COVID-19 Therapies: Protease Inhibitions and Novel Degrader Strategies

M. Reboud-Ravaux, C. El Amri
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引用次数: 2

Abstract

The global spread of severe acute respiratory syndrome corona virus-2 (SARS-CoV-2) variants is alarming. In addition to vaccines, effective antiviral agents are urgently needed to combat corona virus disease 2019 (COVID-19). In this review, we will give insights on several canonical approaches using current medicinal chemistry. They target host (TMPRSS2, cathepsins B/L, furin) and viral (3CLpro and PLPro) proteases involved in virus cell entry and virus production, respectively. Innovative mechanisms of drug action are now explored whereby the drug triggers a cellular event that reduces the level of disease-implicated protein or RNA. The potential therapeutic power of induced degradations of viral proteins by PROTACs and of RNA by RIBOTACs for the treatment of COVID-19 will be discussed. Degraders of host cell RNA-binding proteins (RNA-PROTACs) may also constitute a therapeutical opportunity. First applicated to oncology, these novel technologies may be of a particular interest to obtain therapeutics susceptible to act on mutated viruses.
新冠肺炎治疗:蛋白酶抑制剂和新型降解剂策略
严重急性呼吸综合征冠状病毒2型变异株在全球的传播令人担忧。除了疫苗外,还迫切需要有效的抗病毒药物来对抗2019冠状病毒病(新冠肺炎)。在这篇综述中,我们将对使用当前药物化学的几种经典方法进行深入了解。它们分别靶向参与病毒细胞进入和病毒产生的宿主(TMPRSS2、组织蛋白酶B/L、弗林蛋白酶)和病毒(3CLpro和PLPro)蛋白酶。目前正在探索药物作用的创新机制,通过该机制,药物触发细胞事件,降低与疾病相关的蛋白质或RNA水平。将讨论PROTAC诱导的病毒蛋白降解和RIOTACs诱导的RNA降解对治疗新冠肺炎的潜在治疗作用。宿主细胞RNA结合蛋白(RNA-PROTACs)的降解物也可能构成治疗机会。这些新技术首先应用于肿瘤学,可能对获得对变异病毒敏感的治疗方法特别感兴趣。
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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