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The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation.
Flegel, Jana; Shaaban, Saad; Jia, Zhi Jun; Schulte, Britta; Lian, Yilong; Krzyzanowski, Adrian; Metz, Malte; Schneidewind, Tabea; Wesseler, Fabian; Flegel, Anke; Reich, Alisa; Brause, Alexandra; Xue, Gang; Zhang, Minghao; Dötsch, Lara; Stender, Isabelle D; Hoffmann, Jan-Erik; Scheel, Rebecca; Janning, Petra; Rastinejad, Fraydoon; Schade, Dennis; Strohmann, Carsten; Antonchick, Andrey P; Sievers, Sonja; Moura-Alves, Pedro; Ziegler, Slava; Waldmann, Herbert.
Afiliación
  • Flegel J; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Shaaban S; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Jia ZJ; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Schulte B; Faculty of Chemistry, Institute of Organic Chemistry, University of Vienna Währinger Str. 38, Vienna 1090, Austria.
  • Lian Y; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Krzyzanowski A; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
  • Metz M; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Schneidewind T; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Wesseler F; Ludwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, United Kingdom.
  • Flegel A; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Reich A; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Brause A; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Xue G; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Zhang M; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Dötsch L; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Stender ID; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Hoffmann JE; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Scheel R; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Janning P; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Rastinejad F; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Schade D; Nuffield Department of Medicine, Target Discovery Institute, University of Oxford, Oxford, OX3 7FZ, UK.
  • Strohmann C; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Antonchick AP; Faculty of Chemistry, Chemical Biology, Technical University Dortmund, Dortmund 44227, Germany.
  • Sievers S; Protein Chemistry Facility, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Moura-Alves P; Protein Chemistry Facility, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
  • Ziegler S; Faculty of Chemistry, Inorganic Chemistry, Technical University Dortmund, Dortmund 44227, Germany.
  • Waldmann H; Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
J Med Chem ; 65(24): 16268-16289, 2022 12 22.
Article en En | MEDLINE | ID: mdl-36459434
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Receptores de Hidrocarburo de Aril / Proteínas Hedgehog Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Receptores de Hidrocarburo de Aril / Proteínas Hedgehog Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article