A potent EGFR inhibitor
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Compound 56

Item No. 17254

Technical Information
Formal Name
N-(3-bromophenyl)-6,7-diethoxy-4-quinazolinamine
CAS Number
171745-13-4
Molecular Formula
C18H18BrN3O2
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 2 mg/mlDMSO: 2 mg/mlDMSO:PBS(pH 7.2) (1:2): 0.25 mg/mlEthanol: 2 mg/ml
λmax
208, 230, 252, 333 nm
SMILES
BrC1=CC(NC2=NC=NC3=C2C=C(OCC)C(OCC)=C3)=CC=C1
InChi Code
InChI=1S/C18H18BrN3O2/c1-3-23-16-9-14-15(10-17(16)24-4-2)20-11-21-18(14)22-13-7-5-6-12(19)8-13/h5-11H,3-4H2,1-2H3,(H,20,21,22)
InChi Key
YXOXHAUUTIOBDA-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Compound 56 is a highly potent inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR; IC50 = 0.006 nM).1 It has been used to inhibit EGFR activity in pancreatic cancer cell lines and to induce the differentiation of rat mesenchymal stem cells.2,3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bridges, A.J., Zhou, H., Cody, D.R., et alTyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor. J. Med. Chem. 39(1), 267-276 (1996).

    2. Chandana, S.R., Leece, C.M., Gallo, K.A., et alInhibition of MLK3 decreases proliferation and increases antiproliferative activity of epidermal growth factor receptor (EGFR) inhibitor in pancreatic cancer cell lines. Cancer Growth Metastasis 3, 1-9 (2010).

    3. Hwang, K.C., Kim, J.Y., Chang, W., et alChemicals that modulate stem cell differentiation. Proc. Natl. Acad. Sci. USA 105(21), 7467-7471 (2008).