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保护风蚀地的刺山柑
引用本文:何江波, 欧阳芬, 张燊, 等. 刺山柑化学成分研究[J]. 云南农业大学学报(自然科学), 2018, 33(3): 558-562. DOI: 10.12101/j.issn.1004-390X(n).201704015
作者姓名:何江波  欧阳芬  张燊  王波  句红萍  陶剑  张雪梅  芮丹云  牛燕芬
作者单位:1.昆明学院,昆明市呼吸系统疾病防治重点实验室,云南 昆明 650214;2.昆明市艺术学校,云南 昆明 650216;3.昆明学院 农学院,云南 昆明 650214
基金项目:云南省科技厅青年基金项目(2016FD109);云南省教育厅资助项目(2017ZZX091)
摘    要:ttttt目的ttttt研究刺山柑(Capparis spinosa L.)的化学成分。tttttttttttttttttt方法ttttt运用硅胶柱色谱、凝胶柱色谱(Sephadex LH-20)和反相RP-18柱色谱对乙酸乙酯部位进行分离纯化,然后通过现代波谱学鉴定方法(1H-NMR,13C-NMR,MS),结合文献数据分析确定化合物的结构。tttttttttttttttttt结果ttttt从刺山柑乙酸乙酯部位分离得到12个化合物,依次确定为(R)-2-甲基-2,4-二甲氧基-6H-吡喃-3-酮(1),1H-吲哚-3-乙腈-4-O-β-吡喃型葡萄糖苷(2),3-吲哚甲酸(3),尿嘧啶(4),5-(methoxymethyl)-1H-pyrrole-2-carbaldehyde(5),4-羟基-5-甲基呋喃-3-羧酸(6),苯甲酸(7),水杨酸(8),(2R,4aR,8aR)-3,4,4a,8a-tetrahydro-4a-hydroxy-2,6,7,8a-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-chromene-5,8-dione (9),α-生育酚(10),异槲皮苷(11),芸香苷(12)。tttttttttttttttttt结论ttttt化合物1,3,5,6,9,10均为首次从刺山柑中分离得到。tttt

关 键 词:刺山柑  提取分离  化学结构  结构鉴定
收稿时间:2017-04-08
修稿时间:2017-05-12

1H-Indole-3 acetonitrile glycosides from Capparis spinosa fruits
Jiangbo HE, Fen OUYANG, Shen ZHANG, et al. Chemical Constituents from Capparis spinosa L.[J]. JOURNAL OF YUNNAN AGRICULTURAL UNIVERSITY(Natural Science), 2018, 33(3): 558-562. DOI: 10.12101/j.issn.1004-390X(n).201704015
Authors:Jiangbo HE  Fen OUYANG  Shen ZHANG  Bo WANG  Hongping JU  Jian TAO  Xuemei ZHANG  Danyun RUI  Yanfen NIU
Affiliation:1.Kunming Key Laboratory of Respiratory Disease, Kunming University, Kunming 650214, China;2.Kunming Arts School, Kunming 650216, China;3.School of Agriculture, Kunming University, Kunming 650214, China
Abstract:tttttPurposetttttThe chemical constituents of Capparis spinosa L. were analyzed.ttttttttttttttttttMethodtttttThe compounds were isolated by silica column chromatography, Sephadex LH-20 column chromatography and RP-18 reverse-phase column chromatography from the EtOAc extract. The structures were characterized by various spectroscopic (1H-NMR, 13C-NMR and MS) and comparison with the data of literatures.ttttttttttttttttttResulttttttTwelve compounds were isolated from the EtOAc extract, and identified as (R)-2,4-dimethoxy-2-methyl-6H-pyran-3-one (1), capparilosides A (2), indole-3-carboxylic acid (3), uracil (4), 5-(methoxymethyl)-1H-pyrrole-2-carbaldehyde (5), 4-hydroxy-5-methylfuran-3-carboxylic acid (6), benzoic acid (7), salicylic acid (8), (2R,4aR,8aR)-3,4,4a,8a-Tetrahydro-4a-hydroxy-2,6,7,8a-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-chromene-5,8-dione (9), α-tocopherol (10), isoquercitrin (11), rutin (12).ttttttttttttttttttConclusiontttttCompounds 1, 3, 5, 6, 9, 10 were isolated from C. spinosa L. for the first time.ttttttttt
Keywords:Capparis spinosa L.  extraction and isolation  chemical constituents  structural identification
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