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作 者:冉小库[1] 王晓彤[1] 刘培培[1] 迟玉新[1] 王博佳[1] 窦德强[1] 康廷国[1] 熊伟
机构地区:[1]辽宁中医药大学药学院,大连116600 [2]大连快活林生物技术有限公司,大连116600
出 处:《中国天然药物》2013年第3期269-273,共5页
摘 要:目的:研究构树叶的化学成分。方法:采用D101型大孔吸附树脂、硅胶、ODS和半制备型高效液相色谱等分离方法对构树叶提取物分离纯化,通过1D,2DNMR技术确定其结构,并采用MTT法对分得化合物进行细胞毒活性测定,同时比色法和采用高效液相色谱法建立了对构树叶中总黄酮和cosmosiin的含量测定方法。结果:分离鉴定了6个化合物,它们的结构鉴定为:(+)-pinoresinol-4′-O-β-D-glucopyransyl-4″-O-β-D-apiofuranoside(1),cosmosiin(2),luteolin-7-O-β-D-glucopyranoside(3),liriodendrin(4),3,5,4′-trihydroxy-bibenzyl-3-O-β-D-glucoside(5),apigenin-6-C-β-D-glycopyranside(6)。结论:化合物1为一个新的木脂素,化合物5,6为首次从该属植物中分离,化合物1,4,6对HepG-2细胞株有不同程度的抑制活性,而化合物2,3,5对HepG-2细胞株没有活性;根据含量测定结果得知,确定构树叶的最佳采收时间为9月份。AIM: To investigate the chemical constituents from the leaves of Broussonetia papyrifera. METHODS: The chemical constituents were isolated and purified by macroporous adsorptive resin D101, silica gel, and ODS column chromatography and prepa- rative HPLC. Their structures were elucidated on the basis of 1D and 2D NMR analyses. In addition, their cytotoxic activity against human hepatoma carcinoma cells (HepG-2) were evaluated by the MTT method Furthermore, RP-HPLC and colorimetric methods were used for the analysis of cosmosiin and total flavonoids. RESULTS: A new lignan, together with five known compounds were obtained, and their structures were characterized as (+)-pinoresinol-4'-O-fl-D-glucopyranosyl-4"-O-fl-D-apiofuranoside (1), cosmosiin (2), luteolin-7-O-fl-D-glucopyranoside (3), liriodendrin (4), 3, 5, 4'-trihydroxy-bibenzyl-3-O-fl-D-glucoside (5), and apigenin-6-C-fl-D- glucopyranside (6). Furthermore, RP-HPLC and colorimetric methods were established for the analysis of cosmosiin and total flavon- oids. CONCLUSION: Compound 1 was a new lignan, and compounds 5 and 6 were isolated for the first time from the title plant. Compounds 1, 4 and 6 showed definite activities against HepG-2, while the other compounds didn't show inhibitory effects. The opti- mal harvest time of B. papyrifera (L.) Vent. is September.
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