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机构地区:[1]北京大学药学院天然药物及仿生药物国家重点实验室,北京100191 [2]首都医科大学中医药学院,北京100069
出 处:《中国天然药物》2012年第5期358-362,共5页
基 金:supported by the National Natural Science Foundation of China (No. 30973629);China Postdoctoral Science Foundation (No. 20110490251);Foundation of State Key Laboratory of Natural and Biomimetic Drugs in Peking University (No. K20120213);Capital TCM & Nursing Foundation ( No.11ZYH08)~~
摘 要:目的:研究南刘寄奴中化学成分。方法:采用硅胶和 ODS 等柱层析分离手段以及半制备高效液相, 运用 NMR、MS 以及理化性质鉴定化合物的结构。结果:从南刘寄奴中分离得到 8 个化合物, 其结构鉴定为 3β-ethoxytanapartholide (1), ((4S*,5S*)-dihydro-5-[(1R*, 2S*)-2-hydroxy-2-methyl-5-oxo-3-cyclopenten-1-yl]-3-methylene-4-(3-oxobutyl)-2(3H)-furanone) (2), ligucy-peronol (3), cyperusol C (4), santamarin (5), 1α, 2α, 3α, 4α, 10α-pentahydroxyguaia-11(13)-ene-12, 6α-olide (6), balanophonin (7),methyl 3-(2’-hydroxy-4’-methoxyphenyl) propanoate (8)。结论:化合物 1 是新人工产物, 化合物 4 和 8 为首次从蒿属中分离得到, 化合物 2–3, 5–7 为首次从该植物中分离得到。AIM: To study chemical constituents of the aerial parts of Artemisia anomala (Asteraceae). METHODS: The constituents were isolated with silica gel, ODS column chromatography and semi-preparative HPLC, and their structures were elucidated on the basis of physical characteristics and spectral data. RESULTS: Eight compounds were obtained, and their structures were identified as 3,8-ethoxytanapartholide (1), (4S*, 5S*)-dihydro-5-[(1R*, 2S*)-2-hydroxy-2-methyl-5-oxo-3-cyclopenten-1-yl]-3-methylene-4-(3-oxobutyl)- 2(3H)-furanone (2), ligucyperonol (3), cyperusol C (4), santamarin (5), la, 2a, 3a, 4a, 10a -pentahydroxyguala-11(13)-ene-12, 6a-olide (6), balanophonin (7), methyl 3-(2'-hydroxy-4'-methoxyphenyl) propanoate (8). CONCLUSION: Compound 1 was a new artifact, 4 and 8 were isolated from the genus Artemisia for the first time, and compounds 2-3, 5-7 were isolated from this plant for the first time.
关 键 词:南刘寄奴 蒿属 化学成分 1 10-裂环愈创木烷型倍半萜
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