2021
DOI: 10.1139/cjpp-2020-0734
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Ribavirin shows antiviral activity against SARS-CoV-2 and downregulates the activity of TMPRSS2 and the expression of ACE2 in vitro

Abstract: Ribavirin is a guanosine analog and has a broad-spectrum antiviral activity against RNA viruses. Based on this, we aimed to show the anti-SARS-CoV-2 activity of this drug molecule via in vitro, in silico and molecular techniques. Ribavirin showed antiviral activity in Vero E6 cells following SARS-CoV-2 infection whereas the drug itself did not show any toxic effect over the concentration range tested. In silico analysis suggested that Ribarivin has a broad-spectrum impact on SARS-CoV-2, acting at different vir… Show more

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Cited by 43 publications
(28 citation statements)
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“…It also inhibits RNA-dependent RNA polymerase activity. Following their bioinformatics studies, it has been claimed that the drug could bind to the active site of the enzyme and, by inhibiting it, could be a potent inhibitor for SARS-CoV-2 infection [ 47 , 48 ].…”
Section: Interventions Of Ifns and Their Agonists With Sars-cov-2 Infectionmentioning
confidence: 99%
“…It also inhibits RNA-dependent RNA polymerase activity. Following their bioinformatics studies, it has been claimed that the drug could bind to the active site of the enzyme and, by inhibiting it, could be a potent inhibitor for SARS-CoV-2 infection [ 47 , 48 ].…”
Section: Interventions Of Ifns and Their Agonists With Sars-cov-2 Infectionmentioning
confidence: 99%
“…The paths linking viral proteins to the process of viral entry implicate IMPDH2 in the viral entry pathway. Consistently, IMPDH inhibitors have been shown to interfere with coronavirus replication in Vero E6 cells [28,29]. Likewise, PIK3C3 was found to be crossed over by paths connecting viral proteins to processes of virus entry, ER stress, and innate response to dsRNA and stress granules.…”
Section: Exploring the Function Of Sars-cov2 Interacting Proteinsmentioning
confidence: 76%
“…Firstly, SYBYL-X2.0 software was used for protein pretreatment, including extraction of ligand small molecules, removal of water molecules, and hydrogenation. Then, SYBYL-X2.0 was used to conduct molecular docking between key ingredients and proteins, and the interaction between small molecules and targets was scored by combining the CSCORE and Total-score scoring functions of Surflex-Dock molecular docking module results, and the molecular docking results of ribavirin were used as the control group [ 5 , 6 ]. The docking results were visualized using TBTools software and Discovery Studio 2016 Client.…”
Section: Methodsmentioning
confidence: 99%