Organic sodium salts

Sigma Aldrich Fine Chemicals Biosciences Poly-L-glutamic acid sodium salt | 26247-79-0 | MFCD00081868 | 100mg

Poly-L-glutamic acid sodium salt | Mol Wt: 15,000-50,000 | 26247-79-0 | MFCD00081868 | 100mg

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Sigma Aldrich Fine Chemicals Biosciences Carboxymethylcellulose sodium salt Medium viscosity | 9004-32-4 | MFCD00081472 | 1kg

Carboxymethylcellulose sodium salt Medium viscosityPurity: MW: | 9004-32-4 | MFCD00081472 | 1kg

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000724322 DNQX DISODIUM SALT 50MG

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000724337 DNQX DISODIUM SALT 100MG

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000691031 DNQX DISODIUM SALT 25MG

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Thermo Scientific Production Chemicals and Services DOE AND INGALLS

NC3894470 SODIUM ACETATE TRIHY USP 85LB

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eMolecules​ 865-47-4 | Potassium tert-butoxide 20% solution in tetrahydrofuran | Oakwood Chemical | MFCD00012162 | 112.213 | C4H9KO | 0.000 | [K+].CC(C)(C)[O-] | 25g | 537708080

Potassium tert-butoxide 20% solution in tetrahydrofuran | Oakwood Chemical | 865-47-4 | MFCD00012162 | 112.213 | C4H9KO | 0.000 | [K+].CC(C)(C)[O-] | 25g | 537708080

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eMolecules​ 865-47-4 | Potassium tert-butoxide, Trace metals grade 99.8% | Oakwood Chemical | MFCD00012162 | 112.213 | C4H9KO | 99.000 | [K+].CC(C)(C)[O-] | 25g | 537709487

Potassium tert-butoxide, Trace metals grade 99.8% | Oakwood Chemical | 865-47-4 | MFCD00012162 | 112.213 | C4H9KO | 99.000 | [K+].CC(C)(C)[O-] | 25g | 537709487

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eMolecules​ 865-47-4 | Potassium tert-butoxide 20% solution in tetrahydrofuran | Oakwood Chemical | MFCD00012162 | 112.213 | C4H9KO | 0.000 | [K+].CC(C)(C)[O-] | 500g | 537708082

Potassium tert-butoxide 20% solution in tetrahydrofuran | Oakwood Chemical | 865-47-4 | MFCD00012162 | 112.213 | C4H9KO | 0.000 | [K+].CC(C)(C)[O-] | 500g | 537708082

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Medchemexpress LLC DNQX (FG 9041) | 2379-57-9 | C8H4N4O6 | 200 MG

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DNQX (FG 9041) is a quinoxaline derivative and a selective, potent competitive non-NMDA glutamate receptor antagonist. It is characterized by its activity against various glutamate receptors.

• Selective, potent competitive non-NMDA glutamate receptor antagonist
• Targets AMPA receptors with an IC50 of 0.5 μM
• Targets kainate receptors with an IC50 of 2 μM
• Targets NMDA receptors with an IC50 of 40 μM
• Selectively depolarizes thalamic reticular nucleus (TRN) neurons in vitro
• Diminishes phencyclidine (PCP) induced hsp70 induction in vivo

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Apexbio Technology LLC DIBUTYRYL-CAMP SODI. SALT 50MG

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DIBUTYRYL-CAMP SODI. SALT 50MG APEXBIO TECHNOLOGIES

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Medchemexpress LLC Glycerophosphoric acid (disodium salt hydrate) (α and β mixture) | 98.0% | 500 MG

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Glycerophosphoric acid (disodium salt hydrate) (α and β mixture) is a complex that contains both alpha and beta glycerophosphoric acid isomers.

• Is a complex mixture of isomers.
• Suitable for biochemical assay applications.

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Medchemexpress LLC CNQX | 115066-14-3 | C9H4N4O4 | 1 ML

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CNQX (FG9065) is a potent and competitive AMPA/kainate receptor antagonist with IC50s of 0.3 μM and 1.5 μM, respectively. It is also a competitive non-NMDA receptor antagonist, capable of blocking the expression of fear-potentiated startle in rats. This product is for research use only.

• Potent and competitive AMPA/kainate receptor antagonist
• IC50s of 0.3 μM for AMPA and 1.5 μM for kainate receptors
• Competitive non-NMDA receptor antagonist
• Blocks expression of fear-potentiated startle in rats
• Purity of 99.38%
• Appears as a white to yellow solid
• Soluble in DMSO at 20 mg/mL

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Medchemexpress LLC NBQX | 118876-58-7 | C12H8N4O6S | 50 MG

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NBQX (FG9202) is a highly selective and competitive antagonist of the AMPA receptor, exhibiting both neuroprotective and anticonvulsant properties.

• Acts as a highly selective and competitive AMPA receptor antagonist.
• Possesses neuroprotective activity.
• Demonstrates anticonvulsant activity.
• Shows high affinity for AMPA and kainate binding sites.
• Exhibits minimal or no affinity for the glutamate recognition site within the NMDA receptor complex.

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Medchemexpress LLC DNQX | 2379-57-9 | C8H4N4O6 | 50 MG

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DNQX (FG 9041) is a quinoxaline derivative that acts as a selective, potent competitive non-NMDA glutamate receptor antagonist. It exhibits IC50 values of 0.5 μM for AMPA receptors, 2 μM for kainate receptors, and 40 μM for NMDA receptors.

• Selective non-NMDA glutamate receptor antagonist
• Potent competitive antagonist
• IC50s: 0.5 μM (AMPA), 2 μM (kainate), 40 μM (NMDA)
• High purity (99.67%)
• Available as solid and solution
• In vivo dissolution protocols provided
• In vitro, depolarizes thalamic reticular nucleus (TRN) neurons
• In vivo, diminishes phencyclidine (PCP) hsp70 induction

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