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Updated: Jul 10, 2026

Studies of Chaperone-Cochaperone Interactions using Homogenous Bead-Based Assay
Published on: July 21, 2021
Derrubone, an inhibitor of the Hsp90 protein folding machinery
M Kyle Hadden1, Lakshmi Galam, Jason E Gestwicki
1Department of Medicinal Chemistry, Malott 4070, The University of Kansas, Lawrence, KS 66045-7563, USA.
Abstract:
High-throughput screening of a library of diverse molecules has identified derrubone ( 1), an isoflavone natural product from Derris robusta, as a potent Hsp90 inhibitor. Subsequent testing in several cellular-based assays established 1 as a low micromolar inhibitor in vitro. In addition, derrubone induced the degradation of numerous Hsp90 client proteins, a hallmark effect resulting from Hsp90 inhibition. The identification of 1 as an Hsp90 inhibitor provides a new natural product scaffold upon which the development of novel Hsp90 inhibitors can be pursued.
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