Modjinan Kayangar, N. R. Nono, T. R. Fouedjou, T. B. Tchegnitegni, K. B. Ponou, B. R. Teponno, J. K. Siems, F. M. Melzig, L. Barboni, A. L. Tapondjou
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引用次数: 1

摘要

背景:木参属五加科植物,传统上用于治疗淋病感染、腹泻、疟疾和糖尿病等多种外来疾病。根据体外和体内的科学评价,该植物具有抗菌、抑菌、降血糖、抗疟原虫和抗癌等主要药理活性。研究目的:本文在综述了国内外对这一重要药用植物的传统研究和药理研究的基础上,报道了从Cussonia arborea Hochst茎皮甲醇提取物中分离和鉴定次生代谢产物的研究进展。材料与方法:将木参茎皮MeOH提取物悬浮于水中,分别用乙酸乙酯和正丁醇进行提取。乙酸乙酯提取物(18 g)经重复柱层析得到7(1-7)个化合物。它们的结构通过核磁共振测定,并发表了数据。结果:分离得到的化合物鉴定为:原儿茶酸(1),3、23-dihydroxyolean-12-en-28-oic酸(2)和3,23-dihydroxyurs-12-en-28-oic酸(2 b)比5/4,3点-β-D-xylopyranosylolean-12-en-28-oic酸(3)、3 -α-L-arabinopyranosylolean-12-en-28-oic酸(4)、β-resorcylic酸(5)、混合3 -β-D-glucopyranosyl-23-hydroxyolean-12-en-28-oic酸(6)和3 -β-D-glucopyranosyl-23-hydroxyurs-12-en-28-oic酸(6 b)配给4/1,化合物3、4、5、7、2b和6b均为首次从该植物中分离得到
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Cussonia arborea Hochst (Araliaceae): Ethnobotany, Pharmacology and Phytochemistry
Background:  C. arborea belonging to Araliaceae family is used traditionally to cure many alien diseases including gonorrhoeae infection, diarrhea, malaria, and diabetes mellitus. The plant has been examined on the basis of scientific in vitro and in vivo evaluations possessing the major pharmacological activities including antimicrobial, antibacterial, antihyperglycemic,  antiplasmodial and anticancer properties. Aim of the study: In the present paper, we reported the isolation and characterization of secondary metabolites from the methanol extract of the stem bark of Cussonia arborea Hochst after a short review of the traditional and pharmacological studies done on this important medicinal plant. Materials and methods: MeOH extract of stem bark of C. arborea was suspended in water and successively extracted with EtOAc and n-BuOH. The EtOAc extract (18 g) was subjected to repeated column chromatography to yield seven (1-7) compounds. Their structures were determined by means of NMR, and published data. Results: The isolated compounds were identified as: protocatechuic acid (1), mixture of 3,23-dihydroxyolean-12-en-28-oic acid (2a) and 3,23-dihydroxyurs-12-en-28-oic acid (2b) in ratio 5/4, 3-O-β-D-xylopyranosylolean-12-en-28-oic acid (3), 3-O-α-L-arabinopyranosylolean-12-en-28-oic acid (4), β-resorcylic acid (5), mixture of 3-O-β-D-glucopyranosyl-23-hydroxyolean-12-en-28-oic acid (6a) and 3-O-β-D-glucopyranosyl-23-hydroxyurs-12-en-28-oic acid (6b) in ration 4/1, 3-O-β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl-3β-hydroxyolean-12-en-28-oic acid (7). Compounds 3, 4, 5, 7, 2b and 6b are herein reported for the first time in this plant
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