Biochemistry
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Potent in vitro anti-SARS-CoV-2 activity by gallinamide A and analogues via inhibition of cathepsin L
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Structural basis for the inhibition of the papain-like protease of SARS-CoV-2 by small molecules
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Mechanism of SARS-CoV-2 polymerase inhibition by remdesivir
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TMPRSS2 and ADAM17 interactions with ACE2 complexed with SARS-CoV-2 and B 0 AT1 putatively in intestine, cardiomyocytes, and kidney
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Fragment Binding to the Nsp3 Macrodomain of SARS-CoV-2 Identified Through Crystallographic Screening and Computational Docking
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Structural impact on SARS-CoV-2 spike protein by D614G substitution
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Ebselen, disulfiram, carmofur, PX-12, tideglusib, and shikonin are non-specific promiscuous SARS-CoV-2 main protease inhibitors
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The ACE2-binding interface of SARS-CoV-2 Spike inherently deflects immune recognition
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Mass spectrometric based detection of protein nucleotidylation in the RNA polymerase of SARS-CoV-2
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A Speedy Route to Multiple Highly Potent SARS-CoV-2 Main Protease Inhibitors
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