2019年冠状病毒病(COVID-19)
组合化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
激酶
定向进化
化学
2019-20冠状病毒爆发
纳米技术
病毒学
生物化学
生物
计算生物学
计算机科学
材料科学
医学
病理
突变体
爆发
基因
传染病(医学专业)
疾病
作者
John A. McIntosh,Tamas Benkovics,Steven M. Silverman,Mark A. Huffman,Jongrock Kong,Peter E. Maligres,Tetsuji Itoh,Hao Yang,Deeptak Verma,Weilan Pan,Hsing‐I Ho,Jonathan Vroom,Anders M. Knight,Jessica A. Hurtak,Artis Klapars,Anna Fryszkowska,William Morris,Neil A. Strotman,Grant S. Murphy,Kevin M. Maloney,Patrick S. Fier
出处
期刊:ACS central science
[American Chemical Society]
日期:2021-10-29
卷期号:7 (12): 1980-1985
被引量:112
标识
DOI:10.1021/acscentsci.1c00608
摘要
Molnupiravir (MK-4482) is an investigational antiviral agent that is under development for the treatment of COVID-19. Given the potential high demand and urgency for this compound, it was critical to develop a short and sustainable synthesis from simple raw materials that would minimize the time needed to manufacture and supply molnupiravir. The route reported here is enabled through the invention of a novel biocatalytic cascade featuring an engineered ribosyl-1-kinase and uridine phosphorylase. These engineered enzymes were deployed with a pyruvate-oxidase-enabled phosphate recycling strategy. Compared to the initial route, this synthesis of molnupiravir is 70% shorter and approximately 7-fold higher yielding. Looking forward, the biocatalytic approach to molnupiravir outlined here is anticipated to have broad applications for streamlining the synthesis of nucleosides in general.
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