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product name NMDA


Description: 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. NMDA binds to NMDA-receptor and interacts with it. However, NMDA is proved to be a poor substrate for the uptake transporters, suggesting that the excitatory effect could not be an indirect consequence of glutamate uptake.

References: Curr Opin Neurobiol. 2001 Jun;11(3):327-35; Nature. 1993 Aug 5;364(6437):535-7.



Molecular Weight (MW)

147.13
Formula

C5H9NO4
CAS No.

6384-92-5
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 5 mg/mL (33.98 mM) 
Water: 30 mg/mL (203.9 mM)
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19423374

In Vitro

In vitro activity: NMDA is an excitatory amino acid neurotransmitter, which only binds to the NMDA receptor without effecting other glutamate receptors (such as those for AMPA and kainate). NMDA specifically binds to the NR2 subunits of NMDA receptor, and then stimulates the open of non-specific cation channel which can allow the passage of Ca2+ and Na+ into the cell and K+ out of the cell. Activation of the NMDA receptor is able to produce the excitatory postsynaptic potential (EPSP), and trigger the increase of intracellular Ca2+ content which may further take participating in various signaling pathways. NMDA receptor plays a key role in a wide range of physiological (e.g. long-term potentiation and neuronal plasticity) and pathological processes (e.g. excitotoxicity and epilepsy).


Kinase Assay


Cell Assay

In Vivo  
Animal model  
Formulation & Dosage  
References Curr Opin Neurobiol. 2001 Jun;11(3):327-35.

AZD2015

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Author: Sodium channel