Percentages of inhibition of specific binding at CGRPR, CB2R, and M3R

CompoundDisplacement of radioligand binding (%) (compounds at 10 µM)
hCGRPRhCB2RhM3R
1a−1.0 ± 4.37.3 ± 0.3−4.1 ± 3.1
11a14.3 ± 1.832.8 ± 2.8–3.9 ± 8.6

hCGRPR: human calcitonin gen-related peptide receptor; hCB2R: human cannabinoid receptor, subtype 2; hM3R: human muscarinic receptor, subtype 3. In all cases, data are from two experiments in duplicate. Radioligands used: hCGRPR: [125]hGCRPα, agonist hGCRPα (1 µM); hCB2R: [3H]WIN 55212-2, agonist (5 µM); hM3R: [3H]4-DMAP, agonist 4-DMAP (1 µM)