Ferrocenylchalcone-uracil conjugates: synthesis and cytotoxic evaluation

被引:6
|
作者
Singh, Amandeep [1 ]
Mehra, Vishu [2 ]
Sadeghiani, Neda [3 ]
Mozaffari, Saghar [3 ]
Parang, Keykavous [3 ]
Kumar, Vipan [1 ]
机构
[1] Guru Nanak Dev Univ, Dept Chem, Amritsar 143005, Punjab, India
[2] Hindu Coll, Dept Chem, Amritsar 143001, Punjab, India
[3] Chapman Univ, Sch Pharm, Ctr Targeted Drug Delivery, Irvine, CA 92618 USA
关键词
Click chemistry; Cytotoxic evaluation; Ferrocenylchalcone; Uracil; ANTI-TUBERCULAR EVALUATION; BETA-LACTAM-FERROCENE; ANTICANCER AGENTS; CANCER; CELLS; DERIVATIVES; CHEMISTRY;
D O I
10.1007/s00044-018-2145-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Huisgen's azide-alkyne cycloaddition reaction was employed to synthesize a series of 1H-1,2,3-triazole-tethered uracil-ferrocenyl chalcone conjugates with the aim of evaluating their in vitro anti-proliferative efficacy on human leukemia (CCRF-CEM) and human breast adenocarcinoma (MDA-MB-468) cell lines. Cytotoxic evaluation studies identified a number of synthesized conjugates that inhibited the proliferation of leukemia cancer cells by similar to 70% after 72 h. The selected synthesized conjugates were found to be significantly less cytotoxic against normal kidney cell line (LLC-PK1) when compared with CCRF-CEM cancer cells. [GRAPHICS] .
引用
收藏
页码:1260 / 1268
页数:9
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