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Synthesis of new biologically active polymer bioconjugates based on lupane allylamides

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Abstract

Betulonic and 2-hydroxyiminobetulonic acids were synthesized based on betulin triterpenoid, which can readily be isolated from birch (Bétula) bark. Allylamides of betulonic and 2-hydroxyiminobetulonic acids were prepared by the reaction of the corresponding acids with allylamine in the presence of oxalyl chloride and triethylamine. It was established that the obtained allylamides copolymerize at low rates with acrylonitrile and N-vinylpyrrolidone in the presence of radical initiators to produce random copolymers. The resulting copolymers exhibit the cytotoxic activity against MS cultures and are promising for developing new bioactive polymer bioconjugates.

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Authors and Affiliations

  1. Institute of Technical Chemistry, Ural Branch, Russian Academy of Sciences, ul. Akademika Koroleva 3, Perm, 614013, Russia

    M. N. Gorbunova, G. F. Krainova, I. A. Tolmacheva & V. V. Grishko

Authors
  1. M. N. Gorbunova
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  2. G. F. Krainova
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  3. I. A. Tolmacheva
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  4. V. V. Grishko
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Correspondence to M. N. Gorbunova.

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Original Russian Text © M.N. Gorbunova, G.F. Krainova, I.A. Tolmacheva, V.V. Grishko, 2014, published in Khimiya Rastitel’nogo Syr’ya, 2014, No. 4, pp. 91–99.

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Gorbunova, M.N., Krainova, G.F., Tolmacheva, I.A. et al. Synthesis of new biologically active polymer bioconjugates based on lupane allylamides. Russ J Bioorg Chem 41, 732–738 (2015). https://doi.org/10.1134/S1068162015070043

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  • DOI: https://doi.org/10.1134/S1068162015070043

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