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QI Wei-Yan, OU Na, WU Xiao-Dong, XU Han-Mei. New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity[J]. 中国天然药物, 2016, 14(10): 789-793.
引用本文: QI Wei-Yan, OU Na, WU Xiao-Dong, XU Han-Mei. New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity[J]. 中国天然药物, 2016, 14(10): 789-793.
QI Wei-Yan, OU Na, WU Xiao-Dong, XU Han-Mei. New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity[J]. Chinese Journal of Natural Medicines, 2016, 14(10): 789-793.
Citation: QI Wei-Yan, OU Na, WU Xiao-Dong, XU Han-Mei. New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity[J]. Chinese Journal of Natural Medicines, 2016, 14(10): 789-793.

New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity

New arbutin derivatives from the leaves of Heliciopsis lobata with cytotoxicity

  • 摘要: Heliciopsis lobata is a medicinal plant, which is exclusively used to treat tumor in Li folk region. Two new arbutin derivatives, 6'-((E)2-methoxy-5-hydroxycinnamoyl) arbutin (1) and 2'-((E)2, 5-dihydroxycinnamoyl) arbutin (2) along with five known compounds (3-7), were isolated from the leaves of Heliciopsis lobata. Their structures were elucidated on the basis of extensive spectroscopic interpretations. They were evaluated for their potential anticancer activity. Compounds 6 and 7 exhibited cytotoxicity against MGC-803 cells with IC50 values being 44.1 and 11.3 gmL-1, respectively. Additionally, compounds 1, 2 and 5-7 exhibited a moderate inhibition of MGC-803 cells invasion;compound 2 at 20 gmL-1 inhibited the invasion of MGC-803 cells by 43.0%, compared with the controls.

     

    Abstract: Heliciopsis lobata is a medicinal plant, which is exclusively used to treat tumor in Li folk region. Two new arbutin derivatives, 6'-((E)2-methoxy-5-hydroxycinnamoyl) arbutin (1) and 2'-((E)2, 5-dihydroxycinnamoyl) arbutin (2) along with five known compounds (3-7), were isolated from the leaves of Heliciopsis lobata. Their structures were elucidated on the basis of extensive spectroscopic interpretations. They were evaluated for their potential anticancer activity. Compounds 6 and 7 exhibited cytotoxicity against MGC-803 cells with IC50 values being 44.1 and 11.3 gmL-1, respectively. Additionally, compounds 1, 2 and 5-7 exhibited a moderate inhibition of MGC-803 cells invasion;compound 2 at 20 gmL-1 inhibited the invasion of MGC-803 cells by 43.0%, compared with the controls.

     

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