Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374336 | Bioorganic & Medicinal Chemistry Letters | 2011 | 6 Pages |
Abstract
Through Hsp90-dependent firefly luciferase refolding and Hsp90-dependent heme-regulated eIF2α kinase (HRI) activation assays, silybin was identified as a novel Hsp90 inhibitor. Subsequently, a library of silybin analogues was designed, synthesized and evaluated. Initial SAR studies identified the essential, non-essential and detrimental functionalities on silybin that contribute to Hsp90 inhibition.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Huiping Zhao, Gary E. Brandt, Lakshmi Galam, Robert L. Matts, Brian S.J. Blagg,