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Cat. No. Product Name Information
PC-45528

SYM2206

AMPAR antagonist

SYM2206 is an allosteric, non-competitive antagonist of the AMPA receptor with IC50 of 2.8 uM.
PC-45064

Rapastinel

NMDAR agonist

Rapastinel (GLYX-13, Thr-Pro-Pro-Thr-NH2) is a tetrapeptide (TPPT-amide) that acts as a NMDA receptor glycine site partial agonist.
PC-45533

CIQ

NMDAR potentiator

CIQ is a subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors.
PC-42745

LY450108

AMPAR PAM

LY450108 is a potent, selective, and centrally active positive allosteric modulator of AMPAR-mediated neurotransmission, which increase ion channel flux in the presence of agonist by suppressing desensitization and/or deactivation of the receptors.
PC-42744

LY451395

AMPAR PAM

Mibampator (LY451395) is a potent, selective, and centrally active positive allosteric modulator of AMPAR-mediated neurotransmission, which increase ion channel flux in the presence of agonist by suppressing desensitization and/or deactivation of the receptors.
PC-42691

Rislenemdaz

GluN2B antagonist

Rislenemdaz (MK-0657, CERC-301) is a potent, orally bioavailable brain‐penetrant, NR2B-selective NMDA receptor (GluN2B) antagonist with Ki and IC 50 of 8.1 nM and 3.6 nM respectively, with no off-target activity.
PC-45532

L-701324

NMDAR antagonist

L-701324 (L-701,324) is a potent, orally active antagonist at the glycine modulatory site on NMDA receptor with IC50 of 2 nM.
PC-42742

Aniracetam

AMPAR PAM

Aniracetam (Ro 13-5057) is a positive allosteric modulator of AMPAR, potentiates the iQA responses induced in Xenopus oocytes by rat brain mRNA in a reversible manner.
PC-42743

Ampalex

AMPAR PAM

Ampalex (CX516) is a positive allosteric modulator of AMPA, increases fast, excitatory (glutamatergic) synaptic responses in hippocampal slices by about 50% with an EC50 of 170 uM.
PC-42746

Farampator

AMPAR PAM

Farampator (CX-691, Org24448) is a positive allosteric modulator of AMPAR as ampakine agent.
PC-22610

NS3763

GLUK5 antagonist

NS3763 is a noncompetitive antagonist of GLUK5 receptor, inhibits domoate-induced increase in intracellular calcium mediated through the GLU(K5) of kainate receptors with IC50 of 1.6 uM, with no effect on GLU(K6) subtype.
PC-22609

3-Hydroxykynurenine

iGluR modulator

3-Hydroxykynurenine (3-HK) is a metabolite produced through host tryptophan metabolism, restricts bacterial expansion in macrophages via a systemic mechanism, modulates the activity of iGluR receptors of the AMPAR and KAR subclasses.

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