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Purpose
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A potent and irreversible FAAH (Fatty Acid Amide Hydrolase) inhibitor
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Characteristics
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Cell-permeable. Active site serine (IC50 = 33 nM). It is highly selective for FAAH relative to other mammalian serine hydrolases.
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Purity
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≥ 98 % by TLC
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Chemical Name
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N-Phenyl-4-(quinolin-2-ylmethyl)piperazine-1-carboxamide
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Formula
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C₂₁H₂₂N₄O
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Permeability
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Cell-permeable
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Solubility
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DMSO (~25 mg/ml) or Ethanol (~ 3 mg/ml)
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