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 |