1672691-74-5
1672691-74-5
Chemical Structure
JZP-430
- CAS No.: 1672691-74-5
- Formula:C16H26N4O3S
- Molecular Weight:354.47
IUPAC Name: 4-morpholino-1,2,5-thiadiazol-3-yl cyclooctyl(methyl)carbamate
InChIKey: WKSHMJCYWFOADB-UHFFFAOYSA-N
SMILES: O=C(OC1=NSN=C1N2CCOCC2)N(C3CCCCCCC3)C
Biological Activity: 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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JZP-430 | 99.74% | 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). | ||||||||||||||||||||
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JZP-430 (Standard) | ≥98% | JZP-430 (Standard) is the analytical standard of JZP-430 (HY-101457). This product is intended for research and analytical applications. 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). | ||||||||||||||||||||
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