Selective, active-site directed, irreversible inhibitor of cPLA2 (IC50=5µM) and Ca2+-independent iPLA2 (IC50=0.5µM). Potent, irreversible inhibitor of fatty acid amide hydrolase (FAAH) (IC50=2.5nM), 800 -fold more potent than AACOCF3 (Prod. No. BML-ST335)). Irriversible CB1 receptor antagonist in rat brain membrane (IC50=20nM).
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Regulatory Status |
RUO – Research Use Only |
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