Drug Repurposing Screen for Compounds Inhibiting the Cytopathic Effect of SARS-CoV-2

被引:51
|
作者
Chen, Catherine Z. [1 ]
Shinn, Paul [1 ]
Itkin, Zina [1 ]
Eastman, Richard T. [1 ]
Bostwick, Robert [2 ]
Rasmussen, Lynn [2 ]
Huang, Ruili [1 ]
Shen, Min [1 ]
Hu, Xin [1 ]
Wilson, Kelli M. [1 ]
Brooks, Brianna M. [1 ]
Guo, Hui [1 ]
Zhao, Tongan [1 ]
Klump-Thomas, Carleen [1 ]
Simeonov, Anton [1 ]
Michael, Samuel G. [1 ]
Lo, Donald C. [1 ]
Hall, Matthew D. [1 ]
Zheng, Wei [1 ]
机构
[1] Natl Ctr Adv Translat Sci, Rockville, MD 20850 USA
[2] Southern Res, Birmingham, AL USA
基金
美国国家卫生研究院;
关键词
COVID-19; cytopathic effect; drug repurposing and discovery; HTS; SARS-CoV-2; PHARMACOKINETICS; EFFICACY;
D O I
10.3389/fphar.2020.592737
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug repurposing is a rapid approach to identify therapeutics for the treatment of emerging infectious diseases such as COVID-19. To address the urgent need for treatment options, we carried out a quantitative high-throughput screen using a SARS-CoV-2 cytopathic assay with a compound collection of 8,810 approved and investigational drugs, mechanism-based bioactive compounds, and natural products. Three hundred and nineteen compounds with anti-SARS-CoV-2 activities were identified and confirmed, including 91 approved drugs and 49 investigational drugs. The anti-SARS-CoV-2 activities of 230 of these confirmed compounds, of which 38 are approved drugs, have not been previously reported. Chlorprothixene, methotrimeprazine, and piperacetazine were the three most potent FDA-approved drugs with anti-SARS-CoV-2 activities. These three compounds have not been previously reported to have anti-SARS-CoV-2 activities, although their antiviral activities against SARS-CoV and Ebola virus have been reported. These results demonstrate that this comprehensive data set is a useful resource for drug repurposing efforts, including design of new drug combinations for clinical trials for SARS-CoV-2.
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页数:10
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