Powder: -20°C for 3 years
In solvent: -80°C for 2 years
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
Description | JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL). |
Targets&IC50 | ABHD6:44 nM(Human) |
Molecular Weight | 354.47 |
Formula | C16H26N4O3S |
CAS No. | 1672691-74-5 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
DMSO: 90 mg/mL (253.9 mM), Need ultrasonic
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
JZP-430 1672691-74-5 代谢 Lipase MAGL Monoacylglycerol lipase inhibit JZP 430 JZP430 Inhibitor inhibitor