Few 18F PET radioligand derivatives of potent and selective A2AR antagonist SCH442416 were developed for imaging of the A2ARs. These PET ligands include [18F]MRS5425 ([18F]-FESCH),129,130 [18F]-FPSCH,130 and [18F]MNI-444131 as shown in Figure 5. The A2AR-mediated uptake of [18F]MRS5425 was higher in the striatum of the 6-OHDA lesion-induced rats compared to that of the normal rats, making [18F]MRS5425 a suitable PET radiotracer for imaging of PD patients.129