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Description
JZP 430 is a potent and irreversible α/β-hydrolase domain 6 (ABHD6) inhibitor (IC50 = 44 nM). Exhibits ∽230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
Specifications
Specifications
| Chemical Name or Material | 4-(4-Morpholinyl)-1,2,5-thiadiazol-3-yl N-cyclooctyl-N-methylcarbamate |
| CAS | 1672691-74-5 |
| Quantity | 50 mg |
| Target | Hydrolase Inhibitors |
| Molecular Formula | C16H26N4O3S |
| Formula Weight | 354.47 |
| Purity | >98% |
Product Title
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