Cargando…
Large-Scale Computational Screening Identifies First in Class Multitarget Inhibitor of EGFR Kinase and BRD4
Inhibition of cancer-promoting kinases is an established therapeutic strategy for the treatment of many cancers, although resistance to kinase inhibitors is common. One way to overcome resistance is to target orthogonal cancer-promoting pathways. Bromo and Extra-Terminal (BET) domain proteins, which...
Autores principales: | Allen, Bryce K., Mehta, Saurabh, Ember, Stewart W. J., Schonbrunn, Ernst, Ayad, Nagi, Schürer, Stephan C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657038/ https://www.ncbi.nlm.nih.gov/pubmed/26596901 http://dx.doi.org/10.1038/srep16924 |
Ejemplares similares
-
Identification of a Novel Class of BRD4 Inhibitors by Computational Screening
and Binding Simulations
por: Allen, Bryce K., et al.
Publicado: (2017) -
Acetyl-lysine Binding Site of Bromodomain-Containing
Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors
por: Ember, Stuart W. J., et al.
Publicado: (2014) -
Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival
por: Kannan-Sundhari, Abhiraami, et al.
Publicado: (2020) -
Fluorinated Aromatic Amino Acids Are Sensitive (19)F NMR Probes for Bromodomain-Ligand Interactions
por: Mishra, Neeraj K., et al.
Publicado: (2014) -
Correction to Letter: Fluorinated Aromatic Amino Acids
Are Sensitive (19)F NMR Probes for Bromodomain–Ligand
Interactions
por: Mishra, Neeraj K., et al.
Publicado: (2016)