Acriflavine, a clinically aproved drug, inhibits SARS-CoV-2 and other betacoronaviruses

Author:

Napolitano Valeria,Dabrowska AgnieszkaORCID,Schorpp Kenji,Mourão AndréORCID,Barreto-Duran EmiliaORCID,Benedyk MalgorzataORCID,Botwina PawelORCID,Brandner Stefanie,Bostock MarkORCID,Chykunova YuliyaORCID,Czarna AnnaORCID,Dubin GrzegorzORCID,Fröhlich Tony,Hoelscher Michael,Jedrysik Malwina,Matsuda Alex,Owczarek KatarzynaORCID,Pachota MagdalenaORCID,Plettenburg Oliver,Potempa JanORCID,Rothenaigner Ina,Schlauderer Florian,Szczepanski ArturORCID,Mohn Kristin Greve-Isdahl,Blomberg BjornORCID,Sattler MichaelORCID,Hadian KamyarORCID,Popowicz Grzegorz MariaORCID,Pyrc KrzysztofORCID

Abstract

SummaryThe COVID-19 pandemic caused by SARS-CoV-2 has been socially and economically devastating. Despite an unprecedented research effort, effective therapeutics are still missing to limit severe disease and mortality. Using high-throughput screening, we identified acriflavine as a potent papain-like protease (PLpro) inhibitor. NMR titrations and a co-crystal structure confirm that acriflavine blocks the PLpro catalytic pocket in an unexpected binding mode. We show that the drug inhibits viral replication at nanomolar concentration in cellular models, in vivo in mice and ex vivo in human airway epithelia, with broad range activity against SARS-CoV-2 and other betacoronaviruses. Considering that acriflavine is an inexpensive drug approved in some countries, it may be immediately tested in clinical trials and play an important role during the current pandemic and future outbreaks.

Publisher

Cold Spring Harbor Laboratory

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