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The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation
[Image: see text] 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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791665/ https://www.ncbi.nlm.nih.gov/pubmed/36459434 http://dx.doi.org/10.1021/acs.jmedchem.2c00956 |
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author | 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 |
author_facet | 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 |
author_sort | Flegel, Jana |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-9791665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97916652022-12-27 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 J Med Chem [Image: see text] 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. American Chemical Society 2022-12-02 2022-12-22 /pmc/articles/PMC9791665/ /pubmed/36459434 http://dx.doi.org/10.1021/acs.jmedchem.2c00956 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | 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 The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation |
title | The Highly
Potent AhR Agonist Picoberin Modulates
Hh-Dependent Osteoblast Differentiation |
title_full | The Highly
Potent AhR Agonist Picoberin Modulates
Hh-Dependent Osteoblast Differentiation |
title_fullStr | The Highly
Potent AhR Agonist Picoberin Modulates
Hh-Dependent Osteoblast Differentiation |
title_full_unstemmed | The Highly
Potent AhR Agonist Picoberin Modulates
Hh-Dependent Osteoblast Differentiation |
title_short | The Highly
Potent AhR Agonist Picoberin Modulates
Hh-Dependent Osteoblast Differentiation |
title_sort | highly
potent ahr agonist picoberin modulates
hh-dependent osteoblast differentiation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791665/ https://www.ncbi.nlm.nih.gov/pubmed/36459434 http://dx.doi.org/10.1021/acs.jmedchem.2c00956 |
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