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EGFR-IN-174
Catalog No. T213555 Copy Product Info
🥰Excellent
EGFR-IN-174 is a potent inhibitor of EGFR (IC50= 0.17 μM) and also effectively inhibits VEGFR-2 (IC50= 0.2007 μM). It demonstrates strong anticancer properties with low toxicity towards normal cells. EGFR-IN-174 induces G2/M and Pre-G1 phase cell cycle arrest and significantly triggers apoptosis. It is employed in cancer research, including studies on colorectal cancer, hepatocellular carcinoma, and breast cancer.
EGFR-IN-174
Copy Product Info🥰Excellent
Catalog No. T213555
EGFR-IN-174 is a potent inhibitor of EGFR (IC50= 0.17 μM) and also effectively inhibits VEGFR-2 (IC50= 0.2007 μM). It demonstrates strong anticancer properties with low toxicity towards normal cells. EGFR-IN-174 induces G2/M and Pre-G1 phase cell cycle arrest and significantly triggers apoptosis. It is employed in cancer research, including studies on colorectal cancer, hepatocellular carcinoma, and breast cancer.
EGFR-IN-174
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | EGFR-IN-174 is a potent inhibitor of EGFR (IC50= 0.17 μM) and also effectively inhibits VEGFR-2 (IC50= 0.2007 μM). It demonstrates strong anticancer properties with low toxicity towards normal cells. EGFR-IN-174 induces G2/M and Pre-G1 phase cell cycle arrest and significantly triggers apoptosis. It is employed in cancer research, including studies on colorectal cancer, hepatocellular carcinoma, and breast cancer. |
| Targets&IC50 | VEGFR2:0.2007 μM |
| In vitro | EGFR-IN-174 (compound 3a) exhibits strong cytotoxicity against HCT-116, HepG-2, and MCF-7 cell lines, with IC50 values of 5.58, 4.82, and 11.15 μM, respectively, while showing minimal cytotoxicity toward normal WI-38 cells (IC50 = 86.26 μM). Additionally, EGFR-IN-174 (4.82-11.15 μM, 72 hours) effectively induces cell cycle arrest at the G2/M phase and Pre-G1 phase and significantly triggers apoptosis in HCT-116, HepG-2, and MCF-7 cells. |
| Storage | Powder: -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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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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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