Enisamium Inhibits SARS-CoV-2 RNA Synthesis.
Amizon
COVID-19
FAV00A
RNA polymerase
SARS-CoV-2
molecular dynamics simulation
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
17 Sep 2021
17 Sep 2021
Historique:
received:
28
08
2021
revised:
14
09
2021
accepted:
14
09
2021
entrez:
28
9
2021
pubmed:
29
9
2021
medline:
29
9
2021
Statut:
epublish
Résumé
Pandemic SARS-CoV-2 causes a mild to severe respiratory disease called coronavirus disease 2019 (COVID-19). While control of the SARS-CoV-2 spread partly depends on vaccine-induced or naturally acquired protective herd immunity, antiviral strategies are still needed to manage COVID-19. Enisamium is an inhibitor of influenza A and B viruses in cell culture and clinically approved in countries of the Commonwealth of Independent States. In vitro, enisamium acts through metabolite VR17-04 and inhibits the activity of the influenza A virus RNA polymerase. Here we show that enisamium can inhibit coronavirus infections in NHBE and Caco-2 cells, and the activity of the SARS-CoV-2 RNA polymerase in vitro. Docking and molecular dynamics simulations provide insight into the mechanism of action and indicate that enisamium metabolite VR17-04 prevents GTP and UTP incorporation. Overall, these results suggest that enisamium is an inhibitor of SARS-CoV-2 RNA synthesis in vitro.
Identifiants
pubmed: 34572438
pii: biomedicines9091254
doi: 10.3390/biomedicines9091254
pmc: PMC8467925
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Wellcome Trust
ID : 206579/Z/17/Z
Pays : United Kingdom
Organisme : Wellcome
ID : 206579/Z/17/Z
Organisme : ZonMw
ID : 10430 01 201 0018
Pays : Netherlands
Commentaires et corrections
Type : UpdateOf
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