CNQX disodium salt
Tocris Bioscience, part of Bio-Techne | Catalog # 1045
Potent non-NMDA iGluR antagonist; more water soluble form of CNQX (Cat. No. 0190)
Key Product Details
Description
Potent non-NMDA iGluR antagonist; more water soluble form of CNQX (Cat. No. 0190)
Product Description
CNQX disodium salt is a more water-soluble disodium salt of the AMPA and kainate antagonist CNQX (Cat. No. 0190), which is an AMPA and kainate receptor antagonist (IC50 values are 0.3 μM, 1.5 μM for AMPA and kainate receptors, respectively). CNQX is also an antagonist at the glycine modulatory site on the NMDA receptor complex (IC50 = 25 μM). CNQX can be used to isolate GABAA receptor mediated spontaneous inhibitory postsynaptic currents and antagonizes non-NMDA receptor-mediated responses in cultured cerebellar granule cells. CNQX shows neuroprotective effects in models of ischemia and inhibits seizure-like activity in hippocampal neurons.Product Specifications
Molecular Weight
276.12
Formula
C9H2N4O4Na2
Storage
Desiccate at RT
Purity
≥98% (HPLC)
Chemical Name
6-Cyano-7-nitroquinoxaline-2,3-dione disodium
CAS Number
479347-85-8
PubChem ID
2821
InChI Key
YCXDDPGRZKUGDG-UHFFFAOYSA-L
SMILES
[Na+].[Na+].[O-]C1=C([O-])N=C2C=C(C(=CC2=N1)C#N)[N+]([O-])=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 2.76 | 10 |
Preparing Stock Solutions
for CNQX disodium salt
The following data is based on the product molecular weight 276.12
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 36.22 mL | 181.08 mL | 362.16 mL |
| 0.5 mM | 7.24 mL | 36.22 mL | 72.43 mL |
| 1 mM | 3.62 mL | 18.11 mL | 36.22 mL |
| 5 mM | 0.72 mL | 3.62 mL | 7.24 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Watkins Structure-activity relationships in the development of excitatory amino acid receptor agonists and competitive antagonists. TiPS 1990 PMID: 2155495
- King Antagonism of synaptic potentials in ventral horn neurones by 6-cyano-7-nitroquinoxaline-2,3-dione: a study in the rat spinal cord in vitro. Br.J.Pharmacol. 1992 PMID: 1358390
- Long Effect of 6-cyano-2,3-dihydroxy-7-nitro-quinoxaline (CNQX) on dorsal root-, NMDA-, kainate and quisqualate-mediated depolarization of rat motoneurones in vitro. Br.J.Pharmacol. 1990 PMID: 1976402
- Honore Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonists. Science 1988 PMID: 2899909
Product Specific Notices for CNQX disodium salt
For research use only
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