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Chemistry of Natural Compounds

, Volume 48, Issue 6, pp 930–933 | Cite as

Matsutake alcohol glycosides from Sanchezia nobilis

  • Ahmed E. Abd Ellah
  • Khaled M. Mohamed
  • Enaam Y. Backheet
  • Mahmoud H. Mohamed
Article

Phytochemical investigation of the aerial parts of Sanchezia nobilis Hook. (Acanthaceae) has yielded matsutake alcohol (1-octen-3-ol) (1) and four matsutake alcohol glycosides identified as 3-O-β-glucopyranosyl-1-octen-3-ol (2), 3-O-β-glucopyranosyl-(1→6)-β-glucopyranosyl-1-octen-3-ol (3), 3-O-α-arabinopyranosyl-(1→6)-β-glucopyranosyl-1-octen-3-ol (4), and 3-O-α-arabinopyranosyl-(1→6)-β-glucopyranosyl-(1→6)-β-glucopyranosyl-1-octen-3-ol (5). The structures of the isolated compounds were assigned on the basis of different techniques of NMR spectral analysis. Compounds 1–4 have been isolated here for the first time from the family Acanthaceae, while compound 5 is isolated here for the first time from a natural source.

Keywords

Sanchezia nobilis Hook.f. Acanthaceae matsutake alcohol glycosides 

References

  1. 1.
    K. R. Kirtikar and B. D. Basu, Indian Medicinal Plants, Jayyed press, Delhi-6, Vol. III, 2nd Ed., 1975.Google Scholar
  2. 2.
    J. M. Watt and M. G. Breyer-Brandwijk, The Medicinal and Poisonous Plants of Southern and Eastern Africa, 2nd Ed., E. and S. Livingstone Ltd., Edinburgh and London, 1962.Google Scholar
  3. 3.
    A. E. Abd-Ellah, K. M. Mohamed, E. Y. Bakheet, and H. Mohamed, Bull. Pharm. Sci. Assiut Univ., 29 (II), 300 (2006).Google Scholar
  4. 4.
    S. Yamamura, K. Ozawa, K. Ohtani, R. Kasai, and K. Yamasaki, Phytochemistry, 48, 131 (1998).CrossRefGoogle Scholar
  5. 5.
    S. Takano, M. Yanase, M. Takahashi, and K. Ogasawara, Chem. Lett., 2017 (1987).Google Scholar
  6. 6.
    T. Kurihara and M. Kikuchi, Yakugaku Zasshi, 93, 1201 (1973).PubMedGoogle Scholar
  7. 7.
    S. Murahashi, Chem. Res., 34, 155 (1938).Google Scholar
  8. 8.
    W. Freytag and K. H. Ney, Eur. J. Biochem., 4, 315 (1968).PubMedCrossRefGoogle Scholar
  9. 9.
    E. Honkanen and T. Moisio, Acta. Chim. Scand., 17, 858 (1963).CrossRefGoogle Scholar
  10. 10.
    M. Yoshikawa, T. Murakami, and M. Kubo, Chem. Pharm. Bull., 46 (5), 886 (1998).PubMedCrossRefGoogle Scholar
  11. 11.
    M. S. Kamel, K. M. Mohamed, H. A. Hassanean, K. Ohtani, R. Kasai, and K. Yamasaki, Phytochemistry, 55, 252 (2000).CrossRefGoogle Scholar
  12. 12.
    H. Bradbury and J. Jenkins, Carbohydr. Res., 125, 126 (1984).Google Scholar
  13. 13.
    S. Wang, E. L. Ghisalberti, and J. Ridsdill, J. Nat. Prod., 61 (4), 508 (1998).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2013

Authors and Affiliations

  • Ahmed E. Abd Ellah
    • 1
  • Khaled M. Mohamed
    • 2
  • Enaam Y. Backheet
    • 2
  • Mahmoud H. Mohamed
    • 1
  1. 1.Department of Pharmacognosy, Faculty of PharmacyAl-Azhar UniversityAssiutEgypt
  2. 2.Department of Pharmacognosy, College of PharmacyAl-Taif UniversityAl-TaifEgypt

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