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The crystal structures of the GluA2 ligand-binding domain in complex with the positive allosteric modulator CX516 and its methyl-substituted analogue Me-CX516 show that their binding modes are similar to those of aniracetam and CX614. This supports that CX516 affects receptor deactivation. The structures also show that there is limited space for substitutions at the piperidine ring of CX516.