Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C8H2N4O6
- Molecular weight
- 250.12 g/mol
- IUPAC name
- 6,7-dinitroquinoxaline-2,3-dione
- SMILES
- C1=C(C(=CC2=NC(=O)C(=O)N=C21)[N+](=O)[O-])[N+](=O)[O-]
- InChIKey
- YEUPBRRGMWBCEB-UHFFFAOYSA-N
- XLogP
- -0.7
- Polar surface area
- 151 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Research
1,155 papers- DNQX in the nucleus accumbens inhibits cocaine-induced conditioned place preference.Brain research · 1995
- DNQX-induced toxicity in cultured rat hippocampal neurons: an apparent AMPA receptor-independent effect?Neurochemistry international · 2003
- Selective excitatory actions of DNQX and CNQX in rat thalamic neurons.Journal of neurophysiology · 2010
- Aniracetam and DNQX affect the acquisition of rapid tolerance to ethanol in mice.Pharmacology, biochemistry, and behavior · 2009
- DNQX inhibits phencyclidine (PCP) and ketamine induction of the hsp70 heat shock gene in the rat cingulate and retrosplenial cortex.Brain research · 1995
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 249.997
Show 3 more facts
- chemical formula
- C₈H₂N₄O₆
- canonical SMILES
- C1=C(C(=CC2=NC(=O)C(=O)N=C21)[N+](=O)[O-])[N+](=O)[O-]
- Commons category
- DNQX
Sources (2)
via Wikidata · CC0