Design, synthesis and biological evaluation of novel quinazoline derivatives as potential anti-cancer agents

被引:4
|
作者
Alafeefy, Ahmed M. [1 ]
Ashour, Abdelkader E. [2 ]
机构
[1] AlKharj Univ, Coll Pharm, Dept Pharmaceut Chem, AlKharj, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh, Saudi Arabia
关键词
Anti-tumour; dasatinib; quinazoline; synthesis; NF-KAPPA-B; O-ALKYLATION; INHIBITORS; DISCOVERY; LEUKEMIA;
D O I
10.3109/14756366.2011.601302
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
Twenty-two quinazoline derivatives have been synthesised and examined for their anti-tumour activity against three tumour cell lines, namely human breast cancer cell line (MCF-7), human cervical cancer cell line (HeLa) and human hepatoma cell line (HepG2). Twelve of the tested compounds have shown promising anti-tumour activity with an IC50 range of 5.0-9.7 mu g/mL. Regarding the spectrum of activity, five compounds exhibited interesting anti-proliferative properties against the three tested cell lines comparable to the reference drug (dasatinib).
引用
收藏
页码:541 / 545
页数:5
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