Many of the flavonoids inhibited threeβHSD2 and CYP17A1 substantially, when the inhibition of downstream enzymes, CYP21A2 and CYP11B1, was both of those substrate and flavonoid distinct. The dihydrochalcones inhibited the exercise of CYP21A2, but not that of CYP11B1. Although rutin, orientin and vitexin inhibited deoxycortisol conversion by CYP1

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