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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 |