Chemical Structure : JZP-430
CAS No.: 1672691-74-5
货号: PC-20129Not For Human Use, Lab Use Only.
JZP-430 (JZP430) is potent, selective and irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with IC50 of 44 nM (hABHD6), 230-fold selectivity over FAAH and lysosomal acid lipase (LAL).
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---|---|---|---|
1 mg | ¥880 | In stock | |
5 mg | ¥1580 | In stock | |
10 mg | ¥2480 | In stock | |
25 mg | ¥4280 | In stock | |
50 mg | ¥7280 | In stock | |
100 mg | Get quote |
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JZP-430 (JZP430) is potent, selective and irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with IC50 of 44 nM (hABHD6), 230-fold selectivity over FAAH and lysosomal acid lipase (LAL).
JZP-430 is highly selective for ABHD6 over the other detectable brain serine hydrolases, including FAAH, MAGL and ABHD12.
分子量 | 354.47 | |
分子式 | C16H26N4O3S | |
外观性状 | Solid | |
储存条件 |
|
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
4-morpholino-1,2,5-thiadiazol-3-yl cyclooctyl(methyl)carbamate |
1. Jayendra Z Patel, et al. ChemMedChem. 2015 Feb;10(2):253-65.
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