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J Am Chem Soc ; 144(9): 3761-3765, 2022 03 09.
Artigo em Inglês | MEDLINE | ID: mdl-35224970

RESUMO

The Covid-19 pandemic highlights the urgent need for cost-effective processes to rapidly manufacture antiviral drugs at scale. Here we report a concise biocatalytic process for Molnupiravir, a nucleoside analogue recently approved as an orally available treatment for SARS-CoV-2. Key to the success of this process was the development of an efficient biocatalyst for the production of N-hydroxy-cytidine through evolutionary adaption of the hydrolytic enzyme cytidine deaminase. This engineered biocatalyst performs >85 000 turnovers in less than 3 h, operates at 180 g/L substrate loading, and benefits from in situ crystallization of the N-hydroxy-cytidine product (85% yield), which can be converted to Molnupiravir by a selective 5'-acylation using Novozym 435.


Assuntos
Antivirais , Tratamento Farmacológico da COVID-19 , Citidina Desaminase/metabolismo , Citidina/análogos & derivados , SARS-CoV-2 , Biocatálise , Citidina/biossíntese , Citidina/metabolismo , Citidina Desaminase/genética , Escherichia coli/enzimologia , Escherichia coli/genética , Hidroxilaminas , Engenharia Metabólica , Engenharia de Proteínas , Uridina/metabolismo
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