D0540

DNQX

≥98% (TLC)

• Synonyme(s) : 6,7-Dinitroquinoxaline-2,3(1H,4H)-dione
• Formule empirique (notation de Hill): C₈H₄N₄O₆
• Numéro CAS: 2379-57-9
• Poids moléculaire : 252.14
• Numéro MDL: MFCD00069257
• Code UNSPSC : 51111800
• ID de substance PubChem : 24277973
• Nomenclature NACRES : NA.77

Propriétés

• Niveau de qualité: 200
• Pureté: ≥98% (TLC)
• Forme: powder
• Chaîne SMILES: [O-][N+](=O)c1cc2NC(=O)C(=O)Nc2cc1[N+]([O-])=O
• 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)
• Clé InChI: RWVIMCIPOAXUDG-UHFFFAOYSA-N
• Informations sur le gène: human ... GRIA1(2890) , GRIA2(2891) , GRIK1(2897) , GRIK2(2898) , GRIK3(2899) , GRIK4(2900) , GRIK5(2901) ; mouse ... Gria1(14799) ; rat ... Gria1(50592) , Grik1(29559) , Grik4(24406) , Grin2a(24409)

Description

Application

DNQX has been used to block N-Methyl-D-aspartic acid (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors in various experiments.

Actions biochimiques/physiologiques

DNQX is a quinoxaline derivative.

A competitive kainate, quisqualate (non-NMDA) glutamate receptor antagonist.

Caractéristiques et avantages

This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound is featured on the Glutamate Receptors (Ion Channel Family) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.