| Name | PF-06795071 |
|---|
| Description | PF-06795071 is a potent and selective covalent MAGL inhibitor with an IC50 of 3 nM[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 3 nM (MAGL)[1] |
| In Vitro | PF-06795071 shows excellent selectivity against FAAH with an IC50 of 3.1 μM[1]. |
| References |
| Molecular Formula | C18H17F4N3O3 |
|---|---|
| Molecular Weight | 399.34 |