Title : Novel Amide Derivatives as Potent Tyrosinase Inhibitors; In-vitro, In-vivo Antimelanogenic Activity and Computational Studies.

Pub. Date : 2019

PMID : 30892163






1 Functional Relationships(s)
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1 Furthermore, the molecular docking demonstrates that 5c interact with copper ions and multiple amino acids in the active site of tyrosinase with best glide score (-5.387 kcal/mol), essential for mushroom tyrosinase inhibition and the ability of diminishing the melanin synthesis in-vitro and in-vivo. Copper tyrosinase Mus musculus