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中药黄蜀葵花化学成分的分离与鉴定(III)
引用本文:李春梅,安雅婷,王 涛,尚海花,高秀梅,张 祎. 中药黄蜀葵花化学成分的分离与鉴定(III)[J]. 沈阳药科大学学报, 2011, 28(7): 520-525
作者姓名:李春梅  安雅婷  王 涛  尚海花  高秀梅  张 祎
作者单位:(1. 天津市中药化学与分析重点实验室,天津 300193;2. 天津中医药大学 中医药研究院,天津 300193)
摘    要:目的 研究中药黄蜀葵(Abelmoschus manihot (L.)Medic)花的化学成分。方法 采用正相硅胶、反相ODS、Sephadex LH-20等柱色谱以及HPLC等手段进行分离纯化,并通过理化性质与光谱分析方法鉴定了化合物的结构。结果 从黄蜀葵花体积分数为95%的乙醇提取物中分离鉴定了9个化合物,分别为棉皮素 8-O-β-D-葡萄糖醛酸苷(gossypetin 8-O-β-D-glucuronide,1)、棉皮素 3-O-β-葡萄糖-8-O-β-葡萄糖醛酸(gossypetin 3-O-β-glucopyranoside-8-O-β-glucuronopyranoside,2)、棉皮素 3'-O-β-D-葡萄糖苷(gossypetin 3'-O-β-D-glucopyranoside,3)、tiliroside(4)、山奈酚3-O-[(3"-O-乙酰基-6"-O-(E)-对羟基桂皮酰基)]-β-D-葡萄糖苷(kaempferol 3-O-[3"-O-acetyl -6"-O-(E)-p-coumaroyl)]-β-D-glucopyranoside,5)、槲皮素 3-O-[β-D-木糖基(1→2)-a-L-鼠李糖基(1→6)]-β-D-半乳糖苷(quercetin 3-O-[β-D-xylopyranosyl(1→2)-a-L-rhamnopyranosyl(1→6)-β-D-galactopyranoside,6)、4-羟基苯甲酸 β-D-葡萄糖酯(4-hydroxybenzoic acid β-D-glucose ester,7)、原儿茶酸(protocatechuic acid,8)、原儿茶酸 3-O-β-D-葡萄糖苷(protocatecheuic acid 3-O-β-D-glucoside,9)。结论 其中化合物2、4-9为首次从秋葵属中分离得到,并首次报道了化合物5、6、9在DMSO-d6中的光谱数据。

关 键 词:秋葵属  黄蜀葵花  化学成分  结构鉴定,
收稿时间:2010-12-28

Isolation and identification of chemical constituents from the flowers of Abelmoschus manihot (L.) Medic (III)
LI Chun-mei,An Ya-ting,WANG Tao,Shang Hai-hua,GAO Xiu-mei,ZHANG Yi. Isolation and identification of chemical constituents from the flowers of Abelmoschus manihot (L.) Medic (III)[J]. Journal of Shenyang Pharmaceutical University, 2011, 28(7): 520-525
Authors:LI Chun-mei  An Ya-ting  WANG Tao  Shang Hai-hua  GAO Xiu-mei  ZHANG Yi
Affiliation:(1. Key Laboratory of Traditional Chinese Medicinal Chemistry and Analytical Chemistry of Tianjin, Tianjin 300193, China; 2. Institute of Traditional Chinese Medicine Research, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China)
Abstract:Objective To study the chemical constituents from the flowers of Abelmoschus manihot (L.) Medic. Method The compounds were isolated by chromatographies such as silica gel, ODS, Sephadex LH-20 and HPLC, and identified by the chemical and physical methods, especially spectral analysis. Results Nine compounds were isolated. The structures of them were identified as gossypetin 8-O-β-D-glucuronide (1), gossypetin 3-O-β-glucopyranoside-8-O-β-glucuronopyranoside (2), gossypetin 3'-O-β-glucopyranoside (3), tiliroside (4), kaempferol 3-O-[3"-O-acetyl -6"-O-(E)-p-coumaroyl)]-β-D-glucopyranoside (5), quercetin 3-O-[β-D-xylopyranosyl(1→2)-a-L-rhamnopyranosyl(1→6)]-β-D-galactopyranoside (6), 4-hydroxybenzoic acid β-D-glucose ester (7), protocatechuic acid (8), protocatecheuic acid-3-O-β-glucoside (9), respectively. Conclusion Seven compounds 2, 4-9 are obtained from Abelmoschus genus for the first time, and the spectral data in DMSO-d6 solution of 5, 6 and 9 are reported firstly.
Keywords:Abelmoschus genus')"  >Abelmoschus genus  Abelmoschus manihot (L.) Medic')"  >Abelmoschus manihot (L.) Medic  chemical constituent  ')"  >structure identification
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