FAAH
Fatty Acid Amide Hydrolase (FAAH) is an enzyme that breaks down fatty acid amides, including endocannabinoids like anandamide. These compounds are involved in the regulation of pain, mood, appetite, and memory. Inhibition of FAAH can increase the levels of these signaling molecules, offering potential therapeutic benefits for pain, anxiety, and neurodegenerative diseases. At CymitQuimica, we offer a selection of FAAH inhibitors to support your research in neuroscience, pain management, and endocannabinoid signaling.
Found 64 products of "FAAH"
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FAAH/MAGL-IN-2
CAS:FAAH/MAGL-IN-2: potent, reversible, oral FAAH & MAGL inhibitor, IC50: 11/36 nM, may research neuropathic pain, no locomotion issue.Formula:C15H13Cl2N3O3SColor and Shape:SolidMolecular weight:386.25FAAH/MAGL-IN-3
FAAH/MAGL-IN-3 irreversibly inhibits FAAH (IC50: 179 nM) & MAGL (IC50: 759 nM) with low PAMPA permeability.Formula:C21H25N3O6SColor and Shape:SolidMolecular weight:447.5Dual FAAH/sEH-IN-1
CAS:Dual FAAH/sEH-IN-1 inhibits both sEH (IC50: 9.6 nM) and FAAH (IC50: 7 nM), offering potent anti-inflammatory effects.
Formula:C25H22ClN3O3S2Purity:99.89%Color and Shape:SolidMolecular weight:512.04TC-F 2
CAS:TC-F 2 is a FAAH inhibitor.Formula:C26H25N5O2Purity:98%Color and Shape:SolidMolecular weight:439.51
