Center for Translational Antiviral Research, Georgia State University, Atlanta, Georgia, USA.
DNA Cell Biol. 2022 Aug;41(8):699-704. doi: 10.1089/dna.2022.0312. Epub 2022 Jul 5.
The COVID-19 pandemic has highlighted the urgent need for the development of broad-spectrum antivirals to enhance preparedness against future spillover of zoonotic viruses with pandemic potential into the human population. Currently, the direct-acting orally available SARS-CoV-2 inhibitors molnupiravir and paxlovid are approved for human use under emergency use authorization. A promising next-generation therapeutic candidate is the orally available ribonucleoside analog 4'-fluorouridine (4'-FlU) that had potent antiviral efficacy against different viral targets, including SARS-CoV-2 in human organoids and animal models. Although a nucleoside analog inhibitor such as molnupiravir that targets the viral RNA-dependent RNA polymerase (RdRP) complex, 4'-FlU showed a distinct mechanism of activity, delayed chain termination, compared with molnupiravir's induction of viral error catastrophe. This review will focus on some currently approved and emerging medicines developed against SARS-CoV-2, examining their potential to form a pharmacological first-line defense against zoonotic viruses with pandemic potential.
新冠疫情突出表明,迫切需要开发广谱抗病毒药物,以增强对未来具有大流行潜力的人畜共患病毒溢出到人类群体的准备。目前,直接作用的口服可用 SARS-CoV-2 抑制剂莫努匹韦和帕昔洛韦已根据紧急使用授权获准用于人体。一种有前途的下一代治疗候选药物是口服可用的核苷类似物 4'-氟尿嘧啶(4'-FlU),它对不同的病毒靶点具有强大的抗病毒功效,包括人类类器官和动物模型中的 SARS-CoV-2。虽然核苷类似物抑制剂(如靶向病毒 RNA 依赖性 RNA 聚合酶(RdRP)复合物的莫努匹韦),但 4'-FlU 的作用机制不同,与莫努匹韦诱导的病毒错误灾难相比,它会延迟链终止。本综述将重点介绍一些针对 SARS-CoV-2 开发的已批准和新兴药物,研究它们对具有大流行潜力的人畜共患病毒形成药理学一线防御的潜力。