Chemistry of Natural Compounds

, Volume 49, Issue 5, pp 845–847 | Cite as

Flavonoids from the Aerial Part of Polygonum persicaria

  • A. V. Kurkina
  • T. K. Ryazanova
  • V. A. Kurkin

The known flavonoids pinostrobin (5-hydroxy-7-methoxyflavanone), 2',6'-dihydroxy-4',5'-dimethoxychalcone (polygochalcone), astragalin, isoquercitrin, quercitrin, and also the new natural compound 6'-hydroxy2',4'-dimethoxychalcone (persicochalcone) were isolated from the aerial part of lady’s thumb (Polygonum persicaria L.) and characterized using PMR and UV spectroscopy and mass spectrometry.


lady’s thumb Polygonum persicariaaerial part flavonoids flavanones chalcones flavonols pinostrobin 6'-hydroxy-2',4'-dimethoxychalcone 2',6'-dihydroxy-4',5'-dimethoxychalcone astragalin isoquercitrin quercitrin 


  1. 1.
    State Registry of Drugs [in Russian], Vol. 1, Official Edition, Moscow, 2008, 1238 pp.Google Scholar
  2. 2.
    V. A. Kurkin, Pharmacognosy [in Russian], 2nd Ed., Revised and Supplemented, Handbook, OOO Ofort, GOU VPO SamGMU, Samara, 2007, 1239 pp.Google Scholar
  3. 3.
    Plant Resources of Russia: Wild Flowering Plants, Their Component Composition and Biological Activity, Vol. 1, Families Magnoliaceae-Juglandaceae, Ulmaceae, Moraceae, Cannabiaceae, Urticaceae [in Russian], Chief Ed. A. L. Budantsev, Tovarishchestvo Nauchnykh Izdanii KMK, St. Petersburg, Moscow, 2008, 421 pp.Google Scholar
  4. 4.
    Plant Resources of the USSR. Flowering Plants, Their Chemical Composition and Use. Families Magnoliaceae-Limoniaceae [in Russian], Nauka, Leningrad, 1985, 460 pp.Google Scholar
  5. 5.
    M. M. Mukhamed'yarova, Khim. Prir. Soedin., 131 (1968).Google Scholar
  6. 6.
    H. D. Smolarz, Acta Pol. Pharm., 59 (2), 145 (2002).PubMedGoogle Scholar
  7. 7.
    H. Yoon, S. Eom, J. Hyun, G. Jo, D. Hwang, S. Lee, Y. Yong, J. C. Park, Y. H. Lee, and Y. Lim, Bull. Korean Chem. Soc., 32 (6), 2101 (2011).CrossRefGoogle Scholar
  8. 8.
    J. P. Dzoyem, A. H. L. Nkuete, V. Kuete, M. F. Tala, H. K. Wabo, S. K. Guru, V. S. Rajput, A. Sharma, P. Tane, I. A. Khan, A. K. Saxena, H. Laatsch, and N. H. Tan, Planta Med., 78 (8), 787 (2012).PubMedCrossRefGoogle Scholar
  9. 9.
    A. V. Kurkina, T. K. Ryazanova, and V. A. Kurkin, Khim. Prir. Soedin., 717 (2013).Google Scholar
  10. 10.
    D.-Y. Lee, H.-N. Lyu, H.-Y. Kwak, L. Jung, Y.-H. Lee, D.-K. Kim, I.-S. Chung, S. H. Kim, and N.-I. Baek, J. Appl. Biol. Chem., 50 (3), 144 (2007).Google Scholar
  11. 11.
    T. Nanamura, T. Hagiwara, and H. Kawagishi, Biosci. Biotechnol. Biochem., 69 (2), 280 (2005).CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2013

Authors and Affiliations

  • A. V. Kurkina
    • 1
  • T. K. Ryazanova
    • 1
  • V. A. Kurkin
    • 1
  1. 1.Samara State Medical UniversitySamaraRussia

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