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  Indian J Med Microbiol
 

Figure 2: The effects of Bangpungtongseong-san on the activities of CYP1A2 (a), CYP2B6 (b), CYP2C9 (c), CYP2C19 (d), CYP2D6 (e), CYP2E1 (f), and CYP3A4 (g). The fluorescence-based enzyme assays of the CYP450 isozymes were established in vitro . a-Naphthoflavone, sulfaphenazole, quinidine, sodium diethyldithiocarbamate trihydrate, and ketoconazole were used as positive controls for CYP1A2, CYP2C9, CYP2D6, CYP2E1, and CYP3A4, respectively. Miconazole was used as a positive control for CYP2B6 and CYP2C19. The data are presented as the mean ± standard error of the mean (n = 3)

Figure 2: The effects of <i>Bangpungtongseong-san</i> on the activities of CYP1A2 (a), CYP2B6 (b), CYP2C9 (c), CYP2C19 (d), CYP2D6 (e), CYP2E1 (f), and CYP3A4 (g). The fluorescence-based enzyme assays of the CYP450 isozymes were established <i>in vitro</i> . a-Naphthoflavone, sulfaphenazole, quinidine, sodium diethyldithiocarbamate trihydrate, and ketoconazole were used as positive controls for CYP1A2, CYP2C9, CYP2D6, CYP2E1, and CYP3A4, respectively. Miconazole was used as a positive control for CYP2B6 and CYP2C19. The data are presented as the mean ± standard error of the mean (<i>n</i> = 3)