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毛草龙化学成分及其细胞毒活性研究

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为探究毛草龙(Ludwigia octovalvis)中的活性成分,该研究采用硅胶、Sephadex LH-20、C18中低压和半制备液相等色谱方法对毛草龙的 80%乙醇提取物进行分离纯化,根据理化性质及波谱数据鉴定化合物结构,并通过MTS法检测单体化合物对 5 种肿瘤细胞增殖的抑制活性.结果表明:(1)从毛草龙中分离得到20 个化合物,分别鉴定为(-)-南烛木树脂酚(1)、8,8′-bisdihydrosiringenin(2)、5-甲氧基-(-)-异落叶松脂素(3)、(-)-isolariciresinol(4)、3,4′-二甲氧基鞣花酸(5)、3,3′,4′-三甲氧基鞣花酸(6)、1,3,6-tri-O-galloyl-β-glucospyranose(7)、柯里拉京(8)、没食子酸甲酯(9)、没食子酸乙酯(10)、terminaliate A(11)、丁香酸(12)、3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone(13)、木犀草素(14)、山柰酚(15)、5,8-dihydroxy-7-methoxyflavone(16)、川陈皮素(17)、桔皮素(18)、α-托可醌(19)、5-O-(E)-p-coumaroyl quinic acid ethyl ester(20).其中,化合物 1-5、7、8、11、13、16-20 为首次从该属植物中分离得到,化合物 6、9、10、12、15 为首次从该植物中分离得到.(2)化合物 19 对白血病 HL-60 细胞显示细胞毒活性,IC50 为 10.31 μmol·L-1;化合物6-8、19 对非小细胞肺癌细胞A549 显示细胞毒活性,IC50分别为25.82、42.05、36.94、17.54 μmol·L-1;化合物 6、7、11、14、19 对肝癌 SMMC-7721 显示细胞毒活性,IC50 分别为 24.24、26.35、26.51、33.34、20.44 μmol·L-1;化合物 6 和化合物 19 对乳腺癌MDA-MB-231 显示细胞毒活性,IC50 分别为 34.91、21.13 μmol·L-1;化合物6、7、19 对结肠癌SW480 显示细胞毒活性,IC50分别为36.03、39.97、5.52 μmol·L-1.该研究结果丰富了毛草龙的化学成分,为毛草龙抗肿瘤活性研究奠定了基础.
Chemical constituents and cytotoxic activity of Ludwigia octovalvis
To study the chemical constituents of Ludwigia octovalvis,the 80%ethanol extract from L.octovalvis was isolated by silica gel,Sephadex LH-20,Flash C18 and semi-preparative liquid chromatography,and the structures of obtained compounds were identified by physicochemical properties and spectral data.The cytotoxic activity of the isolates were evaluated by MTS method.The results were as follows:(1)Twenty compounds were isolated from L.octovalvis,and their structures were identified as(-)-lyoniresinol(1),8,8′-bisdihydrosiringenin(2),5-methoxy-(-)-isolariciresinol(3),(-)-isolariciresinol(4),3,4′-di-O-methylellagic acid(5),3,3′,4′-tri-O-methylellagic acid(6),1,3,6-tri-O-galloyl-β-glucospyranose(7),corilagin(8),methyl gallate(9),ethyl gallate(10),terminaliate A(11),syringic acid(12),3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone(13),luteolin(14),kaempferol(15),5,8-dihydroxy-7-methoxyflavone(16),nobiletin(17),tangeretin(18),α-tocopherolquinone(19),5-O-(E)-p-coumaroyl quinic acid ethyl ester(20).Compounds 1-5,7,8,11,13,16-20 were isolated from Ludwigia for the first time.Compounds 6,9,10,12,15 were isolated from this plant for the first time.(2)Compound 19 showed inhibitory activity against the leukemia HL-60 with the IC50 value of 10.31 μmol·L-1.Compounds 6-8,19 showed inhibitory activity against the lung cancer cells A549 with the IC50 values of 25.82,42.05,36.94,17.54 μmol·L-1,respectively.Compounds 6,7,11,14,19 showed inhibitory activity against the liver cancer SMMC-7721 with the IC50 values of 24.24,26.35,26.51,33.34,20.44 μmol·L-1,respectively.Compounds 6,19 showed inhibitory activity against the breast cancer MDA-MB-231 with the IC50 values of 34.91,21.13 μmol·L-1,respectively.Compounds 6,7,19 showed inhibitory activity against the colon cancer SW480 with the IC50 values of 36.03,39.97,5.52 μmol·L-1,respectively.The results of this study enrich the chemical constituents of L.octovalvis and provide a basis for the development of anti-tumor activity.

Ludwigia octovalvisZhuang MedicineLudwigiaα-tocopherolquinonecytotoxic activity

曾雨娴、廖广凤、李金玲、李敏、李兵、朱小勇、卢汝梅

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广西中医药大学 药学院,南宁 530200

毛草龙 壮药 丁香蓼属 α-托可醌 细胞毒活性

广西自然科学基金面上项目广西中医药大学桂派中医药传承创新团队资助项目

2020GXNSFAA2971722022B005

2024

广西植物
广西壮族自治区广西植物研究所,中国科学院广西植物研究所,广西植物学会

广西植物

CSTPCD北大核心
影响因子:0.719
ISSN:1000-3142
年,卷(期):2024.44(6)