1373347-49-9Relevant academic research and scientific papers
Synthesis and biological evaluation of 1-cyano-2-Amino-benzimidazole derivatives as a novel class of antitumor agents
Hu, Zhang,Ou, Lili,Li, Sidong,Yang, Lei
, p. 3029 - 3038 (2014/05/06)
A series of 1-cyano-2-Amino-benzimidazole derivatives were synthesized and evaluated for their cytotoxic activities in vitro against three human cancer cell lines (human lung carcinoma cell line: A549, human leukemia cell line: K562, and human prostate cancer cell line: PC-3). Most of these compounds showed potent activities against these tumor cell lines, especially against A549 and K562 cell lines. The preliminary structure-Activity relationships of 1-cyano-2-Amino-benzimidazole derivatives were also discussed. The cell cycle analysis was carried out in K562 cells and the results showed that compound 4d caused a marked increase of cells in G 2/M phase.
Copper(I)-catalyzed intramolecular C-N coupling reactions to form 1-cyanobenzimidazoles
Hu, Zhang,Li, Si-Dong,Hong, Peng-Zhi,Wu, Zhanxia
, p. 147 - 155 (2012/02/04)
Employing a CuI/2,2'-biimidazole catalyst system, the intramolecular C-N coupling reactions of various substituted aryl guanidines could be successfully carried out under mild conditions. A variety of 1-cyanobenzimidazoles were synthesized in good to excellent yields. ARKAT-USA, Inc.
