Department of Medical Biotechnologies, University of Siena, Siena, Italy.
Expert Opin Ther Pat. 2021 Apr;31(4):325-337. doi: 10.1080/13543776.2021.1880568. Epub 2021 Mar 3.
: The current SARS-CoV-2 pandemic urgently demands for both prevention and treatment strategies. RNA-dependent RNA-polymerase (RdRp), which has no counterpart in human cells, is an excellent target for drug development. Given the time-consuming process of drug development, repurposing drugs approved for other indications or at least successfully tested in terms of safety and tolerability, is an attractive strategy to rapidly provide an effective medication for severe COVID-19 cases.: The currently available data and upcominSg studies on RdRp which can be repurposed to halt SARS-CoV-2 replication, are reviewed.: Drug repurposing and design of novel compounds are proceeding in parallel to provide a quick response and new specific drugs, respectively. Notably, the proofreading SARS-CoV-2 exonuclease activity could limit the potential for drugs designed as immediate chain terminators and favor the development of compounds acting through delayed termination. While vaccination is awaited to curb the SARS-CoV-2 epidemic, even partially effective drugs from repurposing strategies can be of help to treat severe cases of disease. Considering the high conservation of RdRp among coronaviruses, an improved knowledge of its activity can provide useful information for drug development or drug repurposing to combat SARS-CoV-2 as well as future pandemics.
当前的 SARS-CoV-2 大流行迫切需要预防和治疗策略。RNA 依赖性 RNA 聚合酶(RdRp)在人类细胞中没有对应物,是药物开发的理想靶点。鉴于药物开发过程耗时漫长,重新利用已批准用于其他适应症的药物,或者至少在安全性和耐受性方面经过成功测试,是为严重 COVID-19 病例快速提供有效药物的一种有吸引力的策略。本文回顾了可用于阻止 SARS-CoV-2 复制的 RdRp 的现有数据和即将进行的研究,以进行药物再利用。药物再利用和新型化合物的设计正在并行进行,以分别提供快速反应和新的特定药物。值得注意的是,校对 SARS-CoV-2 外切酶活性可以限制设计为即时链终止剂的药物的潜在作用,并有利于通过延迟终止起作用的化合物的开发。虽然疫苗接种正在等待以遏制 SARS-CoV-2 流行,但即使是来自再利用策略的部分有效药物也可以帮助治疗严重疾病。鉴于 RdRp 在冠状病毒之间高度保守,对其活性的更深入了解可以为药物开发或药物再利用提供有用信息,以对抗 SARS-CoV-2 以及未来的大流行。