Identification of [18F]TRACK, a Fluorine-18-Labeled Tropomyosin Receptor Kinase (Trk) Inhibitor for PET Imaging

Changes in expression and dysfunctional signaling of TrkA/B/C receptors and oncogenic Trk fusion proteins are found in neurological diseases and cancers. Here, we describe the development of a first 18F-labeled optimized lead suitable for in vivo imaging of Trk, [18F]­TRACK, which is radiosynthesize...

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Veröffentlicht in:Journal of medicinal chemistry 2018-02, Vol.61 (4), p.1737-1743
Hauptverfasser: Bernard-Gauthier, Vadim, Mossine, Andrew V, Mahringer, Anne, Aliaga, Arturo, Bailey, Justin J, Shao, Xia, Stauff, Jenelle, Arteaga, Janna, Sherman, Phillip, Grand’Maison, Marilyn, Rochon, Pierre-Luc, Wängler, Björn, Wängler, Carmen, Bartenstein, Peter, Kostikov, Alexey, Kaplan, David R, Fricker, Gert, Rosa-Neto, Pedro, Scott, Peter J. H, Schirrmacher, Ralf
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Sprache:eng
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Zusammenfassung:Changes in expression and dysfunctional signaling of TrkA/B/C receptors and oncogenic Trk fusion proteins are found in neurological diseases and cancers. Here, we describe the development of a first 18F-labeled optimized lead suitable for in vivo imaging of Trk, [18F]­TRACK, which is radiosynthesized with ease from a nonactivated aryl precursor concurrently combining largely reduced P-gp liability and improved brain kinetics compared to previous leads while displaying high on-target affinity and human kinome selectivity.
ISSN:0022-2623
1520-4804
DOI:10.1021/acs.jmedchem.7b01607