| Literature DB >> 19610616 |
Paul A Brough1, Xavier Barril, Jenifer Borgognoni, Patrick Chene, Nicholas G M Davies, Ben Davis, Martin J Drysdale, Brian Dymock, Suzanne A Eccles, Carlos Garcia-Echeverria, Christophe Fromont, Angela Hayes, Roderick E Hubbard, Allan M Jordan, Michael Rugaard Jensen, Andrew Massey, Angela Merrett, Antony Padfield, Rachel Parsons, Thomas Radimerski, Florence I Raynaud, Alan Robertson, Stephen D Roughley, Joseph Schoepfer, Heather Simmonite, Swee Y Sharp, Allan Surgenor, Melanie Valenti, Steven Walls, Paul Webb, Mike Wood, Paul Workman, Lisa Wright.
Abstract
Inhibitors of the Hsp90 molecular chaperone are showing considerable promise as potential molecular therapeutic agents for the treatment of cancer. Here we describe novel 2-aminothieno[2,3-d]pyrimidine ATP competitive Hsp90 inhibitors, which were designed by combining structural elements of distinct low affinity hits generated from fragment-based and in silico screening exercises in concert with structural information from X-ray protein crystallography. Examples from this series have high affinity (IC50 = 50-100 nM) for Hsp90 as measured in a fluorescence polarization (FP) competitive binding assay and are active in human cancer cell lines where they inhibit cell proliferation and exhibit a characteristic profile of depletion of oncogenic proteins and concomitant elevation of Hsp72. Several examples (34a, 34d and 34i) caused tumor growth regression at well tolerated doses when administered orally in a human BT474 human breast cancer xenograft model.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19610616 DOI: 10.1021/jm900357y
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446