Skip to main content
SpringerLink
Log in

Flavanones and Flavones from Bashkir Propolis

  • Published:
Chemistry of Natural Compounds Aims and scope

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

References

  1. S. Almutairi, R. Edrada-Ebel, J. Fearnley, J. O. Ogoli, W. Alotabi, C. J. Clements, A. I. Gray, and D. G. Watson, Phytochem. Lett., 10, 160 (2014).

    Article  CAS  Google Scholar 

  2. M. A. E. Watanabe, M. K. Amarante, B. J. Conti, and J. M. Sforcin, J. Pharm. Pharmacol., 63, 1378 (2011).

    Article  CAS  Google Scholar 

  3. M. P. Popova, K. Graikou, I. Chikon, and V. S. Bankova, J. Agric. Food Chem., 58, 3167 (2010).

    Article  CAS  Google Scholar 

  4. A. Petrova, M. Popova, C. Kuzmanova, I. Tsvetkova, H. Naydenski, E. Muli, and V. Bankova, Fitoterapia, 81, 509 (2010).

    Article  CAS  Google Scholar 

  5. J. M. Alvarez-Suarez, Bee Products – Chemical and Biological Properties, Springer International Publishing AG, 2017, pp. 99–111.

  6. Sh. Huang, C.-P. Zang, K. Wang, G. Q. Li, and F.-L. Hu, Molecules, 19, 19610 (2014).

    Article  Google Scholar 

  7. B.-N. Su, E. J. Park, J. S. Vigo, J. G. Graham, F. Cabieses, H. H. S. Fong, J. M. Pezzuto, and A. D. Kinghorn, Phytochemistry, 63, 335 (2003).

    Article  CAS  Google Scholar 

  8. A. G. Gonzalez, Z. E. Aguiar, J. G. Luis, A. G. Ravelo, J. T. Vazquez, and X. A. Dominguez, Phytochemistry, 28, 2871 (1989).

    Article  CAS  Google Scholar 

  9. K. Ichino, H. Tanaka, and K. Ito, Tetrahedron, 44, 3251 (1988).

    Article  CAS  Google Scholar 

  10. H. Haberlein and K.-P. Tschiersch, Phytochemistry, 35, 765 (1994).

    Article  CAS  Google Scholar 

  11. J.-Q. Gu, E. J. Park, J. S. Vigo, J. G. Graham, H. H. S. Fong, J. M. Pezzuto, and A. D. Kinghorn, J. Nat. Prod., 65, 1616 (2002).

    Article  CAS  Google Scholar 

  12. N. M. Cuong, T. V. Sung, C. Kamperdick, and G. Adam, Pharmazie, 51, 128 (1996).

    CAS  Google Scholar 

  13. M. G. Carvalho, D. C. Cranchi, and A. G. Carvalho, J. Braz. Chem. Soc., 7, 187 (1996).

    Article  Google Scholar 

  14. V. I. Yamovoi, E. A. Kulmagambetova, A. T. Kulyyasov, K. M. Turdybekov, and S. M. Adekenov, Chem. Nat. Compd., 37, 424 (2001).

    Article  Google Scholar 

  15. K. J. Hodgetts, Tetrahedron, 61, 6860 (2005).

    Article  CAS  Google Scholar 

  16. T. Korenada, K. Hayashi, Y. Kaki, R. Maenishi, and T. Sakai, Org. Lett., 13, 2022 (2011).

    Article  Google Scholar 

  17. J. McNulty, J. J. Nair, E. Bollareddy, K. Keskar, A. Thorat, D. J. Crankshaw, A. C. Holloway, G. Khan, G. D. Wright, and L. Ejim, Phytochemistry, 70, 2040 (2009).

    Article  CAS  Google Scholar 

  18. D. Bertelli, G. Papotti, L. Bortolotti, G. L. Marcazzan, and M. Plessi, Phytochem. Anal., 23, 260 (2012).

    Article  CAS  Google Scholar 

  19. G. Jerz, R. Waibel, and H. Achenbach, Phytochemistry, 66, 1698 (2005).

    Article  CAS  Google Scholar 

  20. S. Grecco, A. C. Dorigueto, I. M. Landre, M. G. Soares, K. Martho, R. Lima, R. C. Pascon, M. A. Vallim, T. M. Capello, P. Romoff, P. Sartorelli, and J. H. G. Lago, Molecules, 19, 7528 (2014).

    Article  Google Scholar 

  21. S. Grecco, J. Q. Reimao, A. G. Tempone, P. Sartorelli, R. L. O. R. Cunha, P. Romoff, M. J. P. Ferreira, O. A. Favero, and J. H. G. Lago, Exp. Parasitol., 130, 141 (2012).

    Article  CAS  Google Scholar 

  22. J.-M. Fang, W. Ch. Su, and Y.-Sh. Cheng, Phytochemistry, 27, 1385 (1988).

    Google Scholar 

  23. V. A. Kurkin, G. G. Zapesochnaya, and V. B. Braslavskii, Chem. Nat. Compd., 26, 224 (1990).

    Article  Google Scholar 

Download references

Acknowledgment

The work was financially supported by the Russian Foundation for Basic Research and the Academy of Sciences of the Republic of Bashkortostan (Project No. 17-43-020483 p_a). Structures of compounds were established using PMR and 13C NMR spectra with 2D experiments (COSY, HSQC, HMBC, NOESY) and MALDI TOF/TOF mass spectra obtained at the Agidel Common Use Center at the IPC, RAS.

Author information

Authors and Affiliations

  1. Ufa State Petroleum Technological University, 145 Chernyshevskogo St., Ufa, 450062, Russia

    R. A. Zainullin, R. V. Kunakova & V. F. Gareev

  2. Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 141 Prosp. Oktyabrya, Ufa, 450075, Russia

    I. V. Galyautdinov, Z. R. Sadretdinova, Z. S. Muslimov & V. N. Odinokov

Authors
  1. R. A. Zainullin
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. R. V. Kunakova
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. V. F. Gareev
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. I. V. Galyautdinov
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Z. R. Sadretdinova
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Z. S. Muslimov
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. V. N. Odinokov
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to R. A. Zainullin.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 5, September–October, 2018, pp. 827–829.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zainullin, R.A., Kunakova, R.V., Gareev, V.F. et al. Flavanones and Flavones from Bashkir Propolis. Chem Nat Compd 54, 975–977 (2018). https://doi.org/10.1007/s10600-018-2526-5

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10600-018-2526-5

Keywords

Search

Navigation