Cargando…
Discovery of potent and noncovalent KRAS(G12D) inhibitors: Structure-based virtual screening and biological evaluation
KRAS(G12D), the most common oncogenic KRAS mutation, is a promising target for the treatment of pancreatic cancer. Herein, we identified four potent and noncovalent KRAS(G12D) inhibitors (hits 1–4) by using structure-based virtual screening and biological evaluation. The in vitro assays indicated th...
Autores principales: | Wang, Yuting, Zhang, Hai, Li, Jindong, Niu, Miao-Miao, Zhou, Yang, Qu, Yuanqian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815544/ https://www.ncbi.nlm.nih.gov/pubmed/36618907 http://dx.doi.org/10.3389/fphar.2022.1094887 |
Ejemplares similares
-
Identification of novel and potent dual-targeting HDAC1/SPOP inhibitors using structure-based virtual screening, molecular dynamics simulation and evaluation of in vitro and in vivo antitumor activity
por: Yang, Yingxue, et al.
Publicado: (2023) -
Discovery of potent heat shock protein 90 (Hsp90) inhibitors: structure-based virtual screening, molecular dynamics simulation, and biological evaluation
por: Xu, Yonghua, et al.
Publicado: (2023) -
KRAS inhibitors: going noncovalent
por: Drosten, Matthias, et al.
Publicado: (2022) -
Discovery of High-Affinity Noncovalent Allosteric
KRAS Inhibitors That Disrupt Effector Binding
por: McCarthy, Michael J., et al.
Publicado: (2019) -
Discovery of Potent Disheveled/Dvl Inhibitors Using Virtual Screening Optimized With NMR-Based Docking Performance Index
por: Hori, Kiminori, et al.
Publicado: (2018)