Bulletin of the Korean Chemical Society

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New 5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one Derivative Has Both Tyrosinase Inhibitory and Antioxidant Properties

  • Published : 2007.03.20
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References

  1. Burdock, G. A.; Soni, M. G.; Carabin, I. G. Regulatory Toxicology and Pharmacology 2001, 33, 80 https://doi.org/10.1006/rtph.2000.1442
  2. Futamura, T.; Okabe, M.; Tamura, T.; Toda, K.; Matsunobu, T.; Park, Y. S. J. Biosci. Bioeng. 2001, 91, 272 https://doi.org/10.1263/jbb.91.272
  3. Ohyama, Y.; Mishima, Y. Fragrance J. 1990, 6, 53
  4. Kobayashi, Y.; Kayahara, H.; Tadasa, K.; Tanaka, H. Bioorg. Med. Chem. Lett. 1996, 6, 1303 https://doi.org/10.1016/0960-894X(96)00221-1
  5. Mitani, H.; Koshiishi, I.; Sumita, T.; Imanari, T. Eur. J. Pharmacol. 2001, 411, 169 https://doi.org/10.1016/S0014-2999(00)00873-6
  6. Yuen, V. G.; Caravan, P.; Gelmini, L.; Glover, N.; Mcneill, J. H.; Setyawati, I. A.; Zhou, Y.; Orvig, C. J. Inorg. Biochem. 1997, 68, 109 https://doi.org/10.1016/S0162-0134(97)00082-2
  7. Kim, M. S.; Lee, S.; Rho, H. S.; Kim, D. H.; Chang, I. S.; Chung, J. H. Clinica. Chimica. Acta 2005, 362, 161 https://doi.org/10.1016/j.cccn.2005.06.016
  8. Pomerantz, S. H. J. Biol. Chem. 1963, 238, 2351
  9. Peus, D.; Meves, A.; Pott, M.; Beyerle, A.; Pittelkow, M. R. Free Radic. Biol. Med. 2001, 30, 425 https://doi.org/10.1016/S0891-5849(00)00488-3
  10. Delicado, E. N.; Ferrer, A. S.; Carmona, F. G. Biochim. Biophys. Acta. General Subjects 1997, 1335, 127 https://doi.org/10.1016/S0304-4165(96)00130-4
  11. Saffari, Y.; Hossein Sadrzadeh, S. M. Life Sciences 2004, 74, 1513 https://doi.org/10.1016/j.lfs.2003.08.019
  12. Bors, W.; Michel, C. Free Radic. Biol. Med. 1999, 27, 1413 https://doi.org/10.1016/S0891-5849(99)00187-2
  13. Rho, H. S.; Baek, H. S.; Lee, B. S.; Kim, J. H.; Kim, D. H.; Chang, I. S. Bull. Korean Chem. Soc. 2006, 27, 115 https://doi.org/10.5012/bkcs.2006.27.1.115

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