Cart
sales@molnova.com
CNQX
CAS No. 115066-14-3
CNQX( FG9065 )
Catalog No. M20706 CAS No. 115066-14-3
CNQX is a competitive non-NMDA glutamate receptor antagonist (IC50s = 0.3 and 1.5 μM for AMPA and kainate receptors respectively).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 43 | In Stock |
|
| 5MG | 39 | In Stock |
|
| 10MG | 54 | In Stock |
|
| 25MG | 118 | In Stock |
|
| 50MG | 183 | In Stock |
|
| 100MG | 294 | In Stock |
|
| 200MG | 443 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCNQX
-
NoteResearch use only, not for human use.
-
Brief DescriptionCNQX is a competitive non-NMDA glutamate receptor antagonist (IC50s = 0.3 and 1.5 μM for AMPA and kainate receptors respectively).
-
DescriptionCNQX is a competitive non-NMDA glutamate receptor antagonist (IC50s = 0.3 and 1.5 μM for AMPA and kainate receptors respectively).
-
In Vitro——
-
In VivoAnimal Model:Male Wistar rats weighing 180-200 g Dosage:0.75, 1.5, and 3 mg/kg Administration:IP; 20 min before testing Result:Decreased the number of cocaine (IV; 0.25 mg/infusion) responses in a dose-dependent manner during the first 15-min cocaine-free interval.
-
SynonymsFG9065
-
PathwayNeuroscience
-
TargetGluR
-
RecptorAMPA
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number115066-14-3
-
Formula Weight232.15
-
Molecular FormulaC9H4N4O4
-
Purity>98% (HPLC)
-
SolubilityDMSO:30 mg/mL (129.23 mM)
-
SMILES[O-][N+](=O)c1cc2[nH]c(=O)c(=O)[nH]c2cc1C#N
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Blake J F Brown M W Collingridge G L . CNQX blocks acidic amino acid induced depolarizations and synaptic components mediated by non-NMDA receptors in rat hippocampal slices[J]. Neuroscience letters 1988 89(2):182-186.
molnova catalog
related products
-
Ro0711401
Ro0711401 is an agonist of mGlu1 receptor.
-
VU 0469650
VU 0469650 is a potent and selective negative allosteric modulator of mGluR1 (IC50 = 99 nM).
-
MMPIP hydrochloride
MMPIP hydrochloride is a selective antagonist of allosteric mGluR7. MMPIP hydrochloride can be used in research on the roles of mGluR7 on central nervous system functions.
