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Lookup NU author(s): Professor Martin NobleORCiD,
Dr Ian HardcastleORCiD,
Professor Jane Endicott
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The interaction between murine double minute (MDM2) and p53 is a major target in anticancer drug design. Several potent compound series, including the nutlins and spirooxindoles, have previously been established as high-affinity antagonists of MDM2. In this paper, we describe the interaction of isoindolinone inhibitors with MDM2, as characterized by nuclear magnetic resonance spectroscopy. Isoindolinone inhibitors bind specifically to the MDM2 p53 binding site and exploit all sub-pockets used by p53, nutlins and spirooxindoles. Furthermore, isoindolinones bind with low micromolar to high nanomolar affinities, with the best compound approaching the potency of nutlin-3.
Author(s): Riedinger C, Noble ME, Wright DJ, Mulks F, Hardcastle I, Endicott JA, McDonnell JM
Publication type: Article
Publication status: Published
Journal: Chemical Biology and Drug Design
Print publication date: 01/03/2011
ISSN (print): 1747-0277
ISSN (electronic): 1747-0285
Publisher: Wiley-Blackwell Publishing, Inc.
PubMed id: 21244642
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