Several FDA-Approved Drugs Effectively Inhibit SARS-CoV-2 Infection in vitro

To identify drugs that are potentially used for the treatment of COVID-19, the potency of 1403 FDA-approved drugs were evaluated using a robust pseudovirus assay and the candidates were further confirmed by authentic SARS-CoV-2 assay. Four compounds, Clomiphene (citrate), Vortioxetine, Vortioxetine...

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Published inFrontiers in pharmacology Vol. 11; p. 609592
Main Authors Xiong, Hua-Long, Cao, Jia-Li, Shen, Chen-Guang, Ma, Jian, Qiao, Xiao-Yang, Shi, Tian-Shu, Ge, Sheng-Xiang, Ye, Hui-Ming, Zhang, Jun, Yuan, Quan, Zhang, Tian-Ying, Xia, Ning-Shao
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Published Switzerland Frontiers Media S.A 05.02.2021
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Abstract To identify drugs that are potentially used for the treatment of COVID-19, the potency of 1403 FDA-approved drugs were evaluated using a robust pseudovirus assay and the candidates were further confirmed by authentic SARS-CoV-2 assay. Four compounds, Clomiphene (citrate), Vortioxetine, Vortioxetine (hydrobromide) and Asenapine (hydrochloride), showed potent inhibitory effects in both pseudovirus and authentic virus assay. The combination of Clomiphene (citrate), Vortioxetine and Asenapine (hydrochloride) is much more potent than used alone, with IC50 of 0.34 μM.
AbstractList To identify drugs that are potentially used for the treatment of COVID-19, the potency of 1403 FDA-approved drugs were evaluated using a robust pseudovirus assay and the candidates were further confirmed by authentic SARS-CoV-2 assay. Four compounds, Clomiphene (citrate), Vortioxetine, Vortioxetine (hydrobromide) and Asenapine (hydrochloride), showed potent inhibitory effects in both pseudovirus and authentic virus assay. The combination of Clomiphene (citrate), Vortioxetine and Asenapine (hydrochloride) is much more potent than used alone, with IC50 of 0.34 μM.
Author Shen, Chen-Guang
Yuan, Quan
Ge, Sheng-Xiang
Ye, Hui-Ming
Ma, Jian
Shi, Tian-Shu
Xia, Ning-Shao
Zhang, Tian-Ying
Xiong, Hua-Long
Qiao, Xiao-Yang
Cao, Jia-Li
Zhang, Jun
AuthorAffiliation 3 Shenzhen Key Laboratory of Pathogen and Immunity, National Clinical Research Center for Infectious Disease, State Key Discipline of Infectious Disease, Shenzhen Third People’s Hospital, Second Hospital Affiliated to Southern University of Science and Technology, Shenzhen , China
1 State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Life Sciences and School of Public Health, Xiamen University, Xiamen , China
4 School of Public Health, Southern Medical University, Guangzhou , China
2 Department of Clinical Laboratory, Women and Children’s Hospital, School of Medicine, Xiamen University, Xiamen , China
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  surname: Xia
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  organization: State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Life Sciences and School of Public Health, Xiamen University, Xiamen, China
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Copyright Copyright © 2021 Xiong, Cao, Shen, Ma, Qiao, Shi, Ge, Ye, Zhang, Yuan, Zhang and Xia.
Copyright © 2021 Xiong, Cao, Shen, Ma, Qiao, Shi, Ge, Ye, Zhang, Yuan, Zhang and Xia. 2021 Xiong, Cao, Shen, Ma, Qiao, Shi, Ge, Ye, Zhang, Yuan, Zhang and Xia
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Keywords SARS-CoV-2
pseudovirus assay
drug screening
drug combination
vesicular stomatitis virus
Language English
License Copyright © 2021 Xiong, Cao, Shen, Ma, Qiao, Shi, Ge, Ye, Zhang, Yuan, Zhang and Xia.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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Reviewed by: Xuping Xie, University of Texas Medical Branch at Galveston, United States
This article was submitted to Pharmaceutical Medicine and Outcomes Research, a section of the journal Frontiers in Pharmacology
These authors have contributed equally to this work
Edited by: Rafael Maldonado, Pompeu Fabra University, Spain
Silvia Spoto, Policlinico Universitario Campus Bio-Medico, Italy
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Snippet To identify drugs that are potentially used for the treatment of COVID-19, the potency of 1403 FDA-approved drugs were evaluated using a robust pseudovirus...
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SubjectTerms drug combination
drug screening
Pharmacology
pseudovirus assay
SARS-CoV-2
vesicular stomatitis virus
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Title Several FDA-Approved Drugs Effectively Inhibit SARS-CoV-2 Infection in vitro
URI https://www.ncbi.nlm.nih.gov/pubmed/33613282
https://search.proquest.com/docview/2492279387
https://pubmed.ncbi.nlm.nih.gov/PMC7892437
https://doaj.org/article/99c6bb154816476bab9f54ea1e62d03a
Volume 11
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