黄宇希, 严禹瑶, 李小翠, 刘菲, 熊亮, 戴鸥. 蓬莪术正丁醇部位中一个新的紫罗兰酮成分J. 药学学报, 2025, 60(10): 3139-3145. DOI: 10.16438/j.0513-4870.2025-0528
引用本文: 黄宇希, 严禹瑶, 李小翠, 刘菲, 熊亮, 戴鸥. 蓬莪术正丁醇部位中一个新的紫罗兰酮成分J. 药学学报, 2025, 60(10): 3139-3145. DOI: 10.16438/j.0513-4870.2025-0528
HUANG Yu-xi, YAN Yu-yao, LI Xiao-cui, LIU Fei, XIONG Liang, DAI Ou. A new ionone from n-butanol fraction of Curcuma phaeocaulisJ. Acta Pharmaceutica Sinica, 2025, 60(10): 3139-3145. DOI: 10.16438/j.0513-4870.2025-0528
Citation: HUANG Yu-xi, YAN Yu-yao, LI Xiao-cui, LIU Fei, XIONG Liang, DAI Ou. A new ionone from n-butanol fraction of Curcuma phaeocaulisJ. Acta Pharmaceutica Sinica, 2025, 60(10): 3139-3145. DOI: 10.16438/j.0513-4870.2025-0528

蓬莪术正丁醇部位中一个新的紫罗兰酮成分

A new ionone from n-butanol fraction of Curcuma phaeocaulis

  • 摘要: 采用反相中压液相色谱、凝胶柱色谱、硅胶柱色谱、制备薄层色谱及反相半制备高液相色谱等分离技术, 对蓬莪术正丁醇部位进行了分离纯化。随后, 运用高分辨质谱、红外、核磁共振等波谱技术对化合物进行了结构鉴定。最终, 从蓬莪术正丁醇部位中分离鉴定了3个紫罗兰酮苷类化合物, 分别为(6Z, 9S)-4, 6-megastigmadien-3-one-9-O-β-D-glucopyranoside (1)、(3R, 9S)-megastigman-5-en-3, 9-diol 3-O-β-D-glucopyranoside (2) 和blumenol C glucoside (3), 其中化合物1为新的紫罗兰酮苷, 化合物23为首次从蓬莪术中分离得到。对分得的化合物进行细胞毒和抗炎活性研究, 结果表明, 3个化合物均具有一定的细胞毒及抗炎活性。

     

    Abstract: The n-butanol fraction of Curcuma phaeocaulis was separated and purified using a combination of chromatographic techniques, including reversed-phase medium-pressure liquid chromatography, gel column chromatography, silica gel column chromatography, preparative thin-layer chromatography and reversed-phase semi-preparative high-performance liquid chromatography. The structures of the isolated compounds were elucidated through comprehensive spectroscopic analyses, including high-resolution mass spectrometry, infrared spectroscopy, and nuclear magnetic resonance spectroscopy. Finally, three ionone glycosides were isolated from C. phaeocaulis and identified as (6Z, 9S)-4, 6-megastigmadien-3-one-9-O-β-D-glucopyranoside (1), (3R, 9S)-megastigman-5-en-3, 9-diol 3-O-β-D-glucopyranoside (2), and blumenol C glucoside (3). Notably, compound 1 was a new ionone, while compounds 2 and 3 were isolated from C. phaeocaulis for the first time. Subsequent evaluation of cytotoxic and anti-inflammatory activities revealed that all three compounds exhibited cytotoxic and anti-inflammatory effects.

     

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