| Literature DB >> 28833911 |
Lea Kremer1,2, Carsten Schultz-Fademrecht3, Matthias Baumann3, Peter Habenberger3, Axel Choidas3, Bert Klebl3, Susanne Kordes3,4, Hans R Schöler4, Jared Sterneckert4,5, Slava Ziegler1, Gisbert Schneider6, Herbert Waldmann1,2.
Abstract
Cell-based assays enable monitoring of small-molecule bioactivity in a target-agnostic manner and help uncover new biological mechanisms. Subsequent identification and validation of the small-molecule targets, typically employing proteomics techniques, is very challenging and limited, in particular if the targets are membrane proteins. Herein, we demonstrate that the combination of cell-based bioactive-compound discovery with cheminformatic target prediction may provide an efficient approach to accelerate the process and render target identification and validation more efficient. Using a cell-based assay, we identified the pyrazolo-imidazole smoothib as a new inhibitor of hedgehog (Hh) signaling and an antagonist of the protein smoothened (SMO) with a novel chemotype. Smoothib targets the heptahelical bundle of SMO, prevents its ciliary localization, reduces the expression of Hh target genes, and suppresses the growth of Ptch+/- medulloblastoma cells.Entities:
Keywords: chemoinformatics; hedgehog signaling; inhibitors; target identification; target prediction
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Year: 2017 PMID: 28833911 DOI: 10.1002/anie.201707394
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336