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Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design

The Petasis borono-Mannich reaction was employed for an alternative entry towards three-branched cereblon ligands. Such compounds are capabable of making multiple interactions with the protein surface and possess a suitable linker exit vector. The high-affinity ligands were used to assemble prototyp...

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Autores principales: Kuchta, Robert, Heim, Christopher, Herrmann, Alexander, Maiwald, Samuel, Ng, Yuen Lam Dora, Sosič, Izidor, Keuler, Tim, Krönke, Jan, Gütschow, Michael, Hartmann, Marcus D., Steinebach, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9994103/
https://www.ncbi.nlm.nih.gov/pubmed/36908700
http://dx.doi.org/10.1039/d2cb00223j
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author Kuchta, Robert
Heim, Christopher
Herrmann, Alexander
Maiwald, Samuel
Ng, Yuen Lam Dora
Sosič, Izidor
Keuler, Tim
Krönke, Jan
Gütschow, Michael
Hartmann, Marcus D.
Steinebach, Christian
author_facet Kuchta, Robert
Heim, Christopher
Herrmann, Alexander
Maiwald, Samuel
Ng, Yuen Lam Dora
Sosič, Izidor
Keuler, Tim
Krönke, Jan
Gütschow, Michael
Hartmann, Marcus D.
Steinebach, Christian
author_sort Kuchta, Robert
collection PubMed
description The Petasis borono-Mannich reaction was employed for an alternative entry towards three-branched cereblon ligands. Such compounds are capabable of making multiple interactions with the protein surface and possess a suitable linker exit vector. The high-affinity ligands were used to assemble prototypic new molecular glues and proteolysis targeting chimeras (PROTACs) targeting BRD4 for degradation. Our results highlight the importance of multicomponent reactions (MCRs) in drug discovery and add new insights into the rapidly growing field of protein degraders.
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spelling pubmed-99941032023-03-09 Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design Kuchta, Robert Heim, Christopher Herrmann, Alexander Maiwald, Samuel Ng, Yuen Lam Dora Sosič, Izidor Keuler, Tim Krönke, Jan Gütschow, Michael Hartmann, Marcus D. Steinebach, Christian RSC Chem Biol Chemistry The Petasis borono-Mannich reaction was employed for an alternative entry towards three-branched cereblon ligands. Such compounds are capabable of making multiple interactions with the protein surface and possess a suitable linker exit vector. The high-affinity ligands were used to assemble prototypic new molecular glues and proteolysis targeting chimeras (PROTACs) targeting BRD4 for degradation. Our results highlight the importance of multicomponent reactions (MCRs) in drug discovery and add new insights into the rapidly growing field of protein degraders. RSC 2023-01-03 /pmc/articles/PMC9994103/ /pubmed/36908700 http://dx.doi.org/10.1039/d2cb00223j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kuchta, Robert
Heim, Christopher
Herrmann, Alexander
Maiwald, Samuel
Ng, Yuen Lam Dora
Sosič, Izidor
Keuler, Tim
Krönke, Jan
Gütschow, Michael
Hartmann, Marcus D.
Steinebach, Christian
Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title_full Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title_fullStr Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title_full_unstemmed Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title_short Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
title_sort accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9994103/
https://www.ncbi.nlm.nih.gov/pubmed/36908700
http://dx.doi.org/10.1039/d2cb00223j
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