Shao Xia, Butch Elizabeth R, Kilbourn Michael R, Snyder Scott E
Division of Nuclear Medicine, Department of Radiology, University of Michigan Medical Center, Ann Arbor, MI 48109, USA.
Nucl Med Biol. 2003 Jul;30(5):491-500. doi: 10.1016/s0969-8051(03)00031-3.
A series of N-fluoroethylpiperidinyl (1), N-fluoroethylpiperidinemethyl (2) and N-fluoroethylpyrrolidinyl (3) esters were synthesized and examined as new (18)F-labeled radiotracers for measuring brain cholinesterase activity. The fluoroethyl group, instead of methyl group, results in slower in vitro enzymatic cleavage rates and higher selectivity for AChE. Based on metabolism in mouse blood and PET time-activity curves in rats, two radiotracers were identified as potential candidates for further in vivo evaluation in higher species.
合成了一系列N-氟乙基哌啶基(1)、N-氟乙基哌啶甲基(2)和N-氟乙基吡咯烷基(3)酯,并将其作为用于测量脑胆碱酯酶活性的新型(18)F标记放射性示踪剂进行了研究。氟乙基取代甲基导致体外酶促裂解速率较慢,对乙酰胆碱酯酶(AChE)的选择性更高。基于小鼠血液中的代谢情况和大鼠的正电子发射断层扫描(PET)时间-活度曲线,确定了两种放射性示踪剂作为在高等物种中进行进一步体内评估的潜在候选物。