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M pro has a catalytic active site motif consisting of His41 and Cys145 residues ( in silico docking studies with allicin revealed the formation of S -thioallylations at Cys145, Cys85 and Cys156 of M pro and of Cys622 of RdRp, indicating the potential of allicin to attenuate SARS-CoV-2 replication ( pro active site ( pro in silico , including the diallyl di- and trisulfides with promising docking scores ( 2+ levels released from host proteins inhibited the RdRp of SARS coronavirus ( S -thioallylation or via elevated Zn 2+ levels to exert immunomodulatory and antiviral effects

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