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4. The solvent was evaporated in vacuo and the precipitated solids were recrystallized from an appropriate solvent or purified by column chromatography.
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43049149384
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note
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2)
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43049092267
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note
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2 for 2 h. The assay solutions were transferred to a scintillation microplate and mixed with a solution of antimouse YSi SPA beads and anticortisol antibody in assay buffer (50 mM Tris-HCl, pH 7.0; 300 mM NaCl, 1 mM EDTA, 5% glycerol). The plate was incubated for 2 h at room temperature and read on a scintillation counter. The percentage of inhibition was determined relative to a non-inhibited control.
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43049133562
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note
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x were the glycemia values at +1, +3, +5, and +7 h, respectively. All values were expressed as means ± SEM. Statistical significance was estimated by analysis of variance (ANOVA), p < 0.05 and p < 0.01 implies significance.
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