Description
A GPR18 agonist (EC50 = 0.56 µM in a β-arrestin recruitment assay using CHO cells expressing the human receptor); selective for GPR18 over GPR55, as well as CB1 and CB2, at 10 µM but also binds to the adenosine A2A receptor (Ki = 0.33 µM for the rat receptor)
Formal name: 6,7,8,9-tetrahydro-9-[2-(1H-indol-3-yl)ethyl]-1,3-dimethyl-pyrimido[2,1-f]purine-2,4(1H,3H)-dione
Synonyms:
Molecular weight: 378.4
CAS: 955121-65-0
Purity: ≥98%
Formulation: A crystalline solid