Search results for 'Anandamide'

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  • (-)-5'-DMH-CBD

    (-)-5'-DMH-CBD is an anandamide membrane transport inhibitor (IC50 = 14 μM) that is relatively metabolically stable, which displays some affinity for CB2 receptors but has only weak affinity for CB1 receptors and has no activity at VR1 receptors or FAAH. Learn More

    Starting at: $149.00

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  • Anandamide - d4

    Anandamide - d4 is a deuterated anandamide that is used as an internal standard for the quantification of AEA by GC- or LC-mass spectrometry. Learn More

    Starting at: $149.00

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  • Anandamide

    Anandamide is an endogenous cannabinoid and TRPV1 receptor agonist that also blocks TNF-α-induced NF-κB activation via direct inhibition of IKK. Learn More

    Starting at: $59.00

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  • OMDM-2

    OMDM-2 is a metabolically stable inhibitor of anandamide cellular uptake that displays relatively low affinity for CB1 and CB2 receptors with Ki values of 5.1 and > 10 μM and for vanilloid VR1 receptors with EC50 value of 10 μM. Learn More

    Starting at: $65.00

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  • Olvanil

    Olvanil, a potent vanilloid receptor agonist, blocks anandamide uptake (IC50 = 9 μM) and may bind to CB1 cannabinoid receptors. Learn More

    Starting at: $99.00

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  • O-1918

    O-1918 is a selective, silent antagonist of a putative endothelial anandamide receptor distinct from CB1 or CB2 receptors. Learn More

    Starting at: $149.00

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  • O-2093

    O-2093 is an inhibitor of anandamide uptake (IC50 = 17.3 μM) with little or no activity at CB1, CB2, TRPV1 and FAAH. Learn More

    Starting at: $99.00

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  • UCM 707

    UCM 707 is a potent endocannabinoid transport inhibitor. IC50 values are 0.8 and 30 μM for inhibition of the anandamide transporter and FAAH respectively. Ki values are 4700, 67 and > 5000 nM for CB1, CB2 and VR1 receptors respectively. Learn More

    Starting at: $125.00

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  • VDM 11

    VDM 11 is a potent and selective inhibitor of the anandamide membrane transporter (AMT) with IC50 values of 4-11 μM, which displays negligible agonist activity at the hVR1 receptor and very weak action at CB1 and CB2 receptors. Learn More

    Starting at: $75.00

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  • Virodhamine

    Virodhamine endogenous cannabinoid receptor mixed agonist/antagonist found in higher concentrations peripherally than anandamide. Learn More

    Starting at: $79.00

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  • AM 1172

    AM 1172 metabolically stable anandamide uptake inhibitor (IC50 = 2.1 - 2.5 μM) and fatty acid amide hydrolase (FAAH) inhibitor (Ki = 3.18 μM). Learn More

    Starting at: $139.00

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  • AM 404

    AM 404 is a competitive and selective inhibitor of carrier-mediated anandamide transport (IC50 = 1 μM). Does not activate CB1 receptors or inhibit anandamide hydrolysis but has been shown to activate native and cloned vanilloid receptors (pEC50 = 7.4). Active in vivo. Also available in water soluble emulsion . Learn More

    Starting at: $65.00

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  • Palmitoylisopropylamide

    Palmitoylisopropylamide is an inhibitor of fatty acid amide hydrolase (FAAH); pIC50 = 4.89 for inhibition of [3H]-anandamide metabolism. Learn More

    Starting at: $65.00

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  • MAFP

    MAFP is a potent, irreversible inhibitor of fatty acid amide hydrolase (FAAH, anandamide amidase), the enzyme responsible for anandamide hydrolysis (IC50 = 2.5 nM). It also binds irreversibly to CB1 receptors (IC50 = 20 nM). Learn More

    Starting at: $98.00

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  • N-Arachidonylglycine

    N-Arachidonylglycine is an endogenous anandamide-like compound. Learn More

    Starting at: $85.00

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  • (R)-(+)-Methanandamide

    (R)-(+)-Methanandamide is a stable anandamide analog that is a selective agonist for the CB1 receptor (Ki values are 20 and 815 nM for CB1 and CB2 receptors respectively), which also displays agonist activity at vanilloid receptors. Learn More

    Starting at: $65.00

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  • DEA

    DEA is a potent endocannabinoid and anandamide analog that activates CB1 receptors in microglia and binds to rat synaptosomal membranes (Ki = 34.4 nM). Learn More

    Starting at: $80.00

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  • AACOCF3

    AACOCF3 is an inhibitor of cytosolic (85 kDa) phospholipase A2. It also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Learn More

    Starting at: $65.00

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  • PALDA

    PALDA is an endogenous fatty acid dopamide that displays 'entourage' effects on endovanilloids NADA and anandamide. Learn More

    Starting at: $75.00

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  • Arvanil

    Arvanil is a cannabinoid CB1 and vanilloid TRPV1 (VR1) agonist (Ki values are 0.5 and 0.3 μM respectively), which also inhibits the anandamide transporter (IC50 = 3.6 μM). Learn More

    Starting at: $50.00

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