Cargando…
Small-molecule MDM2/X inhibitors and PROTAC degraders for cancer therapy: advances and perspectives
Blocking the MDM2/X–P53 protein–protein interaction has been widely recognized as an attractive therapeutic strategy for the treatment of cancers. Numerous small-molecule MDM2 inhibitors have been reported since the release of the structure of the MDM2–P53 interaction in 1996, SAR405838, NVP-CGM097,...
Autores principales: | Fang, Yuan, Liao, Guochao, Yu, Bin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452049/ https://www.ncbi.nlm.nih.gov/pubmed/32874827 http://dx.doi.org/10.1016/j.apsb.2020.01.003 |
Ejemplares similares
-
Non-small molecule PROTACs (NSM-PROTACs): Protein degradation kaleidoscope
por: Ma, Sinan, et al.
Publicado: (2022) -
Targeted Protein Degradation by Chimeric Small Molecules, PROTACs and SNIPERs
por: Naito, Mikihiko, et al.
Publicado: (2019) -
Design of stapled peptide-based PROTACs for MDM2/MDMX atypical degradation and tumor suppression
por: Chen, Si, et al.
Publicado: (2022) -
Small-Molecule PROTACs for Cancer Immunotherapy
por: Liu, Zefan, et al.
Publicado: (2022) -
Homo-PROTAC mediated suicide of MDM2 to treat non-small cell lung cancer
por: He, Shipeng, et al.
Publicado: (2021)