期刊文献+

笔管草中Megastigmane及黄酮苷类化学成分(英文) 被引量:17

Megastigmanes and Flavonoid Glycosides of Equisetum debile
下载PDF
导出
摘要 目的 :研究木贼科植物笔管草 (Equisetumdebile)的化学成分。方法 :采用硅胶、sephadexLH 2 0凝胶柱色谱进行分离纯化 ,通过理化方法和光谱分析鉴定化合物结构。结果 :从笔管草全草乙酸乙酯和正丁醇提取物中分离得到 4个megastigmane型化合物和 4个黄酮苷 ,分别鉴定为blumenolA(1) ,corchoinosideC(2 ) ,sammangaosideA(3) ,(3S ,5R ,6R ,7E ,9S)- megastigmane-7-ene-3-hydroxy-5 ,6-epoxy-9-O-β- D-glucopyranoside(4) ,山柰酚-3,7-双葡萄糖苷 (5 ) ,camelliasideC(6 ) ,山柰酚-3-槐糖苷 (7)andclematine(8) .化合物 1-4 ,6 。 AIM: To study the chemical constituents of Equisetum debile. METHODS: Compounds were isolated by column chromatography on silica gel, sephadex LH-20, ODS-18 and their structures were elucidated based on the spectroscopic methods including 2D NMR (COSY, HMQC, HMBC). RESULTS: Four megastigmane type compounds were isolated, one aglycone and three glucosides, identified as blumenol A (1), corchoinoside C (2), sammangaoside A (3), and (3S, 5R, 6R, 7E, 9S)-megastigmane-7-ene-3-hydroxy-5, 6-epoxy-9-O-β-D- glucopyranoside (4). Four flavonoid glycosides, kaempferol-3, 7-di-β-D-glucoside (5), camelliaside C (6), kaempferol 3-O-β-sophoroside (7), clematine (8) were also obtained from this plant. CONCLUSION: All megasigmane compounds and compound 6, 8 were obtained from Equisetaceae family for the first time.
出处 《中国天然药物》 SCIE CAS CSCD 2005年第2期93-96,共4页
关键词 木贼科 笔管草 化学成分 Megastigmane类化合物 黄酮苷 中药材 光谱分析 Equisetsaceae Equisetum debile Chemical constituents Megastigmane Flavonoid glycosides
  • 相关文献

参考文献10

  • 1[1]Goda Y, Hoshino K, Akiyama H, et al. Inhibitors of histamine release from RBL-2H3 cells induced by antigen stimulation[J]. Biol Pharm Bull. 1999, 22 (12): 1319-1326.
  • 2[2]Ito H, Kobayashi E, Li SH, et al. Antitumor activity of compounds isolated from leaves of Eriobotrya japonica[J]. J Agric Food Chem. 2002, 50: 2400-2403.
  • 3[3]Chang FL, Chen CY, Hsieh TJ, et al. Chemical constituents from Annona glabra Ⅲ[J]. J Chin Chem Soc(中国化学), 2000, 47: 913-910.
  • 4[4]Kanchanapoom T, Kasai R, Chumsri P, et al. Megastigmane and iridoid glucosides from Clerodendrum inerme[J]. Phytochemistry. 2001, 58: 333-336.
  • 5[5]Yoshikawa M, Shimada H, Saka M, et al. Medicinal Foodstuff. V. Moroheiya. (1): Absolute stereostructure of corchoinosides A, B, and C, Histamine release inhibitors from the leaves of Vietnamese Corchorus olitorius L. (Tiliaceae)[J]. Chem Pharm Bull. 1997, 45(3): 464-469.
  • 6[6]Otsuka H, Hirata E, Shinzato T, et al. Stereochemistry of megastigmane glucosides from Glochidion zeylanicum and Alangium premnifolium[J]. Phytochemistry, 2003, 62(5): 763-768.
  • 7[7]Markham K R, Ternai B, Stanley R, et al. Carbon-13 NMR studies of flavonoids-Ⅲ naturally occurring flavonoid glycosides and their acylated derivatives[J]. Tetrahedron. 1978, 34: 1389-1397.
  • 8[8]Sekine T, Arai Y, Ikegami F, et al. Isolation of camelliaside C from "tea seed cake" and inhibitory effects of its derivatives on arachidonate 5-lipoxygenase[J]. Chem Pharm Bull. 1993, 41(6): 1185-1187.
  • 9[9]Yoshizaki M, Fujino H, Masuyama M, et al. A chemotaxonomic study of flavonoids in the leaves of six Trichosanthes species[J]. Phytochemistry, 1987, 26(9): 2557-2558.
  • 10[10]Chen LF, Liu J, Stephen Davidson R, et al. Isolation and structure of clematine, A new flavanone glycoside from Clematis armandii Franch[J]. Teterahedron, 1993, 49(23): 5169-5176.

同被引文献234

引证文献17

二级引证文献128

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