From the "One-Molecule, One-Target, One-Disease" Concept towards Looking for Multi-Target Therapeutics for Treating Non-Polio Enterovirus (NPEV) Infections.

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2024-09-16 DOI:10.3390/ph17091218
Hugo Roux, Franck Touret, Pascal Rathelot, Patrice Vanelle, Manon Roche
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引用次数: 0

Abstract

Non-polio enteroviruses (NPEVs), namely coxsackieviruses (CV), echoviruses (E), enteroviruses (EV), and rhinoviruses (RV), are responsible for a wide variety of illnesses. Some infections can progress to life-threatening conditions in children or immunocompromised patients. To date, no treatments have been approved. Several molecules have been evaluated through clinical trials without success. To overcome these failures, the multi-target directed ligand (MTDL) strategy could be applied to tackle enterovirus infections. This work analyzes registered clinical trials involving antiviral drugs to highlight the best candidates and develops filters to apply to a selection for MTDL synthesis. We explicitly stated the methods used to answer the question: which solution can fight NPEVs effectively? We note the originality and relevance of this proposal in relation to the state of the art in the enterovirus-inhibitors field. Several combinations are possible to broaden the antiviral spectrum and potency. We discuss data related to the virus and data related to each LEAD compound identified so far. Overall, this study proposes a perspective on different strategies to overcome issues identified in clinical trials and evaluate the "MTDL" potential to improve the efficacy of drugs, broaden the antiviral targets, possibly reduce the adverse effects, drug design costs and limit the selection of drug-resistant virus variants.

从 "一分子、一靶点、一疾病 "概念到寻找治疗非脊髓灰质炎肠道病毒 (NPEV) 感染的多靶点疗法。
非脊髓灰质炎肠道病毒(NPEVs),即柯萨奇病毒(CV)、埃可病毒(E)、肠道病毒(EV)和鼻病毒(RV),可导致多种疾病。在儿童或免疫力低下的患者中,有些感染可发展为危及生命的疾病。迄今为止,还没有治疗方法获得批准。通过临床试验对几种分子进行了评估,但都没有成功。为了克服这些失败,多靶点定向配体(MTDL)策略可用于解决肠病毒感染问题。这项工作分析了已登记的抗病毒药物临床试验,以突出最佳候选药物,并开发了过滤器,用于选择 MTDL 合成。我们明确阐述了用于回答以下问题的方法:哪种方案能有效对抗 NPEV?我们注意到这一建议在肠病毒抑制剂领域的独创性和相关性。可以通过几种组合来扩大抗病毒谱和效力。我们讨论了与病毒有关的数据以及迄今发现的每种 LEAD 化合物的相关数据。总之,本研究从不同的角度提出了克服临床试验中发现的问题的策略,并评估了 "MTDL "在提高药物疗效、拓宽抗病毒靶点、减少不良反应、降低药物设计成本和限制耐药病毒变种的选择方面的潜力。
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
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.
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