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Triterpenoid Saponins from Elsholtzia bodinieri

  • Hu, Hao-Bin (College of Chemistry and Chemical Engineering, Longdong University) ;
  • Zheng, Xu-Dong (College of Chemistry and Chemical Engineering, Longdong University) ;
  • Hu, Huai-Sheng (College of Chemistry and Chemical Engineering, Longdong University) ;
  • Jian, Yu-Feng (Department of Biology, Longdong University)
  • Published : 2007.09.20

Abstract

A new oleanane-type triterpenoid estersaponin, bodinierin C (1), along with two known saponins, mazusaponin I (2) and ciwujianoside C (3), were isolated from the water-soluble part of the root barks of Elsholtzia bodinieri. The structure of bodinierin C was characterized by spectroscopic means and chemical hydrolysis as 3β -Ocaffeoyl- 23-hydroxylechinocystic acid 28-O-α -L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β- D-glucopyranosyl ester. The known compounds were identified by comparing their spectral data with those of authentic samples or data reported in the literature. All compounds were firstly isolated from Elsholtzia bodinieri family.

Keywords

References

  1. Delectis Florae Reipublicae Popularis Sinicae Agendae Academiae Sinicae Edita. Flora Reipublicae Popularis Sinicae; Science Press: Beijing, 1990; Vol. 60, p 336
  2. Jiangsu New Medical College. Dictionary of Traditional Chinese Drug; Shanghai Science and Technology Press: Shanghai, 1985; Vol. 1, p 489
  3. Zhu, W. M.; He, H. P.; Wang, S. Z.; Zuo, G. Y.; Hao, X. J. Chin. Chem. Lett. 2000, 13, 253
  4. Li, R. T.; Li, J. T.; Wang, J. K. Helv. Chim. Acta 2005, 88, 252 https://doi.org/10.1002/hlca.200590006
  5. Zhao, D. B.; Yang, Y. X.; Zhang, W.; Liu, X. H.; Zhai, C. P.; Wang, H. Q. J. Chin. Med. Mat. 2005, 28, 94
  6. Hu, H. B.; Liu, J. X.; Zheng, X. D. Chin. Tradit. Herb Drugs 2006, 37, 18
  7. Hu, H. B.; Jian, Y. F.; Zheng, X. D.; Cao, H. Bull. Korean Chem. Soc. 2007, 28, 351 https://doi.org/10.5012/bkcs.2007.28.3.467
  8. Yaguchi, E.; Miyase, T.; Ueno, A. Phytochemistry 1995, 39, 185 https://doi.org/10.1016/0031-9422(94)00857-P
  9. Shao, C. J.; Kesai, R.; Xu, J. D.; Tanaka, O. Chem. Pharm. Bull. 1988, 36, 601 https://doi.org/10.1248/cpb.36.601
  10. Ikuta, A.; Itokawa, H. Phytochemistry 1988, 27, 2813 https://doi.org/10.1016/0031-9422(88)80668-X
  11. Conrad, J.; Vogler, B.; Klaiber, I.; Roos, G.; Walter, U.; Kraus, W. Phytochemistry 1998, 48, 647 https://doi.org/10.1016/S0031-9422(98)00154-X
  12. Mahato, S. B.; Kundu, A. P. Phytochemistry 1994, 37, 1517 https://doi.org/10.1016/S0031-9422(00)89569-2
  13. Zhang, Y. J.; Yang, C. R. Phytochemistry 1994, 36, 997 https://doi.org/10.1016/S0031-9422(00)90478-3
  14. Niranjan, P. S.; Shashi, B. M. Phytochemistry 1994, 37, 1425 https://doi.org/10.1016/S0031-9422(00)90425-4
  15. Yun, B. S.; Ryoo, I. J.; Lee, I. K.; Park, K. H.; Choung, D. H.; Han, K. H.; Yoo, I. D. J. Nat. Prod. 1999, 62, 764 https://doi.org/10.1021/np9804637
  16. Li, X. C.; Wang, D. Z.; Wu, S. G. Phytochemistry 1990, 29, 595 https://doi.org/10.1016/0031-9422(90)85123-W
  17. Teng, R. W.; Zhong, H. M.; Chen, C. X.; Wang, D. Z. Chin. J. Magn. Reson. 1999, 16, 389
  18. Teng, R. W.; Wang, D. Z.; Chen, C. X. Chin. Chem. Lett. 2000, 11, 337
  19. He, Z. D.; Qiao, C. F.; Han, Q. B.; Wang, Y.; Ye, W. C.; Xu, H. X. Tetrahedron 2005, 61, 2211 https://doi.org/10.1016/j.tet.2004.12.032
  20. Agrawal, P. K. Phytochemistry 1992, 31, 3307 https://doi.org/10.1016/0031-9422(92)83678-R
  21. Haddad, M.; Miyamoto, T.; Laurens, V.; Lacaille-Dubois, M. A. J. Nat. Prod. 2003, 66, 372 https://doi.org/10.1021/np020391q

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  2. vol.99, pp.3, 2016, https://doi.org/10.1002/hlca.201500195
  3. pp.1478-6427, 2018, https://doi.org/10.1080/14786419.2018.1477144
  4. Human Acyl-CoA: Cholesterol Acyltransferase (hACAT) Inhibitory Activities of Triterpenoids from Roots of Glycine max (L.) Merr vol.29, pp.3, 2007, https://doi.org/10.5012/bkcs.2008.29.3.615
  5. Triterpenoids vol.27, pp.1, 2007, https://doi.org/10.1039/b808530g
  6. Two new oleanane triterpenoid saponins from Elsholtzia bodinieri vol.5, pp.3, 2012, https://doi.org/10.1016/j.phytol.2012.05.016
  7. Three new 18,19-seco-ursane glycosides from Elsholtzia bodinieri vol.12, pp.None, 2007, https://doi.org/10.1016/j.phytol.2015.04.028
  8. Two new ursane-type triterpenoid saponins from Elsholtzia bodinieri vol.39, pp.6, 2007, https://doi.org/10.1007/s12272-016-0750-8
  9. Two new oleanane triterpenoid saponins from Elsholtzia bodinieri vol.35, pp.21, 2021, https://doi.org/10.1080/14786419.2020.1721489