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The main protease and RNA-dependent RNA polymerase are two prime targets for SARS-CoV-2.
Jin, Zhenming; Wang, Haofeng; Duan, Yinkai; Yang, Haitao.
  • Jin Z; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China; School of Life Sciences and School of Medicine, Tsinghua University, Beijing, China.
  • Wang H; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China; School of Life Sciences, Tianjin University, Tianjin, China. Electronic address: wanghf@tju.edu.cn.
  • Duan Y; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
  • Yang H; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China. Electronic address: yanght@shanghaitech.edu.cn.
Biochem Biophys Res Commun ; 538: 63-71, 2021 01 29.
Article in English | MEDLINE | ID: covidwho-1125596
ABSTRACT
The coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), poses an unprecedented global health crisis. It is particularly urgent to develop clinically effective therapies to contain the pandemic. The main protease (Mpro) and the RNA-dependent RNA polymerase (RdRP), which are responsible for the viral polyprotein proteolytic process and viral genome replication and transcription, respectively, are two attractive drug targets for SARS-CoV-2. This review summarizes up-to-date progress in the structural and pharmacological aspects of those two key targets above. Different classes of inhibitors individually targeting Mpro and RdRP are discussed, which could promote drug development to treat SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Enzyme Inhibitors / Coronavirus Protease Inhibitors / Coronavirus RNA-Dependent RNA Polymerase / Coronavirus 3C Proteases / SARS-CoV-2 Type of study: Prognostic study Limits: Humans Language: English Journal: Biochem Biophys Res Commun Year: 2021 Document Type: Article Affiliation country: J.bbrc.2020.10.091

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Enzyme Inhibitors / Coronavirus Protease Inhibitors / Coronavirus RNA-Dependent RNA Polymerase / Coronavirus 3C Proteases / SARS-CoV-2 Type of study: Prognostic study Limits: Humans Language: English Journal: Biochem Biophys Res Commun Year: 2021 Document Type: Article Affiliation country: J.bbrc.2020.10.091