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构树叶的化学成分
引用本文:冯卫生,李红伟,郑晓珂,匡海学,陈随清,王彦志,臧新钰. 构树叶的化学成分[J]. 药学学报, 2008, 43(2): 173-180
作者姓名:冯卫生  李红伟  郑晓珂  匡海学  陈随清  王彦志  臧新钰
作者单位:1. 河南中医学院药学院
2. 河南中医学院基础医学院,河南,郑州,450008
3. 河南中医学院黑龙江中医药大学,黑龙江,哈尔滨,150040
基金项目:2004 Chinese Medicine Technology Research Project of the State Administration of Traditional Chinese Medicine of the People’s Republic of China (04-05ZP43)
摘    要:为研究构树叶(Broussonetia papyrifera)的化学成分,用Diaion HP-20,Toyopearl HW-40C,Sephadex LH-20,silica gel等柱色谱方法进行分离,根据其理化性质和波谱数据鉴定化合物结构。分离得到了19个化合物,分别鉴定为芹菜素(1),芹菜素-7-O-β-D-吡喃葡糖苷(2),柯伊利素-7-O-β-D-吡喃葡糖苷(3),芹菜素-7-O-β-D-吡喃葡糖醛酸苷(4),牡荆素-7-O-β-D-吡喃葡糖苷(5),木犀草素(6),5,7,4′-三羟基-6-C-[a-L-鼠李糖(1→2)]-β-D-葡糖黄酮碳苷(7),5,7,4′-三羟基-8-C-[α-L-鼠李糖(1→2)]-β-D-葡糖黄酮碳苷(8),异牡荆素(9),牡荆素(10),苯甲酸苯甲酯-2,6-二-O-β-D-吡喃葡糖苷(11),(2R,3R,5R,6S,9R)-3-羟基-5,6-环氧-β-紫罗兰醇-2-O-β-D-葡糖苷(12),(2R,3R,5R,6S,9R)-3-羟基-5,6-环氧-乙酰-β-紫罗兰醇-2-O-β-D-葡糖苷(13),ficustriol (14),(6S,9S)-玫瑰花苷(15),3β-羟基-5α,6α-环氧-β-紫罗兰酮-2α-O-β-D-葡糖苷(16),icariside B1 (17),sammangaoside A (18),3-羟基-5α,6α-环氧-β-紫罗兰酮(19)。化合物11、12、13为新化合物,其余化合物为首次从该属植物中分离得到。

关 键 词:构树叶  黄酮  苯甲酸苯甲酯-2,6-二-O-β-D-吡喃葡糖苷  megastigmanes
文章编号:0513-4870(2008)02-0173-08
收稿时间:2007-09-07
修稿时间:2007-09-07

Chemical constituents from the leaves of Broussonetia papyrifera
FENG Wei-sheng,LI Hong-wei,ZHENG Xiao-ke,KUANG Hai-xue,CHEN Sui-qing,WANG Yan-zhi,ZANG Xin-yu. Chemical constituents from the leaves of Broussonetia papyrifera[J]. Acta pharmaceutica Sinica, 2008, 43(2): 173-180
Authors:FENG Wei-sheng  LI Hong-wei  ZHENG Xiao-ke  KUANG Hai-xue  CHEN Sui-qing  WANG Yan-zhi  ZANG Xin-yu
Affiliation:Henan University of Traditional Chinese Medicine, School of Pharmacy, Zhengzhou 450008, China. fwsh@hactcm.edu.cn
Abstract:To separate and identify the chemical constituents from the leaves of Broussonetia papyrifera (Linn.) Vent, various columns including Diaion HP-20, Toyopearl HW-40C, Sephadex LH-20, silica gel were employed for the isolation and purification of compounds from the leaves of B. papyrifera. The structures of the compounds were elucidated by their physiochemical characteristics and spectral data. Nineteen compounds were isolated from the leaves of B. papyrifera and their structures were identified as apigenin (1), apigenin-7-O-beta-D-glucopyranoside (2), chrysoerid-7-O-beta-D-glucopyranoside (3), apigenin-7-O-beta-D-glucopyranuronide (4), vitexin-7-O-beta-D-glucopyranoside (5), luteolin (6), 5,7,4'-trihydroxyl-6-C-[a-L-rhamnopyranosyl (1-->2)]-beta-D-glucopyranosyl flavone (7), 5,7,4'-trihydroxyl-8-C-[a-L-rhamnopyranosyl (1-->2)]-beta-D-glucopyranosyl flavone (8), saponaretin (9), vitexin (10), benzyl benzoate-2, 6-di-O-beta-D-glucopyranoside (11), (2R, 3R, 5R, 6S, 9R)-3-hydroxy-5,6-epoxy-beta-ionol-2-O-beta-D-glucopyranoside (12), (2R, 3R, 5R, 6S, 9R)-3-hydroxyl-5,6-epoxy-acetyl-beta-ionol-2-O-beta-D-glucopyranoside (13), ficustriol (14), (6S, 9S)-roseoside (15), 3beta-hydroxy-5alpha,6alpha-epoxy-beta-ionone-2alpha-O-beta-D-glucopyranoside (16), icariside B1 (17), sammangaoside A (18), 3-hydroxy-5alpha,6alpha-epoxy-beta-ionone (19). Compounds 11, 12 and 13 are new compounds, the others are isolated from this genus Broussonetia for the first time.
Keywords:Broussonetia papyrifera  flavonoids  benzyl benzoate-2,6-di-O-β-D-glucopyranoside  megastigmanes
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