结核靶点的新兴景观:药物化学方法。

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL
Baji Baba Shaik, Kimeshni Moodley, Safiyah Ghumran, Muhammad D. Bala, Parvesh Singh, Rajshekhar Karpoormath
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引用次数: 0

摘要

近十年来,抗结核药物的发现进展,特别是对其生物学功能、靶点抑制和结核病诊断的研究取得了长足的进展。基于靶点的药物发现技术的应用已经成为药物化学家开发新的治疗策略的有力工具,例如它在新靶点、新先导物和具有最佳疗效的候选药物的鉴定/验证中的应用。最近批准delamanid和bedaquiline分别用于治疗耐多药结核病和广泛耐药结核病进一步证明了这一点。虽然结核病药物管道已经显示出巨大的发展,但高损耗率必须不断补充管道,通过抑制新靶点来发挥作用的高质量先导。这篇综述提供了一个关键的分析方法,用于推进击中化合物成为可行的先导候选,以及新靶点在不久的将来可能对药物开发的影响。最后,我们总结了目前结核病药物开发面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Emerging Landscape of Tubercular Targets: A Medicinal Chemistry Approach

Antitubercular drug discovery progress in the last decade, especially research on the biological function, target inhibition and diagnosis of tuberculosis (TB) diagnosis has considerably advanced. The application of target-based drug discovery techniques have become a more powerful tool for medicinal chemists in developing new therapeutic strategies, such as its application in the identification/validation of new targets, new leads, and drug candidates with optimized efficacy. This has been further evidenced by the recent approval of delamanid and bedaquiline for the treatment of MDR-TB and XDR-TB, respectively. While a TB drug pipeline has shown great development, high attrition rates must constantly replenish the pipeline with high-quality leads acting through the inhibition of new targets. This review provides a critical analysis of the approaches used to advance hit compounds into viable lead candidates as well as the possible influence of new targets on drug development in the near future. Finally, we concluded with the present challenges that are faced in TB drug development.

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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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