1. Academic Validation
  2. UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors

UCM-A86 is a selective positive allosteric modulator of GluN1/GluN3 NMDA receptors

  • bioRxiv. 2025 Nov 16:2025.11.14.688378. doi: 10.1101/2025.11.14.688378.
Avery J Benton 1 Mia R Johns 1 Emil Diamant 1 2 Nirvan Rouzbeh 1 Valdemar P Sørensen 1 2 Carly M Anderson 1 Davide Secci 2 Zhucheng Zhang 2 Andrew R Rau 1 Rasmus P Clausen 2 Kasper B Hansen 1
Affiliations

Affiliations

  • 1 Center for Structural and Functional Neuroscience, Center for Biomolecular Structure and Dynamics, Division of Biological Sciences, University of Montana, Missoula, MT.
  • 2 Department for Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Abstract

N-methyl-d-aspartate (NMDA) receptors are ionotropic glutamate receptors that mediate excitatory neurotransmission in the central nervous system (CNS) where they play critical roles in normal and pathological brain functions and neurodevelopment. While the glutamate/glycine-activated GluN2-containing NMDA receptors (GluN1/GluN2) have been extensively studied, the physiological roles and pharmacology of glycine-activated GluN3-containing receptors (GluN1/GluN3) remain less understood. Although GluN1/GluN3 receptors exhibit unique functional properties and play distinct roles in neuronal development and synapse maturation, studies of their precise roles in neurophysiology and circuit function are impeded by limited availability of GluN3-selective pharmacological tools. This study describes UCM-A86, a novel GluN3-selective positive allosteric modulator, with EC50 values of 21 μM and 19 μM at GluN1/GluN3A and GluN1/GluN3B receptors, respectively. UCM-A86 selectively potentiates recombinant GluN1/GluN3A and GluN1/GluN3B receptors by 436% and 174%, respectively, relative to activation by glycine, with no activity at recombinant GluN1/GluN2A-D receptors. Furthermore, UCM-A86 selectively potentiates responses from native GluN1/GluN3A receptors expressed in somatostatin-expressing interneurons of the somatosensory cortex with no modulation of hippocampal AMPA receptor- and GluN1/2 NMDA receptor-mediated excitatory postsynaptic currents. Mechanistic studies suggest that UCM-A86 modulation is facilitated by agonist binding (or channel gating) and that UCM-A86 primarily potentiates GluN1/GluN3A by increasing open probability with no effects on mean channel conductance. These findings advance the synthetic pharmacology of GluN1/GluN3 receptors and provide a novel tool for modulation of native GluN3-containing NMDA receptors.

Keywords

Ionotropic glutamate receptors; allosteric modulation; drug discovery; ligand-gated ion channels; neuropharmacology; synaptic transmission.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-179573
    98.64%, Positive Allosteric Modulator Of GluN1/GluN3 NMDA Receptors