Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Synthesis and Antioxidant Activity of 3-Methoxyflavones

  • Yoo, Ho (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Kim, Seung-Hwan (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Lee, Ji-Yong (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Kim, Hyoung-Ja (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Seo, Seon-Hee (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Chung, Bong-Young (Department of Chemistry, Korea University) ;
  • Jin, Chang-Bae (Life Sciences Division, Korea Institute of Science & Technology) ;
  • Lee, Yong-Sup (Kyung Hee East-West Pharmaceutical Research Institute and Department of Pharmaceutical Science, College of Pharmacy, Kyung Hee University)
  • Published : 2005.12.20
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References

  1. Haraguchi, H.; Ishikawa, H.; Sanchez, Y.; Ogura, T.; Kubo, Y.; Kubo, I. Bioorg. Med. Chem. 1997, 5, 865 https://doi.org/10.1016/S0968-0896(97)00029-1
  2. Cai, Q.; Rahn, R. O.; Zhang, R. Cancer Lett. 1997, 119, 99 https://doi.org/10.1016/S0304-3835(97)00261-9
  3. Choi, C. W.; Kim, S. C.; Hwang, S. S.; Choi, B. K.; Ahn, H. J.; Lee, M. Y.; Park, S. H.; Kim, S. K. Plant Science 2002, 163, 1161 https://doi.org/10.1016/S0168-9452(02)00332-1
  4. Braca, A.; Fico, G.; Morelli, I.; De Simone, F.; Tomè, F.; De Tommasi, N. J. Ethnopharm. 2003, 86, 63 https://doi.org/10.1016/S0378-8741(03)00043-6
  5. Dugas, Jr., A. J.; Castaneda-Acosta, J.; Bonin, G. C.; Price, K. L.; Fischer, N. H.; Winston, G. W. J. Nat. Prod. 2000, 63, 327 https://doi.org/10.1021/np990352n
  6. Lee, E. H.; Kim, H. J.; Song, Y. S.; Jin, C.; Lee, K.-T.; Cho, J.; Lee, Y. S. Arch. Pharm. Res. 2003, 26, 1018 https://doi.org/10.1007/BF02994752
  7. Dok-Go, H.; Lee, K. H.; Kim, H. J.; Lee, E. H.; Lee, J.; Song, Y. S.; Lee, Y.-H.; Jin, C.; Lee, Y. S.; Cho, J. Brain Research 2003, 965(1-2), 130 https://doi.org/10.1016/S0006-8993(02)03844-1
  8. Boers, F.; Deng, B.-L.; Lemiere, G.; Lepoivre, J.; De Groot, A.; Dommisse, R.; Vlietinck, A. J. Arch. der Pharm. 1997, 330, 313 https://doi.org/10.1002/ardp.19973300909
  9. Bouktaib, M.; Lebrun, S.; Atmani, A.; Rolando, C. Tetrahedron 2002, 58, 10001 https://doi.org/10.1016/S0040-4020(02)01306-6
  10. De Meyer, N.; Haemers, A.; Mishra, L.; Pandey, H. K.; Pieters, L. A. C.; Berghe, D. A. V.; Vlietinck, A. J. J. Med. Chem. 1991, 34, 736 https://doi.org/10.1021/jm00106a039
  11. Lee, J. S.; Kim, H. J.; Park, H.; Lee, Y. S. J. Nat. Prod. 2002, 65, 1367 https://doi.org/10.1021/np020048l
  12. Toda, S.; Kumura, M.; Ohnishi, M. Planta Med. 1991, 57, 8 https://doi.org/10.1055/s-2006-960005
  13. Sanz, M. J.; Ferrandiz, M. L.; Cejudo, M.; Terencio, M. C.; Gil, B.; Bustos, G.; Ubeda, A.; Gunasegaran, R.; Alcaraz, M. J. Xenobiotica 1994, 24, 689 https://doi.org/10.3109/00498259409043270

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