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
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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Auteurs

Stefano Elli (S)

Istituto di Ricerche Chimiche e Biochimiche "G. Ronzoni", Via Giuseppe Colombo 81, 20133 Milano, Italy.

Denisa Bojkova (D)

Institute of Medical Virology, University Hospital Frankfurt am Main, Goethe University, Paul-Ehrlich-Straße 40, 60596 Frankfurt am Main, Germany.

Marco Bechtel (M)

Institute of Medical Virology, University Hospital Frankfurt am Main, Goethe University, Paul-Ehrlich-Straße 40, 60596 Frankfurt am Main, Germany.

Thomas Vial (T)

Division of Virology, Department of Pathology, Addenbrooke's Hospital, University of Cambridge, Hills Road, Cambridge CB2 2QQ, UK.

David Boltz (D)

IIT Research Institute, 10 W 35th St, Chicago, IL 60616, USA.

Miguel Muzzio (M)

IIT Research Institute, 10 W 35th St, Chicago, IL 60616, USA.

Xinjian Peng (X)

IIT Research Institute, 10 W 35th St, Chicago, IL 60616, USA.

Federico Sala (F)

Istituto di Ricerche Chimiche e Biochimiche "G. Ronzoni", Via Giuseppe Colombo 81, 20133 Milano, Italy.

Cesare Cosentino (C)

Istituto di Ricerche Chimiche e Biochimiche "G. Ronzoni", Via Giuseppe Colombo 81, 20133 Milano, Italy.

Andrew Goy (A)

Farmak Joint Stock Company, Kyrylivska Street, 04080 Kyiv, Ukraine.

Marco Guerrini (M)

Istituto di Ricerche Chimiche e Biochimiche "G. Ronzoni", Via Giuseppe Colombo 81, 20133 Milano, Italy.

Lutz Müller (L)

Regenold GmbH, Zöllinplatz 4, 79410 Badenweiler, Germany.

Jindrich Cinatl (J)

Institute of Medical Virology, University Hospital Frankfurt am Main, Goethe University, Paul-Ehrlich-Straße 40, 60596 Frankfurt am Main, Germany.

Victor Margitich (V)

Farmak Joint Stock Company, Kyrylivska Street, 04080 Kyiv, Ukraine.

Aartjan J W Te Velthuis (AJW)

Division of Virology, Department of Pathology, Addenbrooke's Hospital, University of Cambridge, Hills Road, Cambridge CB2 2QQ, UK.

Classifications MeSH