Substituted aminophenols and flavonoids as potential components for test-systems for total antioxidant activity

Kinetics of ortho -phenylenediamine (PDA) oxidation has been investigated in the “pseudoperoxidase” system, Methemalbumin-H 2 O 2 , in the presence of 2-amino-4- tert -butylphenol (ATBP), 2-amino-4,6-di tert -butylphenol (ADTBP) and its four N-acyl derivates, as well as flavonoids (quercetin, morin,...

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Published inBiochemistry (Moscow). Supplement. Series B, Biomedical chemistry Vol. 2; no. 1; pp. 75 - 81
Main Authors Grigorenko, Yu. A., Karaseva, E. I., Metelitza, D. I., Sorokin, V. L., Ksendsova, G. A., Shadyro, O. I.
Format Journal Article
LanguageEnglish
Published Moscow Nauka/Interperiodica 2008
Springer Nature B.V
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Summary:Kinetics of ortho -phenylenediamine (PDA) oxidation has been investigated in the “pseudoperoxidase” system, Methemalbumin-H 2 O 2 , in the presence of 2-amino-4- tert -butylphenol (ATBP), 2-amino-4,6-di tert -butylphenol (ADTBP) and its four N-acyl derivates, as well as flavonoids (quercetin, morin, silibin, hesperidin and naringin). Under standard experimental conditions (20°C, phosphate buffered saline, pH 7.4, containing 5.25% ethanol and DMF) ATBP, ADTBP and two its N-acyl-derivatives and also all five flavonoids inhibited PDA oxidation with different efficiency, which was characterized in terms of the inhibition constants, K i , M, or the percent of inhibition degree at the maximal concentrations of these inhibitors. Quercetin (K i = 7.7 × 10 −5 M) and ATBP (K i = 1.26 × 10 −4 M) were the most effective antioxidants. Using these characteristics and other required criteria, the pairs PDA-quercetin and PDA-ATBP were proposed for a practical application in the test-systems for evaluation of total antioxidant activity of biological objects.
ISSN:1990-7508
1990-7516
DOI:10.1007/s11828-008-1008-x