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NMDA Receptors
More Information »NMDA receptors are members of the ionotropic class of glutamate receptors, which also includes Kainate and AMPA receptors. NMDA receptors consist of NR1 subunits combined with NR2 (A-D) or NR3 (A-B) subunits. The ligand-gated channel is permeable to cations.
NMDA Receptor Products
Agonists |
|
Cat.No. |
Product Name / Activity |
| 0186 | cis-ACPD |
| Potent NMDA agonist. Also group II mGluR agonist | |
| 0213 | D-Aspartic acid |
| NMDA agonist | |
| 0214 | L-Aspartic acid |
| NMDA agonist | |
| 0216 | L-Cysteinesulfinic acid |
| NMDA and mGlu agonist | |
| 3406 | GLYX 13 |
| NMDA receptor partial agonist; acts at the glycine site | |
| 0281 | (R)-(+)-HA-966 |
| NMDA partial agonist/antagonist, acts at glycine site | |
| 0197 | Homoquinolinic acid |
| Selective, potent NMDA agonist | |
| 0285 | Ibotenic acid |
| Non-selective NMDA agonist | |
| 2277 | MNI-caged-D-aspartate |
| Caged D-aspartate; NMDA agonist | |
| 0114 | NMDA |
| Selective NMDA agonist | |
| 0959 | Spermidine trihydrochloride |
| Agonist at polyamine site | |
| 0312 | (RS)-(Tetrazol-5-yl)glycine |
| Highly potent NMDA receptor agonist | |
Antagonists |
|
Cat.No. |
Product Name / Activity |
| 0258 | ACBC |
| NMDA antagonist, acts at glycine site | |
| 3693 | DL-AP5 Sodium salt |
| Sodium salt of DL-AP5 (Cat. No. 0105) | |
| 0106 | D-AP5 |
| Potent, selective NMDA antagonist. More active form of DL-AP5 (Cat. No. 0105) | |
| 0105 | DL-AP5 |
| Potent, selective NMDA antagonist | |
| 0107 | L-AP5 |
| Potent, selective NMDA antagonist. Less active form of DL-AP5 (Cat. No. 0105) | |
| 0164 | D-AP7 |
| Specific NMDA antagonist. More active form of DL-AP7 (Cat. No. 0104) | |
| 0104 | DL-AP7 |
| Specific NMDA antagonist | |
| 0389 | Arcaine sulfate |
| Competitive NMDA antagonist | |
| 0322 | (R)-4-Carboxyphenylglycine |
| Moderately potent NMDA antagonist | |
| 1469 | CGP 37849 |
| Potent selective NMDA antagonist | |
| 1409 | CGP 39551 |
| Potent, selective and competitive NMDA antagonist | |
| 1493 | CGP 78608 hydrochloride |
| Potent, selective glycine-site NMDA antagonist | |
| 1241 | CGS 19755 |
| Potent, competitive NMDA antagonist | |
| 3697 | 7-Chlorokynurenic acid sodium salt |
| Sodium salt of 7-Chlorokynurenic acid (Cat. No. 0237) | |
| 0237 | 7-Chlorokynurenic acid |
| NMDA antagonist, acts glycine site | |
| 0817 | (2R,3S)-Chlorpheg |
| Weak NMDA antagonist | |
| 0190 | CNQX |
| NMDA antagonist, acts glycine site. Also AMPA/kainate antagonist | |
| 2456 | Co 101244 hydrochloride |
| Highly selective NR2B antagonist | |
| 3125 | Conantokin-R |
| Potent non-competitive NMDA receptor antagonist | |
| 3122 | Conantokin-T |
| Non-competitive NMDA receptor antagonist | |
| 0247 | (R)-CPP |
| Potent NMDA antagonist. More active enantiomer of (RS)-CPP (Cat. No. 0173) | |
| 0173 | (RS)-CPP |
| Potent NMDA antagonist | |
| 1265 | D-CPP-ene |
| Potent, competitive NMDA antagonist | |
| 3071 | Dextromethorphan hydrobromide |
| NMDA receptor antagonist | |
| 0286 | 5,7-Dichlorokynurenic acid |
| Potent NMDA antagonist, acts glycine site | |
| 3698 | 5,7-Dichlorokynurenic acid sodium salt |
| Sodium salt of 5,7-Dichlorokynurenic acid (Cat. No. 0286). Potent NMDA antagonist, acts at glycine site | |
| 0360 | (±)-1-(1,2-Diphenylethyl)piperidine maleate |
| NMDA antagonist, acts ion channel site | |
| 4491 | DQP 1105 |
| Selective NR2C/NR2D receptor antagonist | |
| 2195 | Eliprodil |
| Non-competitive NR2B-selective NMDA antagonist | |
| 0869 | Felbamate |
| NMDA antagonist, acts glycine site | |
| 2867 | Flupirtine maleate |
| Indirect NMDA receptor antagonist | |
| 2348 | Gavestinel |
| Potent and selective glycine site antagonist. Orally available and active in vivo | |
| 0282 | (S)-(-)-HA-966 |
| NMDA antagonist/partial agonist | |
| 2861 | HU 211 |
| NMDA receptor antagonist. Also NF-κB inhibitor | |
| 0290 | N-(4-Hydroxyphenylacetyl)spermine |
| Wasp toxin analog | |
| 0545 | Ifenprodil hemitartrate |
| Non-competitive NMDA antagonist. Also σ ligand | |
| 2892 | threo Ifenprodil hemitartrate |
| NR2B-selective NMDA antagonist. Also σ agonist | |
| 3131 | Ketamine hydrochloride |
| Non-competitive NMDA receptor antagonist | |
| 4379 | (S)-(+)-Ketamine hydrochloride |
| NMDA receptor antagonist; enantiomer of ketamine hydrochloride (Cat. No. 3131) | |
| 0742 | L-689,560 |
| Very potent NMDA antagonist | |
| 0705 | L-701,252 |
| NMDA antagonist, acts glycine site | |
| 0907 | L-701,324 |
| NMDA antagonist, acts at glycine site | |
| 0840 | Loperamide hydrochloride |
| NMDA antagonist, reduces Ca2+ flux | |
| 1521 | LY 233053 |
| Competitive NMDA receptor antagonist | |
| 1019 | LY 235959 |
| Competitive NMDA antagonist | |
| 0773 | Memantine hydrochloride |
| NMDA antagonist; acts at ion channel site | |
| 0955 | (-)-MK 801 maleate |
| NMDA antagonist, less active enantiomer | |
| 0924 | (+)-MK 801 maleate |
| Non-competitive NMDA antagonist, acts at ion channel site | |
| 1970 | Norketamine hydrochloride |
| Potent, non-competitive NMDA antagonist | |
| 4230 | NPEC-caged-D-AP5 |
| Caged D-AP5 (Cat.No. 0106); NMDA antagonist | |
| 3277 | Pentamidine isethionate |
| Antimicrobial that antagonizes NMDA receptors | |
| 2557 | Phencyclidine hydrochloride |
| Non-competitive NMDA receptor antagonist | |
| 2273 | PMPA (NMDA antagonist) |
| Competitive NMDA antagonist | |
| 2530 | PPDA |
| Subtype-selective NR2C/NR2D antagonist | |
| 2274 | PPPA |
| Competitive NR2A antagonist | |
| 1622 | Remacemide hydrochloride |
| NMDA antagonist; blocks ion channel and allosteric modulatory site | |
| 2005 | Ro 04-5595 hydrochloride |
| Selective NR2B antagonist | |
| 1594 | Ro 25-6981 maleate |
| Subtype-selective NR2B antagonist | |
| 3254 | Ro 61-8048 |
| NMDA antagonist; increases kynurenic acid levels | |
| 3343 | Ro 8-4304 hydrochloride |
| Selective NR2B antagonist | |
| 1251 | SDZ 220-040 |
| Potent, competitive NMDA antagonist | |
| 1250 | SDZ 220-581 |
| Competitive NMDA antagonist | |
| 0635 | Synthalin sulfate |
| Non-competitive NMDA antagonist | |
| 4154 | TCN 201 |
| Selective NR1/NR2A receptor antagonist | |
| 4163 | TCN 213 |
| NMDA antagonist; selective for NR2A over NR2B | |
| 4072 | TCN 237 dihydrochloride |
| Highly potent and selective NR2B antagonist | |
| 2782 | TCS 46b |
| Orally active, subtype-selective NR1A/NR2B antagonist | |
Ligand Sets |
|
Cat.No. |
Product Name / Activity |
| 1825 | Mixed NMDA Receptor Tocriset™ |
| Selection of 5 mixed NMDA receptor ligands (Cat. Nos. 0114, 0312, 0106, 0924 and 1241) | |
| 1823 | NMDA Receptor - Glycine Site Tocriset™ |
| Selection of 5 NMDA receptor (glycine site) ligands (Cat. Nos. 0219, 0281, 0742, 1493 and 0237) | |
Other |
|
Cat.No. |
Product Name / Activity |
| 1238 | CCMQ |
| Used to characterize NR2B-containing NMDA receptors | |
| 4105 | CIQ |
| Potentiator of NMDA receptors containing NR2C/NR2D | |
| 0219 | Glycine |
| Endogenous potentiator, co-transmitter | |
| 1636 | IEM 1460 |
| Open-channel blocker of NMDA currents. Also blocks AMPA currents | |
| 2224 | MNI-caged-NMDA |
| Caged NMDA | |
| 2213 | N20C hydrochloride |
| Non-competitive NMDA receptor open-channel blocker | |
| 2851 | Nefiracetam |
| Cognitive enhancer; potentiates NMDA currents | |
| 0225 | Quinolinic acid |
| Endogenous NMDA agonist and transmitter candidate | |
| 0226 | D-Serine |
| Potentiator, acts glycine site | |
| 0958 | Spermine tetrahydrochloride |
| Modulator at polyamine site | |
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