Synthesis and In Vitro Anticancer Evaluation of Flavone-1,2,3-Triazole Hybrids

被引:8
|
作者
Nemeth-Rieder, Alexandra [1 ]
Keglevich, Peter [1 ]
Hunyadi, Attila [2 ]
Latif, Ahmed Dhahir [3 ,4 ]
Zupko, Istvan [3 ]
Hazai, Laszlo [1 ]
机构
[1] Budapest Univ Technol & Econ, Fac Chem Technol & Biotechnol, Dept Organ Chem & Technol, Muegyet Rkp 3, H-1111 Budapest, Hungary
[2] Univ Szeged, Inst Pharmacognosy, Eotvos U 6, H-6720 Szeged, Hungary
[3] Univ Szeged, Dept Pharmacodynam & Biopharm, Eotvos Str 6, H-6720 Szeged, Hungary
[4] Wasit Univ, Fac Med, Dept Pharmacol & Toxicol, Wasit 52001, Iraq
来源
MOLECULES | 2023年 / 28卷 / 02期
关键词
flavones; chrysin; kaempferol; hybrids; 1,2,3-triazole; anticancer activity; CLICK CHEMISTRY; DERIVATIVES; FEASIBILITY; CHRYSIN;
D O I
10.3390/molecules28020626
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
Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hybrids were investigated on 60 cell lines of 9 common cancer types (NCI60) in vitro as antitumor agents. Some of them proved to have a significant antiproliferative effect.
引用
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页数:16
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