Name | PF-06795071 |
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Description | PF-06795071 is a potent and selective covalent MAGL inhibitor with an IC50 of 3 nM[1]. |
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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 |
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Molecular Weight | 399.34 |