Literature DB >> 24900194

Allosteric IGF-1R Inhibitors.

Timo Heinrich1, Ulrich Grädler1, Henning Böttcher1, Andree Blaukat1, Adam Shutes2.   

Abstract

Targeting allosteric protein sites is a promising approach to interfere selectively with cellular signaling cascades. We have discovered a novel class of allosteric insulin-like growth factor-I receptor (IGF-1R) inhibitors. 3-Cyano-1H-indole-7-carboxylic acid {1-[4-(5-cyano-1H-indol-3-yl)butyl]piperidin-4-yl}amide (10) was found with nanomolar biochemical, micromolar, cellular IGF-1R activity and no relevant interference with cellular insulin receptor signaling up to 30 μM. The allosteric binding site was characterized by X-ray crystallographic studies, and the structural information was used to explain the unique mode of action of this new class of inhibitors.

Entities:  

Keywords:  IGF-1R; allosteric inhibition; indole-butyl-amine; kinase inhibitor

Year:  2010        PMID: 24900194      PMCID: PMC4007842          DOI: 10.1021/ml100044h

Source DB:  PubMed          Journal:  ACS Med Chem Lett        ISSN: 1948-5875            Impact factor:   4.345


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