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Computed structural comparison and binding features (visualization using UCSF Chimera and AutoDock) of Chlorogenic acid (A), Tigecycline (B), Podophyllotoxin (C), Ervacycline (D), Quercetin (E), and Minocycline (F), with SARS-COV2 main protease. The lower the binding energy, the greater will be the binding affinity.
