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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-iGluR

Request The Product List ofiGluR iGluR

Cat. No. Product Name Information
PC-61514

Traxoprodil

NR2B antagonist

Traxoprodil (CP101606) is a potent, selective N-methyl-D-aspartate (NMDA) antagonist with selectivity for the NR2B subunit, potently protects cultured hippocampal neurons from glutamate toxicity (IC50=10 nM).
PC-61501

NS-1209

AMPA antagonist

NS-1209 is a selective, water-soluble, in vivo long-lasting AMPA antagonist with Ki of 43 nM.
PC-61239

(S)93-31

GluN2B antagonist

(S)93-31 is a pH-dependent, GluN2B-selective inhibitor of NMDA receptor with IC50 of 0.19 uM at pH6.9, 10-fold selecivity over brain tissue pH 7.6 (IC50=1.8 uM).
PC-60899

LY3130481

AMPAR antagonist

LY3130481 (CERC611) is a potent, selective, noncompetitive TARP γ8-associated AMPA receptors with IC50 of 65.3 nM (GluA1/TARP γ-8), with no activity for γ-2 (cerebellum) or other TARP members.
PC-60783

AICP

GluN2C agonist

AICP is a potent, selective GluN2C-selective NMDA receptor glycine site superagonist with EC50 of 1.7 nM at GluN1/2C.
PC-60772

UBP 296

UBP 296 (UBP296, UBP-296) is a potent, and selective GluR5-subunit containing kainate receptor antagonist with Kd of 1.09 uM.
PC-60771

UBP 302

iGluR antagonist

UBP 302 (UBP-302) is a potent, and selective GluR5-subunit containing kainate receptor antagonist with Kd of 402 nM.
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.

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