참고문헌
- H. Kim, J. Choi, J. K. Cho, S. Y. Kim, and Y. S. Lee, Solid-phase synthesis of kojic acid-tripeptides and their tyrosinase inhibitory activity, storage stability, and toxicity, Bioorganic & Medicinal Chemistry Letters, 14, 2843 (2004). https://doi.org/10.1016/j.bmcl.2004.03.046
- D. S. King, C. G. Fields, and G. B. Fields, A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis, Int. J. Pept. Protein Res., 36, 255 (1990).
- T. K. von Almen, G. A. Olson, and R. D. Olson, Behavioral effects of melanocyte stimulating hormone release-inhibiting factor-1, Neuroscience & Biobehavioral Reviews, 7(2), 257 (1983). https://doi.org/10.1016/0149-7634(83)90018-0
- WO2007137015A2, Dermatological uses of tri-, tetra-, penta-, and polypeptides
- A. M. Lopez-Contreras, J. H. Martinez-Liarte, F. Solano, P. Samaraweera, J. M. Newton, and J. T. Bagnara, The amphibian melanization inhibiting factor (MIF) blocks the alpha-MSH effect on mouse malignant melanocytes, Pigment Cell Res., 9(6), 311 (1996). https://doi.org/10.1111/j.1600-0749.1996.tb00123.x
- K. Schallreuter, A. Slominski, J. M. Pawelek, K. Jimbow, and B. A. Gilchrest, What controls melanogenesis?, Exp. Dermatol., 7, 143 (1998). https://doi.org/10.1111/j.1600-0625.1998.tb00315.x
- A. Perez-Bernal, M. A. Munoz-perez, and F. Camacho, Management of facial hyperpigmentation, Am. J. Clin. Dermatol., 1(5), 261 (2000). https://doi.org/10.2165/00128071-200001050-00001
- Y. J. Kima and H. Uyamab, Tyrosinase inhibitors from natural and synthetic sources:structure, inhibition mechanism and perspective for the future, Cell. Mol. Life Sci., 62, 1707 (2005). https://doi.org/10.1007/s00018-005-5054-y
- S. Parvez, M. Kang, H. Chung, C. Cho, M. Hong, M. Shin, and H. Bae, Survey and mechanism of skin depigmenting and lightening agents, Phytother. Res., 20, 921 (2006). https://doi.org/10.1002/ptr.1954
- D. Kim, S. Park, S. Kwon, K. Li, S. Youn, and K. Park, (-)-Epigallocatechin-3-gallate and hinokitiol reduce melanin synthesis via decreased MITF production, Arch. Pharm. Res., 27(3), 334 (2004). https://doi.org/10.1007/BF02980069
- S. Boonanuntanasarn, G. Yoshizaki, and T. Takeuchi, Specific gene silencing using small interfering RNAs in fish embryos. Biochem. Biophys. Res. Commun., 310, 1089 (2003). https://doi.org/10.1016/j.bbrc.2003.09.127
- J. W. Wiechers, A. V. Rawlings, C. Garcia, C. Chesne, P. Balaguer, J. C. Nicolas, S. Corre, and M.-D. Galibert, A new mechanism of action for skin whitening agents: binding to the peroxisome proliferator activated receptor, Int. J. Cosmetic Sci., 27, 123 (2005). https://doi.org/10.1111/j.1467-2494.2004.00256.x
- K. Sato, H. Takahashi, R. Iraha, and M. Toriyama, Down-regulation of tyrosinase expression by acetylsalicylic acid in murine B16 melanoma, Biol. Pharm. Bull., 31(1), 33(2008). https://doi.org/10.1248/bpb.31.33
- J. Koo, H. T. Kim, H. Yoon, K. Kwon, I. Choi, S. H. Jung, H. Kim, B. Park, and J. Park, Effect of xanthohumol on melanogenesis in B16 melanoma cell, Exp. Mol. Medicine, 40(3), 313 (2008). https://doi.org/10.3858/emm.2008.40.3.313
- K. Sato and M. Toriyama, Depigmenting Effect of Catechins, Molecules, 14, 4425 (2009). https://doi.org/10.3390/molecules14114425
- K. Ohguchi, C. Nakajima, M. Oyama, M. Iinuma, T. Itoh, Y. Akao, Y. Nozawa, and M. Ito, Inhibitory effects of flavonoid glycosides isolated from the peel of Japanese Persimmon (Diospyros kaki 'Fuyu') on melanin biosynthesis, Biol. Pharm. Bull., 33(1), 122 (2010). https://doi.org/10.1248/bpb.33.122
- K. V. Bossche, J. Naeyaert, and J. Lambert, The quest for the mechanism of melanin transfer, Traffic, 7(7), 769 (2006). https://doi.org/10.1111/j.1600-0854.2006.00425.x
- R. E. Boissy, Melanosome transfer to and translocation in the keratinocyte, Experimental Dermatology, 12, 5 (2003). https://doi.org/10.1034/j.1600-0625.12.s2.1.x
- S. Bonettoa, I. Carlavan, and D. Baty, Isolation and agonist peptides to the human melanocortin 1 receptor, Peptides, 26, 2302 (2005). https://doi.org/10.1016/j.peptides.2005.04.002
- C. Haskell-Luevano, J. R. Holder, E. K. Monck, and R. M. Bauzo, Characterization of melanocortin NDPMSH agonist peptide fragments at the mouse central and peripheral melanocortin receptors, J. Med. Chem., 44, 2247 (2001). https://doi.org/10.1021/jm010061n
- M. Tsatmali, J. Ancans, and A. J. Thody, Melanocyte function and its control by melanocortin peptides, J. Histochem. Cytochem., 50(2), 125 (2002). https://doi.org/10.1177/002215540205000201
- L. H. Brinckerhoff, V. V. Kalashnikov, L. Thompson, G. V. Yamshchikov, R. A. Pierce, H. S. Galavotti, V. H. Engelgard, and C. L. Slingluff, Terminal modifications inhibit proteolytic degradation of an immunogenic MART-1(27-35) peptide: implications for peptide vaccines, Int. J. Cancer, 83, 326 (1999). https://doi.org/10.1002/(SICI)1097-0215(19991029)83:3<326::AID-IJC7>3.0.CO;2-X
- M. F. Powell, T. Stewart, L. Otvos, L. Urge, F. C.A. Gaeta, A. Sette, T. Arrhenius, D. Thomson, K. Soda, and S. M. Colon, Peptide stability in drug development. II. Effects of single amino acid substitution and glycosylation on peptide reactivity in human serum, Pharm. Res., 10, 1268 (1993). https://doi.org/10.1023/A:1018953309913
- D. I. Jang, B. G. Lee, C. O. Jeon, N. S. Jo, and J. S. Koh, Melanogenesis inhibitor from paper mulberry, Cosmet. Toiletries, 112(3), 59 (1997).
- A. Andrawis and V. Kahn, Effect of methimazole on the activity of mushroom tyrosinase, Biochem. J., 235, 91 (1986). https://doi.org/10.1042/bj2350091
- E. Kaiser, R. L. Colescott, C. D. Bossinger, and P. Cook, Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides, Anal. Biochem. 34, 595 (1970). https://doi.org/10.1016/0003-2697(70)90146-6
- Synthetic Peptides: A User's Guide (G.A. Grant, ed.), W. H. Freeman and Company, New York, (1992).