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SID: 26758178

Inhibitor Resource

Inhibitor Libraries

Inhibitor Database
  AGL 2263
Cat. No. 121850  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Tyrosine Kinase (PTK) » Receptor

AG 2263

Yellow solid. PROTECT FROM LIGHT. PACKAGED UNDER INERT GAS. A cell-permeable benzoxazolone-containing bioisostere of tyrphostin AG 538 (Cat. No. 658403) that acts as a potent, substrate-competitive, but not ATP-competitive, inhibitor of insulin receptor (IR) and insulin-like growth factor-1 receptor (IGF-1R). It is selective towards IR and IGF-1R (IC50 = 0.4 and 0.43 µM, respectively) and inhibits Src and PKB only at much higher concentrations (IC50 = 2.2 and 55 µM, respectively) in kinase assays. Shown to prevent IGF-1-induced cellular IGF-1R autophosphorylation and down stream signalling. Specifically inhibits IGF-1-induced, but not PDGF-induced, activation of PKB in cells. Effectively blocks the formation of colonies in soft agar by breast and prostate cancer cells. Exhibits improved cellular oxidative stability than AG 538. Purity: ≥97% by HPLC.

Ref.: Blum, G., et al. 2003. J. Biol. Chem. 278, 40442.

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5 mgY€190


SolubilityMolecular FormulaMol. Wt.
DMSO C17H10N2O5 322.3 


Related Literature:

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Inhibitor Sourcebook

Material Safety Data Sheets:
121850: AGL 2263 - English
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Related Categories:
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Tyrosine Kinase (PTK) » Receptor