The most active inhibitors were identified based on docking score, ligand–protein interactions, and toxicity analysis studies including Molecular Weight (MW), Hydrogen Bond Donner (HBD), Hydrogen Bond Acceptor (HBA), partial coefficient logP, Polar Surface Area (PSA), rotatable bonds, rings, Blood–Brain Barrier and Ames Toxicity etc. The compounds showing the least binding affinity, high lead likenesses, and best interactions were selected as potential inhibitors of Scm (Fms10).

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