时珍国医国药
時珍國醫國藥
시진국의국약
LISHIZHEN MEDICINE AND MATERIA MEDICA RESEARCH
2010年
4期
905-906
,共2页
三叶木通%化学成分%酚醇%酚醇苷
三葉木通%化學成分%酚醇%酚醇苷
삼협목통%화학성분%분순%분순감
目的 研究三叶木通Akebia trifoliata茎中强极性化学成分.方法 采用硅胶、凝胶、制备型HPLC等对三叶木通的水提取液进行分离,根据波谱方法(EI-MS、ESI-MS、~1H-NMR、~(13)C-NMR、DEPT、HSQC、HMBC、~1H-~1H COSY)对分离所得的化合物进行结构鉴定.结果分离并鉴定了6个化合物,分别为4-羟基-3,5-二甲氧基苯甲醇 (4-hydroxy-3,5-dimethoxybenzenemethanol) ①;赤式-1-苯-(4'羟基-3'甲氧基)-2-苯(4''-羟基-3''-甲氧基)-1,3-丙二醇) [erythro-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3''-methoxy)-1,3-propanediol]②;苏式-1-苯-(4'-羟基-3'-甲氧基)-2-苯-(4''-羟基-3''–甲氧基)-1,3-丙二醇[threo-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3'' -methoxy)-1,3-propanediol]③;(7S,8S)-1-(4-羟基-3,5-二甲氧基苯)-1,2,3 –丙三醇 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol]④;2-(4-羟基-3-甲氧基苯)-乙醇1-O-β-D-葡萄糖苷[2-(4-hydroxy-3-methoxyphenyl)-ethanol-1-O-β-D-glucopyranoside]⑤;(7S,8S)-1-(4-羟基-3,5-二甲氧基苯)-1,2,3-丙三醇-2-O-β-D-葡萄糖苷 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol-2-O-β-D-glucopyranoside]⑥.结论 6个化合物全部为首次从该属植物中分离获得.
目的 研究三葉木通Akebia trifoliata莖中彊極性化學成分.方法 採用硅膠、凝膠、製備型HPLC等對三葉木通的水提取液進行分離,根據波譜方法(EI-MS、ESI-MS、~1H-NMR、~(13)C-NMR、DEPT、HSQC、HMBC、~1H-~1H COSY)對分離所得的化閤物進行結構鑒定.結果分離併鑒定瞭6箇化閤物,分彆為4-羥基-3,5-二甲氧基苯甲醇 (4-hydroxy-3,5-dimethoxybenzenemethanol) ①;赤式-1-苯-(4'羥基-3'甲氧基)-2-苯(4''-羥基-3''-甲氧基)-1,3-丙二醇) [erythro-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3''-methoxy)-1,3-propanediol]②;囌式-1-苯-(4'-羥基-3'-甲氧基)-2-苯-(4''-羥基-3''–甲氧基)-1,3-丙二醇[threo-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3'' -methoxy)-1,3-propanediol]③;(7S,8S)-1-(4-羥基-3,5-二甲氧基苯)-1,2,3 –丙三醇 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol]④;2-(4-羥基-3-甲氧基苯)-乙醇1-O-β-D-葡萄糖苷[2-(4-hydroxy-3-methoxyphenyl)-ethanol-1-O-β-D-glucopyranoside]⑤;(7S,8S)-1-(4-羥基-3,5-二甲氧基苯)-1,2,3-丙三醇-2-O-β-D-葡萄糖苷 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol-2-O-β-D-glucopyranoside]⑥.結論 6箇化閤物全部為首次從該屬植物中分離穫得.
목적 연구삼협목통Akebia trifoliata경중강겁성화학성분.방법 채용규효、응효、제비형HPLC등대삼협목통적수제취액진행분리,근거파보방법(EI-MS、ESI-MS、~1H-NMR、~(13)C-NMR、DEPT、HSQC、HMBC、~1H-~1H COSY)대분리소득적화합물진행결구감정.결과분리병감정료6개화합물,분별위4-간기-3,5-이갑양기분갑순 (4-hydroxy-3,5-dimethoxybenzenemethanol) ①;적식-1-분-(4'간기-3'갑양기)-2-분(4''-간기-3''-갑양기)-1,3-병이순) [erythro-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3''-methoxy)-1,3-propanediol]②;소식-1-분-(4'-간기-3'-갑양기)-2-분-(4''-간기-3''–갑양기)-1,3-병이순[threo-1-phenyl-(4'-hydroxy-3'-methoxy)-2-phenyl-(4''-hydroxy-3'' -methoxy)-1,3-propanediol]③;(7S,8S)-1-(4-간기-3,5-이갑양기분)-1,2,3 –병삼순 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol]④;2-(4-간기-3-갑양기분)-을순1-O-β-D-포도당감[2-(4-hydroxy-3-methoxyphenyl)-ethanol-1-O-β-D-glucopyranoside]⑤;(7S,8S)-1-(4-간기-3,5-이갑양기분)-1,2,3-병삼순-2-O-β-D-포도당감 [(7S,8S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-1,2,3-propanetriol-2-O-β-D-glucopyranoside]⑥.결론 6개화합물전부위수차종해속식물중분리획득.
