Chemistry of Natural Compounds

, Volume 47, Issue 5, pp 802–804 | Cite as

Chemical study of Panzerina lanata

  • D. N. OlennikovEmail author
  • L. M. Tankhaeva

Panzerina lanata (L.) Sojak. is a plant species of the family Lamiaceae. It is widely distributed over the territory of Buryatia. P. lanata is used in Tibetian medicine under the name gang ga' chung as a substitute for Gentiana urnula Smith. (Gentianaceae) to treat stomach, intestinal, and gynecological diseases [1]. A chemical study of this plant found ballonigrine, 13-hydroxyballonigrine [2], stachydrin [3], and phenolic compounds [4]. The goal of our work was to study the chemical composition of the aerial part of P. lanata growing in Buryatia.

The aerial part of P. lanata was collected in the vicinity of Naryn-Atsagat (Republic of Buryatia, Russia, June 17, 2009; 52°01′65″ N, 108°27′95″ E). The species was determined by Doctor of Pharmaceutical Sciences T. A. Aseeva (IGEB, SB, RAS). A sample of the raw material was preserved in the herbarium of the Department of Biologically Active Compounds, IGEB, SB, RAS (No. L/L2111-09).

Ground raw material of P. lanata(340 g) was extracted...


Rutin EtOAc Caffeic Acid Chlorogenic Acid Ursolic Acid 
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.



The work was supported financially by SB RAS Project No. VI.52.1.3.


  1. 1.
    Tibetian Medicine in Buryatia [in Russian], RAS, Novosibirsk, 2008.Google Scholar
  2. 2.
    G. Savona, F. Piozzi, and J. R. Hanson, Phytochemistry, 17, 2132 (1978).CrossRefGoogle Scholar
  3. 3.
    T. A. Khokhrina and V. A. Peshkova, Chem. Nat. Comp., 10, 284 (1975).CrossRefGoogle Scholar
  4. 4.
    Plant Resources of the USSR. Families Hippuridaceae-Lobeliaceae [in Russian], Nauka, Leningrad, 1991.Google Scholar
  5. 5.
    F. H. Foppen, Chromatogr. Rev., 14, 133 (1971).PubMedCrossRefGoogle Scholar
  6. 6.
    T. Kurihara, M. Kikuchi, S. Suzuki, and E. Toyoda, Yakugaku Zasshi, 96, 1407 (1976).PubMedGoogle Scholar
  7. 7.
    M. Kates, Techniques of Lipidology: Isolation, Analysis, and Identification of Lipids, Elsevier, New York, 1972.Google Scholar
  8. 8.
    J. S. Choi, H. S. Young, J. C. Park, J.-H. Choi, and W. S. Woo, Arch. Pharm. Res., 9, 233 (1986).CrossRefGoogle Scholar
  9. 9.
    M.-H. Yang and L.-Y. Kong, Chem. Nat. Comp., 44, 98 (2008).CrossRefGoogle Scholar
  10. 10.
    E.-R. Woo and M. S. Piao, Arch. Pharm. Res., 27, 173 (2004).PubMedCrossRefGoogle Scholar
  11. 11.
    G. M. Pettit, A. Numata, T. Takemura, R. H. Ore, A. S. Narula, J. M. Schmidt, G. M. Cragg, and C. P. Pase, J. Nat. Prod., 53, 456 (1990); H. Ravn, S. Nishibe, M. Sasahara, and L. Xuebo, Phytochemistry, 29, 3627 (1990).Google Scholar
  12. 12.
    Y.-S. Liang, H. K. Kim, A. W. M. Lefeber, C. Erkelens, Y. H. Choi, and R. Verpoorte, J. Chromatogr. A, 1112, 148 (2006); H. Tazaki, M. Ito, M. Miyoshi, J. Kawabata, E. Fukushi, T. Fujita, M. Motouri, T. Furuki, and K. Nabeta, Biosci. Biotechnol. Biochem., 66, 255 (2002).Google Scholar
  13. 13.
    H. A. Jung, J. C. Park, H. Y. Chung, J. Kim, and J. S. Choi, Arch. Pharm. Res., 22, 213 (1999).PubMedCrossRefGoogle Scholar
  14. 14.
    V. M. Malikov and M. P. Yuldashev, Chem. Nat. Comp., 38, 358, 473 (2002).CrossRefGoogle Scholar
  15. 15.
    T. Ohsugi, R. Nishida, and H. Fukami, Appl. Entomol. Zool., 26, 29 (1991); I. Uriarte-Pueyo, M. Goicoechea, A. G. Gil, A. L. de Cerain, A. L. de Munain, and M. I. Calvo, J. Agric. Food Chem., 57, 11055 (2009).Google Scholar

Copyright information

© Springer Science+Business Media, Inc. 2011

Authors and Affiliations

  1. 1.Institute of General and Experimental Biology, Siberian BranchRussian Academy of SciencesUlan-UdeRussia

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