Please use this identifier to cite or link to this item: https://dspace.uzhnu.edu.ua/jspui/handle/lib/35058
Full metadata record
DC FieldValueLanguage
dc.contributor.authorКороль, Наталія Іванівна-
dc.contributor.authorГоловко-Камошенкова, Оксана Миколаївна-
dc.contributor.authorСливка, М.В.-
dc.contributor.authorПаллаг, Олександра Володимирівна-
dc.contributor.authorБойко, Надія Володимирівна-
dc.contributor.authorЛендєл, Василь Георгійович-
dc.date.accessioned2021-05-12T08:33:28Z-
dc.date.available2021-05-12T08:33:28Z-
dc.date.issued2020-
dc.identifier.citationСинтез та біоактивність 5,5’-бутан-біс-4-заміщених-4Н-1,2,4-триазол-3-тіонів / Н. І. Король, О. М. Головко-Каамошенкова, М. В. Сливка [та ін.] // Науковий вісник Ужгородського університету : серія: Хімія; зб. наук. пр. / редкол.: І.Є. Барчій, С.М. Сухарев, В.П. Антонович та ін. – Ужгород : УжНУ, 2020. – вип.1 (43). – C. 32–39. – Рез. англ. – Бібліогр. : с. 35–37 (35 назв).uk
dc.identifier.issn2414-0260-
dc.identifier.urihttps://dspace.uzhnu.edu.ua/jspui/handle/lib/35058-
dc.description.abstractDerivatives of 1,2,4-triazole have a number of valuable pharmacological properties and are used in medicine, agriculture, photography. At the same time, information on bis-triazole derivatives is limited. In particular, there is a known method of synthesis of Mannich bases - derivatives of 5,5'- butane-bis-1,2,4-triazole-3-thions, some of which exhibit antioxidant, antifungal and antibacterial properties. Another study was aimed at obtaining 4-amino-substituted derivatives of 5,5'-butane-bis- 1,2,4-triazole-3-thione, as well as their 2-adamantanone-substituted Schiff bases, the toxicity of which was also studied. The possibility of using the compound 3,3′-butane-1,4-diyl) bis [4-amino-1H-1,2,4- triazole-5-(4H)-thione] as a corrosion inhibitor is described. The source also characterizes a series of 4-amino-substituted derivatives of 5,5'-butane-bis-1,2,4-triazole-3-thions, their condensation reaction with the formation of triazolothiadiazoles, some of the compounds showed antibacterial properties. Due to the lack of data on compounds of this class, the lack of research on the effect of substituent in position 4 of the triazole cycle on the biological properties of compounds, as well as due to the high pharmacological potential of substances containing 1,2,4-triazole - the aim of this research is obtaining and studying the biological action of 5,5'-butane-bis-1,2,4-triazole-3-thione derivatives with aliphatic and aromatic substituents in position 4 of the triazole nucleus. In this study, a number of derivatives of 5,5'-butane-bis-1,2,4-triazoles with methyl, phenyl, pnitrophenyl, hexyl, heptyl and octyl substituents in the fourth position of the triazole nucleus were obtained, their structure was proved by NMR spectroscopy and elemental analysis, the study of biological action on microorganisms selected from collection test strains and clinical isolates, the study of quantitative microbiological characteristics by culturing the obtained compounds with preselected microorganisms. The high biological action of newly synthesized compounds indicates the prospects for their further functionalization and study. Keywords: bis-1,2,4-triazoles; isothiocyanates, acid hydrazides; condensation; biological activity.uk
dc.language.isoukuk
dc.publisherГоверлаuk
dc.relation.ispartofseriesХімія;-
dc.subjectbis-1,2,4-triazolesuk
dc.subjectisothiocyanatesuk
dc.subjectacid hydrazidesuk
dc.subjectcondensationuk
dc.subjectbiological activityuk
dc.titleСинтез та біоактивність 5,5’-бутан-біс-4-заміщених-4Н-1,2,4-триазол-3-тіонівuk
dc.title.alternativeSynthesis and bioactivity of 5,5'-butane-bis-4-substituted-4h-1,2,4- Triazole-3-thiols)uk
dc.typeTextuk
dc.pubTypeСтаттяuk
Appears in Collections:Науковий вісник УжНУ Серія Хімія Випуск 1 (43) 2020

Files in This Item:
File Description SizeFormat 
СИНТЕЗ ТА БІОАКТИВНІСТЬ.pdf175.03 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.