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Chemistry of Natural Compounds

, Volume 53, Issue 2, pp 375–376 | Cite as

Polyphenols from Several Psammopelitohalophytes

  • G. A. Seitimova
  • B. K. Eskalieva
  • G. Sh. Burasheva
  • M. Iqbal Choudhary
  • Achyut Adhikari
Article

The plants Climacoptera obtusifolia and Kochia prostrata are psammopelitohalophytes that are typically highly tolerant to the soil mechanical composition and have significant resources in Kazakhstan [1, 2]. Therefore, phytochemical research on the aerial part of the Kazakhstan variety of K. prostrata was initiated and studies of the chemical composition of C. obtusifolia were continued [3, 4].

Fractional extraction and adsorption-distribution and gel chromatography isolated pure phenolic compounds 18 (14 from C. obtusifolia; 58, K. prostrata). The compounds were identified using chemical and spectral analyses and comparison with the literature and authentic samples. Compounds 58 were observed for the first time in plants of the genus Kochia. Compounds 24 were isolated for the first time from plants of the family Chenopodiaceae.

Quercetin 3-O-β-D-Glucopyranosyl-(6→1)-α-L-rhamnopyranoside (rutin) (1). C27H30O16, light-yellow crystals, mp 214–216°C. UV spectrum (MeOH, λmax, nm):...

Keywords

MeOH Quercetin Rutin CD3OD White Needle 
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.

References

  1. 1.
    N. I. Akzhigitova, Halophilic Flora of Central Asia and Its Signatures [in Russian], Fan, Tashkent, 1982, pp. 26-30.Google Scholar
  2. 2.
    Flora of Kazakhstan [in Russian], Vol 3, Academy of Sciences of the Kazakh SSR, Alma-Ata, 1960, pp. 179–226, 231–234.Google Scholar
  3. 3.
    B. Yeskaliyeva, M. A. Mesaik, A. Abbaskhan, A. Kulsoom, G. Sh. Burasheva, Zh. A. Abilov, M. I. Choudhary, and Atta-ur-Rahman, Phytochemistry, 67, 2392 (2006).CrossRefPubMedGoogle Scholar
  4. 4.
    G. A. Seitimova, B. K. Eskalieva, G. Sh. Burasheva, and M. I. Choudhary, Chem. Nat. Compd., 50, 537 (2014).CrossRefGoogle Scholar
  5. 5.
    A. K. Kipchakbaeva, R. A.-A. Khamid, B. K. Eskalieva, G. Sh. Burasheva, Zh. A. Abilov, S. R. Numonov, and H. A. Aisa, Chem. Nat. Compd., 52, 322 (2016).CrossRefGoogle Scholar
  6. 6.
    B. P. Silva, R. R. Bernardo, and J. P. Parente, Phytochemistry, 53, 87 (2000).CrossRefPubMedGoogle Scholar
  7. 7.
    Q. Xiong, D. Shi, and M. Mizuno, Phytochemistry, 39, 723 (1995).CrossRefGoogle Scholar
  8. 8.
    A. F. Barrero, A. Haidour, M. Munoz-Dorado, M. Akssira, A. Sedqui, and I. Mansour, Phytochemistry, 48, 1237 (1998).CrossRefGoogle Scholar
  9. 9.
    C. A. Buschi, A. B. Pomilio, and E. G. Gros, Phytochemistry, 18, 1249 (1979).CrossRefGoogle Scholar
  10. 10.
    N. A. Ser, Phytochemistry, 27, 3708 (1988).CrossRefGoogle Scholar
  11. 11.
    H. C. Kwon and K. R. Lee, Arch. Pharm. Res., 24, 194 (2001).CrossRefPubMedGoogle Scholar
  12. 12.
    C. J. Baker, B. D. Whitaker, D. P. Roberts, N. M. Mock, C. P. Rice, K. L. Deahl, and A. A. Aver′yanov, Physiol. Mol. Plant Pathol., 66, 90 (2005).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2017

Authors and Affiliations

  • G. A. Seitimova
    • 1
  • B. K. Eskalieva
    • 1
  • G. Sh. Burasheva
    • 1
  • M. Iqbal Choudhary
    • 2
  • Achyut Adhikari
    • 2
  1. 1.Al-Farabi Kazakh National University, Faculty of Chemistry and Chemical EngineeringAlmatyRepublic of Kazakhstan
  2. 2.Research Institute of Chemistry, International Center of Chemical and Biological SciencesUniversity of KarachiKarachiPakistan

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