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Synthesis and Bioactivity of Furoxan-Based Nitric Oxide-Releasing Colchicine Derivatives as Anticancer Agents

机译:呋喃喃基一氧化氮秋水仙碱衍生物作为抗癌剂的合成及生物活性

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摘要

A series of novel nitric oxide-donating colchicine derivatives (9a-j) were synthesized by coupling furoxan with N-methyl colchiceinamide through an appropriate spacer arm and their cytotoxicity against four human cancer cell lines in vitro were evaluated by MTT method. It was found that many of the derivatives displayed significant activity, particularly, compound 9f showed more potent cytotoxic activities than colchicine.
机译:通过适当的间隔臂将呋喃喃与N-甲基乙酰水杨酰胺偶联,合成了一系列新型的一氧化氮供体秋水仙碱衍生物(9a-j),并通过MTT法评估了它们对四种人类癌细胞系的体外细胞毒性。发现许多衍生物表现出显着的活性,特别是化合物9f显示出比秋水仙碱更有效的细胞毒性活性。

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