| Literature DB >> 24900194 |
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