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Cat. No. Product Name Information
PC-60146

APD-371

CB2 agonist

APD-371 (APD371, Olorinab) is a potent, selective and orally available CB2 agonist with EC50 of 6.2 nM.
PC-60086

AM-6538

AM-6538 (AM6538) is a potent, selective cannabinoid receptor CB1 antagonist with Ki of 5.1 nM..
PC-45531

JD-5037

CB1 antagonist

JD-5037 is a potent, selective and peripherally restricted cannabinoid-1 (CB1) receptor blocker with IC50 of 2 nM, does not inhibit CB2 receptor (IC50>1000 nM).
PC-42171

Bay 59-3074

CB1/CB2 agonist

Bay 59-3074 is a potent, selective cannabinoid CB1/CB2 receptor partial agonist with Ki of 48.3, and 45.5 nM for human CB1 and human CB2 receptors, respectively.
PC-42063

Taranabant

CB1 inverse agonist

Taranabant (MK-0364) is a potent, selective and orally active cannabinoid-1 receptor (CB1R) inverse agonist with IC50 of 2.8 nM, Ki of 0.13 nM.
PC-42723

Otenabant

CB1 antagonist

Otenabant (CP-945598) is a potent, and selective CB1 receptor antagonist with Ki of 0.7 nM/0.12 nM in binding and functional assays respectively.
PC-22188

SR141716

CB1 antagonist

Rimonabant (SR141716) is a highly potent, brain penetrated and selective central cannabinoid receptor (CB1) antagonist with Ki of 1.8 nM, no affinity for peripheral cannabinoid receptor.
PC-22167

AM10257

CB2 antagonist

AM10257 is a potent, selective cannabinoid receptor 2 (CB2) antagonist with IC50 of 47 nM.
PC-22115

SMM-189

CB2 inverse agonist

SMM-189 is a selective cannabinoid receptor 2 (CB2) inverse agonist with Ki of 121.3 nM, 40-fold selective over CB1 receptor.
PC-21983

BAY38-7271

CB1/CB2 agonist

BAY 38-7271 is selective, highly potent and cannabinoid CB1/CB2 receptor agonist with 0.46-1.85 nM for rat brain, human cortex, or recombinant human CB1 receptors.
PC-21521

AM4113

CB1 neutral antagonist

AM4113 is a high affinity, selective cannabinoid CB1 neutral antagonist with Ki of 0.89 nM, exhibits 100-fold selectivity over CB2 receptors.
PC-21463

AM6527

CB1 antagonist

AM6527 is a highly potent, selective cannabinoid CB1 receptor antagonist with binding Ki of 4.88 nM, 100-fold selective over CB2 receptors.

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