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EGFR-IN-16 (AG473) is an inhibitor of EGFR in human A431 cells.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $122 | 6-8 weeks | 6-8 weeks | |
| 10 mg | $195 | 6-8 weeks | 6-8 weeks | |
| 25 mg | $370 | 6-8 weeks | 6-8 weeks |
| Description | EGFR-IN-16 (AG473) is an inhibitor of EGFR in human A431 cells. |
| Targets&IC50 | HER2:4.74 (pIC50), EGFR:4.85 (pIC50) |
| In vivo | Expressed the EGFR-IN-16 lipoprotein from Neisseria meningitides, flagellin FlaB from Vibrio vulnificus and heat shock protein 70 from Mycobacterium tuberculosis (mHsp70) in Escherichia coli as single proteins and fusion proteins with VP2 protein of infectious bursal disease virus (IBDV).Both cellular and humoral adjuvanticities of the three TLR ligands were compared by immunization of mice in two different ways.Among the three co-administered TLR ligands, recombinant EGFR-IN-16 lipoprotein exhibited the highest cellular and humoral adjuvanticities, including promotion of IL-4, IL-12, IFN-γ and IBDV VP2-specific antibody production.Among the three genetically fused TLR ligands, fusion with EGFR-IN-16 D1 domain exhibited the highest cellular and humoral adjuvanticities. |
| Synonyms | AG473 |
| Molecular Weight | 265.26 |
| Formula | C16H11NO3 |
| Cas No. | 133550-22-8 |
| Smiles | C(=C(/C(=O)C1=CC=CC=C1)\C#N)\C2=CC(O)=C(O)C=C2 |
| Relative Density. | 1.350 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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.
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.
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