Structure—hemolytic activity relationship in isobornylphenol derivatives

O. G. Shevchenko; S. N. Plyusnina; E. V. Buravlev; I. Yu. Chukicheva; I. V. Fedorova; O. V. Shchukina; A. V. Kutchin

doi:10.1007/s11172-017-1962-x

Structure—hemolytic activity relationship in isobornylphenol derivatives

Autores: Shevchenko O.G.¹, Plyusnina S.N.¹, Buravlev E.V.², Chukicheva I.Y.², Fedorova I.V.², Shchukina O.V.², Kutchin A.V.²
Afiliações:
1. Institute of Biology, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
2. Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences
Edição: Volume 66, Nº 10 (2017)
Páginas: 1881-1890
Seção: Full Articles
URL: https://ogarev-online.ru/1066-5285/article/view/241451
DOI: https://doi.org/10.1007/s11172-017-1962-x
ID: 241451

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Resumo

A structure — hemolytic activity relationship in isobornylphenol derivatives was analysed. The morphological transformation of erythrocytes under the influence of some representatives of this class of compounds was demonstrated by scanning electron microscopy. The hemolytic activity of the test compounds can vary within wide limits, depending on the structure and position of substituents determining the nature of the interaction of the compound with the cell membrane.

Palavras-chave

terpenylphenols, isobornylphenols, aminomethylphenols, alkoxymethylphenols, antioxidants, erythrocyte, biomembrane, hemolysis, morphological transformation of erythrocytes, scanning electron microscopy

Sobre autores

O. Shevchenko

Institute of Biology, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: chukichevaiy@mail.ru
Rússia, 28 ul. Kommunisticheskaya, Syktyvkar, 167982