Discovery of [ 11 C]MK-8056: A Selective PET Imaging Agent for the Study of mGluR 2 Negative Allosteric Modulators
Modification of potent, selective metabotropic glutamate receptor 2 negative allosteric modulator (mGluR NAM) led to a series of analogues with excellent binding affinity, lipophilicity, and suitable physicochemical properties for a PET tracer with convenient chemical handles for incorporation of a...
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Veröffentlicht in: | ACS medicinal chemistry letters 2023-07, Vol.14 (7), p.986-992 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Modification of potent, selective metabotropic glutamate receptor 2 negative allosteric modulator (mGluR
NAM) led to a series of analogues with excellent binding affinity, lipophilicity, and suitable physicochemical properties for a PET tracer with convenient chemical handles for incorporation of a
C or
F radiolabel. [
C]MK-8056 was synthesized and evaluated
and demonstrated appropriate affinity, selectivity, and physicochemical properties to be used as a positron emission tomography tracer for mGluR
. |
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ISSN: | 1948-5875 1948-5875 |
DOI: | 10.1021/acsmedchemlett.3c00175 |