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Ripretinib

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Catalog No. T8482Cas No. 1442472-39-0
Alias DCC-2618

Ripretinib (DCC-2618) is an orally bioavailable inhibitor of (KIT) and (PDGFRA).

Ripretinib

Ripretinib

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Purity: 99.62%
Catalog No. T8482Alias DCC-2618Cas No. 1442472-39-0
Ripretinib (DCC-2618) is an orally bioavailable inhibitor of (KIT) and (PDGFRA).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$68In StockIn Stock
2 mg$98In StockIn Stock
5 mg$168In StockIn Stock
10 mg$289In StockIn Stock
25 mg$455In StockIn Stock
50 mg$683In StockIn Stock
100 mg$957-In Stock
1 mL x 10 mM (in DMSO)$213In 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:99.62%
Appearance:Solid
Color:White
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Product Introduction

Ripretinib AI Summary
Ripretinib exhibits cytotoxicity in mouse BA/F3 cells and shows potent inhibitory activity against various Kit mutations, specifically Kit exon 11 deletion, D816H, and T670I mutants, demonstrating IC50 values of 13.0 nM and 9.2 nM for the wild-type KIT and T670I mutant, respectively. Its inhibition activity is weaker against KIT D816V mutant and PDGFRalpha D842V mutant with IC50 values of 25000.0 nM and 36000.0 nM respectively. Additionally, the compound displays potent inhibitory effects against TEL-fused PDGFRalpha and PDGFRbeta, indicating a broad spectrum of bioactivity against multiple cellular targets and demonstrating a selectivity index over KDR..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Ripretinib (DCC-2618) is an orally bioavailable inhibitor of (KIT) and (PDGFRA).
SynonymsDCC-2618
Chemical Properties
Molecular Weight510.36
FormulaC24H21BrFN5O2
Cas No.1442472-39-0
SmilesCCn1c2cc(NC)ncc2cc(-c2cc(NC(=O)Nc3ccccc3)c(F)cc2Br)c1=O
Relative Density.1.544 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 41.67 mg/mL (81.65 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 2 mg/mL (3.92 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 mM1.9594 mL9.7970 mL19.5940 mL97.9701 mL
5 mM0.3919 mL1.9594 mL3.9188 mL19.5940 mL
10 mM0.1959 mL0.9797 mL1.9594 mL9.7970 mL
20 mM0.0980 mL0.4899 mL0.9797 mL4.8985 mL
50 mM0.0392 mL0.1959 mL0.3919 mL1.9594 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

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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