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NBQX disodium

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Catalog No. T25853Cas No. 479347-86-9
Alias NBQX 2Na, FG9202 disodium

NBQX disodium is a highly selective, competitive AMPA receptor antagonist with neuroprotective and anticonvulsant activity. NBQX disodium is a salt of NBQX. NBQX disodium 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.

NBQX disodium

NBQX disodium

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🥰Excellent
Purity: 97.6%
Catalog No. T25853Alias NBQX 2Na, FG9202 disodiumCas No. 479347-86-9
NBQX disodium is a highly selective, competitive AMPA receptor antagonist with neuroprotective and anticonvulsant activity. NBQX disodium is a salt of NBQX. NBQX disodium 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.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$35In StockIn Stock
5 mg$80In StockIn Stock
10 mg$123In StockIn Stock
25 mg$247In StockIn Stock
50 mg$372In StockIn Stock
100 mg$558In StockIn Stock
1 mL x 10 mM (in DMSO)$88In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:97.6%
Appearance:Solid
Color:Yellow to Brown
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Product Introduction

Bioactivity
Description
NBQX disodium is a highly selective, competitive AMPA receptor antagonist with neuroprotective and anticonvulsant activity. NBQX disodium is a salt of NBQX. NBQX disodium 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.
Targets&IC50
AMPA:0.7 ± 0.1 μM, Kainic acid:0.7 ± 0.03 μM
In vitro
In HIP-009 cells, NBQX disodium salt inhibited both AMPA or kainic acid (KA) induced signals in a concentration-dependent manner, with IC50 values being 0.7 ± 0.1 and 0.7 ± 0.03 μM, respectively. The AMPA-evoked calcium rise was completely inhibited by NBQX disodium salt, whereas 68.6% ± 1.3% inhibition of the KA-induced signal was observed with 30 μM of NBQX disodium salt treatment.[1]
In vivo
Administration of NBQX disodium (FG9202; 20 mg/kg, i.p.; for 3 days) exhibits a reduction in PTZ-induced seizures. [2]
In a rat model of focal ischemia, NBQX disodium demonstrates neuroprotective effects when administered intravenously as a bolus dose of 30 mg/kg at the time of MCA occlusion, followed by an additional dose at 1 hour post-occlusion. [3]
SynonymsNBQX 2Na, FG9202 disodium
Chemical Properties
Molecular Weight380.2415
FormulaC12H6N4Na2O6S
Cas No.479347-86-9
SmilesO=C1[N-]C2=C([N-]C1=O)C3=CC=CC(S(=O)(N)=O)=C3C([N+]([O-])=O)=C2.[Na+].[Na+]
Storage & Solubility Information
Storagestore at low temperature,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 30 mg/mL (78.9 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.26 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM2.6299 mL13.1495 mL26.2991 mL131.4954 mL
5 mM0.5260 mL2.6299 mL5.2598 mL26.2991 mL
10 mM0.2630 mL1.3150 mL2.6299 mL13.1495 mL
20 mM0.1315 mL0.6575 mL1.3150 mL6.5748 mL
50 mM0.0526 mL0.2630 mL0.5260 mL2.6299 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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