1区 · 医学
Article
作者: Brause, Alexandra ; Dötsch, Lara ; Krzyzanowski, Adrian ; Schulte, Britta ; Scheel, Rebecca ; Antonchick, Andrey P. ; Waldmann, Herbert ; Metz, Malte ; Hoffmann, Jan-Erik ; Flegel, Jana ; Shaaban, Saad ; Schneidewind, Tabea ; Schade, Dennis ; Stender, Isabelle D. ; Zhang, Minghao ; Sievers, Sonja ; Xue, Gang ; Flegel, Anke ; Wesseler, Fabian ; Lian, Yilong ; Janning, Petra ; Rastinejad, Fraydoon ; Reich, Alisa ; Jia, Zhi Jun ; Ziegler, Slava ; Strohmann, Carsten ; Moura-Alves, Pedro
Identification and analysis of small molecule bioactivity in target-agnostic cellular assays and monitoring changes in phenotype followed by identification of the biological target are a powerful approach for the identification of novel bioactive chemical matter in particular when the monitored phenotype is disease-related and physiologically relevant. Profiling methods that enable the unbiased analysis of compound-perturbed states can suggest mechanisms of action or even targets for bioactive small molecules and may yield novel insights into biology. Here we report the enantioselective synthesis of natural-product-inspired 8-oxotetrahydroprotoberberines and the identification of Picoberin, a low picomolar inhibitor of Hedgehog (Hh)-induced osteoblast differentiation. Global transcriptome and proteome profiling revealed the aryl hydrocarbon receptor (AhR) as the molecular target of this compound and identified a cross talk between Hh and AhR signaling during osteoblast differentiation.