Synthesis and characterization of the two enantiomers of a chiral sigma-1 receptor radioligand: (S)-(+)- and (R)-(-)-[18F]FBFP
Synthesis and characterization of the two enantiomers of a chiral sigma-1 receptor radioligand: (S)-(+)- and (R)-(-)-[18F]FBFP
复制标题
手性 sigma-1 受体放射性配体的两种对映体的合成和表征：(S)-( )- 和 (R)-(-)-[18F]FBFP
DOI：
10.1016/j.cclet.2022.03.099
复制
发表时间：
2022-05-27
影响因子：
9.1
通讯作者：
Jia, Hongmei
中科院分区：
文献类型：
--
作者：
Wang, Tao;Zhang, Ying;Jia, Hongmei
Racemic [F-18]FBFP ([F-18]1) proved to be a potent sigma(1) receptor radiotracer with superior imaging properties. The pure enantiomers of unlabeled compounds (S)- and (R)-1 and the corresponding iodonium ylide precursors were synthesized and characterized. The two enantiomers (S)1 and (R)-1 exhibited comparable high affinity for sigma(1) receptors and selectivity over a 2 receptors. The Ca2+ fluorescence assay indicated that (R)-1 behaved as an antagonist and (S)-1 as an agonist for sigma(1) receptors. The F-18-labeled enantiomers (S)- and (R)-[F-18]1 were obtained in >99% enantiomeric purity from the corresponding enantiopure iodonium ylide precursors with radiochemical yield of 24.4% +/- 2.6% and molar activity of 86-214 GBq/mu mol. In ICR mice both (S)- and (R)-[F-18]1 displayed comparable high brain uptake, brain-to-blood ratio, in vivo stability and binding specificity in the brain and peripheral organs. In micro-positron emission tomography (PET) imaging studies in rats, (S)-[F-18]1 exhibited faster clearance from the brain than (R)-[F-18]1, indicating different brain kinetics of the two enantiomers. Both (S)- and (R)-[F-18]1 warrant further evaluation in primates to translate a single enantiomer with more suitable kinetics for imaging the sigma(1) receptors in humans. (C) 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
