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Metabolism | CY3A4 |
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Formula | C23H20F3N5O2 |
Molar mass | 455.441 g·mol−1 |
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JZP150 (formerly PF-04457845) is an inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC50 of 7.2nM, and both analgesic and antiinflammatory effects in animal studies comparable to naproxen.[1]
JZP150 is currently being developed by Jazz Pharmaceuticals and is in a Phase 2 trial in the US for PTSD.[citation needed]
See also[edit]
- FAAH inhibitor
- 4-Nonylphenylboronic acid
- LY-2183240
- URB-597
- BIA 10-2474, problems in phase 1
References[edit]
- ^ Johnson DS, Stiff C, Lazerwith SE, Kesten SR, Fay LK, Morris M, et al. (February 2011). "Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor". ACS Medicinal Chemistry Letters. 2 (2): 91–96. doi:10.1021/ml100190t. PMC 3109749. PMID 21666860.