天然产物研究与开发 ›› 2017, Vol. 29 ›› Issue (增刊1): 1-5.doi: 10.16333/j.1001-6880.2017.S.001

• 研究论文 •    下一篇

桑叶中的紫罗兰酮类化合物和脂肪酸类化合物研究

王洪庆,陈晓燕,康洁,刘超,李保明,陈若芸*   

  1. 中国医学科学院北京协和医学院药物研究所,天然药物活性物质基础与应用国家重点实验室,北京 100050
  • 出版日期:2017-08-02 发布日期:2017-08-02

Ionone Derivatives and Fatty Acid from Morus alba L.Leaves

WANG Hong-qing,CHEN Xiao-yan,KANG Jie,LIU Chao,LI Bao-ming,CHEN Ruo-yun*   

  1. State Key Laboratory for Functions of Natural Medinices,Institute of Materia Medica,Chinese Academy of Medical Sciences &Peking Union Medical College,Beijing 100050,China
  • Online:2017-08-02 Published:2017-08-02

摘要: 对桑叶的化学成分进行分离鉴定。通过硅胶、反相ODS、Sephadex LH-20柱色谱和prep-HPLC进行分离纯化,从桑叶中分离得到18个化合物,运用现代波谱技术分别鉴定为(3R)-3-羟基-β-紫罗兰酮(1)、(6S,7E,9S)-9-hydroxy-megastigma-4,7-dien-3-one(2)、dehydro-vomifol(3)、 (3S,9R)-3-hydroxy-7,8-didehydro-β-ionol 9-O-β-D-glucopyranoside(4)、(6R,9R)-3-oxo-α-ionol 9-O-β-D-glucopyranoside(5)、(E)-6-[9-(β-D-glucopyranosyloxy)butylidene]-1,1,5-trimethyl-4-cyclohexen-3-one(6)、(Z)-6-[9-(β-D-glucopyranosyloxy) butylidene]-1,1,5-trimethyl-4-cyclohexen-3-one(7)、(6S,9S)-3-α-oxo-ionol 9-O-β-D-glucopyranoside(8)、blumenol C 9-O-β-D-glucopyranoside(9)、lcariside B1(10)、(3S)-O-β-D-glucopyranosyl-6-[3-oxo-(2S)-butenylidenyl]-1,1,5-trimethylcyclohexan-(5R)-ol(11)、(E)-4-((1S,3R,4R)-1-hydroxy-4,5,5-trimethyl-7-oxabicyclo [4.1.0]-heptan-1-yl)but-1-en-3-one(12)、(6R,9S)-vomifoliol-9-O-β-apiofuranosyl-(1′′→6′)-O-β-glucopy-ranoside(13)、(9R)-羟基-(10E,12Z,15Z)-十八碳三烯酸(14)、(2E)-十二碳烯二酸(15)、2,5-dihydro-5-oxo-5furanoctanoic acid(16)、1-glyceryl linolenate(17)、正三十二烷醇(18)。以上化合物均为首次从该植物中分离得到。

关键词: 桑叶, 化学成分, 紫罗兰酮类化合物

Abstract: The chemical constituents of Morus alab L.were isolated by column chromatography on silica gel,Rp-18,Sephadex LH-20 and prep-HPLC by chemical and spectral analyses.Eighteen compounds were finally isolated and purified from the leaves of Morus alab L..Their structures were elucidated as (3R)-3-hydroxy-β-ionone (1),(6S,7E,9S)-9-hydroxy-megastigma-4,7-dien-3-one (2),dehydrovomifol (3),(3S,9R)-3-hydroxy-7,8-didehydro-β-ionol 9-O-β-D-glucopyranoside (4),(6R,9R)-3-oxo-α-ionol 9-O-β-D-glucopyranoside (5),(E)-6-[9-(β-D-glucopyranosyloxy) butyl-idene]-1,1,5-trimethyl-4-cyclohexen-3-one (6),(Z)-6-[9-(β-D-glucopyranosyloxy)buty-lidene]-1,1,5-trimethyl-4-cyclohexen-3-one (7),(6S,9S)-3-oxo-β-ionol 9-O-β-D-glucopyranoside (8),blumenol C 9-O-β-Dglucopyranoside (9),lcariside B1 (10),(3S)-O-β-D-glucopy ranosyl-6-[3-oxo-(2S)-butenylidenyl]-1,1,5-trimethylcyclohexan-(5R)-ol (11),(E)-4-((1S,3R,4R)-1-hydroxy-4,5,5-trimethyl-7-oxabicyclo[4.1.0]-heptan-1-yl)but-1-en-3-one (12),(6R,9S)-vomifoliol-9-O-β-apiofuranosyl-(1′′→6′)-O-β-glucopyranoside (13),(9R)-hydroxy-(10E,12Z,15Z)-octadecatrienoic acid (14),(2E)-dodecenedioic acid (15),2,5-dihydro-5-oxo-5-furanoctanoic acid (16),1-glyceryl linolenate (17),ndotfiacontanol (18)。Compounds 1-18 were obtained from this plant or the first time.

Key words: Morus alab L., chemical constituents, ioone derivatives