Format

Send to

Choose Destination
Bioorg Med Chem. 2008 Jan 15;16(2):783-93. Epub 2007 Oct 13.

Synthesis, in vitro characterization, and radiolabeling of reboxetine analogs as potential PET radioligands for imaging the norepinephrine transporter.

Author information

1
Department of Radiology, Division of Radiological Sciences, Emory University, Atlanta, GA 30322, USA.

Abstract

Six new (S,S)-enantiomers of reboxetine derivatives were synthesized and their binding affinities were determined via competition binding assays in cells expressing the human norepinephrine transporter (NET), serotonin transporter (SERT) or dopamine transporter (DAT). All six compounds prepared exhibit high affinity for the NET (K(i)<or=2nM) and selectivity versus the SERT and DAT. Radiolabeling methods were also developed to prepare these ligands in moderate to high radiochemical yield with high radiochemical purity via O- or S-methylation with [(11)C]CH(3)I, or O-alkylation with [(18)F]fluoroethyl brosylate or [(18)F]fluoropropyl brosylate, and their logP(7.4) was measured. These new C-11- and F-18-labeled tracers will be utilized in comparative microPET studies to evaluate their potential as PET radioligands for imaging brain NET in nonhuman primates.

PMID:
17983754
DOI:
10.1016/j.bmc.2007.10.025
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center