Cargando…
Discovery of potent histone deacetylase inhibitors with modified phenanthridine caps
In discovery of novel HDAC inhibitory with anticancer potency, pharmacophores of phenanthridine were introduced to the structure of HDAC inhibitors. Fatty and aromatic linkers were evaluated for their solubility and activity. Both enzyme inhibitory and in vitro antiproliferative (against U937 cells)...
Autores principales: | Fan, Wenli, Zhang, Lin, Wang, Xuejiang, Jia, Haiyong, Zhang, Lei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7939570/ https://www.ncbi.nlm.nih.gov/pubmed/33663315 http://dx.doi.org/10.1080/14756366.2021.1892089 |
Ejemplares similares
-
Discovery of indole-3-butyric acid derivatives as potent histone deacetylase inhibitors
por: Chen, Yiming, et al.
Publicado: (2021) -
Synthesis and Anticancer Activity Evaluation of Novel Phenanthridine Derivatives
por: Wan, Minghui, et al.
Publicado: (2019) -
Discovery of N-(2-Aminophenyl)-4-(bis(2-chloroethyl)amino)Benzamide as a Potent Histone Deacetylase Inhibitor
por: Zhang, Lihui, et al.
Publicado: (2019) -
Discovery and SAR analysis of 5-chloro-4-((substituted phenyl)amino)pyrimidine bearing histone deacetylase inhibitors
por: Zhang, Lin, et al.
Publicado: (2022) -
Discovery of the First N-Hydroxycinnamamide-Based
Histone Deacetylase 1/3 Dual Inhibitors with Potent Oral Antitumor
Activity
por: Li, Xiaoyang, et al.
Publicado: (2014)