Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs

Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral...

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Published inAntimicrobial agents and chemotherapy Vol. 64; no. 7
Main Authors Jeon, Sangeun, Ko, Meehyun, Lee, Jihye, Choi, Inhee, Byun, Soo Young, Park, Soonju, Shum, David, Kim, Seungtaek
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 23.06.2020
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Online AccessGet full text
ISSN0066-4804
1098-6596
1098-6596
DOI10.1128/AAC.00819-20

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Abstract Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects.
AbstractList Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects.
Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects. Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC 50 s), and in particular, two FDA-approved drugs—niclosamide and ciclesonide—were notable in some respects.
Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects.
Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects.Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which were preselected by an assay of SARS-CoV. We identified 24 potential antiviral drug candidates against SARS-CoV-2 infection. Some drug candidates showed very low 50% inhibitory concentrations (IC50s), and in particular, two FDA-approved drugs-niclosamide and ciclesonide-were notable in some respects.
Author Lee, Jihye
Byun, Soo Young
Kim, Seungtaek
Park, Soonju
Ko, Meehyun
Jeon, Sangeun
Choi, Inhee
Shum, David
Author_xml – sequence: 1
  givenname: Sangeun
  surname: Jeon
  fullname: Jeon, Sangeun
  organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 2
  givenname: Meehyun
  surname: Ko
  fullname: Ko, Meehyun
  organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 3
  givenname: Jihye
  surname: Lee
  fullname: Lee, Jihye
  organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 4
  givenname: Inhee
  surname: Choi
  fullname: Choi, Inhee
  organization: Medicinal Chemistry, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 5
  givenname: Soo Young
  surname: Byun
  fullname: Byun, Soo Young
  organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 6
  givenname: Soonju
  surname: Park
  fullname: Park, Soonju
  organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 7
  givenname: David
  surname: Shum
  fullname: Shum, David
  organization: Screening Discovery Platform, Institut Pasteur Korea, Seongnam, South Korea
– sequence: 8
  givenname: Seungtaek
  surname: Kim
  fullname: Kim, Seungtaek
  organization: Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, South Korea
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32366720$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1002/cpt1976196802
10.1016/j.jiac.2020.04.007
10.1038/s41467-019-13659-4
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10.1056/NEJMoa2001316
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Keywords COVID-19
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Citation Jeon S, Ko M, Lee J, Choi I, Byun SY, Park S, Shum D, Kim S. 2020. Identification of antiviral drug candidates against SARS-CoV-2 from FDA-approved drugs. Antimicrob Agents Chemother 64:e00819-20. https://doi.org/10.1128/AAC.00819-20.
Sangeun Jeon and Meehyun Ko contributed equally to this work. Author order was determined alphabetically.
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SSID ssj0006590
Score 2.7080052
Snippet Drug repositioning is the only feasible option to immediately address the COVID-19 global challenge. We screened a panel of 48 FDA-approved drugs against...
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SubjectTerms Animals
Anti-Inflammatory Agents - pharmacology
Antiviral Agents
Antiviral Agents - pharmacology
Betacoronavirus
Betacoronavirus - drug effects
Cell Line
Chlorocebus aethiops
Coronavirus Infections
Coronavirus Infections - drug therapy
COVID-19
Drug Evaluation, Preclinical - methods
Drug Repositioning
Editor's Pick
Humans
Niclosamide
Niclosamide - pharmacology
Pandemics
Pneumonia, Viral
Pneumonia, Viral - drug therapy
Pregnenediones
Pregnenediones - pharmacology
SARS-CoV-2
Vero Cells
Title Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs
URI https://www.ncbi.nlm.nih.gov/pubmed/32366720
https://journals.asm.org/doi/10.1128/AAC.00819-20
https://www.proquest.com/docview/2398631162
https://pubmed.ncbi.nlm.nih.gov/PMC7318052
Volume 64
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