高山红景天黄酮类化合物的分离与鉴定  被引量:10

Separation and identification of flavone compounds from root and rhizome of Rhodiola sachalinensis A.Bor.

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作  者:韩颖[1] 金艺淑[2] 于建婷[1] 李军[1] 李玉山[1] 

机构地区:[1]沈阳药科大学中药学院,辽宁沈阳110016 [2]沈阳医学院沈洲医院,辽宁沈阳110002

出  处:《沈阳药科大学学报》2011年第2期116-119,共4页Journal of Shenyang Pharmaceutical University

摘  要:目的对高山红景天药材的化学成分进行研究。方法采用反复硅胶柱色谱、ODS柱色谱、Sephadex LH-20柱色谱和半微量制备高效液相色谱分离纯化,根据ESI-MS、1H-NMR和13C-NMR等谱学数据进行结构鉴定。结果从高山红景天根和根茎的乙醇提取物中分离得到8个单体化合物,分别鉴定为黄酮类化合物herbacetin 3-O-[α-L-rhamnopyranosyl(1→2)-β-D-glucopyranosyl]-7-O-α-L-rhamnopyranoside(1)、三叶豆苷(trifolin,2)、草质素苷(rhodionin,3)、山奈酚(kaempferol,4)、山奈酚7-O-α-L-鼠李糖苷(kaempferol7-O-α-L-rhamnopyranoside,5)、小麦黄素(tricin,6)和大花红景天素(rhodiolinin,7);另外还得到2(3H)-苯并噻唑硫酮(2(3H)-benzothiazolethione,8)。结论化合物1为新化合物,化合物2和8为首次从景天科植物中分离得到。Objective To study chemical constituents of root and rhizome of Rhodiola sachalinensis A. Bor. Methods The chemical constituents were isolated by silica, Sephadex LH-20, ODS column chromatography and HPLC. Chemical characters and spectroscopic analysis were employed for the structural identification. Results Eight compounds were obtained and their structures were identified as: herbacetin 3-O-E α-L-rham- nopyranosyl ( 1→2 ) -β-D-glucopyranosyl ] -7-O-α-L-rhanmopyranoside ( 1 ), trifolin ( 2 ), rhodionin ( 3 ), kaempferol ( 4 ), kaempferol 7 -O-α-L-rhanmopyranoside ( 5 ), tricin ( 6 ), rhodiolinin ( 7 ) and 2 (3H) -benzothiazolethione (8). Conclusions Herbacetin 3-O- [ α-L-rhanmopyranosyl ( 1→2 ) -β-D-glucopyranosyl ] -7-O-α-L- rhamnopyranoside(1 )is a new flavonol glucoside which has not been reported before. Compounds 2 and 8 are isolated from family Crassulaceae for the first time.

关 键 词:高山红景天 黄酮 2(3H)0苯并噻唑硫酮 结构鉴定 

分 类 号:R914[医药卫生—药物化学] R284[医药卫生—药学]

 

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