Abstract
The methanol extract of the rhizomes of Curcuma longa was found to inhibit tyrosinase activity. After partition, various column chromatographic and preparative HPLC procedures were used for bioassay guided isolation from the active ethyl acetate-soluble fraction. Various spectroscopic (1D-, 2D-NMR) and mass spectrometric techniques, and Mosher's esterification were applied to elucidate the structures of the isolated compounds. The isolates were tested using an in vitro mushroom tyrosinase assay. Inhibition of melanin formation by the active compounds was further evaluated using B16 mouse melanoma cells. Eleven compounds (
