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SA57 is a potent, selective inhibitor of FAAH(IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH).
Pack Size | Price | Availability | Quantity |
---|---|---|---|
1 mg | 74 € | 35 days | |
5 mg | 275 € | 35 days | |
10 mg | 437 € | 35 days |
Description | SA57 is a potent, selective inhibitor of FAAH(IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH). |
Targets&IC50 | ABHD6 (mouse):850 nM , MAGL (mouse):410 nM , FAAH (human):1.9 nM , MAGL (human):1.4 μM , FAAH (mouse):3.2 nM |
In vitro | SA57 exhibits clear time-dependent inhibition of FAAH and MAGL, suggesting a covalent mechanism of inactivation, presumably through carbamylation of the active site serine nucleophiles of these enzymes[1]. |
In vivo | In vivo SA57 (0.01-12.5 mg/kg; intraperitoneal injection; for 2 hours; C57Bl/6 mice) treatment shows distinct dose-responsive activity against brain serine hydrolases (FAAH, MAGL and ABHD6)[1]. |
Molecular Weight | 338.83 |
Formula | C17H23ClN2O3 |
Cas No. | 1346169-63-8 |
Relative Density. | 1.31g/cm3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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