摘要：SummaryThe emergence of SARS-CoV-2 has led to a global health crisis that, in addition to vaccines and immunomodulatory therapies, calls for the identification of antiviral therapeutics. The papain-like protease (PLpro) activity of nsp3 is an attractive drug target as it is essential for viral polyprotein cleavage and for deconjugation of ISG15, an antiviral ubiquitin-like protein. We show here that 6-Thioguanine (6-TG), an orally available and widely available generic drug, inhibits SARS-CoV-2 replication in Vero-E6 cells with an EC50 of approximately 2 μM. 6-TG also inhibited PLpro-catalyzed polyprotein cleavage and de-ISGylation in cells and inhibited proteolytic activity of the purified PLpro domainin vitro. We therefore propose that 6-TG is a direct-acting antiviral that could potentially be repurposed and incorporated into the set of treatment and prevention options for COVID-19.Graphical abstractDisplay OmittedHighlights•6-Thioguanine (6-TG) is a direct-acting antiviral against SARS-CoV-2•6-TG targets the papain-like protease (PLpro) activity of the viral nsp3 protein•6-TG is a well-characterized and inexpensive orally-delivered drug•6-TG is a potentially useful therapeutic for COVID-19Therapeutics; Drugs; Virology
