DNQX

DNQX

Names
Preferred IUPAC name 6,7-Dinitro-1,4-dihydroquinoxaline-2,3-dione
Identifiers
CAS Number	2379-57-9 N
3D model (JSmol)	Interactive image
ChemSpider	3123097 Y
DrugBank	DB03759 Y
PubChem CID	3899541
UNII	62T278S1MX
CompTox Dashboard (EPA)	DTXSID50274395
InChI InChI=1S/C8H4N4O6/c13-7-8(14)10-4-2-6(12(17)18)5(11(15)16)1-3(4)9-7/h1-2H,(H,9,13)(H,10,14) Y Key: RWVIMCIPOAXUDG-UHFFFAOYSA-N Y InChI=1S/C8H4N4O6/c13-7-8(14)10-4-2-6(12(17)18)5(11(15)16)1-3(4)9-7/h1-2H,(H,9,13)(H,10,14) Key: RWVIMCIPOAXUDG-UHFFFAOYSA-N
SMILES O=c2[nH]c1cc(N(=O)=O)c(N(=O)=O)cc1[nH]c2=O
Properties
Chemical formula	C8H4N4O6
Molar mass	252.142 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YN ?)
Infobox references

DNQX (6,7-dinitroquinoxaline-2,3-dione) is a competitive antagonist at AMPA and kainate receptors, two ionotropic glutamate receptor (iGluR) subfamilies.^[1] It is used in a variety of molecular biology subfields, notably neurophysiology, to assist researchers in determining the properties of various types of ion channels and their potential applications in medicine.

See also[]

• Quinoxalinedione
• CNQX

References[]

External links[]

• DNQX MSDS

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