A novel synthesis of EGFR-tyrosine-kinase inhibitors with 4-(indol-3-yl)quinazoline structure

Autor: Werner Löwe, Anja Lüth
Rok vydání: 2008
Předmět:
Zdroj: Journal of Heterocyclic Chemistry. 45:703-708
ISSN: 1943-5193
0022-152X
DOI: 10.1002/jhet.5570450311
Popis: The epidermal growth factor (EGF) family of membrane receptors has been identified as a key element in the complex signaling network that is utilized by various classes of cell-surface receptors. A new synthetic pathway of 4-(indol-3-yl)quinazolines 15 and 16 is described using cross coupling reactions with quinazoline- and indole moieties. The synthesized compound 15 is a new dual and high potent EGFR- and HER-2-tyrosine kinase inhibitor with excellent cytotoxic properties at different cell lines. Furthermore this substance class shows remarkably strong fluorescence.
Databáze: OpenAIRE