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Five times the Km amount of the substrates: (A) O6BG, (B) DACA, (C) zaleplon, (D) phthalazine, (E) BIBX1382, and (F) zoniporide were incubated with purified expressed human AOX (HAO, 0.0192 μM) in the same way as HLC to compare the time-course plots and ensure that AOX is the enzyme responsible for metabolism. Fitting to product formation was performed using the MAM (n = 3, P < 0.001).
