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• W2099643039 abstract "Phencyclidine (PCP) is a mechanism-based inactivator of cytochrome P450 (P450) 2B6. We have analyzed several steps in the P450 catalytic cycle to determine the mechanism of inactivation of P450 2B6 by PCP. Spectral binding studies show that binding of benzphetamine, a type I ligand, to P450 2B6 was significantly affected as a result of the inactivation, whereas binding of the inhibitor <i>n</i>-octylamine, a type II ligand, was not compromised. Binding of these ligands to P450 2B6 occurs in two phases. Stopped-flow spectral analysis of the binding kinetics of benzphetamine to PCP-inactivated 2B6 revealed a 15-fold decrease in the rate of binding during the second phase of the kinetics (<i>k</i>₁ = 5.0 s^–1, A₁ = 30%; <i>k</i>₂ = 0.02 s^–1, A₂ = 70%, where A₂ indicates the fractional magnitude of the second phase) compared with the native enzyme (<i>k</i>₁ = 8.0 s^–1, A₁ = 58%; <i>k</i>₂ = 0.3 s^–1, A₂ = 42%). Analysis of benzphetamine metabolism by the inactivated protein using liquid chromatography/electrospray ionization/mass spectrometry showed that the rates of formation of <i>nor</i>-benzphetamine and hydroxylated <i>nor</i>-benzphetamine were decreased by 75 and 69%, respectively, whereas the rates of formation for amphetamine, hydroxybenzphetamine, and methamphetamine showed slight but statistically insignificant decreases after the inactivation. The rate of reduction of P450 2B6 by NADPH and reductase was decreased by 6-fold as a result of the modification by PCP. In addition, the extent of uncoupling of NADPH oxidation from product formation, a process leading to futile production of H₂O₂, increased significantly during the metabolism of ethylbenzene as a result of the inactivation." @default.
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• W2099643039 date "2009-01-14" @default.
• W2099643039 modified "2023-09-28" @default.
• W2099643039 title "Mechanistic Analysis of the Inactivation of Cytochrome P450 2B6 by Phencyclidine: Effects on Substrate Binding, Electron Transfer, and Uncoupling" @default.
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• W2099643039 doi "https://doi.org/10.1124/dmd.108.024661" @default.
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