A novel synthesis of EGFR-tyrosine-kinase inhibitors with 4-(indol-3-yl)quinazoline structure
Autor: | Werner Löwe, Anja Lüth |
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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 |
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