Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 24, Pages 5197-5209Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob00854f
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Funding
- United States NIH [NS061025, NS075527, NS058714, MH092797]
- American Parkinson Disease Association (APDA) Advanced Center for Parkinson Disease Research at Washington University
- Greater St. Louis Chapter of the APDA
- Barnes-Jewish Hospital Foundation
- Barbara & Sam Murphy Fund
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The vesicular acetylcholine transporter (VAChT) is a reliable biomarker for assessing cholinergic dysfunction associated with dementia. We recently reported three new potent and selective carbon-11 labeled VAChT radiotracers. Herein, we report the resolution with a Chiralcel OD column of three additional fluorine containing VAChT ligands in which a fluoroethoxy or fluoroethylamino moiety was substituted for the methoxy group. An in vitro competitive binding assay showed that (-)-7 had high potency for VAChT (Ki-VAChT = 0.31 +/- 0.03 nM) and excellent selectivity for VAChT versus sigma receptors (Ki-sigma 1 = 1870 +/- 250 nM, Ki-sigma 2 = 5480 +/- 140 nM). Three different radiolabeling approaches were explored; the radiosynthesis of (-)-[F-18]7 was successfully accomplished via a stepwise two-pot, three-step method with moderate yield (11 +/- 2%) and high radiochemical purity (>98%). PET imaging studies in a nonhuman primate indicated that (-)-[F-18]7 rapidly entered the brain and accumulated in the VAChT-enriched striatum. The uptake of (-)-[F-18]7 in the target striatal area peaked at 10 min and displayed improved clearance kinetics compared to the VAChT tracer [F-18] VAT, which has been approved by the Food and Drug Administration (FDA) for first-in-man studies. These studies justify further investigation of (-)-[F-18]7 and exploration of the structure-activity relationships of these fluoroethoxy and fluoroethylamino analogs.
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