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BCR-ABL-IN-13

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Catalog No. T212936 Copy Product Info
Purity: 99.92%
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BCR-ABL-IN-13 is a dual c-Src and Abl inhibitor, with a Ki value of 0.55 μM against c-Src, 0.10 μM against wild-type Abl, and 0.40 μM against the AblT315I mutant. BCR-ABL-IN-13 exerts competitive/mixed-type inhibitory effects on wild-type Abl, and non-competitive inhibitory effects on the drug-resistant AblT315I mutant. BCR-ABL-IN-13 is used in chronic myeloid leukemia research models to study kinase inhibition profiles, resistance-associated Abl mutations, and signaling pathway modulation in oncogenic tyrosine kinase systems.

BCR-ABL-IN-13

Cas No. 607702-99-8
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$39-In Stock
5 mg$89-In Stock
10 mg$139-In Stock
25 mg$278-In Stock
50 mg$446-In Stock
100 mg$712-In Stock
1 mL x 10 mM (in DMSO)$98-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Batch Information

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Purity:99.92%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
BCR-ABL-IN-13 is a dual c-Src and Abl inhibitor, with a Ki value of 0.55 μM against c-Src, 0.10 μM against wild-type Abl, and 0.40 μM against the AblT315I mutant. BCR-ABL-IN-13 exerts competitive/mixed-type inhibitory effects on wild-type Abl, and non-competitive inhibitory effects on the drug-resistant AblT315I mutant. BCR-ABL-IN-13 is used in chronic myeloid leukemia research models to study kinase inhibition profiles, resistance-associated Abl mutations, and signaling pathway modulation in oncogenic tyrosine kinase systems.
Targets & IC50
Abl:0.10 μM (Ki), c-Src:0.55 μM (Ki), Abl (T315I):0.40 μM (Ki)
In vitro
Methods:The effects of BCR-ABL-IN-13 on mouse myeloid clones expressing imatinib-sensitive and drug-resistant Bcr-Abl were detected.
Results:BCR-ABL-IN-13 exerted potent cytotoxicity against all the above cell lines [1].
Chemical Properties
Molecular Weight363.41
FormulaC16H11F2N3OS2
Cas No.607702-99-8
SmilesO=C(NC1=NN=C(S1)SCC2=CC=C(F)C=C2)C3=CC=C(F)C=C3
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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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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Related Tags: BCR-ABL-IN-13 in vitro | BCR-ABL-IN-13 formula | BCR-ABL-IN-13 molecular weight