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Ketoconazole displacement

Insertion of a triazole ring in place of an imidazole ring is consistent in some cases with retention of antifungal activity. The synthesis of one such agent, azoconazole (64), proceeds simply by displacement of halide with 1,2,4-triazole. The route to terconazole (65) is rather like that to ketoconazole (34). ... [Pg.137]

If the displacement reaction is carried out between imidazole derivative and thiophene analogue the antifungal agent tiaconazole (40) results. A rather slight variant of this sequence produces antifungal sulconazole (41).Obvious variants of the route explicated above for ketoconazole (34) lead to parconazole (42)and doconazole (43),instead. [Pg.1182]

Carbamazepine is metabolized to an active 10,11-epoxide metabolite, thus medications that inhibit 3A4 isoenzymes may result in carbamazepine toxicity (e.g., cimetidine, dUtiazem, erythromycin, fluoxetine, fluvoxamine, isoniazid, itraconazole, ketoconazole, nefa-zodone, propoxyphene, and verapamil). " When carbamazepine is combined with valproate, the carbamazepine dose should be reduced because valproate displaces carbamazepine from protein binding sites, thus increasing free levels." Combining clozapine and carbamazepine is not recommended because of the possibdity of bone marrow suppression with both agents. ... [Pg.1277]


See other pages where Ketoconazole displacement is mentioned: [Pg.132]    [Pg.1181]    [Pg.74]    [Pg.274]    [Pg.922]    [Pg.973]    [Pg.158]    [Pg.1971]    [Pg.103]    [Pg.490]    [Pg.1534]   
See also in sourсe #XX -- [ Pg.103 , Pg.118 ]




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