为提高5-氟尿嘧啶抗癌的靶向性,降低其不良反应,合成了5种新型卟啉-5-氟尿嘧啶衍生物及其Mn3+配合物,优化了合成反应条件,探索了目标化合物的分离方法.通过IR、UV-Vis、1H NMR和ESI-MS对化合物结构和组成进行了确认.采用四甲基偶氮唑蓝(MTT)比色法,以5-氟尿嘧啶为阳性对照药,测试了卟啉化合物对5种肿瘤细胞的体外抑制活性.初筛结果显示,化合物D3对人卵巢癌细胞Sk-ov-3有较强的抑制作用.
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