Molecular Formula | C26H32N8 |
Molar Mass | 456.59 |
Appearance | powder |
Color | white to beige |
Storage Condition | room temp |
In vitro study | PF-4981517 (cyp3ide) is a highly potent, time-specific inhibitor of human CYP3A4. PF-4981517 reversible inhibition of some human cytochrome P450 activities. PF-4981517 acts on CYP3A4, 3A5, and 3A7 with an IC50 of 0.03 μm, 17 μm, and 70 μm, respectively. PF-4981517 co-inhibited all CYP3A activity with Ketoconazole. |
WGK Germany | 3 |
biological activity | PF-4981517 (CYP3cide, PF-04981517) is an effective and selective CYP3A4(P450) inhibitor with an IC50 of 0.03 μM, which is more than 500 times more selective than CYP3A5 and CYP3A7. |
target | TargetValue CYP3A4 30 nM |
Target | Value |
CYP3A4 | 30 nM |
In vitro studies | PF-4981517(CYP3cide) is a highly effective, time-dependent human CYP3A4 inhibitor. PF-4981517 reversibly inhibits some human cytochrome P450 activities. PF-4981517 act on CYP3A4, 3A5, and 3A7, IC50 are 0.03 μM, 17 μM, and 70 μM, respectively. PF-4981517 and Ketoconazole together inhibit all CYP3A activities. |