Organic Letters · 2004 · 40 citations · 7 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryMolecular PharmacologyFluorescence ImagingFluorescence SpectroscopyMolecular Probe DevelopmentEgfr InhibitionEpidermal Growth Factor Receptor Targeting LigandsFluorescence Imaging ProbesFluorescence-based AssaysFluorescent ProbesLabelingMolecular TargetingPhotoaffinity Probes
[structure: see text] The synthesis of a photoaffinity probe for EGFR is described. O-Alkylation of 4-(meta-azidoanilino)-6-methoxy-7-hydroxy-quinazoline with a protected tetraethyleneglycol linker followed by the attachment of tetramethylrhodamine yielded the fluorescent probe AX7593. Photoaffinity labeling of EGFR by AX7593 (K(b) = 280 nM) was shown to have an efficiency of 34% and to be competitive with the EGFR inhibitors PP2 and AG1478.
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Gordon W. Rewcastle, William A. Denny, Alexander J. Bridges et al. · Journal of Medicinal Chemistry · 1995 · 261 citations · Full text