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Relutrigine

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Catalog No. T69652Cas No. 2392951-29-8
Alias PRAX-562, PRAX562, PRAX 562

Relutrigine (PRAX-562) is an orally active, long-acting sodium current inhibitor that preferentially suppresses sustained INa induced by TX-II or SCN8A N1768D mutations (IC50=141/75 nM). It reduces neuronal intrinsic excitability and may be used for anticonvulsant therapy.

Relutrigine

Relutrigine

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Purity: 99.68%
Catalog No. T69652Alias PRAX-562, PRAX562, PRAX 562Cas No. 2392951-29-8
Relutrigine (PRAX-562) is an orally active, long-acting sodium current inhibitor that preferentially suppresses sustained INa induced by TX-II or SCN8A N1768D mutations (IC50=141/75 nM). It reduces neuronal intrinsic excitability and may be used for anticonvulsant therapy.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$289-In Stock
5 mg$723-In Stock
10 mg$1,120-In Stock
25 mg$1,670-In Stock
50 mg$2,180-In Stock
100 mg$2,800-In Stock
1 mL x 10 mM (in DMSO)$648-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:99.68%
Appearance:Solid
Color:Orange
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Product Introduction

Bioactivity
Description
Relutrigine (PRAX-562) is an orally active, long-acting sodium current inhibitor that preferentially suppresses sustained INa induced by TX-II or SCN8A N1768D mutations (IC50=141/75 nM). It reduces neuronal intrinsic excitability and may be used for anticonvulsant therapy.
In vitro
Relutrigine (0.001–10,000 µM) inhibits the hNaV1.6 sustained sodium channel with a persistent INa preference. Relutrigine (0.3 µM) significantly reduces intrinsic excitability in wild-type CA1 pyramidal neurons [1].
In vivo
Relutrigine (0.3–40 mg/kg; oral; single dose) dose-dependently protected against maximal electroconvulsive seizure (MES)-induced tonic hindlimb seizures in male CD-1 mice [1].
SynonymsPRAX-562, PRAX562, PRAX 562
Chemical Properties
Molecular Weight407.27
FormulaC15H11F6N5O2
Cas No.2392951-29-8
SmilesC(OCC)(F)(F)C=1N2C(=NN1)C=NC(=C2)C=3C=C(F)C(OCC(F)(F)F)=NC3
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 (196.43 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4554 mL12.2769 mL24.5537 mL122.7687 mL
5 mM0.4911 mL2.4554 mL4.9107 mL24.5537 mL
10 mM0.2455 mL1.2277 mL2.4554 mL12.2769 mL
20 mM0.1228 mL0.6138 mL1.2277 mL6.1384 mL
50 mM0.0491 mL0.2455 mL0.4911 mL2.4554 mL
100 mM0.0246 mL0.1228 mL0.2455 mL1.2277 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:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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