Chemical Structure : A-796260
Catalog No.: PC-26033Not For Human Use, Lab Use Only.
A-796260 is a potent, selective cannabinoid CB2 receptor agonist with binding Ki of 4.37 nM and 13.0 nM for human and rat CB2 receptors respectively, >30-fold selective over CB1 receptor.
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A-796260 is a potent, selective cannabinoid CB2 receptor agonist with binding Ki of 4.37 nM and 13.0 nM for human and rat CB2 receptors respectively, >30-fold selective over CB1 receptor.
a potent and efficacious agonist at human and rat CB2 receptors with EC50 values of 0.710 nM (Emax of 78%) and 1.63 nM (Emax of 69%), respectively.
A-796260 is highly selective at CB2 receptors, exhibiting 1380- and 175-fold selectivity at human and rat CB2 receptors compared to CB1 receptors of the respective species.
A-796260 dose-dependently attenuated CFA-induced thermal hyperalgesia (ED50=2.8 mg kg−1 i.p.,).
A-796260 dose-dependently attenuated dose-dependently attenuated tactile allodynia on skin incision-induced acute postoperative pain.
| M.Wt | 354.49 | |
| Formula | C22H30N2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Yao BB, et al. Br J Pharmacol. 2008 Jan;153(2):390-401.

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