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Resolution: standard / high Figure 4.
Metabolic profile of eupatorin (10 μM) metabolism by CYP1 family enzymes and identification
of cirsiliol as the primary metabolite. (a) Typical high-pressure liquid chromatography (HPLC) traces of 20-minute incubation
of CYP1 enzymes with eupatorin. (b) Expansion of (a) showing metabolites E2 and E3. (c) Co-elution studies of eupatorin with cirsiliol. A 20-minute CYP1B1 incubate of eupatorin
was spiked with cirsiliol (0.2 μM). Reaction mixtures contained eupatorin, NADPH (nicotinamide
adenine dinucleotide phosphate), and recombinant microsomes purchased from Gentest
Corporation (now part of BD Biosciences). Reactions were terminated by the addition
of 1% acetic acid in methanol. (d) HPLC trace of metabolism of eupatorin in MDA-MB-468 cells. Samples were analysed by
HPLC using a UV detector at 350 nm. Experiments were performed in triplicate. A350: absorption of light at wavelength 350 nm. AU: arbitrary units.
Androutsopoulos et al. Breast Cancer Research 2008 10:R39 doi:10.1186/bcr2090 |