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作 者:宋龙[1] 吕律[1] 王远红[1] 姜廷福[1] 吕志华[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,山东青岛266003
出 处:《中国海洋药物》2016年第1期50-54,共5页Chinese Journal of Marine Drugs
基 金:山东省海洋经济创新发展区域示范项目(鲁财建指[2013]361号)资助
摘 要:目的从罗氏海盘车(Asterias rollestoni)中分离鉴定生物碱类天然产物,并进行体外抗肿瘤活性评价。方法利用凝胶吸附树脂柱层析、硅胶薄层层析、硅胶柱层析、凝胶Sephadex LH-20柱层析和高效液相色谱等手段对化合物进行了分离纯化;运用NMR、MS等波谱方法并结合文献鉴定化合物的结构;采用SRB、MTT法评价化合物的体外抗肿瘤活性。结果从罗氏海盘车的乙醇提取物中分离鉴定了1个吲哚生物碱N-(2-苯乙基)-1H-吲哚-3-乙胺(1)和1个环二肽生物碱类化合物Fellutanine A(2)。化合物2对MGC803细胞的抑制率为53.99%,具有一定的抗肿瘤活性。结论 2个生物碱类化合物均为首次从罗氏海盘车中分离获得;化合物1为首次分离到的天然产物,其核磁数据为首次报道;化合物2具有一定的抗肿瘤活性。Objective To isolate and identify alkaloids from Asterias rollestoni and evaluate their antitumor activities.Methods Isolation and purification were performed by MCI GEL CHP20 gel adsorption resin,TLC,silica gel column chromatography,Sephadex LH-20 column chromatography,and HPLC.Structural characterization was established by spectroscopic analysis(NMR,MS)and comparison with literature data.Antitumor activities were evaluated by SRB and MTT methods.Results Two alkaloids were isolated and identified as N-(2-phenylethyl)-1H-Indole-3-ethanamine(1)and Fellutanine A(2).Compound 2 exhibited potent cytotoxic activity against MGC803 with the inhibition rate of 53.99%.ConclusionIt's the first report for both alkaloids isolated fromAsterias rollestoni.Compound1 was first isolated as natural product and its NMR spectroscopic data was first reported.Compound 2 exhibited potent cytotoxic activity against cancer cell.
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