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  • AM-404 | Anandamide transport inhibitor
    AM-404 (198022-70-7) inhibits anandamide transport (IC50 = 1 μM) without inhibiting anandamide amidase or activating cannabinoid receptors.1,2 Vanilloid receptors are activated by AM-404.3 Active in vivo...

  • Anandamide | Endogenous cannabinoid
    Anandamide (94421-68-8) is an endogenous cannabinoid receptor agonist.1-3 Ki=89 nM for CB1 and 371 nM for CB2 receptors. References/Citations1) Devane et al. (1992), Isolation and structure of a brain constituent that binds...

  • JZL-184 | 1101854-58-3 | Structure | Supplier
    JZL-184 (1101854-58-3) inhibits MAG lipase (IC50=8 nM) selectively over FAAH. Irreversible. Cell permeable. References/Citations1) Long et al. (2009), Selective blockade of 2-arachidonoylglycerol hydrolysis produces...

  • SR-144528 | 192703-06-3 | Structure | Supplier
    SR-144528 (192703-06-3) is a potent and selective antagonist of the cannabinoid CB2 receptor1,2. References/Citations1) Rinaldi-Carmona et al. (1998), SR-144528, the first potent and selective antagonist of the CB2...

  • URB-597 | 546141-08-6 | Structure | Supplier
    URB-597 (546141-08-6) is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor, IC50 = 3-5 nM.1 Produces cannabinoid CB1 and CB2 receptor-mediated analgesia in inflammatory pain states without causing side...

  • WIN-55212-2 mesylate | Cannabinoid CB1/CB2 agonist
    WIN-55212-2 mesylate (131543-23-2) is a high affinity cannabinoid receptor agonist (Ki = 62.3 nM for recombinant human CB1 and 3.3 nM for recombinant human CB2)1 with analgesic2 and anti-inflammatory activities. WIN-55212-2...

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