Name | JZP-430 |
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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]. |
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Related Catalog | |
Target |
IC50: 44 nM (ABHD6, human)[1] |
References |
Molecular Formula | C16H26N4O3S |
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Molecular Weight | 354.47 |
Hazard Codes | Xi |
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