| Bioactivity | PF 750 is a selective and covalent fatty acid amide hydrolase (FAAH) inhibitor, with IC50s varied from 16.2-595 nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile[1]. | |||||||||
| Target | IC50: 16.2-595 nM (FAAH). | |||||||||
| Name | PF 750 | |||||||||
| CAS | 959151-50-9 | |||||||||
| Formula | C22H23N3O | |||||||||
| Molar Mass | 345.44 | |||||||||
| Appearance | Solid | |||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | |||||||||
| Storage |
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| Reference | [1]. Ahn K, et al. Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity. Biochemistry. 2007 Nov 13;46(45):13019-30. |