Abstract
A focused library of novel 2,3-dihydro-1H-1,5-benzodiazepin-2-ones containing sites for 11C-, 18F- and 123I- labelling have been prepared and evaluated against membrane expressing human recombinant metabotropic glutamate 2 receptor (mGluR2). The compounds were found to be non-competitive antagonists with nanomolar affinity. HPLC evaluation of the physiochemical properties of these compounds identified two candidates for PET and SPECT imaging of mGluR2. © 2013 The Royal Society of Chemistry.
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CITATION STYLE
Gilfillan, L., Blair, A., Morris, B. J., Pratt, J. A., Schweiger, L., Pimlott, S., & Sutherland, A. (2013). Synthesis and biological evaluation of novel 2,3-dihydro-1H-1,5- benzodiazepin-2-ones; Potential imaging agents of the metabotropic glutamate 2 receptor. MedChemComm, 4(7), 1118–1123. https://doi.org/10.1039/c3md00110e
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