2-[(3-Aminoalkyl-(alkaryl-,aryl-))- 1 H-1,2,4-triazol-5-yl]anilines: synthesis and anticonvulsant activity

dc.contributor.authorMartynenko, Yu.
dc.contributor.authorBerest, G.
dc.contributor.authorBukhtiyarova, N.
dc.contributor.authorBelenichev, I. F.
dc.contributor.authorVoskoboinik, O.
dc.contributor.authorKovalenkо, S.
dc.contributor.authorМартиненко, Юлія Вікторівна
dc.contributor.authorБерест, Галина Григорівна
dc.contributor.authorБухтіярова, Ніна Вікторівна
dc.contributor.authorБеленічев, І.
dc.contributor.authorВоскобойнік, Олексій Юрійович
dc.contributor.authorКоваленко, Сергій Іванович
dc.date.accessioned2021-06-30T05:27:58Z
dc.date.available2021-06-30T05:27:58Z
dc.date.issued2020
dc.description.abstract: The presented work is devoted to the development of synthesis methods for novel 2-[(3-aminoalkyl-(alkaryl-, aryl-))-1H -1,2,4-triazolo]anilines. Abovementioned compounds were obtained via hydrazinolysis (Ing-Manske procedure) and acid hydrolysis of corresponding N -acylated{([1,2,4]triazolo[1,5- c ]quinazolin-2-yl)alkyl-(alkaryl-, aryl-)}amines. The regioselectivity of hydrazinolysis and hydrolysis were established. The features of spectral characteristics were studied and discussed. Characteristic patterns of protons signals splitting in 1 H NMR of the synthesized compounds were established. The effect of the synthesized compounds on the pentylenetetrazol seizures was studied. It was found that according to some indicators, anticonvulsant activity of 2-[(3-aminoalkyl-(alkaryl-, aryl-))-1H -1,2,4-triazolo]anilines superior or comparable with effect of the reference drug “Lamotrigine”. It is a valid argument for their further structural modification, in-depth study of activity mechanisms and further study of anticonvulsant activity on other experimental seizures models.uk_UK
dc.identifier.citation2-[(3-Aminoalkyl-(alkaryl-,aryl-))- 1 H-1,2,4-triazol-5-yl]anilines: synthesis and anticonvulsant activity / Yu. Martynenko, G. Berest, N. Bukhtiyarova, I. Belenichev, O. Voskoboinik, S. Kovalenkо // Turkish Journal of Chemistry. - 2020. - Vol. 44, № 3. -P. 746-755. - https://doi.org/10.3906/kim-2002-24uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/14217
dc.language.isoenuk_UK
dc.subjectN -acylated{([1,2,4]triazolo[1,5- c ]quinazolin-2-yl)alkyl-(alkaryl-, aryl-)}aminesuk_UK
dc.subject2-[(3-aminoalkyl-(alkaryl-, aryl-))-1H -1,2,4-triazolo]anilinesuk_UK
dc.subjecthydrazinolysisuk_UK
dc.subjectacidic hydrolysisuk_UK
dc.subjectanticonvulsant activityuk_UK
dc.title2-[(3-Aminoalkyl-(alkaryl-,aryl-))- 1 H-1,2,4-triazol-5-yl]anilines: synthesis and anticonvulsant activityuk_UK
dc.typeArticleuk_UK

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