Cargando…
Design, synthesis and biological evaluation of a series of dianilinopyrimidines as EGFR inhibitors
This paper described our efforts to develop dianilinopyrimidines as novel EGFR inhibitors. All the target compounds were tested for inhibitory effects against wild type EGFR (EGFR(wt)) and three tumour cells, including A549, PC-3, and HepG2. Some of the compounds performed well in antitumor activiti...
Autores principales: | Yan, Longjia, Wang, Qin, Liu, Li, Le, Yi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920385/ https://www.ncbi.nlm.nih.gov/pubmed/35260020 http://dx.doi.org/10.1080/14756366.2022.2046567 |
Ejemplares similares
-
Design, synthesis and in vitro biological evaluation of quinazolinone derivatives as EGFR inhibitors for antitumor treatment
por: Le, Yi, et al.
Publicado: (2020) -
Synthesis and preliminary structure-activity relationship study of 3-methylquinazolinone derivatives as EGFR inhibitors with enhanced antiproliferative activities against tumour cells
por: Zhang, Yan, et al.
Publicado: (2021) -
Design, synthesis and antitumor activity of 5-trifluoromethylpyrimidine derivatives as EGFR inhibitors
por: Zuo, Yaqing, et al.
Publicado: (2022) -
Design, synthesis and biological evaluation of novel thiazole-naphthalene derivatives as potential anticancer agents and tubulin polymerisation inhibitors
por: Wang, Guangcheng, et al.
Publicado: (2021) -
Discovery of Novel 2,4-Dianilinopyrimidine Derivatives Containing 4-(Morpholinomethyl)phenyl and N-Substituted Benzamides as Potential FAK Inhibitors and Anticancer Agents
por: Han, Chun, et al.
Publicado: (2021)