After a thorough analysis of docking results, drug likeness and toxicity characteristics were identified through pkCSM [34], ProTox-II [35], and SwissADME [36], which are reported as useful tools in calculating important drug-like descriptors, such as adsorption, distribution, metabolism, excretion, and toxicity (ADMET), as well as use for predicting lead likeness with respect to mutagenicity and carcinogenicity.

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