| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10916021 | Nuclear Medicine and Biology | 2014 | 7 Pages |
Abstract
'Click chemistry' was successfully applied to the synthesis of [18 F]FPTC resulting in high radiochemical yields. [18 F]FPTC showed specific binding in vitro, but not in vivo. Based on the logP value and its ability to block [125I]ICYP binding to C6 cells, FPTC may be a lead to suitable cerebral β-AR ligands.
Keywords
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Authors
Leila Mirfeizi, Anna A. Rybczynska, Aren van Waarde, Lachlan Campbell-Verduyn, Ben L. Feringa, Rudi A.J.O. Dierckx, Philip H. Elsinga,
![First Page Preview: [18Â F]-(fluoromethoxy)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)propan-2-ol ([18Â F FPTC) a novel PET-ligand for cerebral beta-adrenoceptors [18Â F]-(fluoromethoxy)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)propan-2-ol ([18Â F FPTC) a novel PET-ligand for cerebral beta-adrenoceptors](/preview/png/10916021.png)