GdCl3 promoted synthesis of novel pyrimidine fused indazole derivatives and their anticancer activity

被引:24
|
作者
Yakaiah, T. [1 ]
Kurumurthy, C. [1 ]
Lingaiah, B. P. V. [1 ]
Narsaiah, B. [1 ]
Pamanji, R. [2 ]
Velatooru, L. R. [2 ]
Rao, J. Venkateswara [2 ]
Gururaj, S. [4 ]
Parthasarathy, T. [4 ]
Sridhar, B. [3 ]
机构
[1] Indian Inst Chem Technol, Fluoroorgan Div, Hyderabad 500007, Andhra Pradesh, India
[2] Indian Inst Chem Technol, Div Toxicol, Hyderabad 500007, Andhra Pradesh, India
[3] Indian Inst Chem Technol, Lab Xray Crystallog, Hyderabad 500007, Andhra Pradesh, India
[4] Nizam Coll, Dept Chem, Hyderabad 500001, Andhra Pradesh, India
关键词
Indazoles; Aliphatic/aromatic aldehydes; Pyrimidines; Electron rich olefins; Anticancer activity; Rho-kinase (2F2U) protein; GENETIC ALGORITHM;
D O I
10.1007/s00044-011-9962-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The three component Grieco condensation of indazoles, aliphatic/aromatic aldehydes, and electron rich olefins in the presence of GdCl3 resulted in a novel pyrimidine fused indazoles in single pot under mild conditions. Representative examples were screened for in vitro anti-cancer activity and some of the compounds exhibited promising cytotoxic activity against U937 cell lines in comparable with standard drug etoposide. The data were further compared with structure-based investigations using docking studies with the crystal structure of Rho-kinase (2F2U) protein. The fitness values estimated by genetic algorithm were found to have a good correlation with the experimental inhibitory potencies.
引用
收藏
页码:4261 / 4273
页数:13
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