Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives

In this study, thirteen novel 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives were synthesized and characterized by elemental analyses and IR, 1H NMR,13C NMR and UV spectral data. The synthesized compounds were analyzed for their in vitro potential antioxidant activities in three different methods. T...

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Main Authors: O. Gursoy Kol, H. Yuksek
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2010/407603
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author O. Gursoy Kol
H. Yuksek
author_facet O. Gursoy Kol
H. Yuksek
author_sort O. Gursoy Kol
collection DOAJ
description In this study, thirteen novel 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives were synthesized and characterized by elemental analyses and IR, 1H NMR,13C NMR and UV spectral data. The synthesized compounds were analyzed for their in vitro potential antioxidant activities in three different methods. Those antioxidant activities were compared to standard antioxidants such as BHA, BHT and α-tocopherol. The data reveal that the compounds demonstrate a marked capacity for iron binding, especially 5a and 7c In addition to this, the compounds 4 were titrated potentiometrically with TBAH in non-aqueous solvents because of the weak acidic properties of 4,5-dihydro-1H-1,2,4-triazol-5-one ring N-H group.
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publishDate 2010-01-01
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series E-Journal of Chemistry
spelling doaj-art-8a01472973be42839104fffaa2fe5b572025-02-03T05:58:54ZengWileyE-Journal of Chemistry0973-49452090-98102010-01-017112313610.1155/2010/407603Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one DerivativesO. Gursoy Kol0H. Yuksek1Department of Chemistry, Kafkas University, 36100 Kars, TurkeyDepartment of Chemistry, Kafkas University, 36100 Kars, TurkeyIn this study, thirteen novel 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives were synthesized and characterized by elemental analyses and IR, 1H NMR,13C NMR and UV spectral data. The synthesized compounds were analyzed for their in vitro potential antioxidant activities in three different methods. Those antioxidant activities were compared to standard antioxidants such as BHA, BHT and α-tocopherol. The data reveal that the compounds demonstrate a marked capacity for iron binding, especially 5a and 7c In addition to this, the compounds 4 were titrated potentiometrically with TBAH in non-aqueous solvents because of the weak acidic properties of 4,5-dihydro-1H-1,2,4-triazol-5-one ring N-H group.http://dx.doi.org/10.1155/2010/407603
spellingShingle O. Gursoy Kol
H. Yuksek
Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
E-Journal of Chemistry
title Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
title_full Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
title_fullStr Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
title_full_unstemmed Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
title_short Synthesis and In Vitro Antioxidant Evaluation of Some Novel 4, 5-Dihydro-1H, 2, 4-triazol-5-one Derivatives
title_sort synthesis and in vitro antioxidant evaluation of some novel 4 5 dihydro 1h 2 4 triazol 5 one derivatives
url http://dx.doi.org/10.1155/2010/407603
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AT hyuksek synthesisandinvitroantioxidantevaluationofsomenovel45dihydro1h24triazol5onederivatives