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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 Vashchuk, V.
dc.date.accessioned 2025-03-21T22:15:45Z
dc.date.available 2025-03-21T22:15:45Z
dc.date.issued 2022
dc.identifier.citation Shcherbyna R. Evaluation of Antioxidant Activity of 1, 2, 4-Triazole Derivatives With Morpholine Moiety / R. Shcherbyna, Y. Pruhlo, M. Duchenko, M. Kulagina, V. Kudria, V. Vashchuk // Hacettepe University Journal of the Faculty of Pharmacy. – 2022. – 42 (2). - Р. 73-82 uk_UA
dc.identifier.issn ISSN: 2458 - 8806
dc.identifier.other DOI: 10.52794/hujpharm.1033112
dc.identifier.uri https://dspace.vnmu.edu.ua/123456789/8636
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 pronounced 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 increasing 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.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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