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Modification of C11, C28, C2,3,23 or C2,23,28 Functional Groups on Asiatic Acid and Evaluation of Hepatoprotective Effects

  • Published : 2007.06.20

Abstract

For the development of novel hepatoprotective agents, C11, C28, C2,3,23 or C2,23,28 functional groups on asiatic acid were modified, and their hepatoprotective effects were evaluated. Most of the prepared compounds displayed potent hepatoprotective activities against CCl4- and galactosamine (GaIN)-induced hepatotoxicity. Especially, compounds 16 and 20 showed the most significant hepatoprotective effects against GaIN-induced hepatotoxicity (54.2% and 46.4% protection at 50 mM, respectively).

Keywords

References

  1. Liu, J.; Liu, Y. P.; Klaassen, C. D. J. Ethanopharmacol. 1994, 42, 183 https://doi.org/10.1016/0378-8741(94)90084-1
  2. Wang, B.; Jiang, Z. H. Chinese Pharmaceutical Journal 1992, 27, 393
  3. Yabuchi, T.; Tanaka, T.; Sasatsuka, T.; Yamahara, J.; Fujimura, H. JP 1987, 62126149
  4. Hikino, H.; Ohsawa, T.; Kiso, Y.; Oshima, Y. Planta Medica 1984, 50, 353 https://doi.org/10.1055/s-2007-969730
  5. Ma, X. H.; Zhao, Y. C.; Yin, L.; Han, D. W.; Wan, M. S. Acta Pharmaceutica Sinica 1986, 21, 332
  6. Shukla, B.; Viser, S.; Patnaik, G. K.; Tripathi, S. C.; Srimal, R. C.; Day, S.; Dobhal, P. C. Phytotherapy Res. 1992, 6, 74 https://doi.org/10.1002/ptr.2650060205
  7. Sastri, B. N. In The Wealth of India, Raw Materials; C.S.I.R.: New Delhi, 1950; vol II, p 116
  8. Beljanski, M.; Vapaille, N. Rev. Eur. Etud. Clin. Biol. 1971, 16, 897
  9. Pointel, J. P.; Boccalon, H.; Cloarec, M.; Ledevehat, J. M. Angiology 1987, 38, 46 https://doi.org/10.1177/000331978703800106
  10. Bonte, F.; Dumas, M.; Chaudagne, C.; Meybeck, A. Ann. Pharm. Fr. 1995, 53, 38
  11. Shim, P.-J.; Park, J.-H.; Chang, M.-S.; Lim, M.-J.; Kim, D.-H.; Jung, Y.-H.; Jew, S.-S.; Park, E.-H.; Kim, H. D. Bioorg. Med. Chem. Lett. 1996, 6, 2937
  12. Jeong, B.-S. Arch. Pharm. Res. 2006, 29, 556 https://doi.org/10.1007/BF02969264
  13. Jeong, B.-S.; Lee, M. K.; Kim, Y. C.; Lee, E.-S. Arch. Pharm. Res. 2007, 30, 282 https://doi.org/10.1007/BF02977607
  14. Berry, M. N.; Friend, D. S. J. Cell Biol. 1984, 43, 506 https://doi.org/10.1083/jcb.43.3.506
  15. Reitman, S.; Frankel, S. A. Am. J. Clin. Pathol. 1957, 28, 56
  16. Boiteau, P.; Chanez, M. Dissertationes Pharm. 1963, 15, 189
  17. Corey, E. J.; Ursprung, J. J. J. Am. Chem. Soc. 1956, 78, 183 https://doi.org/10.1021/ja01582a052

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