Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1372636 | Bioorganic & Medicinal Chemistry Letters | 2009 | 5 Pages |
Abstract
In this Letter, we report the natural products salvianolic acid A, salvianolic acid B, and caftaric acid as inhibitors of the protein–protein interactions mediated by the SH2 domains of the Src-family kinases Src and Lck, two established disease targets. Moreover, we propose a binding mode for the inhibitors based on molecular modeling, which will facilitate chemical optimization efforts of these important lead structures for drug discovery.
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Related Topics
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Organic Chemistry
Authors
Bianca Sperl, Markus H.J. Seifert, Thorsten Berg,