Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18258
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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.accessioned2021-11-11T09:34:02Z-
dc.date.available2021-11-11T09:34:02Z-
dc.date.issued2021-
dc.identifier.citationDotsenko, V. V., Guz, D. D., Tebiev, D. T., Kindop V. K., Aksenov N. A., Aksenova, I. V., Netreba, E. E. Synthesis and some properties of new 5-Hydroxy-2-[(hetarylthio)methyl]-4H-pyran-4-ones // Russian Journal of General Chemistry. - 2021. - Том 91. - Выпуск 9. - Стр.: 1629 - 1638. - DOI 10.1134/S107036322109005Xru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18258-
dc.description.abstractThe reaction of 2-thioxoazines with chlorokojic acid in the presence of KOH in DMF led to the formation of new hybrid molecules containing fragments of kojic acid and azaheterocycle linked by the SCH2 spacer. In silico prediction of bioavailability parameters was carried out, possible protein targets were predicted by the protein ligand docking method.ru
dc.language.isoenru
dc.publisherPleiades journalsru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subject2-thioxo-1,2-dihydroquinoxalinesru
dc.subject3-cyanopyridine-2(1H)-thionesru
dc.subjectCalculated biological activityru
dc.subjectChlorokojic acidru
dc.subjectS-alkylationru
dc.titleSynthesis and some properties of new 5-Hydroxy-2-[(hetarylthio)methyl]-4H-pyran-4-onesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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