Skip to main content
SpringerLink
Log in

Silenerepin – a New C-Glycosylflavone from Silene repens

  • Published:
Chemistry of Natural Compounds Aims and scope

The new C-glycosylflavone silenerepin or 5-hydroxy-7,4′-dimethoxyflavone-6,8-di-C-β-D-glucopyranoside and 20 known flavonoids were isolated from the herb Silene repens Patrin (Caryophyllaceae). Their structures were elucidated using UV, IR, and NMR spectroscopy and mass spectrometry.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. N. Z. Mamadalieva, R. Lafont, and M. Wink, Diversity, 6, 415 (2014).

    Article  Google Scholar 

  2. D. N. Olennikov, Chem. Nat. Compd., 55, 127 (2019).

    Article  CAS  Google Scholar 

  3. D. N. Olennikov and N. K. Chirikova, Chem. Nat. Compd., 55, 642 (2019).

    Article  CAS  Google Scholar 

  4. D. N. Olennikov and N. I. Kashchenko, Chem. Nat. Compd., 55, 934 (2019).

    Article  CAS  Google Scholar 

  5. D. N. Olennikov, Chem. Nat. Compd., 55, 770 (2019).

    Article  CAS  Google Scholar 

  6. T. J. Mabry, K. R. Markham, and M. B. Thomas, The Systematic Identification of Flavonoids, Springer–Verlag, Berlin, 1970.

    Book  Google Scholar 

  7. N. I. Pryakhina, V. I. Sheichenko, and K. F. Blinova, Chem. Nat. Compd., 20, 554 (1984).

    Article  Google Scholar 

  8. D. N. Olennikov, N. K. Chirikova, N. I. Kashchenko, V. M. Nikolaev, S.-W. Kim, and C. Vennos, Front. Pharmacol., 9, 756 (2018).

    Article  Google Scholar 

  9. C. Xie, N. C. Veitch, P. J. Houghton, and M. S. Simmonds, Chem. Pharm. Bull., 51, 1204 (2003).

    Article  CAS  Google Scholar 

  10. A. K. Whaley, W. Ebrahim, M. El-Neketi, E. U. Ancheeva, F. C. Ozkaya, N. I. Pryakhina, N. U. Sipkina, V. G. Luzhanin, Z. Liu, and P. Proksch, Tetrahedron Lett., 58, 2171 (2017).

    Article  CAS  Google Scholar 

  11. A. Kawase and K. Yagishita, Agric. Biol. Chem., 32, 537 (1968).

    CAS  Google Scholar 

  12. R. A. Hilsenbeck and T. J. Mabry, Phytochemistry, 22, 2215 (1983).

    Article  CAS  Google Scholar 

  13. J. Chopin, G. Dellamonica, M. L. Bouillant, A. Besset, G. Popovici, and G. Weissenbock, Phytochemistry, 16, 2041 (1977).

    Article  CAS  Google Scholar 

  14. J. Peng, G. Fan, Z. Hong, Y. Chai, and Y. Wu, J. Chromatogr. A, 1074, 111 (2005).

    Article  CAS  Google Scholar 

  15. E. Besson, G. Dellamonica, J. Chopin, K. R. Markham, M. Kim, H.-S. Koh, and H. Fukami, Phytochemistry, 24, 1061 (1985).

    Article  CAS  Google Scholar 

  16. M. K. Kim, K. J. Yun, D. H. Lim, J. Kim, and Y. P. Jang, Biomol. Ther., 24, 630 (2016).

    Article  CAS  Google Scholar 

  17. T. Kato and Y. Morita, Chem. Pharm. Bull., 38, 2277 (1990).

    Article  CAS  Google Scholar 

  18. M. Ohkawa, J. Kinjo, Y. Hagiwara, H. Hagiwara, H. Ueyama, K. Nakamura, R. Ishikawa, M. Ono, and T. Nohara, Chem. Pharm. Bull., 46, 1887 (1998).

    Article  CAS  Google Scholar 

  19. M.-A. Dubois, A. Zoll, and J. Chopin, Phytochemistry, 22, 2879 (1983).

    Article  CAS  Google Scholar 

  20. Y.-Q. Zhang, J.-G. Luo, C. Han, J.-F. Xu, and L.-Y. Kong, J. Pharm. Biomed. Anal., 102, 276 (2015).

    Article  CAS  Google Scholar 

  21. A. A. Ahmed, A. M. Shalaby, F. R. Melek, and T. J. Mabry, J. Nat. Prod., 51, 971 (1988).

    Article  CAS  Google Scholar 

  22. T. Iwashina, A. Uehara, J. Kitajima, and T. Yukawa, Bull. Natl. Mus. Nat. Sci., Ser. B, 41, 33 (2015).

    Google Scholar 

  23. A. Bakhtiar, J. Gleye, C. Moulis, I. Fouraste, and E. Stanislas, Phytochemistry, 29, 1339 (1990).

    Article  CAS  Google Scholar 

  24. F. Senatore, M. D’Agostino, and I. Dini, J. Agric. Food Chem., 48, 2659 (2000).

    Article  CAS  Google Scholar 

  25. D. N. Olennikov, N. I. Kashchenko, and N. K. Chirikova, Khim. Rastit. Syr’ya, No. 3, 119 (2019).

  26. G. Cheng, Y. Bai, Y. Zhao, J. Tao, Y. Liu, G. Tu, L. Ma, N. Liao, and X. Xu, Tetrahedron, 56, 8915 (2000).

    Article  CAS  Google Scholar 

  27. M. Jay and M.-R. Viricel, Phytochemistry, 19, 2627 (1980).

    Article  CAS  Google Scholar 

  28. V. Darmograi, Chem. Nat. Compd., 13, 102 (1977).

    Google Scholar 

  29. D. N. Olennikov, N. K. Chirikova, N. I. Kashchenko, T. G. Gornostai, I. Y. Selyutina, and I. N. Zilfikarov, Int. J. Mol. Sci., 18, 2579 (2017).

    Article  Google Scholar 

  30. M. Akabane, A. Yamamoto, S. Aizawa, A. Taga, and S. Kodama, Anal. Sci., 30, 739 (2014).

    Article  CAS  Google Scholar 

Download references

Acknowledgment

The work was sponsored by FASO Russia (AAAA-AA17-117011810037-0).

Author information

Authors and Affiliations

  1. Institute of General and Experimental Biology, Siberian Branch, Russian Academy of Sciences, 6 Sakh’yanovoi St, Ulan-Ude, Russia, 670047

    D. N. Olennikov

Authors
  1. D. N. Olennikov
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to D. N. Olennikov.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 3, May–June, 2020, pp. 367–369.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Olennikov, D.N. Silenerepin – a New C-Glycosylflavone from Silene repens. Chem Nat Compd 56, 423–426 (2020). https://doi.org/10.1007/s10600-020-03053-8

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10600-020-03053-8

Keywords

Search

Navigation