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新型5’-席夫碱取代的补骨脂素衍生物的合成及其抗肿瘤细胞增殖活性研究(英文)
Synthesis and antiproliferative activities of novel 5’-Schiff-base group substituted psoralen derivatives
【摘要】 补骨脂素衍生物与乙酸酐在四氯化碳溶液中可顺利发生Friedel-Crafts酰基化反应,以73%产率得到5’-乙酰基取代的补骨脂素。然后在三氟化硼乙醚作用下,5’-乙酰基补骨脂素与芳香胺或脂肪胺均可顺利反应,以72%~92%产率得到5’-席夫碱取代的补骨脂素衍生物。该合成法具有原料价廉易得、制备条件简单、反应条件温和、收率良好及Friedel-Crafts酰基化反应选择性高等特点。MTT法细胞活性测试表明,所合成的部分补骨脂素衍生物6具有抗增殖活性。
【Abstract】 It was found that psoralen derivative could perform a Friedel-Crafts acylation smoothly with acetic anhydride to give 5’-acetylpsoralen in a 73% yield.In the presence of boron trifluoride etherate,5’-acetylpsoralen reacted with both aromatic amines and aliphatic amine smoothly to afford 5’-Schiff-base group substituted psoralen derivatives in 72%-92% yields.The novel synthetic method has the advantages of cheap materials,mild reaction conditions,good yields and high regioselectivity in the Friedel-Crafts acylation.Cell viability assay by MTT demonstrates that some of the psoralen derivatives 6 have antiproliferative activities.
【Key words】 psoralen derivative; Schiff-base group; synthesis; antiproliferative activity;
- 【文献出处】 药学学报 ,Acta Pharmaceutica Sinica , 编辑部邮箱 ,2011年01期
- 【分类号】R284;R285
- 【下载频次】291