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note
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The detailed synthesis procedure and analytical data for compounds 2a and 2b are given in Supplementary data.
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60449111938
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note
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50 were calculate from the plots of the percentage DPPH transformation after 5 min of reaction against the ratio [Scavenger]/[DPPH]. Values obtained are the average of 3-5 experiments.
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note
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The reaction mixture (50 mM{cyrillic} phosphate buffer, r{cyrillic}N{cyrillic} 7.4) contained 50 μM{cyrillic} xanthine, 75 μM{cyrillic} nitroblue tetrazolium, EDTA (0.1 mM{cyrillic}) and 0.5-2 μM{cyrillic} resorcinarenes 2a,b or 4-hydroxy-TEMPO. Stock solution of compounds 2a,b were prepared in methanol. The volume concentration of the organic solvent in reaction mixture (2 mL) was 2%. The reaction was started by adding 0.008 U of xanthine oxidase to the mixture incubated at 25 °S{cyrillic}.
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60449112170
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note
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2+/MgO as an internal standard. Samples were accommodated in 0.8 mm diameter glass capillaries which were placed in a standard EPR tube.
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46
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60449093712
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note
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Kinetic measurements were performed as reported in Ref. 24. In our experiments, reaction mixture contained 0.05 M phosphate buffer (r{cyrillic}N{cyrillic} 7.4), 0.02% Lubrol, 0.63 mM linoleic acid and 1 mM ABAP. The sample was incubated under air atmosphere at 37 °C and the change in absorbance was monitored over time at 234 nm. Inhibition was started by adding of 5 μL of inhibitor solution to the reaction mixture with the constant rate of autooxidation. The results are expressed in terms of relative antioxidant efficiency defined as the ratio of the antioxidant efficiency of the inhibitor to that of Trolox C. The stoichiometric factors n were determined from the ratio of the lag times for the various concentrations of test antioxidant and Trolox C, the stoichiometric factor of which was taken to be 2. The values of RAE represent mean of three separate determinations and stoichiometric factors n are the average of 3-7 experiments.
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