Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
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JW 642 is an inhibitor of monoacylglycerol lipase (MAGL; IC50s = 3.7, 7.6, and 14 nM for the human, mouse, and rat enzymes, respectively).1 It is selective for MAGL over fatty acid amide hydrolase (FAAH; IC50s = 20.6, 31, and 14 µM for the human, mouse, and rat enzymes, respectively), as well as α/β-hydrolase domain-containing protein 6 (ABHD6; IC50s = 107 and 50 nM for the mouse and rat enzymes, respectively).
WARNING This product is not for human or veterinary use.
1. Highly selective inhibitors of monoacylglycerol lipase bearing a reactive group that is bioisosteric with endocannabinoid substrates. Chem. Biol. 19(5), 579-588 (2012).