Synthesis and preliminary evaluation of [11C]KF17837, a selective adenosine A2A antagonist

An 11C-labeled selective adenosine A2A antagonist, (E)-8-(3,4-dimethoxystyryl)-1,3-dipropyl-7-[11C]-methylxanthine ([11C]KF17837), was prepared by reaction of (E)-8-(3,4-dimethoxytyryl)-1,3-dipropylaxanthine and [11C]methyl iodide with decay-corrected radiochemical yield of 19–50%, radiochemical purity of > 99%, sp. act. of 17–100 GBq/μmol and preparation time of 20–25 min. In mice, the myocardium showed the highest (13.4% ID/g) at 5 min after i.v. injection, which decreased gradually with time. The specific myocardial uptake was visualized by γ-camera. In the brain region the radioactivity level was higher in the A2A receptors-rich striatum than in the cortex and cerebellum. The specific striatal uptake in rats was clearly demonstrated by PET. These results have shown that [11C]KF17837 is a potential PET radioligand for mapping the adenosine A2A receptors in the heart and brain.