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作 者:程灿玲 宫凯凯 李平林[1] 颜洁[1] 梁振[1] 唐旭利[2] 李国强[1]
机构地区:[1]中国海洋大学海洋药物教育部重点实验室,医药学院 [2]中国海洋大学化学化工学院,山东青岛266003
出 处:《中国海洋药物》2014年第1期53-57,共5页Chinese Journal of Marine Drugs
基 金:国家自然科学基金项目(41076084;20975094)资助
摘 要:目的研究红树植物拟海桑Sonneratia paracaseolaris的化学成分。方法利用硅胶柱层析、凝胶Sephadex LH-20柱层析、HPLC等手段对化学成分进行了分离纯化;通过理化性质,结合波谱数据分析并与文献对照,鉴定化合物的结构,分别以MTT和SRB法评价化合物的抗肿瘤活性。结果从红树植物拟海桑Sonneratia paracaseolaris的甲醇提取物中,分离鉴定了9个单体化合物:9-氧橙花叔酮(1),3,7,11-三甲基-1,7(E),10-十二碳三烯-3-羟基-9-酮(2),(22E,24R)5cc,8盯过氧化麦角甾23-甲基-6,22-二烯-3伊醇(3),(22E)-5α,8α-过氧化麦角甾-23甲基-6,9,22-三烯-3β-醇(4),(22E)5α,8α-过氧化麦角甾-6,22-二烯-3β-醇(5),4’-甲氧基偏柏脂素(6),偏柏脂素(7),3’-羟基-4’-甲氧基-4’-脱羟基偏柏脂素(8),1,3二对羟基苯基-4-戊烯-1-酮(9)。化合物6~9对A549、HL-60、P388及K562肿瘤细胞株显示出不同程度的抑制作用,其中化合物8对K562、HL60细胞具有较强的细胞毒活性,IC50值分别为1.99、3.13μmol/L。结论化合物1~9均为首次从拟海桑Sonneratia paracaseolaris中分离得到;首次测定了化合物6~9对A549、HL-60、P388及K562肿瘤细胞株的细胞毒活性,其中化合物8对HL-60、K562细胞显示出较好的抑制活性。Objective To study the chemical constituents of Sonneratia paracaseolaris. Methods The isolation and purification of the compounds were performed by silica gel, Sephadex LH-20 and HPLC methods, their structures were determined by comparison their physieoehemical characters and spectral data with literatures, and their antitumor activities were evaluated by MTT and SRB methods respec- tively. Results From the methanol extracts of Sonneratia paracaseolaris, nine compounds were isolated and identified as 9-oxonerolidol (1), 3, 7, 11-trimethyldodeca-1, 7(E), 10-trien-3-ol-9-one (2), (22E,24R)-5α, 8α-epidioxy-23-methylergosta-6, 22-dien-3β-ol (3), (22E, 24R)-5α, 8α-epidioxy-23-methylergosta-6, 9, 22-trien-3β-ol (4), (22E)-5α, 8α-epidioxy-6, 22-dien-3β-ol (5), 4'-O-methyl-nyasol (6), nyasol (7), 3 -hydroxy-4 -methoxy-4-dehydroxynyasol (8), 1, 3-di-p-hydroxyphenyl-4-penten-1 one (9). Compounds 6-9 showed inhibitory activities against tumor cell lines including A549, HL-60, P388 and K562, and compound 8 had more potential antitumor activities against K562 and HL-60 cells,with ICs0 values of 1.99, 3. 13 mol/L, respectively. Conclusion Compounds 1 -9 were isolated from this Sonneratia paracaseolaris for the first time; Compounds 6-9 were evaluated their cytoxic activi ties against A549, HL-60, P388 and K562 cell lines for the first time, and compound 8 exhibited more potential inhibitory activities against HL-60 and K562 cell lines.
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