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Cat. No. Product Name Information
PC-21029

DQP-1105

GluN2C/2D antagonist

DQP-1105 is a selective GluN2C- and GluN2D-containing NMDARs antagonist with IC50 of 7.0 and 2.7 uM respectively, >50-fold selectivity over GluN2A- or GluN2B-containing receptors.
PC-20695

NYX-2925

NMDAR PAM

NYX-2925 (NYX2925) is a potent, specific NMDAR positive allosteric-modulator, facilitates [3H] MK-801 binding in all four human NMDAR2 subtypes with EC50 of 55 pM, 28 fM, 11 pM, and 55 pM for hNR2A, 2B, 2C, and 2D receptors, respectively.
PC-20370

GNE-5729

GluN2A PAM

GNE-5729 (GNE5729) is a potent, brain penetrant GluN2A-selective NMDAR positive allosteric modulator with EC50 of 37 nM.
PC-20369

GNE-0723

GluN2A PAM

GNE-0723 (GNE0723) is a potent, brain penetrant GluN2A-selective NMDAR positive allosteric modulator with EC50 of 21 nM.
PC-20368

GluN2A PAM (R)-9

GluN2A PAM (R)-9 is a potent, brain penetrant, GluN2A-selective positive allosteric modulator with EC50 of 0.51 uM, Emax 350%.
PC-20320

JNJ-61432059

AMPAR/γ-8 inhibitor

JNJ-61432059 is a potent, TARPγ-8 selective AMPAR negative modulator with pIC50 of 9.7 in FLIPR assay using HEK-293 cells expressing human GluA1o-γ-8.
PC-20090

BPAM344

GluK2 PAM

BPAM344 (BPAM-344) is a positive allosteric modulator of GluK2 kainate receptor, potentiates glutamate-evoked currents of GluK2a 21-fold at 200 uM (EC50=79 uM).
PC-38728

WMS-1410

NR2B receptor antagonist

WMS-1410 is a NR2B selective NMDA receptor antagonist with Ki value of 14 nM, antagonizes glutamate induced excitotoxicity with IC50 of 18.4 nM.
PC-38673

Plazinemdor

NMDA PAM

Plazinemdor (CAD-9303) is a potent N-methyl-D-aspartate (NMDA) receptor positive allosteric modulator with potential for schizophrenia.
PC-73437

Posovolone

GABAA PAM

Posovolone is a GABAA receptor positive allosteric modulator with antidepressant activity.
PC-73433

Onfasprodil

NMDA antagonist

Onfasprodil is a potent, selective N-methyl-D-aspartate (NMDA) receptor antagonist.
PC-38029

D-AP5

D-AP5 is a selective NMDA receptor antagonist that competes with glutamate binding and is commonly used to inhibit NMDA-dependent synaptic plasticity.

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