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

机译:新型喹唑啉衍生物作为潜在抗癌药的设计,合成及生物学评价

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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 μg/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).
机译:已经合成了22种喹唑啉衍生物,并检查了它们对三种肿瘤细胞系(人乳腺癌细胞系(MCF-7),人宫颈癌细胞系(HeLa)和人肝癌细胞系(HepG2))的抗肿瘤活性。十二种测试化合物显示出令人鼓舞的抗肿瘤活性,IC 50 范围为5.0–9.7μg/ mL。关于活性谱,五种化合物对与参考药物(达沙替尼)相当的三种测试细胞系表现出令人感兴趣的抗增殖特性。

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