In Vitro Enzyme Inhibition Experiment
POS. CONTROL: Inhibition of CYP2D6 by quinidine
Inhibition was detected. Cutoff used — High probability of interaction if their IC50 values are less than 1 µM. If IC50 values are between 1 and 10 µM, they have moderate possibility in interaction. Low drug-drug interactions if their IC50 values are greater than 10 µM.
- CYP2D6 4173631
Recombinant expression system Baculovirus-insect cells
Cytochrome B5 No
IC50 values from Table 1
% enzyme inhibition versus precipitant concentration:
Values estimated from Figure 2. In some cases, SEM could not be estimated from the provided figure.
0.02 μM: 47 ± Unknown%
0.2 μM: 79 ± 0%
2 μM: 82 ± Unknown%
20 μM: 87 ± Unknown%
200 μM: See above data
|Sample||Compound measured||Value||Measurement||Study sequence||Additional information||N replicates|
Positive inhibitors which are sulfaphenazole, quinidine and ketoconazole were purchased from Sigma Chemicals (St. Louis, USA). This assay was carried out using the P450-Glo™ Screening Systems from Promega, USA.
NADPH regenerating system