Selective adenosine A2Areceptor antagonist; binds to human and rat A2Areceptors with high affinity (Kivalues are 0.048 and 0.5 nM respectively). Displays > 23000-fold selectivity for hA2Aover hA1in vitrowith minimal affinity for hA2Band hA3receptors (IC50
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
Grade
Moligand™
Product Description
SCH-442416 has been used:
as a selective adenosine A2A antagonist to study its effects on cyclic adenosine monophosphate (cAMP) production in T/C-28a2 chondrocytes or hFOB 1.19 osteoblasts
as a presynaptic A2A receptor antagonists to study its effects on receptor blockade on δ9-Tetrahydrocannabinol (THC) self-administration in squirrel monkeys
as a presynaptic A2A receptor antagonists to study its effects on cocaine-induced locomotion and cocaine-seeking in mice