Cargando…
Macrocyclic FKBP51 Ligands Define a Transient Binding Mode with Enhanced Selectivity
Subtype selectivity represents a challenge in many drug discovery campaigns. A typical example is the FK506 binding protein 51 (FKBP51), which has emerged as an attractive drug target. The most advanced FKBP51 ligands of the SAFit class are highly selective vs. FKBP52 but poorly discriminate against...
Autores principales: | Voll, Andreas M., Meyners, Christian, Taubert, Martha C., Bajaj, Thomas, Heymann, Tim, Merz, Stephanie, Charalampidou, Anna, Kolos, Jürgen, Purder, Patrick L., Geiger, Thomas M., Wessig, Pablo, Gassen, Nils C., Bracher, Andreas, Hausch, Felix |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252719/ https://www.ncbi.nlm.nih.gov/pubmed/33843131 http://dx.doi.org/10.1002/anie.202017352 |
Ejemplares similares
-
FKBP51 and FKBP12.6—Novel and tight interactors of Glomulin
por: Hähle, Andreas, et al.
Publicado: (2019) -
The Many Faces of FKBP51
por: Hähle, Andreas, et al.
Publicado: (2019) -
Picomolar FKBP inhibitors enabled by a single water-displacing methyl group in bicyclic [4.3.1] aza-amides
por: Kolos, Jürgen M., et al.
Publicado: (2021) -
FKBP Ligands—Where We Are and Where to Go?
por: Kolos, Jürgen M., et al.
Publicado: (2018) -
Development of NanoBRET‐Binding Assays for FKBP‐Ligand Profiling in Living Cells
por: Gnatzy, Monika T., et al.
Publicado: (2021)