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Syntheses of 2-Amino and 2-Halothiazole Derivatives as High-Affinity Metabotropic Glutamate Receptor Subtype 5 Ligands and Potential Radioligands for In Vivo Imaging

The structure of the potent selective mGlu(5) ligand, SP203 (1, 3-fluoro-5-[[2-(fluoromethyl)thiazol-4-yl]ethynyl]benzonitrile), was modified by replacing the 2-fluoromethyl substituent with an amino or halo substituent and by variation of substituents in the distal aromatic ring to provide a series...

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Bibliographic Details
Main Authors: Siméon, Fabrice G, Wendahl, Matthew T., Pike, Victor W.
Format: Artigo
Language:Inglês
Published: 2011
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3092816/
https://ncbi.nlm.nih.gov/pubmed/21207959
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm101430m
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