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机构地区:[1]中国药科大学天然药物化学教研室,南京210009 [2]东南大学药物研究中心,南京211187
出 处:《中国药科大学学报》2013年第4期303-306,共4页Journal of China Pharmaceutical University
摘 要:设计合成了一系列以2-甲基-2-取代苯氧基丙酸为离去基团的二价铂配合物,其结构经红外光谱、核磁和质谱确证。采用MTT法对3种肿瘤细胞进行抗增殖活性研究,结果显示化合物对胃癌细胞(SGC-7901)活性较好,对肝癌细胞(HepG2)和非小细胞肺癌细胞(A549)活性较弱或无活性。A class of novel platinum(Ⅱ) complexes with 2-methyl-2-substituted phenoxypropanoic acids as leaving ligands were designed and synthesized.All complexes were characterized by IR,1H NMR and ESI-MS spectra.The in vitro antiproliferative activities were tested by MTT assay against three human cancer cell lines,indicating that the complexes showed selective cytotoxicity to human gastric cancer cell lines(SGC-7901) with only weak antiproliferative activities were observed against human hepatocellular carcinoma cell line(HepG2) and human non-small cell lung cancer cell line(A549).
关 键 词:铂(Ⅱ)配合物 合成 2-甲基-2-取代苯氧丙酸 细胞毒性
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