… Coronavirus protease inhibitors show antiviral activity in vitro. In this study, we used virtual
screening technology to discover potential drugs targeting the 3CL pro of SARS-CoV-2 from …

… a virtual screen with a library of 527 209 natural compounds against the receptor binding
domain of this protein. Top hits from this screen … These findings validate the virtual screening …

… SARS-CoV-1 M pro apo structure has shown the largest outer pocket respect to both
ligand-bounded M pro structures, suggesting that the SARS … virtual screening against the …

… Refined crystal structure (PDB ID: 6Y2G) of a SARS-CoV-2 M pro homodimer with … In
this study, I performed stepwise structure-based virtual screenings using two different docking …

… In this study, a structure-based virtual screening (SBVS) was applied on the high similar …
with strong and stable interactions with the binding pocket residues of SARS-CoV-2 M pro . …

… using high throughput virtual screening tools have been … of SARS-CoV-2–ACE2 receptor.
The results of this study of modeling of S-RBD of SARS-CoV-2, coupled with rapid screening of …

… SARS-CoV-2. 78 natural antiviral compounds database was identified from literature and
virtual screening … active extract of Forsythia suspense as SARS-CoV-2 3CLpro inhibitor that can …

… the SARS coronavirus (SARS-CoV) proteinase. His findings may help scientists to design
SARS … De Groot4 also believed that there were some similarities between SARS-CoV and HIV. …

… Therefore, a virtual screening … virtual screening revealed 21 natural compounds having
higher docking scores and MM-GBSA values for six potent therapeutic targets of SARS-CoV-2 …

… In this study, we have modeled SARS-CoV-2 N7-MTase protein structure in order to decipher
the molecular architecture of the substrate-binding site and to perform virtual screening …