In vitro antitumor activity evaluation of some 1,2,4-triazine derivatives bearing piperazine amide moiety against breast cancer cells

被引:45
作者
Yurttas, Leyla [1 ]
Demirayak, Seref [2 ]
Ilgin, Sinem [3 ]
Atli, Ozlem [3 ]
机构
[1] Anadolu Univ, Dept Pharmaceut Chem, Fac Pharm, TR-26470 Eskisehir, Turkey
[2] Medipol Univ, Sch Pharm, Dept Pharmaceut Chem, TR-34083 Istanbul, Turkey
[3] Anadolu Univ, Dept Pharmaceut Toxicol, Fac Pharm, TR-26470 Eskisehir, Turkey
关键词
1,2,4-Triazine; Piperazine amide; Breast cancer; Antiproliferative activity; Apoptosis; XTT method; ANTICANCER ACTIVITY; AGENTS; ANALOGS; SYSTEMS; THIOGLYCOSIDE; APOPTOSIS;
D O I
10.1016/j.bmc.2014.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of 1,2,4-triazine derivatives bearing piperazine amide moiety has been synthesized and investigated for their potential anticancer activities. 1-[4-(5,6-Bis(4-subtituted phenyl)-1,2,4-triazin-3-yl) piperazin- 1-yl]-2-[4-(3-substituted phenyl) piperazin-1-yl] ethanone derivative (1-32) compounds were synthesized by a four step synthetic procedure. The activity studies were evaluated using XTT method, BrdU method and flow cytometric analysis on MCF-7 breast cancer cells and NIH/3T3 (mouse embryonic fibroblast cells) healthy cells. Compounds 5 with 3-chlorophenyl and compound 7 with 4-chlorophenyl substitutions were found to be promising antiproliferative agents comparing with an effective anticancer drug, cisplatin. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6313 / 6323
页数:11
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