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European Journal of Clinical Pharmacology • 2004 | View Paper
“We also examined the effect of the CYP2D6 inhibitor quinidine , the CYP3A inhibitor ketoconazole, and the dopamine reuptake inhibitor GBR-12935 for their ability to inhibit P450 2D18-mediated metabolism of imipramine.”
Biological & pharmaceutical bulletin • 1993 | View Paper
“ Quinidine was a potent inhibitor of the … site for the 2-hydroxylation of imipramine in microsomes from all three human livers, with apparent Ki-values ranging from 9 to 92 nM. This … strongly suggests that the high affinity enzyme is CYP2D6, the source of the sparteine/debrisoquine oxidation polymorphism.”
British journal of clinical pharmacology • 1992 | View Paper
“On the other hand, lipophilic cationic drugs, such as clonidine, bisoprolol, diphenhydramine, pyrilamine, and imipramine , significantly decreased the uptake of quinidine in MDCK cells.”