Medicinal Polypharmacology in the Clinic - Translating the Polypharmacolome into Therapeutic Benefit.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-03-01 Epub Date: 2024-02-16 DOI:10.1007/s11095-024-03656-8
Muhammad Rafehi, Marius Möller, Wouroud Ismail Al-Khalil, Sven Marcel Stefan
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引用次数: 0

Abstract

Drugs with multiple targets, often annotated as 'unselective', 'promiscuous', 'multitarget', or 'polypharmacological', are widely considered in both academic and industrial research as a high risk due to the likelihood of adverse effects. However, retrospective analyses have shown that particularly approved drugs bear rich polypharmacological profiles. This raises the question whether our perception of the specificity paradigm ('one drug-one target concept') is correct - and if specifically multitarget drugs should be developed instead of being rejected. These questions provoke a paradigm shift - regarding the development of polypharmacological drugs not as a 'waste of investment', but acknowledging the existence of a 'lack of investment'. This perspective provides an insight into modern drug development highlighting latest drug candidates that have not been assessed in a broader polypharmacology-based context elsewhere embedded in a historic framework of classical and modern approved multitarget drugs. The article shall be an inspiration to the scientific community to re-consider current standards, and more, to evolve to a better understanding of polypharmacology from a challenge to an opportunity.

临床中的药用多药理学--将多药组转化为治疗效果。
具有多个靶点的药物通常被注释为 "非选择性"、"杂合性"、"多靶点 "或 "多药理",在学术研究和工业研究中被广泛认为是高风险药物,因为很可能产生不良反应。然而,回顾性分析表明,特别是已获批准的药物具有丰富的多药理特征。这就提出了一个问题:我们对特异性范式("一药一靶点概念")的认识是否正确?这些问题引发了范式的转变--多药理药物的开发不是 "投资浪费",而是承认 "投资不足 "的存在。这一观点为现代药物开发提供了一个视角,突出了在经典和现代已获批准的多靶点药物历史框架内,尚未在更广泛的多药理学背景下进行评估的最新候选药物。这篇文章将激励科学界重新考虑当前的标准,进而更好地理解多药理学,将挑战转化为机遇。
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
7.20
自引率
4.30%
发文量
567
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