References
-
S. J. Kim and M. H. Lee, 3D-QSAR analyses on the inhibition activity of 4-(
$R_1$ )-benzyl alcohol and 4-($R_2$ )-phenol analogues against tyrosinase, J. Soc. Cosmet. Scientists Korea, 35(4), 271 (2009). - W. H. Tollesona, Human melanocyte biology, toxicology, and pathology, J. Environmental Science and Health, Part C, 23(2), 105 (2005). https://doi.org/10.1080/10590500500234970
- J. Ogunnariwo and J. M. T. Hamilton-miller, Brownand red-pigmented pseudomonas: differentiation between melanin and pyorubrin, J. Med. Microbiol., 8, 199 (1975). https://doi.org/10.1099/00222615-8-1-199
- J. H. Park and M. H. Lee, A study of skin color by melanin index according to site, gestational age, birth weight and season of birth in korean neonates, J. Korean Med. Sci., 20, 105 (2005). https://doi.org/10.3346/jkms.2005.20.1.105
- Y. Matoba, T. Kumagai, A. Yamamoto, H. Yoshitsu, and M. Sugiyama, Crystallographic evidence that the dinuclear copper center of tyrosinase is flexible during catalysis, J. Biol. Chem., 281(13), 8981 (2006). https://doi.org/10.1074/jbc.M509785200
- M. Jimenez, S. Chazarra, J. Escribano, J. Cabanes, and F. G. Carmona, Competitive inhibition of mushroom tyrosinase by 4-substituted benzaldehydes, J. Agric. Food Chem., 49(8), 4060 (2001). https://doi.org/10.1021/jf010194h
- E. Neeley, G. Fritch, A. Fuller, J. Wolfe, J. Wright, and W. Flurkey, Variations in IC50 values with purity of mushroom tyrosinase, Int. J. Mol. Sci., 10, 3811 (2009). https://doi.org/10.3390/ijms10093811
- Y. Tokiwa, M. Kitagawa, and T. Raku, Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on mushroom tyrosinase, Biotechnology Letters, 29(3), 481 (2007). https://doi.org/10.1007/s10529-006-9267-4
- K. W. Lam, A. Syahida, Z. U. Haq, M. B. A. Rahman, and N. H. Lajis, Synthesis and biological activity of oxadiazole and triazolothiadiazole derivatives as tyrosinase inhibitors, Bioorg. Med. Chem. Lett., 20(12), 3755 (2010). https://doi.org/10.1016/j.bmcl.2010.04.067
- Y. H. Chung, S. C. Jang, S. J. Kim, and N. D. Sung, 2D-QSAR and HQSAR on the inhibition activity of protein tyrosine phosphatase 1B with oleanolic acid analogues, J. Biol. Chem., 50(2), 52 (2007).
-
S. J. Kim, Y. H. Chung, S. G. Kim, and N. D. Sung, CoMSIA analysis on the inhibition activity of PTP-1B with 3
$\beta$ -Hydroxy-12-oleanen-28-oic acid analogues, J. Korean Soc. Appl. Biol. Chem., 51(3), 171 (2008). - S. J. Kim, N. D. Sung, and H. S. Jung, Holographic quantitative structure-toxicity relationships on the skin sensitization of alkyl-3,4-dihydroxybenzoate and N-alkyl-3,4-dihydroxybenzamide derivatives, J. Soc. Cosmet. Scientist Korea, 31(1), 91 (2005).
- N. D. Sung, H. S. Jung, and S. J. Kim, Hydrolytic reactivity and holographic quantitative structureactivity relationship analyses on the melanogenesis inhibitory activities of alkyl-3,4-dihydro-xybenzoate and N-alkyl-3,4-dihydroxybenzamide derivatives, J. Soc. Cosmet. Scientist Korea, 30(4), 491 (2004).
- T. W. Heritage and D. R. Lowis, Molecular hologram QSAR. Ch. 4., In Rational Drug Design; Novel Methodology and Practical Applications (ed. Parrill, A. L. and M. R. Reddy), ACS Symposium Series 719, American Chemical Society, Washington, DC (1999).
- K. M. Khan, G. M. Maharvi, M. T. H. Khan, A. J. Shaikh, S. Perveen, S. Begum, and M. I. Choudhary, Tetraketones: a new class of tyrosinase inhibitors, Bioorg. Med. Chem., 14(2), 344 (2006). https://doi.org/10.1016/j.bmc.2005.08.029
- Tripos Associates, Inc., 1699 S. Hanley Road, Suite 303, St. Louis, MO. 63144-2913, U.S.A.
- M. G. Sung, S. M. Joo, A. R. Song, and N. D. Sung, QSAR on the inhibition acticity of flavopiridol analogues against breast cancer MCF-7, J. Korean Soc. Appl. Biol. Chem., 50(3), 147 (2007).
- L. Stahle and S. Wold, Multivariate data analysis and experimental design in biomedical research, Progr. Med. Chem., 25, 291 (1988). https://doi.org/10.1016/S0079-6468(08)70281-9
- S. C. Jang and N. D. Sung, Molecular holographic QSAR analysis on the bonding affinity constants between nicotin acetylcholine receptors and New 3-Benzylidenemyosmine analogues and molecular design, J. Korean Soc. Appl. Biol. Chem., 50(2), 127 (2007).
- N. D. Sung, Development of new agrochemicals by quantitative structure-activity relationship (QSAR) methodologies. I. The basic concepts and types of QSAR methodologies, The Korean Journal of Pesticide Science, 6(3), 166 (2002).
- N. D. Sung, Development of new agrochemicals by qnantitative structure-activity relationship (QSAR) methodology. II. The linear free energy relationship (LFER) and descriptors, The Korean Journal of Pesticide Science, 6(4), 231 (2002).
- C. K. Smith and H. Sam, Allergic contact dermatitis, chemical and metabolic mechanisms, Taylor and Francis, London and New York (2001).
- W. G. Landis and M. H. Yu, Introduction to environmental toxicology; impacts of chemicals upon ecological systems. Ch. 5, 110. Lewis Publishers. London (1995).
- M. J. Prival, Evaluation of the TOPKAT system for predicting the carcinogenicity of chemicals, Environ. Mol. Mutagen., 37, 55 (2001). https://doi.org/10.1002/1098-2280(2001)37:1<55::AID-EM1006>3.0.CO;2-5
- D. J. Livingstone, Structure property correlation in molecular design, In Structure-property Correlations in Drug Research (ed. Waterbeemd HVD), Ch. 4. 95, Academic Press, R. G. Landes Company, Austin USA. (1996).
- M. Akamatsu, Current state and perspectives of 3D-QSAR. Curr. Topics Med. Chem., 2(12), 1381 (2002). https://doi.org/10.2174/1568026023392887
- W. S. Choi, Master's thesis dissertation, Chungnam National Univ., Daejeon Korea (2010).