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关苍术不同极性部位化学成分研究及其抗肿瘤活性研究

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目的 研究菊科苍术属植物关苍术(Atractylodes japonica Koidz.ex Kitam)的化学成分.方法 使用关苍术干燥根茎,将其75%乙醇提取物中的二氯甲烷部位与正丁醇部位进行分离纯化,使用正相硅胶色谱、反相ODS和HPLC等方法,并使用各种波谱技术对所得化合物进行结构鉴定.使用人胃癌细胞MGC-803和人宫颈癌细胞HeLa对14个化合物进行抗肿瘤活性测定.结果 从中共得到14种化合物,通过NMR和HR-ESI-MS方法鉴定分别为:五味子甲素(1)、(7S,8R)-dihydrodehydrodiconiferyl alcohol-9'-O-β-D-glucopyranoside(2)、(7S,8R)-dehydrodiconiferyl alcohol 9'-β-glucopyranoside(3)、artemordolignan glycoside A(4)、开环异落叶松脂素-9-O-β-D-葡萄糖苷(5)、2-甲氧基-4-(2-丙烯基)苯基-β-D-吡喃葡萄糖苷(6)、1,2-di-O-β-D-glucopranosyl-4-allylbenzene(7)、白术内酯 Ⅰ(8)、白术内酯 Ⅱ(9)、表白术内酯 Ⅰ(10)、白术内酯Ⅲ(11)、atractylenother(12)、双白术内酯(13)、双表白术内酯(14).从二氯甲烷组分中分离得到化合物1,8~14,正丁醇组分中分离得到化合物2~7.MTT实验结果显示,化合物1,8~14对HeLa细胞具有一定的抗肿瘤活性,化合物8~11,13对MGC-803具有一定的抗肿瘤活性.结论 本次实验共得到14个化合物,其中化合物1~7均为首次从该药用部位中分离获得,部分化合物具有一定的抗肿瘤活性.
Chemical compositions of different polar parts of Atractylodes japonica and its antitumor activity
Objective To determine the chemical components of Atractylodes japonica Koidz.ex Kitam.Methods Dried rhizome of Atractylodes japonica Koidz.ex Kitam was used.The dichloromethane part separated and purified from the n-butanol part of its 75%ethanol extract.The structure of the resulting compounds was identified by normal-phase silica gel chromatography,reversed-phase ODS,HPLC,and other spectroscopic techniques.The antitumor activity was determined for 14 compounds using human gastric cancer cells MGC-803 and human cervical cancer cells HeLa.Results Totally 14 compounds were obtained from Atractylodes japonica Koidz.ex Kitam and identified as deoxyschizandrin(1),(7S,8R)-dihydrodehydrodiconiferyl alcohol-9'-O-β-D-glucopyranoside(2),(7S,8R)-dehydrodiconiferyl alcohol 9'-β-glucopyranoside(3),artemordolignan glycoside A(4),secoisolariciresinol-9-O-β-D-glucopyranoside(5),2-methoxy-4-(2-propenyl)phenyl-β-D-glucopyranoside(6),1,2-di-O-β-D-glucopranosyl-4-allylbenzene(7),atractylenolideⅠ(8),atractylenolide Ⅱ(9),isoatractylenolide Ⅰ(10),atractylenolid Ⅲ(11),atractylenother(12),biatractylenolide(13),and biepiatractylenolide(14).Compounds 1,8~14 were isolated from the dichloromethane fraction while compounds 2~7 were isolated from the n-butanol fraction.The MTT experiments showed that compounds 1,8~14 had certain anti-tumor activity against HeLa cells,and compounds 8~11,13 had certain anti-tumor activity against MGC-803.Conclusion Totally 14 compounds have been obtained.Compounds 1~7 have been isolated from this medicinal part for the first time,several compounds showed certain anti-tumour activity.

Atractylodes japonica Koidz.ex Kitamchemical constituentextraction and separationstructural identificationanti-tumor activity

孙杰、王静、孙朝、王萍、方振兴、于海龙、王道深、周媛媛

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黑龙江中医药大学教育部北药基础与应用研究重点实验室,哈尔滨 150040

黑龙江省中医药科学院,哈尔滨 150036

黑龙江省科学院自然与生态研究所,哈尔滨 150040

哈尔滨市产品质量综合检验检测中心,哈尔滨 150030

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关苍术 化学成分 提取分离 结构鉴定 抗肿瘤活性

2024

中南药学
湖南省药学会

中南药学

CSTPCD
影响因子:0.736
ISSN:1672-2981
年,卷(期):2024.22(12)