Advertisement

A Chemical Study on the Steroidal Glycosides from Atropa belladonna L. Seeds

  • S. A. Shvets
  • N. V. Latsterdis
  • P. K. Kintia
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 404)

Abstract

During recent years steroidal glycosides have attracted a growing interest owing to the wide range of their biological action on living organisms. The substances of this class are able to inhibit the growth of malignant neoplasms, reduce the level of cholesterol in blood, display antioxidant properties, and have antimicrobial and fungicidal actions.1

Keywords

Phthalic Acid Petunia Hybrida Butanolic Extract Physicochemical Constant Monosaccharide Residue 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    P.K. Kintia, G.V. Lazuryevskiy, N.N. Balashova, I.T. Balashova, A.I. Suruzhiu, and V.A. Lyakh, Structure and Biological Activity of Steroidal Glycosides of the Spirostane and Furostane Series,Shtiintsa, Kishinev (In Russian) (1987).Google Scholar
  2. 2.
    C. Sannié and H. Lapin, Recherches sur les sapogenines a noyau sterolique. Identification des genines sur de petites quantites de plantes, Bull. Soc. Chim. Fr. 19: 1080 (1952).Google Scholar
  3. 3.
    S. Kiyosawa, M. Hutoh, T. Komori, T. Nohara, I. Hosokawa, and T. Kawasaki, Detection of prototype compounds of diosgenin and other spirostanol glycosides, Chem. Pharm. Bull. 16: 1162 (1968).PubMedCrossRefGoogle Scholar
  4. 4.
    M.E. Wall, C.R. Eddy, M.L. McClennan, and M.E. Kumpp, Detection and estimation of steroidal sapogenins in plant tissue. Anal. Chem. 24: 1337 (1952).CrossRefGoogle Scholar
  5. 5.
    S. Hakomori, A rapid permethylation of glycolipids and polysaccharides catalyzed by methylsulfonyl carbanion in dimethyl sulfoxide. J. Biochem. 55: 205 (1964).PubMedGoogle Scholar
  6. 6.
    S. Shvets, A. Naibi, P. Kinitia, and K. Spinu, Steroidal glycosides from Petunia hybrida L. seeds. Structure of petuniosides A, C, E, Abstr. III Nation. Meeting of Pharm. of the Moldova Rep. Kishinev, (In Russian) p. 300 (1993).Google Scholar
  7. 7.
    S.A. Shvets, P.K. Kintia, and M.A. Naibi, Steroidal glycosides from Petunia hybrida L. seeds and their biological activity, In Saponins Used in Food and Agriculture, G.R. Waller and K. Yamasaki, Eds., Plenum Publishing Co., New York, NY. In press (1996).Google Scholar
  8. 8.
    C. Shaoxing and J.K. Shyder, Diosgenin-bearing molluscicidal saponins from Allium vineale: NMR approach for the structural assignment of oligosaccharide units, J. Org . Chem. 54: 3679 (1989).CrossRefGoogle Scholar
  9. 9.
    A. Aksel, B.Y. Stephens, J. Lee, Ch.D. Warren, and R.W. Jeanloz, Structure determination of a tetrasaccharide: Transient Overhauser effects in the rotating frame. J. Am. Chem. Soc. 106: 811 (1984).CrossRefGoogle Scholar
  10. 10.
    P.K. Agrawal, D.C. Jain, R.K. Gupta, and R.S. Thakur, Carbon 13-NMR spectroscopy of steroidal sapogenins and steroidal saponins, Phytochemistry 24: 2479 (1984).CrossRefGoogle Scholar
  11. 11.
    V.V. Krokhmalyuk, P.K. Kintia, and V.Ya. Chirva, Gas-liquid chromatography of monosaccharides of triterpene glycosides, Izv. AN MSSR (In Russian) 1: 103 (1975).Google Scholar

Copyright information

© Springer Science+Business Media New York 1996

Authors and Affiliations

  • S. A. Shvets
    • 1
  • N. V. Latsterdis
    • 1
  • P. K. Kintia
    • 1
  1. 1.Institute of GeneticsAcademy of SciencesChisinauMoldova

Personalised recommendations