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dc.contributor.author SHCHERBYNA, R
dc.contributor.author PRUHLO, Y
dc.contributor.author DUCHENKO, M
dc.contributor.author KULAGINA, M
dc.contributor.author KUDRIA, V
dc.contributor.author VALENTYNA, V
dc.date.accessioned 2025-03-18T17:01:13Z
dc.date.available 2025-03-18T17:01:13Z
dc.date.issued 2022
dc.identifier.citation Evaluation of Antioxidant Activity of 1, 2, 4-Triazole Derivatives With Morpholine Moiety / R. Shcherbyna, E. Pryhlo, M. Duchenko, M. Kulagina, V. Kudria, V. Vashchuk // Hacettepe University Journal of the Faculty of Pharmacy. - 2022. - Vol. 42, Iss. 2. - P. 73-82. uk_UA
dc.identifier.issn DOİ: 10.52794/hujpharm.1033112
dc.identifier.uri https://dspace.vnmu.edu.ua/123456789/8012
dc.description.abstract The aim of the work was to study the antioxidant activity of 4-R- 3-(morpholinomethyl)-4H-1,2,4-triazole-5-thioles and their alkyl derivatives in vitro using the method of non-enzymatic initiation of lipid peroxidation. Among the 45 compounds studied, 8 showed varying degrees of AOA. The most pro- nounced AOA has 4-amino-3-(morpholinomethyl)-4H-1,2,4-triazole-5-thiol. It was found that in most cases the introduction in alkyl-derivatives of 4-R- 3-(morpholinomethyl)-4H-1,2,4-triazole-5-thioles free amino group or phenyl substituent to the N4 atom of the 1,2,4-triazole nucleus, accompanied with in- creasing of AOA for test substances. In almost all cases, the presence on the N4 atom of 1,2,4-triazole nucleus methyl or ethyl groups has the opposite effect, even in comparison with control groups. uk_UA
dc.language.iso en uk_UA
dc.publisher Hacettepe University Journal of the Faculty of Pharmacy uk_UA
dc.subject 1,2,4-triazole uk_UA
dc.subject antioxidant activity uk_UA
dc.subject in vitro method uk_UA
dc.title Evaluation of Antioxidant Activity of 1, 2, 4-Triazole Derivatives With Morpholine Moiety uk_UA
dc.type Article uk_UA


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