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10. Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites. Sköld N; Nielsen B; Olsen J; Han L; Olsen L; Madsen U; Kristensen JL; Pickering DS; Johansen TN Bioorg Med Chem; 2014 Oct; 22(19):5368-77. PubMed ID: 25172149 [TBL] [Abstract][Full Text] [Related]
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