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The dried stem and root bark of D. giraldii were obtained from Anguo herbal medicine market (HeBei, China), which were collected from Shanxi Province of China on May, 2012. The plant material was identified by Professor Jin-Cai Lu, Department of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University. A voucher specimen (DG-20120515) was deposited with the Nature Products Laboratory of Shenyang Pharmaceutical University, Shenyang, PR China.
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18 The dried stem and root bark of D. giraldii were obtained from Anguo herbal medicine market (HeBei, China), which were collected from Shanxi Province of China on May, 2012. The plant material was identified by Professor Jin-Cai Lu, Department of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University. A voucher specimen (DG-20120515) was deposited with the Nature Products Laboratory of Shenyang Pharmaceutical University, Shenyang, PR China.
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7 451.1751).
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24
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85043109313
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8 467.1700).
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8 467.1700).
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5Na, 431.1829).
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85043140382
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50 values were calculated with SPSS 16.0 and were determined based on the average results of at least three independent experiments.
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50 values were calculated with SPSS 16.0 and were determined based on the average results of at least three independent experiments.
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31 Raffa, D., Maggio, B., Plescia, F., Cascioferro, S., Raimondi, M.V., Cancemi, G., D'Anneo, A., Lauricella, M., Cusimano, M.G., Bai, R., Bioorg. Med. Chem., 23, 2015, 6305.
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32
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85043131730
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Cell apoptosis was detected using an Annexin V-FITC Apoptosis Detection Kit (Beyotime, Shanghai, China). HepG2 cells were treated with various concentrations of compound 2 for 48 h, followed by washing with ice-cold PBS buffer and resuspended in Annexin V-FITC/PI staining solution for 15 min in the dark. The cell samples were analyzed by a FACScan flow cytometer (Becton Dickinson, USA).
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32 Cell apoptosis was detected using an Annexin V-FITC Apoptosis Detection Kit (Beyotime, Shanghai, China). HepG2 cells were treated with various concentrations of compound 2 for 48 h, followed by washing with ice-cold PBS buffer and resuspended in Annexin V-FITC/PI staining solution for 15 min in the dark. The cell samples were analyzed by a FACScan flow cytometer (Becton Dickinson, USA).
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