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卷叶黄精根中甾体皂苷化学成分及其抗菌活性 被引量:18

Steroid Saponins of Polygonatum cirrhifolium Root and Their Antisepsis Activity
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摘要 利用硅胶、RP-18和Sephadex LH-20等色谱分离手段从卷叶黄精根茎的正丁醇萃取物(总甾体皂苷R)中分离得到2个甾体皂苷化合物,通过理化性质、波谱分析及与文献值对照,鉴定化合物Ⅰ为(25R)-spirost-5-ene-3β-ol-3-O-α-L-rham-nopyranosy(1→2)-[α-L-rhamnopyranosyl(1→4)]-β-D-glucopyranoside,化合物Ⅱ为(25R)-spirost-5-ene-3β-ol-3-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranoside。将化合物Ⅰ进行双相酸水解得到其苷元(化合物Ⅲ),鉴定为薯蓣皂苷元。对总甾体皂苷R、化合物Ⅰ、Ⅱ及Ⅲ的抗菌活性进行测定,结果表明:总甾体皂苷R、化合物Ⅰ及Ⅱ对植物病原菌的抑制效果均比对细菌的抑制效果明显,而化合物Ⅲ对细菌的抑制效果均比对植物病原菌强。 Steroid saponins(R)was extracted from the Polygonatum cirrhifolium root.Two compounds were isolated and purified by the combined use of column chromatography with silical gel,RP-18 and SephadexLH-20 methods.The structure of the compound were elucidated by spectroscopic and the data reported in literature methods.Two compounds were identified as(25R)-spirost-5-ene-3β-ol-3-O-α-L-rham-nopyranosy(1→2)-[α-L-rhamnopyranosyl(1→4)]-β-D-glucopyranoside(Ⅰ)and(25R)-spirost-5-ene-3β-ol-3-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranoside(Ⅱ).The aglycones of compound Ⅰ was obtained by the method of two-phase acid hydrolysis and its structure was identified as diosgenin(Ⅲ).The antisepsis activity of R,compound Ⅰ,Ⅱ and Ⅲ were studied,the results were as follows:Steroid saponins R,compound Ⅰ and Ⅱ had strong inhibition against plant pathogenic fungi growth than bacteria's,but compound Ⅲ had strong inhibition against to bacteria growth than plant pathogenic fungi's.
出处 《林业科学》 EI CAS CSCD 北大核心 2007年第8期91-95,共5页 Scientia Silvae Sinicae
基金 西北农林科技大学校科研专项基金(04ZM027)
关键词 卷叶黄精 甾体皂苷 结构鉴定 抗菌活性 Polygonatum cirrhifolium steroid saponins structure identify antisepsis activity
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