| Name | JZP-430 |
|---|
| Description | JZP-430 is a potent, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with an IC50 of 44 nM, exhibits ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL)[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 44 nM (ABHD6, human)[1] |
| References |
| Molecular Formula | C16H26N4O3S |
|---|---|
| Molecular Weight | 354.47 |
| Hazard Codes | Xi |
|---|