| Cat.No. | Name | Information |
|---|---|---|
| M2767 | Ifenprodil Tartrate | Ifenprodil is an atypical noncompetitive antagonist at the NMDA receptor, it interacts with high affinity at a homogeneous population of NMDA receptors in neonatal rat forebrain with IC50 of 0.3 μM. |
| M9566 | Glycine | Glycine is an inhibitory neurotransmitter in the CNS and also acts as a co-agonist along with glutamate. |
| M2884 | NMDA | NMDA（N-Methyl-D-aspartic acid）is a specific agonist for NMDA receptor mimicking the action of glutamate, the neurotransmitter which normally acts at that receptor. |
| M3003 | CB-839 | Telaglenastat (CB-839) is a potent, selective, and orally bioavailable glutaminase inhibitor with IC50 of 24 nM for recombinant human GAC. |
| M56504 | (S)-(-)-HA 966 | (S)-(-)-HA 966 ((-)-HA 966), a γ-Hydroxybutyrate-like agent, is weakly active as an NMDA-receptor antagonist. |
| M56503 | (2R,3S)-Chlorpheg | (2R,3R)-Chlorpheg is a week antagonist of L-homocysteic acid (L-HCA) induced depolarization.(2R,3R)-Chlorpheg also is a weak N-methyl-D-aspartate (NMDA) antagonist. |
| M56502 | 5-Iodowillardiine | 5-Iodowillardiine is a potent and selective kainate receptor agonist. |
| M56501 | NPEC-caged-(S)-AMPA | NPEC- caged-(S)-AMPA, a caged neurotransmitter analog, is a NPEC photoprotecting group caged the (S)-AMPA to make caged ligands specific for glutamate receptor sub-types. |
| M56500 | NMDAR antagonist 1 | NMDAR antagonist 1 is a potent and orally bioavailable NR2B-selective NMDAR antagonist. |
| M56499 | Neboglamine hydrochloride | Neboglamine (CR-2249, XY-2401) hydrochloride is an orally active NMDA receptor glycine site positive modulator that can be used in schizophrenia research. |
| M56498 | SDZ 220-581 Ammonium salt | SDZ 220-581 Ammonium salt is an orally active, potent, competitive NMDA receptor antagonist with pKi value of 7.7. |
| M56497 | GYKI 52466 dihydrochloride | GYKI 52466 dihydrochloride is an orally active, highly selective and noncompetitive AMPA/kainate receptor antagonist with the IC50 values of 7.5 and 11μM, respectively. |
| M56496 | GYKI-47261 dihydrochloride | GYKI-47261 dihydrochloride is a competitive, orally active, and selective AMPA receptor antagonist with an IC50 of 2.5 μM. |
| M56495 | (R,S)-3,4-Dicarboxyphenylglycine | (R,S)-3,4-Dicarboxyphenylglycine ((RS)-3,4-DCPG) is an AMPA receptor antagonist. |
| M56494 | Pregnanolone sulfate (pyridinium) | Pregnanolone sulfate pyridinium is an endogenous neurosteroid that inhibits NMDA receptors and is neuroprotective. |
| M56493 | 5,7-Dichlorokynurenic acid sodium | 5,7-Dichlorokynurenic acid (sodium) is the sodium form of 5,7-Dichlorokynurenic acid. |
| M56278 | (RS)-APICA | (RS)-APICA is a selective group II metabotropic glutamate receptor (mGluR II) antagonist. |
| M56277 | (RS)-PPG | (RS)-PPG is a potent and selective agonist for group III mGluRs. |
| M56276 | (2R,4R)-APDC | (2R,4R)-APDC is a group II metabotropic glutamate receptor (mGluR) agonist. |
| M56275 | (S)-3,5-DHPG | (S)-3,5-DHPG is a weak, but selective group I metabotropic glutamate receptors (mGluRs) agonist with Ki values of 0.9 µM and 3.9 µM for mGluR1a and mGluR5a, respectively. |
| M56274 | LSN2463359 | LSN2463359 is positive allosteric modulator of metabotropic glutamate 5 (mGlu5). |
| M56273 | (1S,3R)-ACPD | (1S,3R)-ACPD is a mGluR agonist that can depolarize pyramidal cells. |
| M56272 | (±)-LY395756 | (±)-LY395756 is an agonist of mGlu2 receptor and an antagonist of mGlu3 receptor. |
| M56271 | Desmethyl-YM-298198 | Desmethyl-YM-298198 is a high-affinity, selective, and noncompetitive mGluR1 antagonist (IC50: 16 nM). |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
