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Discovery of 4'-O-methylscutellarein as a potent SARS-CoV-2 main protease inhibitor.
Wu, Qianqian; Yan, Shiqiang; Wang, Yujie; Li, Maotian; Xiao, Yibei; Li, Yingxia.
  • Wu Q; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Department of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
  • Yan S; Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
  • Wang Y; Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
  • Li M; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; School of Life Science and Technology, China Pharmaceutical University, Nanjing, 211198, China.
  • Xiao Y; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Department of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 211198, China. Electronic address: yibei.xiao@cpu.ed
  • Li Y; Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China. Electronic address: liyx417@fudan.edu.cn.
Biochem Biophys Res Commun ; 604: 76-82, 2022 05 14.
Article in English | MEDLINE | ID: covidwho-1797136
ABSTRACT
The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in millions of deaths and seriously threatened public health and safety. Despite COVID-19 vaccines being readily popularized worldwide, targeted therapeutic agents for the treatment of this disease remain very limited. Here, we studied the inhibitory activity of the scutellarein and its methylated derivatives against SARS-CoV-2 main protease (Mpro) by the fluorescence resonance energy transfer (FRET) assay. Among all the methylated derivatives we studied, 4'-O-methylscutellarein exhibited the most promising enzyme inhibitory activity in vitro, with the half-maximal inhibitory concentration value (IC50) of 0.40 ± 0.03 µM. Additionally, the mechanism of action of the hits was further characterized through enzyme kinetic studies and molecular docking. Overall, our results implied that 4'-O-methylscutellarein could be a primary lead compound with clinical potential for the development of inhibitors against the SARS-CoV-2 Mpro.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Alkaloids / Viral Protease Inhibitors / Coronavirus 3C Proteases / SARS-CoV-2 / Indoles Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biochem Biophys Res Commun Year: 2022 Document Type: Article Affiliation country: J.bbrc.2022.03.052

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Alkaloids / Viral Protease Inhibitors / Coronavirus 3C Proteases / SARS-CoV-2 / Indoles Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biochem Biophys Res Commun Year: 2022 Document Type: Article Affiliation country: J.bbrc.2022.03.052