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Tritium and deuterium labelling of a kainate receptor antagonist and evaluation as a radioligand

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F24%3A00583406" target="_blank" >RIV/61388963:_____/24:00583406 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/jlcr.4087" target="_blank" >https://doi.org/10.1002/jlcr.4087</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/jlcr.4087" target="_blank" >10.1002/jlcr.4087</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tritium and deuterium labelling of a kainate receptor antagonist and evaluation as a radioligand

  • Original language description

    Kainate receptors play a crucial role in mediating synaptic transmission within the central nervous system. However, the lack of selective pharmacological tool compounds for the GluK3 subunit represents a significant challenge in studying these receptors. Recently presented compound 1 stands out as a potent antagonist of GluK3 receptors, exhibiting nanomolar affinity at GluK3 receptors and strongly inhibiting glutamate-induced currents at homomeric GluK1 and GluK3 receptors in HEK293 cells with Kb values of 65 and 39 nM, respectively. This study presents the synthesis of two potent GluK3-preferring iodine derivatives of compound 1, serving as precursors for radiolabelling. Furthermore, we demonstrate the optimisation of dehalogenation conditions using hydrogen and deuterium, resulting in [2H]-1, and demonstrate the efficient synthesis of the radioligand [3H]-1 with a specific activity of 1.48 TBq/mmol (40.1 Ci/mmol). Radioligand binding studies conducted with [3H]-1 as a radiotracer at GluK1, GluK2, and GluK3 receptors expressed in Sf9 and rat P2 membranes demonstrated its potential applicability for selectively studying native GluK3 receptors in the presence of GluK1 and 2-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor-blocking ligands.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10406 - Analytical chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Labelled Compounds and Radiopharmaceuticals

  • ISSN

    0362-4803

  • e-ISSN

    1099-1344

  • Volume of the periodical

    67

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    120-130

  • UT code for WoS article

    001159520900001

  • EID of the result in the Scopus database

    2-s2.0-85184872172