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dc.contributor.author Shcherbyna, R. en
dc.contributor.author Pruhlo, Y. en
dc.contributor.author Duchenko, M. en
dc.contributor.author Kulagina, M. en
dc.contributor.author Kudria, V. en
dc.contributor.author Vashchuk, V. en
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 [et al.] // Hacettepe University Journal of the Faculty of Pharmacy. – 2022. – Vol. 42, № 2. – P. 73–82. en
dc.identifier.other DOI: 10.52794/hujpharm.1033112
dc.identifier.uri https://dspace.vnmu.edu.ua/123456789/8012 en
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. en
dc.language.iso en en
dc.publisher Hacettepe University Journal of the Faculty of Pharmacy en
dc.subject 1,2,4-triazole en
dc.subject antioxidant activity en
dc.subject in vitro method en
dc.title Evaluation of antioxidant activity of 1, 2, 4-triazole derivatives with morpholine moiety en
dc.type Article en


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