Title : Fluvoxamine is a potent inhibitor of the metabolism of caffeine in vitro.

Pub. Date : 1998 Dec

PMID : 9868741






2 Functional Relationships(s)
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1 The CYP3A4 inhibitors, ketoconazole and bromocriptine, inhibited 1,3,7-trimethyluric acid formation with Kis of 0.75 microM and 5 microM, respectively, thus further supporting the involvement of CYP3A4 in the 8-hydroxylation of caffeine. 1,3,7-trimethyluric acid cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 The CYP3A4 inhibitors, ketoconazole and bromocriptine, inhibited 1,3,7-trimethyluric acid formation with Kis of 0.75 microM and 5 microM, respectively, thus further supporting the involvement of CYP3A4 in the 8-hydroxylation of caffeine. 1,3,7-trimethyluric acid cytochrome P450 family 3 subfamily A member 4 Homo sapiens