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Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata

机译:樟芝樟脑子实体的生物活性类苯胺衍生物的分离与合成

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摘要

A new enynyl-benzenoid, antrocamphin O (1,4,7-dimethoxy-5-methyl-6-(3′-methylbut-3-en-1-ynyl)benzo[d][1,3]dioxide), and the known benzenoids antrocamphin A and 7-dimethoxy-5-methyl-1,3-benzodioxole, were isolated from the fruiting bodies of Antrodia camphorata (Taiwanofungus camphoratus). The structure of antrocamphin O was unambiguously assigned by the analysis of spectral data (including 1D and 2D NMR, high-resolution MS, IR, and UV) and total synthesis. Compound >1 was prepared through the Sonogashira reaction of 5-iodo-4,7-dimethoxy-6-methylbenzene and 2-methylbut-1-en-3-yne as the key step. The benzenoids were tested for cytotoxicity against the HT29, HTC15, DLD-1, and COLO 205 colon cancer cell lines, andactivities are reported herein.
机译:一种新的烯基-苯甲酮,海藻土O(1,4,7-二甲氧基-5-甲基-6-(3'-甲基丁-3-烯-1-炔基)苯并[d] [1,3]二氧化物)和从樟芝Antrodia camphorata(Taiwanofungus camphoratus)的子实体中分离出已知的类苯环化合物前樟脑A和7-二甲氧基-5-甲基-1,3-苯并二恶唑。通过分析光谱数据(包括1D和2D NMR,高分辨率MS,IR和UV)和总合成,明确确定了海马O的结构。化合物> 1 是通过5-碘-4,7-二甲氧基-6-甲基苯和2-甲基丁-1-烯-3-炔的Sonogashira反应制备的,这是关键步骤。测试了该类化合物对HT29,HTC15,DLD-1和COLO 205结肠癌细胞系的细胞毒性,并在此报道了其活性。

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