1. Signaling Pathways
  2. Metabolic Enzyme/Protease
    Neuronal Signaling
  3. FAAH

FAAH

Fatty acid amide hydrolase

FAAH (Fatty acid amide hydrolase) is a membrane-bound protein belonging to serine hydrolase family of enzymes.FAAH is responsible for the hydrolysis of a number of important endogenous fatty acid amides, including the endogenous cannabimimetic agent anandamide (AEA), the sleep-inducing compound oleamide, and the putative anti-inflammatory agent palmitoylethanolamide (PEA). FAAH plays a significant role in termination of signalling of a class of bioactive lipids called fatty acid amides (FAAs) both in the central nervous system (CNS) and peripheral tissues.

FAAH belongs to the amidase signature (AS) superfamily and is widely distributed in multicellular eukaryotes. FAAH has a key role in the control of the cannabinoid signaling, through the hydrolysis of the endocannabinoids anandamide and in some tissues 2-arachidonoylglycerol.

FAAH Related Products (66):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W751418
    N-Nervonoyl taurine
    N-Nervonoyl taurine ((Z)-2-tetracos-15-enamidoethanesulfonic acid) is a fatty acid-taurine conjugate derived from nervonic acid. N-Nervonoyl taurine is a substrate of fatty acid amide hydrolase (FAAH) discovered during metabolite profiling.
    N-Nervonoyl taurine
  • HY-77491
    FAAH/MAGL-IN-5
    Inhibitor 99.17%
    AM6701 is a potent FAAH/MAGL inhibitor (equipotent inhibitory IC50: 1.2 nM) with neuroprotective effects.
    FAAH/MAGL-IN-5
  • HY-120650
    CAY10435
    Inhibitor
    CAY10435 is a β-ketooxazapyridine, selective FAAH inhibitor with antimicrobial activity. CAY10435 binds non-competitively to the FAAH of Dictyostelium discoideum with a Kd value of 0.57 nM.
    CAY10435
  • HY-19636A
    JNJ-42165279 dihydrochloride
    Inhibitor
    JNJ-42165279 (dihydrochloride) is aFAAHinhibitor with IC50 of 70 nM and 313 nM for hFAAH and rFAAH, respectively.
    JNJ-42165279 dihydrochloride
  • HY-111199
    JP83
    Inhibitor
    JP83 is an irreversible fatty acyl amide hydrolase (FAAH) inhibitor with an IC50 of 1.6 nM in competitive activity-based protein profiling (ABPP) experiments.
    JP83
  • HY-U00240
    SA72
    Inhibitor
    SA72 is a highly selective fatty acid amide hydrolase (FAAH) inhibitor.
    SA72