Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Relationships between Structure and Anti-oxidative Effects of Hydroxyflavones

  • Park, Young-Hee (Division of Bioscience and Biotechnology, BMIC, Research Center for Drugs, Konkuk University) ;
  • Lee, Sun-Hee (Division of Bioscience and Biotechnology, BMIC, Research Center for Drugs, Konkuk University) ;
  • Woo, Yoon-Kyung (Division of Bioscience and Biotechnology, BMIC, Research Center for Drugs, Konkuk University) ;
  • Lim, Yoong-Ho (Division of Bioscience and Biotechnology, BMIC, Research Center for Drugs, Konkuk University)
  • Published : 2009.06.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Calderone, V.; Chericoni, S.; Martinelli, C.; Testai, L.; Nardi, A.; Morelli, I.; Breschi, M. C.; Martinotti, E. Naunyn. Schmiedebergs Arch. Pharmacol. 2004, 370, 290. https://doi.org/10.1007/s00210-004-0964-z
  2. Hougee, S.; Sanders, A.; Faber, J.; Graus, Y. M. F.; Berg, W. B.; Garssen, J.; Smit, H. F.; Hoijer, M. A. Biochem. Pharmacol. 2005, 69, 241. https://doi.org/10.1016/j.bcp.2004.10.002
  3. Prasad, L.; Khan, T. H.; Jahangir, T.; Sultana, S. Pharm. Biol. 2007, 45, 116. https://doi.org/10.1080/13880200601113057
  4. Park, Y. H.; Lee, Y. H.; Kim, H. J.; Lee, Y. S.; Yoon, Y. D.; Moon, B. H.; Cheon, Y. H.; Ahn, J. H.; Shim, Y. H.; Lim, Y. H. Bull. Korean Chem. Soc. 2006, 27, 1537. https://doi.org/10.5012/bkcs.2006.27.10.1537
  5. Cramer, R. D.; Patterson, D. E.; Bunce, J. D. J. J. Am. Chem. Soc. 1988, 110, 5959. https://doi.org/10.1021/ja00226a005
  6. Gasteiger, J.; Marsili, M. Tetrahedron 1980, 36, 3219. https://doi.org/10.1016/0040-4020(80)80168-2
  7. Nair, P. C.; Sobhia, M. E. J. Mol. Graph. Model. 2007, 26, 117. https://doi.org/10.1016/j.jmgm.2006.10.002
  8. Young, J. M.; Park, Y. H.; Lee, Y. U.; Kim, H. J.; Shim, Y. H.; Ahn, J. H.; Lim, Y. H. J. Microbiol. Biotechnol. 2007, 17, 530.
  9. Leung, H. W. C.; Kuo, C. L.; Yang, W. H.; Lin, C. H.; Lee, H. Z. Eur. J. Pharmacol. 2006, 534, 12. https://doi.org/10.1016/j.ejphar.2006.01.021
  10. Furusawa, M.; Tanaka, T.; Ito, T.; Nishikawa, A.; Yamazaki, N.; Nakaya, K. I.; Matsuura, M.; Tsuchiya, H.; Nagayama, M.; Iinuma, M. J. Health Sci. 2005, 51, 376. https://doi.org/10.1248/jhs.51.376
  11. Kim, B.; O, K.; Chun, J.; Hwang, K. Bull. Korean Chem. Soc. 2008, 29, 1125. https://doi.org/10.5012/bkcs.2008.29.6.1125
  12. Rahman, A. A.; Moon, S. Bull. Korean Chem. Soc. 2007, 28, 827. https://doi.org/10.5012/bkcs.2007.28.5.827

Cited by

  1. A novel relationship between the radical-scavenging activity of flavonoids and enthalpy of formation revealed with Hartree–Fock computations and thermochemical deduction vol.17, pp.3, 2012, https://doi.org/10.1179/1351000212Y.0000000013
  2. Synthesis and Characterization of Some New Complexes of Magnesium (II) and Zinc (II) with the Natural Flavonoid Primuletin vol.18, pp.7, 2013, https://doi.org/10.3390/molecules18077631
  3. Fast Identification of Radical Scavengers from Securigera varia by Combining 13C-NMR-Based Dereplication to Bioactivity-Guided Fractionation vol.20, pp.8, 2015, https://doi.org/10.3390/molecules200814970
  4. Elucidation of hydroxyl groups-antioxidant relationship in mono- and dihydroxyflavones based on O-H bond dissociation enthalpies vol.21, pp.6, 2015, https://doi.org/10.1007/s00894-015-2669-2
  5. Relationship between Antioxidant and Anticancer Activity of Trihydroxyflavones vol.22, pp.12, 2017, https://doi.org/10.3390/molecules22122169
  6. Protective Effect of Artemisia argyi and Its Flavonoid Constituents against Contrast-Induced Cytotoxicity by Iodixanol in LLC-PK1 Cells vol.19, pp.5, 2018, https://doi.org/10.3390/ijms19051387
  7. Biotransformation of Flavone by CYP105P2 from Streptomyces peucetius vol.22, pp.8, 2009, https://doi.org/10.4014/jmb.1201.01037