期刊文献+

蒜香藤的挥发性成分分析(英文) 被引量:1

Essential Oil Composition of A Novel Garlic Vine Pseudocalymma alliaceum
下载PDF
导出
摘要 采用采用气相色谱-质谱联用技术对蒜香藤不同部位叶、茎与果的挥发性成份进行分析。结果发现,叶、茎、果中可定性定量的化合物分别占挥发性成份总量的97.6%、95.4%与97.4%。在不同部位中,主要的化合物是含硫化合物,分别占挥发性总量的78.4%、54.0%与81.0%。叶、茎、根中主要的挥发性成份有二烯丙基二硫化物(48.9%、25.4%、34.2%)和二烯丙基三硫化物(18.4%、14.0%、29.8%)。蒜香藤的挥发性化学成份与大蒜的相似,尤其体现在含硫化合物上,因此,蒜香藤可以作为大蒜的潜在替代物,其药理活性需要进一步开发研究。 In this study, the leaf, stem, and fruit of Pseudocalymma alliaceum were distilled and the essential oil composi- tion was studied by GC-MS. The identified components constituted 97.6% ,95.4% and 97.4% of the leaf, stem,and fruit oils, respectively. The major components of different parts of P. alliaceum were sulfur-containing compounds, amoun- ting to 78.4% ,54.0% and 81.0% of essential oil composition in leaves, stems, and fruits, respectively. The result showed that the main constituents of the essential oil of leaves, stems, and fruits oils were diallyl disulphide (48.9% ,25. 4% and 34.2% ) and diaUyl trisulfide( 18.4% ,14.0% and 29.8% ). It was concluded that the essential oil composi- tion of P. alliaceum was similar with the garlic Allium sativum, especially to sulfur-containing compounds. The garlic vine P. aUiaceum is a potential substitute of A. sativum and its pharmaceutical effects need to be studied in the future.
作者 唐玲 陈高
出处 《天然产物研究与开发》 CAS CSCD 北大核心 2014年第2期221-224,共4页 Natural Product Research and Development
基金 National Natural Science Foundation of China(NSFC 31100177) West Doctor Fund of the Chinese Academy of Science(Y02F7311W1)
关键词 蒜香藤 含硫化合物 二烯丙基二硫化物 挥发性成份 气相色谱-质谱联用技术 Pseudocalymma alliaceum diallyl disulphide diallyl trisulfide essential oil GC-MS
  • 相关文献

参考文献20

  • 1Lanzotti V. The analysis of onion and garlic. J Chromatogr, 2006,1112:3-22.
  • 2Block E. The organosulfur chemistry of the GenUs Allium - implications for the organic chemistry of sulfur. Angew Chem, 1992,31 : 1135-1178.
  • 3Charma SP, Mohan L, Srivastava CN. Larvicidal activity of Pseudocalyrrmta alliaceum and Allium sativum against Cu/ex quinquefasciatus (Say). Entomol Res ,2011,41:216-220.
  • 4Block E. The chemistry of garlic and onions. Sci Am, 1985, 252 : 114-119.
  • 5Abu-lafi S, Dembicki JW, Goldshlag P, et al. The use of the 'Cryogenic' GC/MS and on-column injection for study of.organosulfur compounds of the Allium sativum. J Food Com- pos Ana/,2004,17:235-245.
  • 6Wattenberg LW, Sparnins VL, Barmy G. Inhibition of N-ni- tros~ethy~amine carcinogenesis in mice by naturally occur- rihg organ0sulfur compounds and monoterpenes. Cancer Res, I989,49 .~'689:2692.
  • 7Shenoy NR, Choughttley ASU. Inhibitory effect of diet related sulphydryl compounds on the formation of carcinogenic ni- / trosamines. Cancer Lett, 1992,65:227 -232.
  • 8Bordia A, Verma SK, Srivastava KC. Effect of garlic (Allium sativum) on blood lipids, blood sugar,fibrinogen and fibrinc~ lytic activity in patients with coronary artery disease. Prosta- glandins Leukot Essent Fatty Acids, 1998,58:257-263.
  • 9Wu CC, Chung JG, Tsai SJ, et al. Differential effects of allyl sulfides from garlic essential oil on cell cycle regulation in human liver tumor cells. Food Chem Toxicol,2004,42 : 1937- 1947.
  • 10Ross SM,King JR,Cesar Izaurralde R,et al.Weed suppression by seven clover species.Agron J,2001,93:820-827.

二级参考文献81

共引文献91

同被引文献18

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部