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EGFR-IN-47

Catalog No. T63185 Copy Product Info
Purity: 98.78%
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EGFR-IN-47 (compound 14aj) is a potent, fourth-generation, and orally active EGFR inhibitor. It specifically targets the EGFR L858R/T790M/C797S triple mutation with an IC50 of 0.01 uM. In NSCLC research, EGFR-IN-47 effectively overcomes C797S-mediated resistance to Osimertinib by inhibiting the phosphorylation of EGFR and its downstream mediators, subsequently inducing cell cycle arrest and apoptosis.

EGFR-IN-47

Copy Product Info
😃Good
Catalog No. T63185

EGFR-IN-47 (compound 14aj) is a potent, fourth-generation, and orally active EGFR inhibitor. It specifically targets the EGFR L858R/T790M/C797S triple mutation with an IC50 of 0.01 uM. In NSCLC research, EGFR-IN-47 effectively overcomes C797S-mediated resistance to Osimertinib by inhibiting the phosphorylation of EGFR and its downstream mediators, subsequently inducing cell cycle arrest and apoptosis.

EGFR-IN-47
Cas No. 3034649-73-2
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$81-In Stock
5 mg$197-In Stock
10 mg$317-In Stock
25 mg$633-In Stock
50 mg$987-In Stock
In stock · Dispatch: USA[1-2d] Global[5-7d]
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:98.78%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
EGFR-IN-47 (compound 14aj) is a potent, fourth-generation, and orally active EGFR inhibitor. It specifically targets the EGFR L858R/T790M/C797S triple mutation with an IC50 of 0.01 uM. In NSCLC research, EGFR-IN-47 effectively overcomes C797S-mediated resistance to Osimertinib by inhibiting the phosphorylation of EGFR and its downstream mediators, subsequently inducing cell cycle arrest and apoptosis.
Targets&IC50
EGFR T790M:0.07 μM, EGFR L858R:0.07 μM, EGFR C797S:0.07 μM
In vitro
EGFR-IN-47 potently inhibits PC-9 cell growth (IC50 = 0.013 uM) and induces G0/G1 arrest [1].
In vivo
Oral EGFR-IN-47 (10-40 mg/kg) shows significant efficacy in xenografts; rat PK reveals 66.05% bioavailability [1].
Chemical Properties
Molecular Weight481.64
FormulaC29H35N7
Cas No.3034649-73-2
SmilesN1=CC=2C=C(N(C2N=C1NC3=CC=C(C=C3)N4CCN(C)CC4)C5CCCC5)CNC=6C=CC=CC6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 16.00 mg/mL (33.22 mM), Sonication is recommmended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0762 mL10.3812 mL20.7624 mL103.8120 mL
5 mM0.4152 mL2.0762 mL4.1525 mL20.7624 mL
10 mM0.2076 mL1.0381 mL2.0762 mL10.3812 mL
20 mM0.1038 mL0.5191 mL1.0381 mL5.1906 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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