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Inhibitor Resource

Inhibitor Libraries

Inhibitor Database
  PD 153035
Cat. No. 234490  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Tyrosine Kinase (PTK) » Receptor

AG 1517
4-[(3-Bromophenyl)amino]-6,7-dimethoxyquinazoline
Compound 32
SU 5271

White solid. PROTECT FROM LIGHT. An extremely potent and specific inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR; IC50 = 25 pM; Ki = 6 pM). Rapidly suppresses autophosphorylation of EGFR at low nanomolar concentrations in fibroblasts or in human epidermoid carcinoma cells. Also selectively blocks EGF-mediated cellular processes including mitogenesis, early gene expression, and oncogenic transformation. Purity: ≥97% by HPLC.

Ref.: Bridges, A.J., et al. 1996. J. Med. Chem. 39, 267. Fry, D.W., et al. 1994. Science 265, 1093.
Sold under license of U.S. Patent 5,457,105 and European Patent 0,566,266.

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SolubilityMolecular FormulaMol. Wt.
DMSO C16H14BrN3O2 360.2 


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234490: PD 153035 - English
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Related Categories:
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Tyrosine Kinase (PTK) » Receptor

Selected Citations:
  1. Nikolay L. Malinin, et al. (2005) Amyloid-b neurotoxicity is mediated by FISH adapter protein and ADAM12 metalloprotease activity. Proceedings of the National Academy of Sciences (USA) 102, 3058-3063.