Cargando…
Heterobifunctional Ligase Recruiters Enable pan-Degradation of Inhibitor of Apoptosis Proteins
[Image: see text] Proteolysis targeting chimeras (PROTACs) represent a new pharmacological modality to inactivate disease-causing proteins. PROTACs operate via recruiting E3 ubiquitin ligases, which enable the transfer of ubiquitin tags onto their target proteins, leading to proteasomal degradation....
Autores principales: | Ng, Yuen Lam Dora, Bricelj, Aleša, Jansen, Jacqueline A., Murgai, Arunima, Peter, Kirsten, Donovan, Katherine A., Gütschow, Michael, Krönke, Jan, Steinebach, Christian, Sosič, Izidor |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108347/ https://www.ncbi.nlm.nih.gov/pubmed/36996313 http://dx.doi.org/10.1021/acs.jmedchem.2c01817 |
Ejemplares similares
-
E3 Ligase Ligands in Successful PROTACs: An Overview of Syntheses and Linker Attachment Points
por: Bricelj, Aleša, et al.
Publicado: (2021) -
Systematic exploration of different E3 ubiquitin ligases: an approach towards potent and selective CDK6 degraders
por: Steinebach, Christian, et al.
Publicado: (2020) -
Leveraging
Ligand Affinity and Properties: Discovery
of Novel Benzamide-Type Cereblon Binders for the Design of PROTACs
por: Steinebach, Christian, et al.
Publicado: (2023) -
Expanding the Structural
Diversity at the Phenylene
Core of Ligands for the von Hippel–Lindau E3 Ubiquitin Ligase:
Development of Highly Potent Hypoxia-Inducible Factor-1α Stabilizers
por: Vu, Lan Phuong, et al.
Publicado: (2023) -
Accessing three-branched high-affinity cereblon ligands for molecular glue and protein degrader design
por: Kuchta, Robert, et al.
Publicado: (2023)