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Tonabersat

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Catalog No. T17116Cas No. 175013-84-0
Alias USL-260, USL260, SB-220453, SB220453

Tonabersat (SB-220453) is a novel and orally available gap-junction modulator and CSD (Cortical spreading depression) inhibitor that regulates cellular communication between trigeminal ganglion neuronal cells and glial cells and inhibits neurogenic inflammation for the treatment of migraine and epilepsy.

Tonabersat

Tonabersat

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Purity: 99.49%
Catalog No. T17116Alias USL-260, USL260, SB-220453, SB220453Cas No. 175013-84-0
Tonabersat (SB-220453) is a novel and orally available gap-junction modulator and CSD (Cortical spreading depression) inhibitor that regulates cellular communication between trigeminal ganglion neuronal cells and glial cells and inhibits neurogenic inflammation for the treatment of migraine and epilepsy.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$997-10 days7-10 days
5 mg$249-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.49%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Tonabersat (SB-220453) is a novel and orally available gap-junction modulator and CSD (Cortical spreading depression) inhibitor that regulates cellular communication between trigeminal ganglion neuronal cells and glial cells and inhibits neurogenic inflammation for the treatment of migraine and epilepsy.
In vitro
Tonabersat is a novel benzopyran derivative that blocks cortical spreading depression, which is thought to be involved in migraine attacks.[1]
In vivo
Methods: Fourteen days after inoculation with MDA231-BrM2 cells, mice were treated with Tonabersat (10 mg/kg), Meclofenamic Acid (10 mg/kg), and Carboplatin. Brain metastatic lesions were quantified by BLI following the indicated regimens.
Results: Treatment with either Tonabersat or Meclofenamic Acid as a single agent significantly inhibited the progression of metastatic lesions. The addition of Carboplatin to either agent significantly inhibited brain metastasis. [2]
SynonymsUSL-260, USL260, SB-220453, SB220453
Chemical Properties
Molecular Weight391.82
FormulaC20H19ClFNO4
Cas No.175013-84-0
SmilesN(C(=O)C1=CC(Cl)=C(F)C=C1)[C@H]2C=3C(OC(C)(C)[C@H]2O)=CC=C(C(C)=O)C3
Relative Density.1.38g/cm3
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (204.18 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (8.42 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
DMSO
1mg5mg10mg50mg
1 mM2.5522 mL12.7610 mL25.5219 mL127.6096 mL
5 mM0.5104 mL2.5522 mL5.1044 mL25.5219 mL
10 mM0.2552 mL1.2761 mL2.5522 mL12.7610 mL
20 mM0.1276 mL0.6380 mL1.2761 mL6.3805 mL
50 mM0.0510 mL0.2552 mL0.5104 mL2.5522 mL
100 mM0.0255 mL0.1276 mL0.2552 mL1.2761 mL

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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:
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2 Enter the in vivo formulation:
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