: </strong>Phenotypic screening was used to assess the effect of pyrazole-benzimidazole derivatives against T. cruzi. Three-dimensional cardiac spheroids were employed to evaluate the toxic effect and drug efficacy. Molecular docking and cysteine protease activity were also performed.</p><p><strong>Results: </strong>Pyrazole-benzimidazole derivatives showed activity against both trypomastigotes and intracellular amastigotes. Compounds 1i (IC50 = 6.6 μM) and 1j (IC50 = 9.4 μM) demonstrated the most potent activity with a high selectivity index (SI > 45) against intracellular amastigotes. Both compounds exhibited high efficacy on 3D cardiac spheroids, effectively reducing the parasite load by over 80%. Molecular docking analysis revealed that both compounds target the catalytic domain of cruzain through pi-stacking and hydrogen bonding interactions and inhibit T. cruzi cysteine protease. These derivatives also showed an additive effect in combination with the reference drug (Bz).</p><p><strong>Conclusion: </strong>Our findings emphasize the significance of pyrazole-benzimidazole hybrids in the search for new anti-T. cruzi agents.</p>","PeriodicalId":10984,"journal":{"name":"Current medicinal chemistry","volume":" ","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0109298673342932241016032905","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Chagas disease (CD), a life-threatening disease caused by Trypanosoma cruzi, remains a significant global public health concern. The limited efficacy of the available drugs (nifurtimox and benznidazole), their severe adverse events, and the unsatisfactory outcomes of clinical trials drive the search for new, effective, and safe drugs.

Objective: This study describes the synthesis, structural characterization, and in vitro antiparasitic activity of novel pyrazole-benzimidazole derivatives against mammalian developmental stages of T. cruzi.

Methods: Phenotypic screening was used to assess the effect of pyrazole-benzimidazole derivatives against T. cruzi. Three-dimensional cardiac spheroids were employed to evaluate the toxic effect and drug efficacy. Molecular docking and cysteine protease activity were also performed.

Results: Pyrazole-benzimidazole derivatives showed activity against both trypomastigotes and intracellular amastigotes. Compounds 1i (IC50 = 6.6 μM) and 1j (IC50 = 9.4 μM) demonstrated the most potent activity with a high selectivity index (SI > 45) against intracellular amastigotes. Both compounds exhibited high efficacy on 3D cardiac spheroids, effectively reducing the parasite load by over 80%. Molecular docking analysis revealed that both compounds target the catalytic domain of cruzain through pi-stacking and hydrogen bonding interactions and inhibit T. cruzi cysteine protease. These derivatives also showed an additive effect in combination with the reference drug (Bz).

Conclusion: Our findings emphasize the significance of pyrazole-benzimidazole hybrids in the search for new anti-T. cruzi agents.

吡唑-苯并咪唑抗克氏锥虫活性的研究。
背景:恰加斯病(CD)是由克氏锥虫引起的一种危及生命的疾病,仍然是一个重大的全球公共卫生问题。现有药物(硝呋替莫和苯硝唑)有限的疗效、严重的不良事件以及临床试验不令人满意的结果促使人们寻找新的、有效的和安全的药物。目的:研究新型吡唑-苯并咪唑衍生物的合成、结构表征及其对哺乳类克氏体发育阶段的体外抗寄生活性。方法:采用表型筛选法评价吡唑-苯并咪唑衍生物对克氏锥虫的作用。采用三维心脏球体评价毒副作用和药物疗效。分子对接和半胱氨酸蛋白酶活性也进行了测试。结果:吡唑-苯并咪唑衍生物对锥乳线虫和细胞内无尾线虫均有抑制作用。化合物1i (IC50 = 6.6 μM)和1j (IC50 = 9.4 μM)对胞内无尾菌丝体的选择性指数最高(SI bbbb45)。这两种化合物对三维心脏球体都有很高的疗效,有效地减少了80%以上的寄生虫负荷。分子对接分析表明,两种化合物通过pi-stacking和氢键相互作用靶向cruzain的催化结构域,抑制T. cruzi半胱氨酸蛋白酶。这些衍生物与对照药物(Bz)联合也显示出加性效应。结论:本研究结果强调了吡唑-苯并咪唑复合物在寻找新的抗t抗体中的重要意义。cruzi代理。
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
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
×
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