Abstract
In the present study, we have performed the in-silico study of SARS-CoV-2
structure with different herbal compounds of medicinal importance. We selected
four viral key proteins of SARS-CoV-2 structure i.e ACE-2
Receptor, Main Protease (Mpro), APO Form, Cryo- electron microscopy structure
for the Molecular docking followed by the molecular dynamic simulation. Using
this simple in silico approach based on the molecular docking and MD simulation of protein and phytochemicals, we have
identified potential lead candidates for the development of low cost nutraceuticals,
which can be used against SARS-CoV-2 virus. Our analysis suggested that
phytochemicals obtained from Phyllanthus emblica and Azadirachta
indica have the highest potential to bind with ACE2 receptor or main protease
of SARS-CoV-2, inhibiting the protease enzymatic activity. The lead compounds
of herbal origin were docked and simulated on viral key proteins of SARS-CoV-2 structure
to evaluate the binding affinity of these phytochemicals along with the type of
interaction and its stability in terms of RMSD and Ramachandran plot. Further, these results were also
verified by drug likeness properties by using SwissADME software. Overall, our
results suggest that out of 14 herbal compounds, Nimbolide and Withaferin-A has
great potential to be developed as low-cost nutraceuticals against SARS-CoV-2 virus,
which is the need of hour.
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