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).
IC50&Target
IC50: 44 nM (ABHD6, human)
分子式
C16H26N4O3S
分子量
354.47
CAS号
1672691-74-5
运输条件
Room temperature in continental US; may vary elsewhere.