AG-1557

- Overview
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    Background
    
    pIC50: 8.194
    AG-1557 is an inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase.
    The epidermal growth factor receptor (EGFR) is a member of the receptor family of tyrosine kinases. Receptor tyrosine kinases are involved in various cancer cell behaviors, such as growth, invasion and blood vessel formation. EGFR is found to be over-expressed in several human solid tumors. Thus, EGFR has received much attention as a target for anticancer drugs.
    In vitro: A pharmacophore model was developed using a dataset of 77 chemically diverse EGFR inhibitors including AG-1557 using PHASE. Statistically valid Three Dimensional Quantitative Structure Activity Relationship (3D-QSAR) equations were generated. Docking of the probable hits into the crystal structure of EGFR was used as a second filter. Calculation of ADME properties of the probable hits arising out of docking further reduced the number of hits. The pharmacophore results indicated that the presence of two aromatic ring features, one acceptor feature, one donor feature and one hydrophobic feature were necessary for potent inhibitory activity. The generated pharmacophore resulted in a 3D-QSAR model, with a correlation coefficient r2 of 0.9905 and q2 of 0.8764. Docking studies as a second filter reduced the hits to 8. Application of drug-likeness as a third filter gave 6 leads. AG-1557 was screening as an inhibitor of EGFR tyrosine kinase with a predicted pIC50 value of 8.62, which was comparable with its experimental determined value of 8.194 [1].
    In vivo: Up to now, there is no animal in vivo data reported.
    Clinical trial: So far, no clinical study has been conducted.
- Properties
  - Alternative Name
    
    Tyrphostin AG-1557; N-(3-iodophenyl)-6,7-dimethoxy-4-quinazolinamine
    
    CAS Number
    
    189290-58-2
    
    Molecular Formula
    
    C16H14IN3O2
    
    Molecular Weight
    
    407.2
    
    Appearance
    
    A crystalline solid
    
    Purity
    
    Purity ≥ 95.00%
    
    Solubility
    
    ≤0.5mg/ml in ethanol;1.5mg/ml in DMSO;1mg/ml in dimethyl formamide
    
    Storage
    
    Store at -20°C
    
    * For Research Use Only