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Synthesis and Biological Activities of 6-Hydroxyaurone Derivatives

机译:6-羟基金龙酮衍生物的合成及生物活性

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摘要

A series of 6-hydroxyaurone derivatives were synthesized in satisfactory yields and characterized by IR, H-1 NMR, C-13 NMR, and HRMS or elemental analysis. The structure of compound 3e was further confirmed by X-ray crystal analysis. Bioassay results indicated that some of the target compounds displayed moderate herbicidal activity against the dicotyledonous plant Brassica campestris L. at 100 mu gmL(-1), and some compounds also showed significant antiproliferative activity against tumor cell lines Hela, HepG-2, and MCF-7.
机译:以令人满意的产率合成了一系列6-羟基金酮衍生物,并通过IR,H-1 NMR,C-13 NMR和HRMS或元素分析进行​​了表征。通过X射线晶体分析进一步证实了化合物3e的结构。生物测定结果表明,某些目标化合物在100μgmL(-1)时对双子叶植物油菜具有中等程度的除草活性,而某些化合物还对肿瘤细胞Hela,HepG-2和MCF具有显着的抗增殖活性。 -7。

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