Molnupiravir as a promising prodrug agent for therapy of COVID-19

L. Birichevskaya, E. Kvasyuk, A. Zinchenko
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Abstract

The ongoing COVID-19 pandemic accompanied by the emergence of new successive pathogenic variants makes problematic the prospects of the approach based on application of exclusively prophylactic vaccines to combat SARSCoV-2. This reason motivated the urgent need in search and development of chemical formulas showing direct antiviral action.The present mini-review provides data on chemical and enzymatic methods of producing molnupiravir regarded so far as one of the most effective pharmaceuticals for treatment of COVID-19. In conclusion of the literature survey it is suggested to administer lipid-containing analog instead of molnupiravir in COVID-19 therapeutic protocols. In this respect the authors reported the successful synthesis catalyzed by bacterial phospholipase D of 5′-dimyristoyl derivative of N4-hydroxycytidine – the compound allegedly more efficient than molnupiravir in inhibiting SARS-CoV-2 replication.
莫努匹拉韦作为治疗COVID-19的前药
持续的COVID-19大流行伴随着新的连续致病变异的出现,使得基于应用专门预防性疫苗来对抗SARSCoV-2的方法的前景存在问题。因此,迫切需要寻找和开发具有直接抗病毒作用的化学配方。本综述提供了迄今为止被认为是治疗COVID-19最有效的药物之一的化学和酶促生产莫努匹拉韦的数据。根据文献调查的结论,建议在COVID-19治疗方案中使用含脂类似物而不是莫努比拉韦。在这方面,作者报告了由细菌磷脂酶D催化成功合成了n4 -羟基胞苷的5 ' -二豆蔻酰基衍生物,据称该化合物在抑制SARS-CoV-2复制方面比莫努皮拉韦更有效。
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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