Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19325
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2022-03-23T14:25:15Z-
dc.date.available2022-03-23T14:25:15Z-
dc.date.issued2022-
dc.identifier.citationDolganov, A. A., Levchenko, A. G., Dahno, P. G., Guz’ D. D., Chikava A. R., Dotsenko, V. V., Aksenov, N. A., Aksenova, I. V. 7-Aryl-3-(hydroxymethyl)-5-oxo-1,2,3,5-tetrahydro[1,2,4]triazolo[1,5-a]pyridine-6,8-dicarbonitriles: Synthesis and Predicted Biological Activity // Russian Journal of General Chemistry. - 2022. - Том 92. - Выпуск 2. - Стр.: 185 - 197. - DOI10.1134/S1070363222020074ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19325-
dc.description.abstractAminomethylation of 1,6-diamino-4-aryl-2-oxo-1,2-dihydropyridine-3,5-dicarbonitriles under the action of excess of formaldehyde in ethanol has led to the formation of 7-aryl-3-(hydroxymethyl)-5-oxo-1,2,3,5-tetrahydro[1,2,4]triazolo[1,5-a]pyridine-6,8-dicarbonitriles. Bioavailability parameters of the obtained compounds have been predicted in silico and the possible protein targets have been predicted via the protein-ligand docking.ru
dc.language.isoenru
dc.publisherPleiades journalsru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectAminomethylationru
dc.subject[1,2,4]triazolo[1,5-a]pyridinesru
dc.subjectCyanoacetohydrazideru
dc.subjectMalononitrileru
dc.subjectOxymethylationru
dc.subjectThe Mannich reactionru
dc.title7-Aryl-3-(hydroxymethyl)-5-oxo-1,2,3,5-tetrahydro[1,2,4]triazolo[1,5-a]pyridine-6,8-dicarbonitriles: Synthesis and Predicted Biological Activityru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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