Cargando…
Synthesis, In Vitro and In Silico Anticancer Activity of New 4-Methylbenzamide Derivatives Containing 2,6-Substituted Purines as Potential Protein Kinases Inhibitors
A novel class of potential protein kinase inhibitors 7–16 was synthesized in high yields using various substituted purines. The most promising compounds, 7 and 10, exhibited inhibitory activity against seven cancer cell lines. The IC(50) values for compounds 7 and 10 were 2.27 and 2.53 μM for K562 c...
Autores principales: | Kalinichenko, Elena, Faryna, Aliaksandr, Bozhok, Tatyana, Panibrat, Alesya |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657793/ https://www.ncbi.nlm.nih.gov/pubmed/34884546 http://dx.doi.org/10.3390/ijms222312738 |
Ejemplares similares
-
Novel Phthalic-Based Anticancer Tyrosine Kinase Inhibitors: Design, Synthesis and Biological Activity
por: Kalinichenko, Elena, et al.
Publicado: (2023) -
Synthesis and Cytotoxic Activity of Some New 2,6-Substituted Purines
por: Kode, Nageswara Rao, et al.
Publicado: (2011) -
Synthesis, Biological Activities and Docking Studies of Novel 4-(Arylaminomethyl)benzamide Derivatives as Potential Tyrosine Kinase Inhibitors
por: Kalinichenko, Elena, et al.
Publicado: (2019) -
Synthesis and anticancer activity of thiosubstituted purines
por: Kowalska, Alicja, et al.
Publicado: (2015) -
N-(2,6-Dichlorophenyl)-4-methylbenzamide
por: Rodrigues, Vinola Z., et al.
Publicado: (2011)