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耳叶牛皮消水溶性部位的化学成分研究
引用本文:张宝,姚成芬,汪洋,蒋礼,马雪,孙佳,张桂青,李勇军.耳叶牛皮消水溶性部位的化学成分研究[J].中草药,2018,49(4):786-790.
作者姓名:张宝  姚成芬  汪洋  蒋礼  马雪  孙佳  张桂青  李勇军
作者单位:贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学 民族药与中药开发应用教育部工程研究中心/国家苗药工程技术研究中心, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学 民族药与中药开发应用教育部工程研究中心/国家苗药工程技术研究中心, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学药学院, 贵州 贵阳 550004,贵州医科大学 贵州省药物制剂重点实验室, 贵州 贵阳 550004;贵州医科大学 民族药与中药开发应用教育部工程研究中心/国家苗药工程技术研究中心, 贵州 贵阳 550004
基金项目:国家自然科学基金资助项目(81760700);贵州省优青项目(201511);贵州省教育厅项目(201304,ZYRC2014012);贵州省创新人才团队项目(20165613/5677)
摘    要:目的对耳叶牛皮消Cynanchum auriculatum水溶性部位的化学成分进行研究。方法综合运用D-101大孔树脂柱色谱、反复硅胶柱色谱、Sephadex LH-20凝胶柱色谱等色谱技术进行分离纯化,并利用MS、NMR等现代波谱学技术对分离得到的化合物进行结构鉴定。结果从耳叶牛皮消水溶性部位分离得到15个化合物,分别鉴定为异莨菪亭(1)、异秦皮啶(2)、去乙酰基萝藦苷元(3)、吐叶醇(4)、4,4-二甲基庚二酸(5)、异落叶松脂素(6)、3-羟基吡啶(7)、3-羟基-2-甲基吡啶(8)、5-羟基-2-羟甲基吡啶(9)、2-甲基-6-(2′,3′,4′-三羟基丁基)吡嗪(10)、kiwiionol(11)、picein(12)、腺苷(13)、cynanoneside B(14)、cynanoneside A(15)。结论化合物1~2、4~13均首次从鹅绒藤属植物中分离得到,化合物15首次从该植物中分离得到。

关 键 词:耳叶牛皮消  鹅绒藤属  异落叶松脂素  吐叶醇  2-甲基-6-(2'',  3'',  4''-三羟基丁基)吡嗪
收稿时间:2017/10/17 0:00:00

Chemical constituents in water fraction of Cynanchum auriculatum
ZHANG Bao,YAO Cheng-fen,WANG Yang,JIANG Li,MA Xue,SUN Ji,ZHANG Gui-qing and LI Yong-jun.Chemical constituents in water fraction of Cynanchum auriculatum[J].Chinese Traditional and Herbal Drugs,2018,49(4):786-790.
Authors:ZHANG Bao  YAO Cheng-fen  WANG Yang  JIANG Li  MA Xue  SUN Ji  ZHANG Gui-qing and LI Yong-jun
Institution:Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;Engineering Research Center for the Development and Application of Ethnic Medicine and TCM, Ministry of Education/National Engineering Research Center of Miao''s Medicines, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;Engineering Research Center for the Development and Application of Ethnic Medicine and TCM, Ministry of Education/National Engineering Research Center of Miao''s Medicines, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China,Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;School of Pharmacy, Guizhou Medical University, Guiyang 550004, China and Guizhou Provincial Key Laboratory of Pharmaceutics, Guizhou Medical University, Guiyang 550004, China;Engineering Research Center for the Development and Application of Ethnic Medicine and TCM, Ministry of Education/National Engineering Research Center of Miao''s Medicines, Guizhou Medical University, Guiyang 550004, China
Abstract:Objective To investigate the chemical constituents of Cynanchum auriculatum. Methods Compounds were isolated and purified by using a combination of various chromatographic techniques including D-101 macroporous adsorptive resins, silica gel, Sephadex LH-20, and other methods. Their structures were elucidated by MS, NMR, and other modern spectroscopies. Results Fifteen compounds were isolated and identified as isocopoletin (1), isofraxidin (2), deacetylmetaplexigenin (3), vomifoliol (4), 4,4-dimethyl heptanedioic acid (5), (+)-isolariciresinol (6), 3-hydroxypyridine (7), 3-hydroxy-2-methylpyridine (8), 5-hydroxyl-2-hydroxymethylpyridine (9), 2-methyl-6-(2'',3'',4''-trihydroxybutyl)-pyrazine (10), kiwiionol (11), picein (12), adenosine (13), cynanoneside B (14), and cynanoneside A (15). Conclusion Compounds 12, 413 are isolated from the plants of genus Cynanchum Linn for the first time, while compound 15 is firstly obtained from C. auriculatum.
Keywords:Cynanchum auriculatum Royle ex Wight  Cynanchum Linn    (+)-isolariciresinol  vomifoliol  2-methyl-6-(2'', 3'', 4''-trihydroxybutyl)-pyrazine
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