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Leucanthoside A, a new allose-containing triterpenoid saponin (1), was isolated from the aerial parts of Cephalaria leucantha L. Its structure was determined by electrospray ionization mass spectrometry and NMR spectroscopy. Complete assignments of the 1H and 13C NMR chemical shifts were achieved by two-dimensional NMR experiments: DQF-COSY, NOESY, TOCSY, HSQC, DINE-HSQC, HMBC, 13C-1H 2D-J-resolved spectroscopy, and 1,1-ADEQUATE.  相似文献   
2.
Three new kaempferol glycosides, kaempferol 3‐Oβ‐D ‐glucopyranosyl‐(1→6)‐β‐D ‐galactopyranosyl‐7‐Oα‐L ‐rhamnopyranoside ( 1 ), kaempferol 3‐O‐β‐D ‐galactopyranosyl‐7‐Oβ‐D ‐glucopyranosyl‐(1→3)‐α‐L ‐rhamnopyranoside ( 2 ), and kaempferol 3‐Oβ‐D ‐glucopyranosyl‐(1→6)‐β‐D ‐galactopyranosyl‐7‐Oβ‐D ‐glucopyranosyl‐(1→3)‐α‐L ‐rhamnopyranoside ( 3 ), were isolated from the whole herbs of Cardamine leucantha, along with three known kaempferol glycosides, kaempferol 7‐Oα‐L ‐rhamnopyranoside, kaempferitrin, and kaempferol 3‐Oβ‐D ‐galactopyranosyl‐7‐Oα‐L ‐rhamnopyranoside. Their structures were elucidated on the basis of spectroscopic methods.  相似文献   
3.
墨西哥鼠尾草与齿叶薰衣草挥发油化学成分比较   总被引:1,自引:0,他引:1  
采用水蒸汽蒸馏法提取墨西哥鼠尾草和齿叶薰衣草挥发油,通过GC-MS分析其化学成分,并用峰面积归一化法计算各组分的相对含量。结果表明,墨西哥鼠尾草和齿叶薰衣草挥发油化学成分和含量有较大差别。  相似文献   
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