Chemical Structure : ISAM-CG557
Catalog No.: PC-25356Not For Human Use, Lab Use Only.
ISAM-CG557 is a potent, selective, and functionally biased CB2 receptor (CB2R) agonist with binding Ki of 54.6 nM, with negligible binding to CB1R, shows strongly biased toward MAPK signaling.
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ISAM-CG557 is a potent, selective, and functionally biased CB2 receptor (CB2R) agonist with binding Ki of 54.6 nM, with negligible binding to CB1R, shows strongly biased toward MAPK signaling.
ISAM-CG557 display notable bias toward MAPK, especially in β-arrestin-MAPK signaling, indicating a selective MAPK pathway activation.
ISAM-CG557 shows EC50 of 0.60 nM and Emax = 60% for CB2R activity.
ISAM-CG557 significantly reduced the production of pro-inflammatory cytokines (TNF-α, IFN-γ, IL-1β, and IL-6) in unstimulated monocytes and macrophages.
ISAM-CG557 elicites a concentration-dependent neuroprotective effect on neurite length in transfected SH-SY5Y cells.
M.Wt | 380.42 | |
Formula | C21H21FN4O2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Gioé-Gallo C, et al. J Med Chem. 2025 Aug 12. doi: 10.1021/acs.jmedchem.5c00604.
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