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http://dspace.zsmu.edu.ua/handle/123456789/14158
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Название: | Study of the structure of products of interaction between some naphthoquinone derivatives and pharmaceutical substances |
Авторы: | Donchenko, А. Miedviediev, K. Voskoboynik, O. Vasyuk, S. Kovalenko, S. Донченко, Анастасія Олександрівна Мєдвєдєва, Катерина Павлівна Воскобойник, О. Ю. Васюк, Світлана Олександрівна Коваленко, Сергій Іванович |
Ключевые слова: | Acetylcysteine β-alanine taurine naphthoquinone derivatives reaction products |
Дата публикации: | 2021 |
Библиографическое описание: | Study of the structure of products of interaction between some naphthoquinone derivatives and pharmaceutical substances / А. Donchenko, K. Miedviedieva, O. Voskoboynik, S. Vasyuk, S. Kovalenko // Ankara Üniversitesi Eczacılık Fakültesi Dergisi. - 2021. - Vol. 45, Iss. 2. - P. 321-331. - https://doi.org/10.33483/jfpau.835875 |
Аннотация: | The purpose of the present work is to detail а study of the interaction between naphthoquinonebased analytical reagents and such pharmacologically active ingredients as acetylcysteine, β-alanine and taurine (2-aminoethanesulfonic acid) including the isolation and structure elucidation of the formed products. Material and Method: UV-visible spectrophotometry was applied to determine the stoichiometric coefficients of reactants in reactions between the pharmaceutical substances and naphthoquinone derivatives. 1Н NMR-spectroscopy, IR spectroscopy, сhromatomass-spectrometry were used to prove the structure of the reaction products. Result and Discussion: The stoichiometric relationships of the reactants in the investigated medicinal substances reactions with quinone derivatives were determined by the methods of saturation and continuous changes. They are 1:1 in each case. According to the determined relationships of components reaction and optimal conditions for reactions path, the products of interaction of acetylcysteine with 2,3-dichloro-1,4-naphthoquinone and taurine, β-alanine with sodium 1,2-naphthoquinone-4-sulfonate were isolated and identified. In order to establish the structure of the compounds, the 1Н NMR-spectroscopy, IR spectroscopy, сhromatomass-spectrometry were used. |
URI: | http://dspace.zsmu.edu.ua/handle/123456789/14158 |
Располагается в коллекциях: | Наукові праці. (Аналітична хімія)
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