Chemical Structure : PM289
Catalog No.: PC-27323Not For Human Use, Lab Use Only.
PM289 is a high affinity, selective Cannabinoid 2 Receptor (CB2R) agonist with Ki of 92.6 nM (hCB2), >300-fold selectivity over hCB1 receptors.
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PM289 is a high affinity, selective Cannabinoid 2 Receptor (CB2R) agonist with Ki of 92.6 nM (hCB2), >300-fold selectivity over hCB1 receptors.
PM289 attenuates NFκB activation in response to TNFα.
PM289 reduces forskolin-stimulated cAMP accumulation in HEK293-CB2R cells in a CB2-dependent manner.
PM289 attenuates TNFα-induced upregulation of ICAM-1.
PM289 reduces barrier disruption in brain microvascular endothelial cells.
PM289 increases wound repair in brain endothelial cells.
PM289 attenuates NFκB activation in response to TNFα.
PM289 modulates morphine-induced antinociceptive effect and withdrawal syndrome in rat model of knee osteoarthritis-associated pain, including both sexes.
| M.Wt | 384.56 | |
| Formula | C24H36N2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Bullock TA, et al. NeuroImmune Pharm Ther. 2023 Oct 16;2(4):387-400.
2. Garcia MM, et al. Neuropharmacology. 2026 Jul 1;299:111090.

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