Cargando…
Synthesis and biological evaluation of 2-aryl-benzimidazole derivatives of dehydroabietic acid as novel tubulin polymerization inhibitors
A series of novel 2-aryl-benzimidazole derivatives of dehydroabietic acid were synthesized and characterized by IR, (1)H NMR, (13)C NMR, MS and elemental analyses. All the target compounds were evaluated for their in vitro cytotoxic activity against SMMC-7721, MDA-MB-231, HeLa and CT-26 cancer cell...
Autores principales: | Miao, Ting-Ting, Tao, Xu-Bing, Li, Dong-Dong, Chen, Hao, Jin, Xiao-Yan, Geng, Yi, Wang, Shi-Fa, Gu, Wen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080489/ https://www.ncbi.nlm.nih.gov/pubmed/35539265 http://dx.doi.org/10.1039/c8ra02078g |
Ejemplares similares
-
Synthesis and biological evaluation of dehydroabietic acid-pyrimidine hybrids as antitumor agents
por: Huang, Lin, et al.
Publicado: (2020) -
Design, synthesis and biological evaluation of 9-aryl-5H-pyrido[4,3-b]indole derivatives as potential tubulin polymerization inhibitors
por: Shi, Lingyu, et al.
Publicado: (2022) -
Biological activity and interaction mechanism of the diketopiperazine derivatives as tubulin polymerization inhibitors
por: Tian, Zhenhua, et al.
Publicado: (2018) -
Synthesis, Computational Analysis, and Antiproliferative Activity of Novel Benzimidazole Acrylonitriles as Tubulin Polymerization Inhibitors: Part 2
por: Beč, Anja, et al.
Publicado: (2021) -
Synthesis and biological evaluation of novel N-(piperazin-1-yl)alkyl-1H-dibenzo[a,c]carbazole derivatives of dehydroabietic acid as potential MEK inhibitors
por: Chen, Hao, et al.
Publicado: (2019)