Recent advances in triazole hybrid molecules for the therapeutic management of neglected tropical diseases.

IF 3.6 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jatin Malik, Gauri Karande, Sankaranarayanan Murugesan, Kondapalli Venkata Gowri Chandra Sekhar
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引用次数: 0

Abstract

The triazole scaffold has garnered considerable attention over the preceding decade as a privileged pharmacophore in the rational design of chemotherapeutic agents targeting neglected tropical diseases (NTDs). This review provides a comprehensive elucidation of the multifaceted research dedicated to the structural optimization of the triazole nucleus and its consequential outcomes on biological efficacy. Emphasis is placed on the methodical investigation of diverse substituents appended to the triazole core, underscoring the profound influence of seemingly marginal modifications on critical pharmacological parameters. Through a comprehensive deconstruction of structure-activity relationships (SAR), this exposition identifies the essential functional moieties underpinning biological efficacy that potentiate anti-parasitic, anti-fungal, and anti-viral activities across a spectrum of NTD-relevant biological targets. These insights deepen the knowledge of triazole based hybrid molecules and guide future rational design of novel compounds. By synthesizing and analyzing findings from a wide array of studies, this review aims to serve as a valuable resource for researchers interested in the continued development of triazole derivatives to manage neglected tropical diseases effectively.

三唑杂化分子治疗被忽视热带病的最新进展。
在过去的十年中,三唑支架作为一种特殊的药效团,在针对被忽视的热带病(NTDs)的化疗药物的合理设计中引起了相当大的关注。本文综述了三唑核结构优化的多方面研究及其对生物功效的影响。重点放在对附加到三唑核心的不同取代基的系统研究上,强调了对关键药理学参数的看似边缘修饰的深刻影响。通过对结构-活性关系(SAR)的全面解构,本文确定了支撑生物功效的基本功能部分,这些功能部分可以增强ntd相关生物靶点的抗寄生虫、抗真菌和抗病毒活性。这些见解加深了对基于三唑的杂化分子的认识,并指导了未来新化合物的合理设计。通过对大量研究结果的综合和分析,本综述旨在为有兴趣继续开发三唑衍生物以有效管理被忽视的热带病的研究人员提供宝贵的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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