Chemistry of Natural Compounds

, Volume 54, Issue 1, pp 66–68 | Cite as

A New Eudesmane-Type Sesquiterpene from the Leaves of Artemisia vulgaris

  • Truong Van Nguyen Thien
  • Lien Thi Kim Tran
  • Nhu Thi Tiet Nhu
  • Toan Phan Duc
  • Lien Thi My Do
  • Dung Duc Tu
  • Phi Phung Nguyen Kim
  • Quang Ton That
Article
  • 3 Downloads

Eight known compounds and one new compound, a eudesmane-type sesquiterpene (1), were isolated from the leaves of Artemisia vulgaris. Their structures were elucidated by HR-ESI-MS, and NMR analyses.

Keywords

Artemisia vulgaris Asteraceae eudesmane-type sesquiterpene 

Notes

Acknowledgment

This work was supported by Grant # 104.01-2011.46 from Vietnam′s National Foundation for Science and Technology Development (NAFOSTED).

References

  1. 1.
    J. A. Duke, M. J. B. Godwin, C. J. Du, and P. N. K. Duke, Handbook of Medicinal Herbs, 2nd Ed., CRC Press, Washington DC, 2002, p. 513.CrossRefGoogle Scholar
  2. 2.
    H. L. Walter, P. F. Memory, and L. Elvin, Medical Botany, 2nd Ed., John Wiley and Sons, New Jersey, 2003, p. 345.Google Scholar
  3. 3.
    S. Lee, H. Chung, C. Maier, and A. Wood, J. Agric. Food. Chem., 46, 3325 (1998).CrossRefGoogle Scholar
  4. 4.
    A. Bamoniri, B. B. F. Mirjalili, A. Mazoochi, and H. J. Batooli, Iran. J. Org. Chem., 2, 533 (2010).Google Scholar
  5. 5.
    P. Wei, H. Ting, W. Yang, B.X. Wen, J. Z. Cheng, and P. Q. Lu, Chem. Nat. Compd., 46, 959 (2011).CrossRefGoogle Scholar
  6. 6.
    N. Tsuneatsu, A. Fumiko, K. Junei, and O. Hikaru, Biol. Pharm. Bull., 25, 875 (2002).CrossRefGoogle Scholar
  7. 7.
    T. Amer, L. Francisco, P. Sara, M. E. Khaled, L. K. Michael, L. Janet, M. Arsala, and J. C. Stephen, J. Nat. Prod., 78, 1461 (2015).CrossRefGoogle Scholar
  8. 8.
    S. Tochiko, M. Takao, S. Yasuhisa, and M. C. Chiu, Chem. Pharm. Bull., 31, 3865 (1983).CrossRefGoogle Scholar
  9. 9.
    D. Yang, H. Xie, B. Yang, and X. Wei, Phytochem. Lett., 7, 217 (2014).CrossRefGoogle Scholar
  10. 10.
    S. Parveen, N. Riaz, M. Saleem, J. Khan, S. Ahmad, A. Ashraf, E. S. Abida, R. T. Bakhsh, and A. Jabbar, J. Chem. Soc. Pak., 34, 1513 (2012).Google Scholar
  11. 11.
    V. Martinez, O. Barbera, S. Parareda, and J. A. Marco, Phytochemistry, 26, 2619 (1987).CrossRefGoogle Scholar
  12. 12.
    A. Berhan, C. Francisco, C. Joee, F. Miguel, J. Ulla, M. Carlos, M. Elisa, and T. Jordi, Tetrahedron, 42, 6003 (1986).CrossRefGoogle Scholar
  13. 13.
    Z. Ke, Q. C. Xiao, Y. C. Xing, W. Qing, F. Qiang, X. Z. Si, and F. T. Peng, Phytochem. Lett., 5, 313 (2012).CrossRefGoogle Scholar
  14. 14.
    S. Glasl, U. Kastner, A. Baumann, W. Robien, J. Jurenitsch, and W. Kubelka, Phytochemistry, 38, 159 (1995).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Truong Van Nguyen Thien
    • 1
  • Lien Thi Kim Tran
    • 1
  • Nhu Thi Tiet Nhu
    • 1
  • Toan Phan Duc
    • 1
  • Lien Thi My Do
    • 2
  • Dung Duc Tu
    • 1
  • Phi Phung Nguyen Kim
    • 1
  • Quang Ton That
    • 1
  1. 1.Faculty of ChemistryUniversity of Science, Vietnam National UniversityHo Chi Minh CityVietnam
  2. 2.Saigon UniversityHo Chi Minh CityVietnam

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