Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374028 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
Abstract
A series of triazole-containing novobiocin analogues has been designed, synthesized and their inhibitory activity determined. These compounds contain a triazole ring in lieu of the amide moiety present in the natural product. The anti-proliferative effects of these compounds were evaluated against two breast cancer cell lines (SKBr-3 and MCF-7), and manifested activities similar to their amide-containing counterparts. In addition, Hsp90-dependent client protein degradation was observed via Western blot analyses, supporting a common mode of Hsp90 inhibition for both structural classes.
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Related Topics
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Authors
Laura B. Peterson, Brian S.J. Blagg,