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Bioorg Med Chem Lett. 2012 May 15;22(10):3498-502. doi: 10.1016/j.bmcl.2012.03.083. Epub 2012 Mar 30.

The central valine concept provides an entry in a new class of non peptide inhibitors of the p53-MDM2 interaction.

Author information

1
Novartis Institutes for BioMedical Research, CH-4002 Basel, Switzerland. pascal.furet@novartis.com

Abstract

Disrupting the interaction between the p53 tumor suppressor and its regulator MDM2 is a promising therapeutic strategy in anticancer drug research. In our search for non peptide inhibitors of this protein-protein interaction, we have devised a ligand design concept exploiting the central position of Val 93 in the p53 binding pocket of MDM2. The design of molecules based on this concept has allowed us to rapidly identify compounds having a 3-imidazolyl indole core structure as the first representatives of a new class of potent inhibitors of the p53-MDM2 interaction.

PMID:
22507962
DOI:
10.1016/j.bmcl.2012.03.083
[Indexed for MEDLINE]

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