References
- Battaini, G, E. Monzani, L. Casella, L. Santagostini, and R. Pagliarin. 2000. Inhibition of the catecholase activity of biomimetic dinuclear copper complexes by kojic acid. J. Biol. Inorg. Chem. 5: 262-268 https://doi.org/10.1007/s007750050370
- Bell, A. A. and M. H. Weeler. 1986. Biosynthesis and function of fungal melanin. Ann. Rev. Phyrophathol. 24: 411-451 https://doi.org/10.1146/annurev.py.24.090186.002211
- Canabas, J., S. Chazarra, and F. Garcia-Carmona. 1994. Kojic acid, a cosmetic skin whitening agent, is a slowbinding inhibitor of catecholase activity of tyrosinase. J. Pharm.Pharmacol. 46: 982-985
- Choi, B. W:, B. H. Lee, K. J. Kang, E. S. Lee, and N. H. Lee. 1998. Screening of the tyrosinase inhibitors from marine algae and medicinal plants. Kor. J. Pharm. 29: 237-242
- Doo1ey, T. P., R. C. Gadwood, K. Ki1gore, and L. M. Thomasco. 1994. Development of an in vitro primary screen for skin depigmentation and antimelanoma agent. Skin Pharmacol. 7: 188-200 https://doi.org/10.1159/000211294
- Hiil, H. Z., W. Li, P. Xin, and D. L. Mitchell. 1997. Melanin: A two edged sword? Pigment Cell Res. 10: 158-161 https://doi.org/10.1111/j.1600-0749.1997.tb00478.x
- Hori, I., K. Nihei, and I. Kubo. 2004. Structural criteria for depigmenting mechanism of arbutin. Phytother. Res. 18: 475-479 https://doi.org/10.1002/ptr.1456
- Ikeda, T. and T. Tsutsumi. 1990. Function and skin depigmental activity of crude drugs. Fragrance J. 18: 59-66
- Kim, Y M., J. Yun, C. K. Lee, H. H. Lee, K. R. Min, and Y. S. Kim. 2002. Oxyresveratrol and hydroxystilbene compounds: Inhibitory effect on tyrosirlase and mechanism of action. J. Biol. Chem. 277: 16340-16344 https://doi.org/10.1074/jbc.M200678200
- Kubo, M. and H. Matsuda. 1995. Development studies of cuticle and medicainal drugs from natural sources on melanin biosynthesis. Fragrance J. 8: 48-55
- Lemer, A. B. and T. B. Fitzpatrick. 1950. Biochemistry of melanin formation. Physiol. Rev. 30: 91-126
- Marotti, I.; A. Bonetti, B. Biavati, P. Catizone, and G Dirlelli. 2007. Biotransformation of common bean (Phaseolus vulgaris L.) flavonoid glycosides by bifidobacterium species from human intestinal origin. J. Agric. Food Chem. 55: 3913-3919 https://doi.org/10.1021/jf062997g
- Matsukarni, M. 1995. Evaluation of antimelanogenic effects. Fragrance J. 19: 14-19
- Matubara, H. 1998. Inhibitory effect of lichen metabolites and their synthetic analogues on me1anin biosynthesis in cultured B-16 mouse mealnoma cells. Natural Product Sciences 4: 161-169
- Mishima, Y, S. Hatta, and Y. Ohyama. 1988. Induction of melanogenesis suppression: cellular pharmacology and mode of differential action. Pigment Cell Res. 1: 367-374 https://doi.org/10.1111/j.1600-0749.1988.tb00136.x
- Nielsen, I. L., W. S. Chee, L. Poulsen, E. Offord-Cavin, S. E. Rasmussen, H. Frederiksen, M. Enslen, D. Barron, M. N. Horcajada, and G. Williamson. 2006. Bioavailability is improved by enzymatic modification of the citrus flavonoid hesperidin in humans: a randomized, double-blind, crossover trial. J. Nutr. 136: 404-408
-
Otieno, D. O. and N. P. Shah. 2007. A comparison of changes in the transformation of isoflavones in soymilk using varying concentrations of exogenous and probioticderived ndogenous
$\beta$ -glucosidases. J. Appl. Microbiol. 103: : 60이1-612 - Peter, E. and I. H. Maibach. 2000. Cosmeceuticals: Drugs vs. Cosmetics. pp. 123-145. Marcel Dekker, New York
- Tomita, K., N. Oda, M. Ohbayashi, H. Kamei, T. Miyaki, and T. Oki. 1990. A new screening method for melanin biosynthesis inhibitiors using Streptomyces bikiniensis. J. Antibiot. 43: 1601-1605 https://doi.org/10.7164/antibiotics.43.1601