Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374186 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
[18F]FEAC ([18F]4a) and [18F]FEDAC ([18F]4b) were developed as two novel positron emission tomography (PET) ligands for peripheral-type benzodiazepine receptor (PBR). [18F]4a and [18F]4b were synthesized by fluoroethylation of precursors 8a and 8b with [18F]FCH2CH2Br ([18F]9), respectively. Small-animal PET scan for a neuroinflammatory rat model showed that the two radioligands had high uptakes of radioactivity in the kainic acid-infused striatum, a brain region where PBR density was increased.
Graphical abstract[18F]FEAC ([18F]4a) and [18F]FEDAC ([18F]4b), two potent PET ligands for peripheral-type benzodiazepine receptor, were synthesized and evaluated.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kazuhiko Yanamoto, Katsushi Kumata, Tomoteru Yamasaki, Chika Odawara, Kazunori Kawamura, Joji Yui, Akiko Hatori, Kazutoshi Suzuki, Ming-Rong Zhang,