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“The probes sulfaphenazole (CYP2C9) and quinidine (CYP2D6) selectively inhibited tolbutamide methylhydroxylation and bufuralol 1'-hydroxylation, respectively.”
Drug metabolism and disposition: the biological fate of chemicals • 1995 | View Paper
“The addition of therapeatic concentrations of salicylic acid, phenylbutazone, and tolbutamide significantly reduced quinidine binding (p < 0.025), but 10 other commonly coadministered drugs did not.”