Inhibition of tyrosinase activity by polyphenol compounds from Flemingia philippinensis roots

Abstract

Flemingia philippinensis is used as a foodstuff or medicinal plant in the tropical regions of China. The methanol (95%) extract of the roots of this plant showed potent tyrosinase inhibition (80% inhibition at 30 mu g/ml). Activity-guided isolation yielded six polyphenols that inhibited both the monophenolase (IC50 = 1.01-18.4 mu M) and diphenolase (IC50 = 5.22-84.1 mu M) actions of tyrosinase. Compounds 1-6 emerged to be three new polyphenols and three known flavanones, flemichin D, lupinifolin and khonk-longinol H. The new compounds (1-3) were identified as dihydrochalcones which we named fleminchalcones (A-C), respectively. The most potent inhibitor, dihydrochalcone (3) showed significant inhibitions against both the monophenolase (IC50 = 1.28 mu M) and diphenolase (IC50 = 5.22 mu M) activities of tyrosinase. Flavanone (4) possessing a resorcinol group also inhibited monophenolase (IC50 = 1.79 mu M) and diphenolase (IC50 = 7.48 mu M) significantly. In kinetic studies, all isolated compounds behaved as competitive inhibitors. Fleminchalcone A was found to have simple reversible slow-binding inhibition against monophenolase. (C) 2013 Elsevier Ltd. All rights reserved.