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Cannabinoid Cannabinoid

Cat.No.  Name Information
M9136 Cannabidiol Cannabidiol is a GPR55 and weak CB1 antagonist with IC50s of 0.445 and 3.35 μM, it is also a CB2 receptor inverse agonist and inhibitor of anandamide uptake with IC50 of 27.5 μM.
M7325 Rimonabant Hydrochloride Rimonabant hydrochloride is a cannabinoid receptor antagonist, which binds selectively to central cannabinoid receptors (CB1) with high affinity
M45352 Tetrahydrocannabivarin Tetrahydrocannabivarin is an antagonist of cannabinoid receptors and may be used in studies related to type 2 diabetes.
M45350 RVD-Hpα RVD-Hpα is an alpha-hemoglobin-derived peptide containing three additional amino acids and a CB1 cannabinoid receptor agonist. In addition, RVD-Hpα is an orthosteric modulator of cannabinoid receptor 2 (CB2).
M25437 Noladin ether Noladin ether is a potent and selective agonist of cannabinoid CB1 receptor, with a Ki of 21.2 nM.
M21427 CB1 agonist 1 CB1 agonist 1 is an agonist of CB1. The pIC50 value of CB1 agonist 1 affinity with CB1 receptor was 5.7. CB1 agonist 1 can be used in the study of brain disorders.
M17348 Olivetol Olivetol is a naturally phenol found in lichens and produced by certain insects, acting as a competitive inhibitor of the cannabinoid receptors CB1 and CB2. Olivetol also inhibits CYP2C19 and CYP2D6 activity, with IC50s of 15.3 μM, 7.21 μM and Kis of 2.71 μM, 2.87 μM, respectively.
M14560 Pregnenolone monosulfate Pregnenolone monosulfate (3β-Hydroxy-5-pregnen-20-one monosulfate) is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones.
M13917 Anandamide Anandamide is an immune modulator in the central nervous system acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55).
M10720 A-836339 A-836339 is a selective agonist of the cb2 receptor and has little effect on the cb1 receptor.
M10719 Yangonin Yangonin has a high affinity for human recombinant cannabinoid CB1 receptors,IC50 and Ki 1.79 μM and 0.72 μM, respectively.
M10718 TM38837 TM38837 is an orally active, peripherally restricted cannabinoid receptor type 1 (CB1) receptor antagonist.TM38837 has limited penetration into the brain and minimizes or prevents CNS adverse effects.
M10652 Voacamine Voacamine is an indole alkaloid, exhibits potent cannabinoid CB1 receptor antagonistic activity. Voacamine also inhibits P-glycoprotein (P-gp) action in multidrug-resistant tumor cells.
M10218 (+)-Gallocatechin (+)-Gallocatechin is found notably in green tea, it has moderate affinity to the human cannabinoid receptor and acts as an antioxidant.
M9691 JD-5037 JD-5037 is a cannabinoid-1 receptor blocker (CB1R antagonist) with IC50 of 1.5 nM.
M9652 CB1-IN-1 CB1-IN-1 is a novel potent restricted CB1R antagonist with Ki of 0.3 nM and 21 nM for CB1R and CB2R, respectively.
M8985 LY2828360 LY2828360 is a novel potent, selective, and efficacious CB2 cannabinoid agonist.
M8919 BAY 59-3074 BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with Ki values of 48.3 and 45.5 nM at human CB1 and CB2 receptors, respectively.
M7613 2-Arachidonyl glycerol 2-Arachidonyl glycerol is an endogenous cannabinoid and also an agonist at cannabinoid receptors.
M6778 GW 405833 GW 405833 is a selective, high affinity CB 2 receptor partial agonist.




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