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首页> 外文期刊>Fitoterapia >Kaemgalangol A: Unusual seco-isopimarane diterpenoid from aromatic ginger ce:italic>Kaempferia galanga/ce:italic>
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Kaemgalangol A: Unusual seco-isopimarane diterpenoid from aromatic ginger ce:italic>Kaempferia galanga/ce:italic>

机译:Kaemgalangol A:来自芳香姜& Ce:斜体> Kaempferia Galanga的异常的Seco-inopimarane diterpenoid& / ce:斜体>

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摘要

A new unusual seco-isopimarane, kaemgalangol A (1) and 12 usual analogs (2?13) were isolated from the rhizomes ofKaempferia galanga(Family: Zingiberaceae). KaemgalangolA (1) represented a rarely isolated 9,10-seco-isopimarane skeleton. The chemical structures of the isolated compounds were mainlyinvestigated by spectroscopic techniques such as 1D, 2D NMR, and HRMS. The absolute configuration of1–3was studied by X-ray diffraction analysis as well as experimental and TDDFT-calculated electronic circular dichroism. Among the isolated diterpenoids,5,6and9exhibited cytotoxic activity against HeLa (IC5075.1, 74.2 and 76.5?μM, respectively) and HSC-2 (IC5069.9, 53.3 and 58.2?μM, respectively) cancer cells.
机译:从Kaempferia Galanga(家族:Zingiberaceae)的根茎中分离出一种新的异常的Seco-Isopimarane,Kaemgalangol A(1)和12个通常类似物(2?13)。 Kaemgalangola(1)代表了很少分离的9,10-秒甲烷骨架骨架。 主要通过光谱技术(如1D,2D NMR和HRM)为分离的化合物的化学结构。 X射线衍射分析研究的1-3瓦斯的绝对配置以及实验和TDDFT计算的电子圆形二色性。 在分离的二萜中,针对Hela(IC5075.1,74.2和76.5Ω,分别)和HSC-2(IC5069.9,53.3和58.2≤m,分别)癌细胞中的5,6和9个exto毒性活性。

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