Organic sodium salts
Apexbio Technology LLC CNQX 115066-14-3 50mg
CNQX (CAS 115066-14-3) is a selective and competitive antagonist of AMPA and kainate subtype ionotropic glutamate receptors In hippocampal slice preparations superfusion with CNQX at concentrations of 2 5 M reversibly inhibits excitatory post-synaptic potentials mediated by Schaffer collaterals and mossy fibers while preserving both fast and slow GABAergic inhibitory responses In behavioral studies bilateral infusion of CNQX into the amygdala or dorsal hippocampus prior to testing partially suppresses the expression of conditioned avoidance responses with complete blockade observed at specific doses CNQX is widely utilized to dissect excitatory synaptic transmission and investigate non-NMDA receptor functions in neurophysiological and behavioral research
Sigma Aldrich Fine Chemicals Biosciences CNQX disodium salt hydrate >=98% (HPLC), solid | 115066-14-3 (free base) | MFCD09953908 | 100MG
CNQX disodium salt hydrate >=98% (HPLC), solid | Purity: >=98% (HPLC) | 115066-14-3 (free base) | MFCD09953908 | 100MG
eMolecules 1907-33-1 | Lithium tert-butoxide | Oakwood Chemical | MFCD00050479 | 80.060 | C4H9LiO | 0.000 | [Li+].CC(C)(C)[O-] | 5g | 703157388
Lithium tert-butoxide | Oakwood Chemical | 1907-33-1 | MFCD00050479 | 80.060 | C4H9LiO | 0.000 | [Li+].CC(C)(C)[O-] | 5g | 703157388
Sigma Aldrich Fine Chemicals Biosciences ADENOSINE-13C10,15N5 52-M 25MG
Adenosine-13C10,15N5 52-monophosphate
Sigma Aldrich Fine Chemicals Biosciences Sodium acetate buffer solution BioXtra, pH 7.0+/-0.05 (25 C), for molecular biology, 3 M, non-sterile; 0.2 mum filtered | 126-96-5 | MFCD00137248 | 1L
Sodium acetate buffer solution BioXtra, pH 7.0+/-0.05 (25 C), for molecular biology, 3 M, non-sterile; 0.2 mum filtered | 126-96-5 | MFCD00137248 | 1L
Sigma Aldrich Fine Chemicals Biosciences Dextran sulfate sodium salt from Leuconostoc spp. average mol wt 9,000-20,000 | 9011-18-1 | MFCD00081551 | 10G
Dextran sulfate sodium salt from Leuconostoc spp. average mol wt 9,000-20,000 | 9011-18-1 | MFCD00081551 | 10G
Medchemexpress LLC CNQX disodium | 479347-85-8 | C9H2N4Na2O4 | 5 MG
CNQX disodium (FG9065 disodium) is a potent and competitive AMPA/kainate receptor antagonist. It blocks the expression of fear-potentiated startle in rats and is a competitive non-NMDA receptor antagonist. It is suitable for in vitro and in vivo research.
- Potent and competitive AMPA/kainate receptor antagonist
- Blocks expression of fear-potentiated startle
- Competitive non-NMDA receptor antagonist
- Suitable for neurological disease research
- Inhibitor of ionotropic glutamate receptors
Pfaltz & Bauer Dimethyldithiocarbamic acid s 100G | 128-04-1
Dimethyldithiocarbamic acid s 100G | 128-04-1
TARGETMOL CHEMICALS INC NBQX DISODIUM 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. NBQX Disodium (FG9202 disodium) is a highly selective competitive AMPA receptor antagonist with neuroprotective and anticonvulsant activity. NBQX Disodium is a salt of NBQX. NBQX is a potent and selective AMPA/rhodosinate receptor antagonist that can be used to antagonize the excitatory toxicity of glutamate. It has anticonvulsant effects in rodent models. purity: 98%
![eMolecules 865-48-5 | Sodium tert-butoxide solution 2M in THF | Oakwood Chemicals | MFCD00040575 | 96.105 | C4H9NaO | 0.000 | [Na+].CC(C)(C)[O-] | 5g | 480149015](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000170084.jpg-250.jpg)
eMolecules 865-48-5 | Sodium tert-butoxide solution 2M in THF | Oakwood Chemicals | MFCD00040575 | 96.105 | C4H9NaO | 0.000 | [Na+].CC(C)(C)[O-] | 5g | 480149015
Sodium tert-butoxide solution 2M in THF | Oakwood Chemicals | 865-48-5 | MFCD00040575 | 96.105 | C4H9NaO | 0.000 | [Na+].CC(C)(C)[O-] | 5g | 480149015
Medchemexpress LLC NBQX (FG9202) | 118876-58-7 | C12H8N4O6S | 1 ML
NBQX (FG9202) is a highly selective and competitive AMPA receptor antagonist. It possesses neuroprotective and anticonvulsant activities. NBQX exhibits high affinity for AMPA and kainate binding sites, with minimal or no affinity for the glutamate recognition site on the NMDA receptor complex.
- Highly selective and competitive AMPA receptor antagonist
- Neuroprotective activity
- Anticonvulsant activity
- High affinity for AMPA and kainate binding sites
- Little to no affinity for the glutamate recognition site on the NMDA receptor complex