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

Авторы: 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
Учреждения:
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
Выпуск: Том 66, № 10 (2017)
Страницы: 1881-1890
Раздел: Full Articles
URL: https://journal-vniispk.ru/1066-5285/article/view/241451
DOI: https://doi.org/10.1007/s11172-017-1962-x
ID: 241451

Цитировать

Полный текст

Открытый доступ
Доступ закрыт

Доступ предоставлен
Доступ закрыт

Только для подписчиков

Аннотация
Об авторах
Список литературы
Дополнительные файлы
Статистика

Аннотация

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.

Ключевые слова

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

Об авторах

O. Shevchenko

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

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