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刺茶美登木中2个新的倍半萜生物碱类化合物

Two novel sesquiterpene alkaloids from Maytenus variabilis

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【作者】 周兰; 邹坤; 李彪; 汪蕾; 程凡;

【Author】 ZHOU Lan;ZOU Kun;LI Biao;WANG Lei;CHENG Fan;College of Hydraulic & Environmental Engineering, China Three Gorges University;Hubei Key Laboratory of Natural Products Research and Utilization, College of Biological and Pharmaceutical Sciences, China Three Gorges University;Yichang Key Laboratory of Modern Pharmaceutical Preparations, College of Medicine and Health Sciences, China Three Gorges University;Public Inspection and Testing Center of Yiling District,Yichang;

【通讯作者】 汪蕾;程凡;

【机构】 三峡大学水利与环境学院; 三峡大学生物与制药学院天然产物研究与利用湖北省重点实验室; 三峡大学健康医学院现代药物制剂宜昌市重点实验室; 宜昌市夷陵区公共检验检测中心;

【摘要】 目的 研究刺茶美登木Maytenus variabilis的倍半萜生物碱类化学成分及其细胞毒活性。方法 运用正相硅胶柱色谱、制备薄层色谱及制备型HPLC等方法进行化合物分离纯化,并用1D NMR、2D NMR、HRMS等现代波谱技术进行化合物的结构鉴定。采用MTT法研究化合物的抗肿瘤活性。结果 从刺茶美登木中分离鉴定2个倍半萜生物碱类化合物,分别鉴定为:(1R,2S,4S,5S,6R,7R,9R,10R)-1,2-dinicotinoyloxy-4-hydroxy-6,15-diacetoxy-9-benzoyloxy-dihydro-β-agarofuran(1)和(1R,2S,4S,5S,6R,7R,9R,10R)-1,6,15-triacetoxy-2,9-dinicotinoyloxy-4-hydroxy-dihydro-β-agarofuran(2)。结论 化合物1和2为新的倍半萜生物碱类化合物,分别命名为美登木宁碱A及美登木宁碱B。细胞毒活性研究显示,化合物1和2对人胃癌HGC-27细胞有一定的体外增殖抑制活性,其半数抑制浓度(median inhibition concentration,IC50)分别为69.44、65.74μmol/L。

【Abstract】 Objective To study the sesquiterpene alkaloids from Maytenus variabilis and their cytotoxic activities. Methods The compounds were isolated and purified by column chromatography over normal phase silica gel, preparative thin-layer chromatography and preparative HPLC. Their structures were elucidated by means of various spectroscopic techniques including one-dimensional nuclear magnetic resonance(1D NMR), two-dimensional nuclear magnetic resonance(2D NMR) and high resolution mass spectrometry(HRMS). The anti-tumor activity of the compound was investigated by MTT assay. Results Two sesquiterpene alkaloids were isolated from M. variabilis, their structures were elucidated as(1R,2S,4S,5S,6R,7R,9R,10R)-1,2-dinicotinoyloxy-4-hydroxy-6,15-diacetoxy-9-benzoyloxy-dihydro-β-agarofuran(1) and(1R,2S,4S,5S,6R,7R,9R,10R)-1,6,15-triacetoxy-2,9-dinicotinoyloxy-4-hydroxy-dihydro-β-agarofuran(2), respectively. Conclusion The cytotoxic activity study revealed that compounds 1 and 2 exhibited certain in vitro proliferation inhibitory activity against human gastric cancer HGC-27 cell with IC50 values of 69.44, 65.74 μmol/L.

【基金】 湖北省中央引导地方科技发展资金项目(2024BSB016);三峡大学人才科研启动基金项目(8253302)
  • 【文献出处】 中草药 ,Chinese Traditional and Herbal Drugs , 编辑部邮箱 ,2025年15期
  • 【分类号】R284.1
  • 【下载频次】63
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