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霍纳-沃兹沃思-埃蒙斯法合成具有强效抗癌活性的胡椒碱类似物。

Horner-Wadsworth-Emmons approach to piperlongumine analogues with potent anti-cancer activity.

作者信息

Han Li-Chen, Stanley Paul A, Wood Paul J, Sharma Pallavi, Kuruppu Anchala I, Bradshaw Tracey D, Moses John E

机构信息

School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.

出版信息

Org Biomol Chem. 2016 Aug 21;14(31):7585-93. doi: 10.1039/c6ob01160h. Epub 2016 Jul 22.

Abstract

Natural products with anti-cancer activity play a vital role in lead and target discovery. We report here the synthesis and biological evaluation of the plant-derived alkaloid, piperlongumine and analogues. Using a Horner-Wadsworth-Emmons coupling approach, a selection of piperlongumine-like compounds were prepared in good overall yield from a novel phosphonoacetamide reagent. A number of the compounds displayed potent anti-cancer activity against colorectal (HCT 116) and ovarian (IGROV-1) carcinoma cell lines, via a mechanism of action which may involve ROS generation. Contrary to previous reports, no selective action in cancer cell (MRC-5) was observed for piperlongumine analogues.

摘要

具有抗癌活性的天然产物在先导化合物和靶点发现中起着至关重要的作用。我们在此报告植物源生物碱派珀长胡椒碱及其类似物的合成与生物学评价。采用霍纳尔-沃兹沃思-埃蒙斯偶联方法,以一种新型膦酰基乙酰胺试剂为原料,以良好的总收率制备了一系列派珀长胡椒碱类化合物。许多化合物通过可能涉及活性氧生成的作用机制,对结肠癌细胞(HCT 116)和卵巢癌细胞(IGROV-1)显示出强大的抗癌活性。与先前的报道相反,未观察到派珀长胡椒碱类似物对癌细胞(MRC-5)有选择性作用。

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