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Cytochrome P450 CYP1A2, induction

The results of in vitro studies indicate that memantine is not likely to cause interactions via induction or inhibition of the major cytochrome P450 isoenzymes involved in drug metabolism (CYP1A2, CYP2C9, CYP3A4). In addition, memantine is not metabolised by this enzyme system, and is therefore not expected to undergo interactions via this mechanism. ... [Pg.695]

H. Toyoshiba, N.J. Walker, J. Bailer, and C.J. Portiera, Evaluation of toxic equivalency factors for induction of cytochromes P450 CYPlAl and CYP1A2 enzyme activity by dioxin-like compounds, Toxicol. Appl. Pharmacol. 194 (2004) 156-168. [Pg.561]

See other pages where Cytochrome P450 CYP1A2, induction is mentioned: [Pg.516]    [Pg.267]    [Pg.32]    [Pg.929]    [Pg.302]    [Pg.187]    [Pg.916]    [Pg.237]    [Pg.47]    [Pg.378]    [Pg.76]    [Pg.1590]    [Pg.314]    [Pg.325]    [Pg.15]    [Pg.144]    [Pg.146]    [Pg.749]    [Pg.755]    [Pg.641]    [Pg.1252]   
See also in sourсe #XX -- [ Pg.192 ]



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