Table 2.
Absorption rate constants for CYP inhibitors involved in in vivo interaction studies
| Inhibitor | CYP enzyme | ka (min−1) | Reference |
|---|---|---|---|
| Sulphaphenazole | 2C9 | 0.030 | [9] |
| Fluconazole | 2C9, 3A4 | 0.061 | [33] |
| Ketoconazole | 2C9, 3A4 | 0.013 | [34] |
| Itraconazole | 3A4 | 0.020 | [35] |
| Quinidine | 2D6, 3A4 | 0.014 | [36] |
| Fluoxetine | 2D6, 3A4 | 0.009 | [37] |
| Fluvoxamine | 2C9, 2D6, 3A4 | 0.008 | [38] |
| Sertraline | 2C9, 2D6 | 0.007 | [37] |
| Citalopram | 2D6 | 0.024 | [37] |
| Nifedipine | 3A4 | 0.056 | [39] |