Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1393437 | European Journal of Medicinal Chemistry | 2008 | 11 Pages |
Abstract
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. The synthesis and pharmacological results of 4-(indole-3-yl)quinazolines are described. The synthesized compounds are new high potent EGFR-tyrosine kinase inhibitors with excellent cytotoxic properties at different cell lines. Furthermore the 4-(indole-3-yl)quinazolines show some tendencies to inhibit the HER-2 TK, too. Moreover this substance class has remarkable strong fluorescence properties.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anja Lüth, Werner Löwe,