Basic information Safety Supplier Related

DNQX disodiumsalt

Basic information Safety Supplier Related

DNQX disodiumsalt Basic information

Product Name:
DNQX disodiumsalt
Synonyms:
  • 3-bis(olate)
  • 3-dione disodium salt
  • sodium 6
  • SODIUM 6;7-DINITROQUINOXALINE-2;3-BIS(OLATE);6;7-DINITROQUINOXALINE-2;3-DIONE DISODIUM SALT
  • DNQX Disodium
  • quinoxaline,inhibit,Inhibitor,iGluR,competitive,DNQX disodium salt,non-NMDA,Ionotropic glutamate receptors,nucleus,selective,FG 9041 disodium,thalamic,reticular
  • DNQX disodium salt, 10 mM in DMSO
CAS:
1312992-24-7
MF:
C8H5N4NaO6
MW:
276.14
Mol File:
1312992-24-7.mol
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DNQX disodiumsalt Chemical Properties

storage temp. 
Store at -20°C
solubility 
5mg/mL in DMSO, 12mg/mL in DMF
form 
solid
color 
Brown
Water Solubility 
Soluble in water (100mM)
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DNQX disodiumsalt Usage And Synthesis

Description

DNQX Disodium is a water-soluble form of selective non-NMDA receptor antagonist DNQX.

Uses

DNQX (FG 9041) disodium salt, a quinoxaline derivative, is a selective, potent competitive non-NMDA glutamate receptor antagonist (IC50s = 0.5, 2 and 40 μM for AMPA, kainate and NMDA receptors, respectively)[1].

in vivo

DNQX (FG 9041), a specific AMPA receptor antagonist, given as either a 5 mg/kg or 10 mg/kg intraperitoneal dose or into the lateral cerebral ventricle (5 μl of 0.5 mg/ml) significantly diminishes phencyclidine (PCP) (40 mg/kg) and ketamine (80, 100, 120 mg/kg) hsp70 induction in the posterior cingulate and retrosplenial cortex[3].

storage

Room temperature (desiccate)

References

[1] Honoré T, et al. Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonists. Science. 1988;241(4866):701-703. DOI:10.1126/science.2899909
[2] Lee SH, et al. Selective excitatory actions of DNQX and CNQX in rat thalamic neurons. J Neurophysiol. 2010;103(4):1728-1734. DOI:10.1152/jn.00540.2009
[3] Sharp JW, et al. DNQX inhibits phencyclidine (PCP) and ketamine induction of the hsp70 heat shock gene in the rat cingulate and retrosplenial cortex. Brain Res. 1995;687(1-2):114-124. DOI:10.1016/0006-8993(95)00477-8

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