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FAAH

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 63 products of "FAAH"

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  • AZ513
    Targetmol
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    AZ513

    CAS:
    <p>AZ513 is a reversible FAAH inhibitor, exhibiting an IC50 of 551 nM for human FAAH and 27 nM for rat FAAH. It inhibits the hydrolysis of arachidonoyl ethanolamide in HEK293 cells transfected with human FAAH, with an IC50 of 360 nM.</p>
    Formula:C14H9Cl2N3O
    Color and Shape:Solid
    Molecular weight:306.147

    Ref: TM-T204429

  • Dual FAAH/sEH-IN-1
    Targetmol
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    Dual FAAH/sEH-IN-1

    CAS:
    <p>Dual FAAH/sEH-IN-1 inhibits both sEH (IC50: 9.6 nM) and FAAH (IC50: 7 nM), offering potent anti-inflammatory effects.</p>
    Formula:C25H22ClN3O3S2
    Purity:99.89%
    Color and Shape:Solid
    Molecular weight:512.04

    Ref: TM-T63536

  • TC-F 2
    Targetmol
    + Info

    TC-F 2

    CAS:
    <p>TC-F 2 is a FAAH inhibitor.</p>
    Formula:C26H25N5O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:439.51

    Ref: TM-T23432

    1mg
    Discontinued
    Discontinued product