Abstract
Currently, aloesin is used in the cosmetic industry as a whitening agent because it inhibits tyrosinase activity. Aloesin is a C-glycosylated chromone compound isolated from aloe, and it is difficult to synthesize because of C-glycosyl moiety in the molecule. The purpose of this study is to search for a new chromone compound which is easy to synthesize and which posesses stronger tyrosinase inhibitory activity than aloesin. Fourteen chromone derivatives were synthesized and screened for their mushroom-tyrosinase inhibitory activity. 5-Methyl-7-methoxy-2-(2′-benzyl-3′-oxobutyl)chromone (15) showed the strongest activity among tested compounds. Its activity was not only stronger than aloesin, but also stronger than arbutin and kojic acid. The kinetic analysis revealed a competitive inhibition of 15 with tyrosinase for the L-tyrosine binding site. © 2002 Pharmaceutical Society of Japan.
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Piao, L. Z., Park, H. R., Park, Y. K., Lee, S. K., Park, J. H., & Park, M. K. (2002). Mushroom tyrosinase inhibition activity of some chromones. Chemical and Pharmaceutical Bulletin, 50(3), 309–311. https://doi.org/10.1248/cpb.50.309
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