Inhibitory effects of coumarin derivatives on tyrosinase

Abstract

In this study, a series of coumarin derivatives were synthesized and their inhibitory effects on the activity of mushroom tyrosinase were evaluated. As a result of measuring the inhibition of tyrosinase activity of these derivatives, the compounds 3e (1.05 µM), 3f (0.83 µM), 3h (0.85 µM), 3i (1.05 µM), and 3k (0.67 µM) of the geranyloxycoumarin derivatives were highly active at a concentration of 0.8%. The geranyloxycoumarin derivatives exhibited better activity than the hydroxycoumarin derivatives. Among the geranyloxycoumarin derivatives, compound 3k was two times more active than arbutin, a positive control, at a concentration of 0.4%. The above results suggest that gerany-loxycoumarin derivatives have great potential for application as functional cosmetic ingredients with tyrosinase-inhibiting activity.