王著禄, 易杨华. 中药商陆有效成分的研究——Ⅱ.商陆皂甙戊、己的分离与鉴定J. 药学学报, 1984, 19(11): 825-829.
引用本文: 王著禄, 易杨华. 中药商陆有效成分的研究——Ⅱ.商陆皂甙戊、己的分离与鉴定J. 药学学报, 1984, 19(11): 825-829.
WANG Zhu-Lu, YI Yang-Hua. STUDIES ON THE ACTIVE PRINCIPLES OF THE CHINESE DRUG "SHANG LU" (PHYTOLACCA ESCULENTA VAN HO UTTE)Ⅱ. THE ISOLATION AND STRUCTURE OF ESCULENTOSIDE E AND FJ. Acta Pharmaceutica Sinica, 1984, 19(11): 825-829.
Citation: WANG Zhu-Lu, YI Yang-Hua. STUDIES ON THE ACTIVE PRINCIPLES OF THE CHINESE DRUG "SHANG LU" (PHYTOLACCA ESCULENTA VAN HO UTTE)Ⅱ. THE ISOLATION AND STRUCTURE OF ESCULENTOSIDE E AND FJ. Acta Pharmaceutica Sinica, 1984, 19(11): 825-829.

中药商陆有效成分的研究——Ⅱ.商陆皂甙戊、己的分离与鉴定

STUDIES ON THE ACTIVE PRINCIPLES OF THE CHINESE DRUG "SHANG LU" (PHYTOLACCA ESCULENTA VAN HO UTTE)Ⅱ. THE ISOLATION AND STRUCTURE OF ESCULENTOSIDE E AND F

  • 摘要: 从商陆科(Phytolaccaceae)植物商陆(Phytolacca esculenta Van Houtte)中分离得到四种结晶,根据化学性质和光谱(UV,IR、NMR,13CNMR和MS)分析,确定结晶Ⅰ为2-羟基商陆酸(2-hydroxyl esculentic acid),结晶Ⅱ为3-O-β-D-吡喃木糖-2-羟基商陆酸,称为商陆皂甙戊,结晶Ⅲ为3-O-(β-D-吡喃葡萄糖-β-D-吡喃木糖)1→4-2-羟基商陆酸,称为商陆皂甙己;结晶Ⅳ的结构正在鉴定中。2-羟基商陆酸有抗炎作用。商陆皂甙戊在本植物中系首次分得,商陆皂甙己为新化合物。

     

    Abstract: In a previous paper we reported the isolation of esculentoside A, B, C and D from Phytolacca eseulenta Van Houtte. In pharmacological experiments the total saponins and esculentoside A exerted considerable enhancement of phagocytic function of leucocytes and promoted DNA synthesis in mice. In further search for active principles, four kinds of crystals (Ⅰ), (Ⅱ), (Ⅲ) and (Ⅳ) were isolated from the 0.01 M pH 7.3 phosphate buffer extract of the plant by silica gel column chromatography. On the basis of chemical properties and spectral data (NMR, 13CNMR, UV, IR, Ms spectra), crystal (Ⅰ) was shown to be 2-hydroxyl esculentic acid, i.e. jaligonic acid which has been considered to have good antiinflammatory action; crystal (Ⅱ) was found to be 3-O-β-D-xylopyranosyl-2-hydroxylesculentic acid and was named as esculentosid E which is identical to phytolaccoside G from Phytolacca americana. Crystal (Ⅲ) is 3-O(β-D-glucopyranosyl-β-D-xylopyranosyl)1→4-2-hydroxyl esculentic acid named as esculentoside F. Esculentoside E was first obtained from this plant and esculentoside F so far has not been reported in literature. Because of the scanty sample of crystal (Ⅳ), its structure is still under investigation.

     

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