Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376336 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
Hsp90 maintains the conformational stability of multiple proteins implicated in oncogenesis and has emerged as a target for chemotherapy. We report here the discovery of a novel small molecule scaffold that inhibits Hsp90. X-ray data show that the scaffold binds competitively at the ATP site on Hsp90. Cellular proliferation and client assays demonstrate that members of the series are able to inhibit Hsp90 at nanomolar concentrations.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Thomas E. Barta, James M. Veal, John W. Rice, Jeffrey M. Partridge, R. Patrick Fadden, Wei Ma, Matthew Jenks, Lifeng Geng, Gunnar J. Hanson, Kenneth H. Huang, Amy F. Barabasz, Briana E. Foley, James Otto, Steven E. Hall,