Design, synthesis, and biological evaluation of quinazoline derivatives containing piperazine moieties as antitumor agents

被引:11
|
作者
Li, Wen [1 ]
Chen, Shu-Yi [1 ]
Hu, Wei-Nan [1 ]
Zhu, Mei [1 ]
Liu, Jia-Min [1 ]
Fu, Yi-Hong [1 ]
Wang, Zhen-Chao [1 ,2 ]
OuYang, Gui-Ping [1 ,2 ,3 ]
机构
[1] Guizhou Univ, Coll Pharm, Guiyang 550025, Peoples R China
[2] Guizhou Med Univ, State Key Lab Funct & Applict Med Plants, Guiyang, Peoples R China
[3] Drug Synthet Engn Lab Guizhou Prov, Guiyang, Peoples R China
基金
中国国家自然科学基金;
关键词
quinazoline derivatives; cytotoxicity; migratory capacity; colonization activity; apoptosis; INHIBITOR GEFITINIB; LUNG-CANCER; IN-VITRO; GROWTH; RADIOTHERAPY; SUPPRESSES; MIGRATION; CELLS;
D O I
10.1177/1747519820910384
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of novel quinazoline derivatives containing piperazine analogs are synthesized via substitution reactions with 6,7-disubstituted 4-chloroquinazoline and benzyl piperazine (amido piperazine). Potent antiproliferative activities are observed against A549, HepG2, K562, and PC-3 withN-(3-chlorophenyl)-2-(4-(7-methoxy-6-(3-morpholino-propoxy)quinazoline-4-yl)piperazine-1-yl)acetamidenameC9showing excellent activity. This active derivative was screened for cell migration ability, proliferation effects, and apoptosis against A549 and PC-3 cells, with the result showing biological activity almost equal to that of the control gefitinib.
引用
收藏
页码:536 / 542
页数:7
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