93 Results for "

N-methyl-D-aspartate (NMDA)

" in MedChemExpress (MCE) Product Catalog:
Products (93)

93 Results for "N-methyl-D-aspartate (NMDA)" in MCE Product Catalog:

7
7 Publications Verification
Cat. No.: HY-100807
CAS No.: 89-00-9
Purity:  99.85%
Quinolinic acid, an endogenous metabolite of tryptophan, is a N-methyl-D-aspartate receptor (NMDA receptor) agonist. Quinolinic acid increases glutamate efflux, induces the generation of ROS, activates nitric oxide synthase, produces excessive NO, leading to calcium ion influx and neuronal apoptosis .
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7
7 Publications Verification
Cat. No.: HY-N2311
CAS No.: 2552-55-8
Synonyms: (RS)-Ibotenic acid; DL-Ibotenic acid
Ibotenic acid has agonist activity at both the N-methyl-D-aspartate (NMDA) and trans-ACPD or metabolotropic quisqualate (Qm) receptor sites.
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6
6 Cited Publications
Cat. No.: HY-17387
CAS No.: 102518-79-6
Synonyms: Huperzine A
(-)-Huperzine A (Huperzine A) is an alkaloid isolated from Huperzia serrata, with neuroprotective activity. (-)-Huperzine A is a potent, highly specific, reversible and blood-brain barrier penetrant inhibitor of acetylcholinesterase (AChE), with an IC50 of 82 nM. (-)-Huperzine A also is non-competitive antagonist of N-methyl-D-aspartate glutamate (NMDA) receptor. (-)-Huperzine A is developed for the research of neurodegenerative diseases, including Alzheimer’s disease .
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4
4 Cited Publications
Cat. No.: HY-100807S
CAS No.: 138946-42-6
Purity:  99.90%
Quinolinic acid-d3 is the deuterium labeled Quinolinic acid. Quinolinic acid, an endogenous metabolite of tryptophan, is a N-methyl-D-aspartate receptor (NMDA receptor) agonist. Quinolinic acid increases glutamate efflux, induces the generation of ROS, activates nitric oxide synthase, produces excessive NO, leading to calcium ion influx and neuronal apoptosis.
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4
4 Cited Publications
Cat. No.: HY-100811
CAS No.: 18000-24-3
Purity:  99.86%
Synonyms: 7-CKA
Target:  

iGluR

Research Areas:  

Neurological Disease

7-Chlorokynurenic acid (7-CKA) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid has potent antinociceptive actions after neuraxial delivery .
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4
4 Cited Publications
Cat. No.: HY-100811A
CAS No.: 1263094-00-3
Purity:  99.79%
Synonyms: 7-CKA sodium salt
Target:  

iGluR

Research Areas:  

Neurological Disease

7-Chlorokynurenic acid sodium salt (7-CKA sodium salt) is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 7-Chlorokynurenic acid sodium salt is also a potent inhibitor of the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM. 7-Chlorokynurenic acid sodium salt has potent antinociceptive actions after neuraxial delivery .
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3
3 Cited Publications
Cat. No.: HY-100714
CAS No.: 76326-31-3
Purity:  ≥98.0%
Synonyms: 2-APV; DL-2-Amino-5-phosphonovaleric acid
Target:  

iGluR

DL-AP5 (2-APV) is a competitive NMDA (N-methyl-D-aspartate) receptor antagonist. DL-AP5 shows significantly antinociceptive activity. DL-AP5 specifically blocks on channels in the rabbit retina .
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3
3 Cited Publications
Cat. No.: HY-101037
CAS No.: 107-97-1
Purity:  ≥98.0%
Synonyms: N-methylglycine; Sarcosin
Sarcosine (N-Methylglycine), an endogenous amino acid, is a competitive glycine transporter type I (GlyT1) inhibitor and N-methyl-D-aspartate (NMDA) receptor co-agonist. Sarcosine increases the glycine concentration, resulting in an indirect potentiation of the NMDA receptor. Sarcosine is commonly used for the research of schizophrenia .
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3
3 Cited Publications
Cat. No.: HY-N2370
CAS No.: 30271-38-6
Category:  

Animals Steroids

Target:  

iGluR LXR

24-Hydroxycholesterol is a natural sterol, which serves as a positive allosteric modulator of N-Methyl-d-Aspartate (NMDA) receptorsR, and a potent activator of the transcription factors LXR.
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3
3 Cited Publications
Cat. No.: HY-100714C
CAS No.: 1303993-72-7
Purity:  99.20%
Synonyms: 2-APV sodium; DL-2-Amino-5-phosphonovaleric acid sodium
Target:  

iGluR

DL-AP5 (2-APV) sodium is a competitive NMDA (N-methyl-D-aspartate) receptor antagonist. DL-AP5 sodium shows significantly antinociceptive activity. DL-AP5 sodium specifically blocks on channels in the rabbit retina .
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2
2 Cited Publications
Cat. No.: HY-B0184
CAS No.: 25451-15-4
Synonyms: W-554; ADD-03055
Target:  

iGluR

Research Areas:  

Neurological Disease

Felbamate (W-554) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA).
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1
1 Cited Publications
Cat. No.: HY-17388
CAS No.: 120786-18-7
(±)-Huperzine A is the racemate of (-)-Huperzine A (HY-17387). (-)-Huperzine A is an alkaloid isolated from Huperzia serrata, with neuroprotective activity. (-)-Huperzine A is a potent, highly specific, reversible and blood-brain barrier penetrant inhibitor of acetylcholinesterase (AChE), with an IC50 of 82 nM. (-)-Huperzine A also is non-competitive antagonist of N-methyl-D-aspartate glutamate (NMDA) receptor. (-)-Huperzine A is developed for the research of neurodegenerative diseases, including Alzheimer’s disease .
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Cat. No.: HY-B1487
CAS No.: 1508-76-5
Synonyms: Tricyclamol hydrochloride; (±)-Procyclidine hydrochloride
Target:  

iGluR mAChR

Research Areas:  

Neurological Disease

Procyclidine (Tricyclamol, (±)-Procyclidine) hydrochloride , an anticholinergic agent, is a muscarinic receptor antagonist that also has the properties of an N-methyl-D-aspartate (NMDA) antagonist. Procyclidine hydrochloride can be used in studies of Parkinson's disease and related psychiatric disorders such as Soman-induced epilepsy .
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Cat. No.: HY-G0021
CAS No.: 6104-71-8
Synonyms: Norclozapine; Desmethylclozapine; Normethylclozapine
N-Desmethylclozapine is a major active metabolite of the atypical antipsychotic agent Clozapine. N-Desmethylclozapine is a potent, allosteric and partial M1 receptors agonist (EC50=115 nM) and is able to potentiate hippocampal N-methyl-d-aspartate (NMDA) receptor currents through M1 receptor activation. N-Desmethylclozapine is also a δ-opioid agonist .
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Cat. No.: HY-109164
CAS No.: 2151842-64-5
Purity:  99.78%
Synonyms: AGN-241751; GATE-251
Target:  

iGluR

Research Areas:  

Neurological Disease

Zelquistinel (AGN-241751) is the orally active N-methyl-D-aspartate (NMDA) receptor partial agonist used for the research of depression, anxiety and other related psychiatric disorders .
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Cat. No.: HY-139580
CAS No.: 2378285-59-5
Purity:  96.61%
Synonyms: CAD-9303
Target:  

iGluR

Research Areas:  

Neurological Disease

Plazinemdor (CAD-9303) is a positive allosteric modulator of N-methyl-D-aspartate (NMDA) receptors, which is used in the research of neurological diseases .
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Cat. No.: HY-106441A
CAS No.: 808732-98-1
Purity:  99.86%
Synonyms: MK-0657; CERC-301
Target:  

iGluR

Research Areas:  

Neurological Disease

Rislenemdaz (CERC-301) is an orally bioavailable and selective N-methyl-D-aspartate (NMDA) receptor subunit 2B (GluN2B) antagonist with Ki and IC 50 of 8.1 nM and 3.6 nM, respectively.
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Cat. No.: HY-15084A
CAS No.: 121917-57-5
Purity:  99.92%
Synonyms: (-)-MK-801 maleate
Target:  

iGluR

Research Areas:  

Neurological Disease

(-)-Dizocilpine maleate ((-)-MK-801 maleate) is a less active (-)-enantiomer of Dizocilpine. (-)-Dizocilpine maleate is a selective and non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist with a Ki of 211.7 nM. (-)-Dizocilpine maleate has antidepressant effects .
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Cat. No.: HY-100807R
CAS No.: 89-00-9
Purity:  99.96%
Quinolinic acid (Standard) is the analytical standard of Quinolinic acid. This product is intended for research and analytical applications. Quinolinic acid, an endogenous metabolite of tryptophan, is a N-methyl-D-aspartate receptor (NMDA receptor) agonist. Quinolinic acid increases glutamate efflux, induces the generation of ROS, activates nitric oxide synthase, produces excessive NO, leading to calcium ion influx and neuronal apoptosis.
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Cat. No.: HY-101178
CAS No.: 139051-78-8
Purity:  ≥99.0%
Target:  

iGluR

Research Areas:  

Neurological Disease

L-689560 is a potent N-methyl-D-aspartate (NMDA) receptor antagonist at the GluN1 glycine binding site. L-689560 is widely used as a radiolabeled ligand in binding studies and used for study the roles of NMDA receptors in normal neurological processes as well as in diseases .
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