Hsp90 Inhibition with Resorcylic Acid Lactones (RALs)

Author(s): Nicolas Winssinger, Jean-Gonzague Fontaine, Sofia Barluenga

Journal Name: Current Topics in Medicinal Chemistry

Volume 9 , Issue 15 , 2009


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Abstract:

Heat shock protein 90 (Hsp90) is an ATP-dependent chaperone which is involved in the post-translational maturation and stabilization of over one hundred proteins (“its clients”). In the absence of Hsp90s chaperoning, its clients are misfolded and degraded via ubiquitin-proteasome pathway. HSP90 has become the focus of intense drug discovery efforts as its activity has been implicated in diverse pathologies ranging from oncology to neurodegenerative and infectious diseases. The most promising inhibitors reported to date inhibit the ATPase activity by binding to the Nterminal ATP pocket. Radicicol, a member of the resorcylic acid lactones (RALs), represents an important pharmacophore to this end. Efforts towards the development of this pharmacophore and its SAR are reviewed herein.

Keywords: Hsp90, resorcylic

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Article Details

VOLUME: 9
ISSUE: 15
Year: 2009
Published on: 01 March, 2012
Page: [1419 - 1435]
Pages: 17
DOI: 10.2174/156802609789895665
Price: $65

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