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Induction troleandomycin

P450 enzymes may also be induced by substrate stabilization, eg, decreased degradation, as is the case with troleandomycin- or clotrimazole-mediated induction of CYP3A enzymes, the ethanol-mediated induction of CYP2E1, and the isosafrole-mediated induction of CYP1A2. [Pg.84]

Pessayre D, Descatoire V, Tinel M, Larrey D (1982) Self-induction by oleandomycin of its own transformation into a metabolite forming an inactive complex with reduced cytochrome P-450. Comparison with troleandomycin. J Pharmacol Exp Ther 221 215-221... [Pg.247]

Especially the inhibition or induction of cytochrome P450 subtype 3A4 (CYP 3A4) is clinically relevant, because a variety of active substances and food substances (e.g. grapefruit juice) are able to affect this enzyme. Substances inhibiting CYP 3A4 include ciclosporin, dihydropyridines, verapamil, midazolam, paclitaxel, simvastatin, lovastatin, atorvastatin, cimetidine, erythromycin, troleandomycin, ketoconazole (and other azoles). Substances inducing CYP 3A4 include steroids, rifampicin, phenobarbital and St John s wort. [Pg.336]


See other pages where Induction troleandomycin is mentioned: [Pg.583]    [Pg.583]    [Pg.516]    [Pg.557]    [Pg.54]    [Pg.446]    [Pg.10]    [Pg.556]    [Pg.562]    [Pg.197]   
See also in sourсe #XX -- [ Pg.621 , Pg.637 ]




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Troleandomycin

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