A series of substituted cinnamic acid esters were synthesized and their inhibitory effects on the diphenolase activity
of mushroom tyrosinase were evaluated. Compound 8 was found to be the most potent inhibitor with IC50 value of
5.60µM. Preliminary structure activity relationships (SARs) were concluded. The inhibition kinetics analyzed by
Lineweaver–Burk plots revealed that compound 8 was anti-competitive inhibitor.
Keywords: Substituted cinnamic acid esters, Tyrosinase inhibitor, Synthesis, Structure activity relationships, Inhibition kinetics,
Rights & PermissionsPrintExport