References
- Mayer, A. M. 1995. Polyphenol oxidases in plants-recent progress. Phytochemistry 26, 11-20 https://doi.org/10.1039/9781847554758-BP011
- Wilcox, D. E., A. G. Porras, Y. T. Hwang, K. Lerch, M. E. Winkler and E. I. Solomon. 1985. Substrate analogue binding to the coupled binuclear copper active site in tyrosinase. J. Am. Chem. Soc. 107, 4015-4027 https://doi.org/10.1021/ja00299a043
- Sanchez-Ferrer, A., J. N. Rodriguez-Lopez, F. Garcia-Ganovas and F, Garcia-Carmona. 1995. Tyrosinase: a comprehensive review of its mechanism. Biochim. Biophys. Acta. 1247, 1-11 https://doi.org/10.1016/0167-4838(94)00204-T
- Whitaker, J. R. 1995. Polyphenol oxidases. In 'Food Enzymes, Structure and Mechanism', pp 271-307. ed. Wong, D. W. S., Chapman & Hall, New York
- McEvily, A. J., R. Iyengar and W. S. Otwell. 1991. Sulfite alternative prevents shrimp melanosis. Food Technol. 45, 80-86
- McEvily, A. J., R. Iyengar and W. S. Otwell. 1992. Inhibition of enzymatic browning in foods and beverage. Crit. Rev. Food Sci. Nutr. 32, 253-273 https://doi.org/10.1080/10408399209527599
- Friedman, M. 1996. Food browning and its prevention: An overview. J. Agric. Food Chem. 44, 631-653. https://doi.org/10.1021/jf950394r
- Rescigno, A., F. Sollai, B. Pisu, A. Rinaldi and E. Sanjust. 2002. Tyrosinase inhibition: general and applied aspects. J. Enzyme Inhib. Med. Chem. 17, 207-218 https://doi.org/10.1080/14756360210000010923
- Mosher, D. B., M. A. Pathak and T. B. Fitzpatrick. 1983. Vitiligo, etiology, pathogenesis, diagnosis, and treatment, eds. Fitzpatrick, T. B., A. Z. Eisen, K. Wolff, I. M. Freedberg and K. F. Austen. pp 205-225. 'Update: Dermathology in general medicine'. McGraw Hill, New York
- Maeda, K. and M. Fukuda. 1991. In vitro effectiveness of several whitening cosmetic components in human melanocytes. J. Soc. Cosmet. Chem. 42, 361-368
- Fu, B., H. Li, X. Wang, F. S. C. Lee and S. Cui. 2005. Isolation and identification of flavonoids in licorice and a study of their inhibitory effects on tyrosinase. J. Agric. Food Chem. 53, 7408-7414 https://doi.org/10.1021/jf051258h
- Miyazawa, M., T. Oshima, K. Koshio, Y. Itsuzaki and J. Anzai. 2003. Tyrosinase inhibitor from black rice bran. J. Agric. Food Chem. 51, 6953-6956 https://doi.org/10.1021/jf030388s
- Nerya, O., R. Musa, S. Khatib, S. Tamir and J. Vaya. 2004. Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers. Phytochemistry 65, 1389-1395 https://doi.org/10.1016/j.phytochem.2004.04.016
- Kubo, I., I. Kinst-Hori, Y. Kubo, Y. Yamagiwa, T. Kamikawa and H. Haraguchi. 2000. Molecular design of antibrowing agents. J. Agric. Food Chem. 48, 1393-1399 https://doi.org/10.1021/jf990926u
- Hano, Y., Y. Matsumoto, J. Y. Sun and T. Nomura. 1990. Structures of four new isoprenylated xanthones, cudraxanthones H, I, J, and K. Planta Med. 56, 478-481 https://doi.org/10.1055/s-2006-961016
- Lee, J. H., B. W. Lee, J. H. Kim, W. D. Seo, K. C. Jang and K. H. Park. 2005. Antioxidant effects of isoflavones from the stem bark of Cudrania tricuspidata. Agric. Chem. Biotechnol. 48, 193-197
- Nomura, T., Y. Hano and T. Fujimoto. 1983. Three new isoprenylated xanthones, cudraxanthone A, B and C, from the root bark of Cudrania Tricuspidata (carr.) bur. Heterocycles 20, 213-218 https://doi.org/10.3987/R-1983-02-0213
- Fujimoto, T., Y. Hano and T. Nomura .1984. Components of root bark of Cudrania tricuspidata1. Structures of four new isoprenylated xanthones, cudraxanthones A, B, C and D. Planta Med. 50, 218-221 https://doi.org/10.1055/s-2007-969682
- Hano, Y., Y. Matsumoto, J. Y. Sun and T. Nomura. 1990. Structures of four new isoprenylated xanthones, cudraxanthones H, I, J, and K. Planta Med. 56, 478-481. https://doi.org/10.1055/s-2006-961016
- Hano, Y., Y. Matsumoto, J. Y. Sun and T. Nomura. 1990. Structures of three new isoprenylated xanthones, cudraxanthones E, F, and G. Planta Med. 56, 399-402 https://doi.org/10.1055/s-2006-960993
- Lee, B. W., J. H. Lee, S. W. Gal, Y. H. Moon and K. H. Park 2006. Selective ABTS radical-scavenging activity of prenylated flavonoids from Cudrania tricuspidata. Biosci. Biotechnol. Biochem. 70, 427-432 https://doi.org/10.1271/bbb.70.427
- Lee, B. W., S. W. Gal, K. M. Park and K. H. Park 2005. Cytotoxic xanthones from Cudrania tricuspidata. J. Nat. Prod. 68, 456-458 https://doi.org/10.1021/np030481a
- Lee, B. W., N. S. Kang and K. H. Park. 2004. Isolation of antibacterial prenylated flavonoids from Cudrania tricuspidata. J. Korean Soc. Appl. Biol. Chem. 47, 270-273
- Khatib, S., O. Nerya, R. Musa, M. Shmuel, S. Tamir and J. Vaya. 2005. Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety. Bioorg. Med. Chem. 13, 433-441 https://doi.org/10.1016/j.bmc.2004.10.010
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