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Razaxaban hydrochloride

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Catalog No. T12694Cas No. 405940-76-3
Alias DPC 906 hydrochloride, BMS 561389 hydrochloride

Razaxaban hydrochloride is a highly potent, selective and orally active inhibitor of factor Xa(Ki of 0.19 nM),has strongly antithrombotic activity.

Razaxaban hydrochloride

Razaxaban hydrochloride

Copy Product Info
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Catalog No. T12694Alias DPC 906 hydrochloride, BMS 561389 hydrochlorideCas No. 405940-76-3
Razaxaban hydrochloride is a highly potent, selective and orally active inhibitor of factor Xa(Ki of 0.19 nM),has strongly antithrombotic activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$1,6706-8 weeks6-8 weeks
50 mg$2,1806-8 weeks6-8 weeks
100 mg$2,8006-8 weeks6-8 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Razaxaban hydrochloride is a highly potent, selective and orally active inhibitor of factor Xa(Ki of 0.19 nM),has strongly antithrombotic activity.
Targets&IC50
Thrombin: 540 nM (ki), FXa:ki:0.19 nM
In vitro
Razaxaban shows good Caco-2 permeability. The anticoagulant activity of Razaxaban is evaluated in the in vitro human plasma activated partial thromboplastin time (aPTT) and human prothrombin time (PT) assays. Razaxaban shows a doubling of aPTT and PT at 6.1 μM and 2.1 μM, respectively. .
In vivo
Traetment with Razaxaban inhibits thrombus formation in a dose-dependent manner (ID50 of 1.6 μmol/kg/h in the rabbit arterio-venous shunt thrombosis model).
SynonymsDPC 906 hydrochloride, BMS 561389 hydrochloride
Chemical Properties
Molecular Weight564.92
FormulaC24H21ClF4N8O2
Cas No.405940-76-3
SmilesCl.O=C(NC1=CC=C(C=C1F)N2C=CN=C2CN(C)C)C3=CC(=NN3C=4C=CC=5ON=C(N)C5C4)C(F)(F)F
Relative Density.1.31g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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

You can also refer to dose conversion for different animals. More Dose Conversion

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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