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Synthetic Analogue of the Natural Product Piperlongumine as a Potent Inhibitor of Breast Cancer Cell Line Migration

机译:天然产物哌隆定的合成类似物作为乳腺癌细胞系迁移的强抑制剂

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>Piperlongumine is a natural amide alkaloid isolated from several species of Piper and is described in the literature as selectively cytotoxic to several cancer cell lines. Inhibiting cell migration has gained considerable interest as an approach for discovering antimetastatic agents because this process is fundamental to metastasis. Piperlongumine, selected from cell-based assay screening of NuBBE Database, inhibited the migration of MDA-MB-231 breast cancer cells with an EC50 of 3.0 ?± 1.0 ?μM by the Boyden chamber assay. A series of five analogous compounds based on the structure of piperlongumine were designed, synthesized and evaluated in cell migration and cytotoxicity assays. The analogue designed by molecular simplification ((E)-N-acryloyl-3-(3,4,5-trimethoxyphenyl)acrylamide) was the most active of the series, with an EC50 of 1.5 ?± 1 ?μM. Additionally, this compound was selectively cytotoxic, with a selectivity index (SI) of 4.4.
机译:哌隆定(Piperlongumine)是从几种Piper物种中分离出来的天然酰胺生物碱,在文献中被描述为对几种癌细胞具有选择性的细胞毒性。作为发现抗转移剂的一种方法,抑制细胞迁移已经引起了极大的兴趣,因为该过程是转移的基础。从NuBBE数据库的基于细胞的试验筛选中选择的哌隆丁通过Boyden室试验抑制了EC50为3.0±±1.0μM的MDA-MB-231乳腺癌细胞的迁移。在细胞迁移和细胞毒性测定中设计,合成和评估了一系列基于哌隆定结构的五个类似化合物。通过分子简化设计的类似物((E)-N-丙烯酰基-3-(3,4,5-三甲氧基苯基)丙烯酰胺)是该系列中活性最高的,EC50为1.5?±1?μM。另外,该化合物具有选择性的细胞毒性,选择性指数(SI)为4.4。

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