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Vodobatinib

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Catalog No. T8882Cas No. 1388803-90-4
Alias K-0706

Vodobatinib (K-0706) is a novel 3rd generation (3G) TKI effective against wild-type and mutated BCR-ABL1 with limited off-target activity.

Vodobatinib

Vodobatinib

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Purity: 99.55%
Catalog No. T8882Alias K-0706Cas No. 1388803-90-4
Vodobatinib (K-0706) is a novel 3rd generation (3G) TKI effective against wild-type and mutated BCR-ABL1 with limited off-target activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$31In StockIn Stock
5 mg$72In StockIn Stock
10 mg$118In StockIn Stock
25 mg$223In StockIn Stock
50 mg$358In StockIn Stock
100 mg$556In StockIn Stock
500 mg$1,343-In Stock
1 mL x 10 mM (in DMSO)$79In StockIn 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:99.55%
Appearance:Solid
Color:White
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Product Introduction

Vodobatinib AI Summary
Vodobatinib demonstrates a brain-to-plasma drug level ratio (BPR) of 0.4 in C57BL6 mice when administered at a dosage of 30 mg/kg orally, suggesting moderate brain distribution compared to plasma after 1 hour, as analyzed by LC/MS. It is a potent inhibitor of wild type BCR-ABL phosphorylation in mouse BaF3 cells, with an IC50 of 0.9 nM, and also shows inhibitory activity against various BCR-ABL mutants (L248R, Y253H, E255V, T315I) with IC50 values ranging from 154.0 nM to 1967.0 nM. The compound exhibits good tissue distribution, evidenced by a plasma concentration of 4798.0 ng/ml and a brain concentration of 1901.0 ng/g at the same dose and time point..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Vodobatinib (K-0706) is a novel 3rd generation (3G) TKI effective against wild-type and mutated BCR-ABL1 with limited off-target activity.
Targets&IC50
BCR-ABL1:7 nM (IC50)
SynonymsK-0706
Chemical Properties
Molecular Weight453.92
FormulaC27H20ClN3O2
Cas No.1388803-90-4
SmilesCc1ccc(cc1C#Cc1cnc2ccccc2c1)C(=O)NNC(=O)c1c(C)cccc1Cl
Relative Density.1.35 g/cm3 (Predicted)
Storage & Solubility Information
Storagekeep away from moisture,store 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: 125 mg/mL (275.38 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 2 mg/mL (4.41 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 mM2.2030 mL11.0152 mL22.0303 mL110.1516 mL
5 mM0.4406 mL2.2030 mL4.4061 mL22.0303 mL
10 mM0.2203 mL1.1015 mL2.2030 mL11.0152 mL
20 mM0.1102 mL0.5508 mL1.1015 mL5.5076 mL
50 mM0.0441 mL0.2203 mL0.4406 mL2.2030 mL
100 mM0.0220 mL0.1102 mL0.2203 mL1.1015 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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