Bulletin of the Korean Chemical Society

  • 제34권4호
  • /
  • Pages.1272-1274
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  • 2013
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Cytotoxicity of Substituted Benzimidazolyl Curcumin Mimics Against Multi-Drug Resistance Cancer Cell

  • Eom, Young Woo (Cell Therapy and Tissue Engineering Center, Yonsei University Wonju College of Medicine) ;
  • Oh, Sangtae (Department of Basic Science, Kwandong University College of Medicine) ;
  • Woo, Ho Bum (Department of Basic Science, Yonsei University Wonju College of Medicine) ;
  • Ham, Jungyeob (Marine Chemomics Laboratory, Natural Medicine Center, Korea Institute of Science and Technology) ;
  • Ahn, Chan Mug (Department of Basic Science, Yonsei University Wonju College of Medicine) ;
  • Lee, Seokjoon (Department of Pharmacology, Kwandong University College of Medicine)
  • 투고 : 2012.12.26
  • 심사 : 2013.01.21
  • 발행 : 2013.04.20
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참고문헌

  1. Srimal, R. C.; Dhawan, B. N. J. Pharm. Pharmacol. 1973, 25, 447. https://doi.org/10.1111/j.2042-7158.1973.tb09131.x
  2. Sharma, O. P. Biochem. Pharmacol. 1976, 25, 1811. https://doi.org/10.1016/0006-2952(76)90421-4
  3. Li, C. J.; Zhang, L. J.; Dezube, B. J.; Crumpacker, C. S.; Pardee, A. B. Proc. Natl. Acad. Sci. 1993, 90, 1839. https://doi.org/10.1073/pnas.90.5.1839
  4. Kawamori, T.; Lubet, R.; Steele, V. E.; Kelloff, G. J.; Kaskey, R. B.; Rao, C. V.; Reddy, B. S. Cancer Res. 1999, 59, 597.
  5. Brouet, I.; Ohshima, H. Biochem. Biophys. Res. Commun. 1995, 206, 533. https://doi.org/10.1006/bbrc.1995.1076
  6. Sidhu, G. S.; Mani, H.; Gaddipati, J. P.; Singh, A. K.; Seth, P.; Banaudha, K. K.; Patnaik, G. K.; Maheshwari, R. K. Wound Rep. Reg. 1999, 7, 362. https://doi.org/10.1046/j.1524-475X.1999.00362.x
  7. Woo, H. B.; Shin, W.-S.; Lee, S.; Ahn, C. M. Bioorg. Med. Chem. Lett. 2005, 15, 3782. https://doi.org/10.1016/j.bmcl.2005.05.064
  8. Ahn, C. M.; Park, B.-G.; Woo, H. B.; Ham, J.; Lee, S. Bioorg. Med. Chem. Lett. 2009, 19, 1481. https://doi.org/10.1016/j.bmcl.2009.01.019
  9. Park, S.-K.; Oh, S.; Shin, H. K.; Kim, S. H.; Ham, J.; Song, J.-S.; Lee, S. Bioorg. Med. Chem. Lett. 2011, 21, 3573. https://doi.org/10.1016/j.bmcl.2011.04.106
  10. Woo, H. B.; Eom, Y. W.; Park, K.-S.; Ham, J.; Ahn, C. M.; Lee, S. Bioorg. Med. Chem. Lett. 2012, 22, 933. https://doi.org/10.1016/j.bmcl.2011.12.074
  11. Nofal, Z. M.; Soliman, E. A.; El-Karim, S. S. A.; El-Zahar, M. I.; Srou, A. M.; Sethumadhavan, S.; Maher, T. J. Acta. Pol. Pharm.-Drug Res. 2011, 68, 519.
  12. Porcari, A. R.; Devivar, R. V.; Kucera, L. S.; Drach, J. C.; Townsend, L. B. J. Med. Chem. 1998, 41, 1252. https://doi.org/10.1021/jm970559i
  13. Kumar, J. R.; Jawahar, J. L.; Pathak, D. P. E-J. Chem. 2006, 3, 278. https://doi.org/10.1155/2006/765712
  14. Aouali, N.; Eddabra, L.; Macadré, J.; Morjani, H. Crit. Rev. Oncol./Hematol. 2005, 56, 61. https://doi.org/10.1016/j.critrevonc.2004.12.010
  15. Chearwae, W.; Anuchapreeda, S.; Nandigama, K.; Ambudkar, S. V.; Limtrakul, P. Biochem. Pharmacol. 2004, 68, 2043. https://doi.org/10.1016/j.bcp.2004.07.009
  16. Anuchapreeda, S.; Leechanachai, P.; Smith, M. M.; Ambudkar, S. V.; Limtrakul, P. Biochem. Pharmacol. 2002, 64, 573. https://doi.org/10.1016/S0006-2952(02)01224-8
  17. Romiti, N.; Tongiani, R.; Cervelli, F.; Chieli, E. Life Sci. 1998, 62, 2349. https://doi.org/10.1016/S0024-3205(98)00216-1
  18. Kim, Y. K.; Song, Y. J.; Seo, D. W.; Kang, D. W.; Lee, H. Y.; Rhee, D. K.; Han, J. W.; Ahn, C. M.; Lee, S.; Kim, S. N. Biochem. Biophys. Res. Commun. 2007, 355, 136. https://doi.org/10.1016/j.bbrc.2007.01.117
  19. Um, Y.; Cho, S.; Woo, H. B.; Kim, Y. K.; Kim, H.; Ham, J.; Kim, S. N.; Ahn, C. M.; Lee, S. Bioorg. Med. Chem. 2008, 16, 3608. https://doi.org/10.1016/j.bmc.2008.02.012
  20. Orjales, A.; Alonso-Cires, L.; López-Tudanca, P.; Tapia, I.; Mosquera, R.; Labeaga, L. Eur. J. Med. Chem. 1999, 34, 415. https://doi.org/10.1016/S0223-5234(99)80091-9
  21. Roggen, H.; Charnock, C.; Gundersen, L.-L. Tetrahedron 2009, 65, 5199. https://doi.org/10.1016/j.tet.2009.04.100
  22. Dess, D. B.; Martin, J. C. J. Org. Chem. 1983, 48, 4155. https://doi.org/10.1021/jo00170a070
  23. Matarrese, M.; Soloviev, D. V.; Moresco, R. M.; Ferri, V.; Simonelli, P.; Magni, F.; Colombo, F.; Todde, S.; Carpinelli, A.; Fazio, F.; Kienle, M. G. Bioorg. Chem. 1998, 26, 91. https://doi.org/10.1006/bioo.1998.1089
  24. Qiang, F.; Lee, B.-J.; Ha, I.; Kang, K. W.; Woo, E.-R.; Han, H.-K. Eur. J. Pharm. Sci. 2010, 41, 226. https://doi.org/10.1016/j.ejps.2010.06.009
  25. Lu, J.-J.; Cai, Y.-J.; Ding, J. Mol. Cell Biochem. 2012, 360, 253. https://doi.org/10.1007/s11010-011-1064-2

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