目的 对一年蓬的化学成分进行分离和结构鉴定。方法 运用Diaion HP-20、Toyopearl HW-40、Sephadex LH-20、硅胶、制备液相等多种柱色谱技术进行分离纯化,并根据化合物的光谱数据和理化性质进行结构鉴定。结果 分离得到20个化合物,分别为香草酸(1),阿魏酸(2),对羟基苯乙酮(3),二氢松柏醇(4),黑麦草内酯(5),4-羟基-3-甲氧基苯丙-8-烯-4-O-β-D-吡喃木糖基-(1→6)-β-D-吡喃葡萄糖苷(6),吲哚-3-甲醛(7),5,7-二羟基色原酮(8),焦袂康酸(9),erigeside D(10),3,5-二甲氧基-4-O-(β-D-吡喃葡萄糖基)-苯甲酸甲酯(11),二氢去氢二愈创木基醇-4′-O-β-D-葡萄糖苷(12),高圣草素(13),二氢高良姜醇(14),白杨素(15),高车前素(16),金圣草素(17),环桑皮素(18),蓟黄素(19)和柚皮素(20)。结论 化合物1~8、11~19为首次从该植物中分到。
Abstract
OBJECTIVE To study the chemical constituents of Erigeron annuus (L.) Pers.. METHODS The compounds were isolated and purified by Diaion HP-20, Toyopearl HW-40, Sephadex LH-20, MCI Gel CHP-20, silica gel column chromatography, and preparative HPLC, and their structures were elucidated on the basis of spectral data and physiochemical properties. RESULTS Twenty compounds were elucidated as vanillic acid(1), ferulic acid(2), 4-hydroxyacetophenone(3), dihydroconiferylalcohol(4), loliolide(5), 4-hydroxy-3-methoxyphenylprop-8-ene 4-O-β-D-xylopyraosyl-(1→6)-β-D-glucopyranoside(6), 1H-indole-3-carbaldehyde(7), 5,7-dihydroxychromone(8), pyromeconic acid(9), erigeside D(10), methyl syringate 4-O-β-D-glucopyranoside(11),(7S,8R)-urolignoside(12), homoeriodictyol(13), pinobaksin(14), chrysin(15), hispidulin(16), chryseriol(17), cyclomorusin(18), cirsimaritin(19), and naringenin(20), respectively. CONCLUSION Compounds 1-8 and 11-19 is isolated from this plant for the first time.
关键词
一年蓬 /
酚酸 /
吡喃酮 /
黄酮
{{custom_keyword}} /
Key words
Erigeron annuus (L.) Pers. /
phenolic acid /
pyrone /
flavonoid
{{custom_keyword}} /
中图分类号:
R284
{{custom_clc.code}}
({{custom_clc.text}})
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] DING B Z, WANG S Y. Flora of Henan(Ⅲ)(河南植物志) [M]. Zhengzhou:Henan Science and Technology Press, 1997:593.
[2] Nanjing University of Traditional Chinese Medicine. Dictionary of Traditional Chinese Medicine(中药大辞典) [M]. Shanghai:Shanghai Science and Technology Press, 2006:3-4.
[3] ZHANG W K, YANG G E, LI Q, et al. Studies on chemical constituents of Euphorbia sorori [J]. China J Chin Mater Med(中国中药杂志), 2006, 31(20):1694-1696.
[4] AN N, ZHANG T T, GUI M, et al. Chemical constituents from the stem bark of Pandanus tectorius [J]. Chin Pharm J(中国药学杂志), 2015, 50(11):931-934.
[5] LIU J, LI G Q, WU X, et al. Chemical constituents from Glechoma longituba [J]. China J Chin Mater Med(中国中药杂志), 2014, 39(4):695-698.
[6] HUANG Y H, ZENG W M, LI G Y, et al. Characterization of a new sesquiterpene and antifungal activities of chemical constituents from Dryopteris fragrans (L. ) Schott [J]. Molecules , 2014, 19(1):507-513.
[7] CHENG W, XU W D, ZHU C G, et al. Glycosides from Machilus wangchiana [J]. China J Chin Mater Med(中国中药杂志), 2015, 40(6):1102-1107.
[8] LU Y, LI Z H, MA L, et al. Study on chemical constituents from cultivated Gynura nepalensis[J]. China J Chin Mater Med(中国中药杂志), 2014, 39(19):3777-3781.
[9] WEI A H, WU G H, XIONG C M, et al. Flavonoids of Macrothelypteris viridifrons [J]. Chin Pharm J (中国药学杂志), 2011, 46(3):177-179.
[10] FAN Q F, NA Z, HU H B, et al. Chemical constituents from stem barks of Garcinia paucinervis[J]. Tradit Herb Drug(中草药杂志), 2012, 43(3):436-439.
[11] CHEN B, LI B G, ZHANG G L. Glycosides from Erigeron breviscapus[J]. Acta Bot Sin, 2002, 44(3):344-348.
[12] KOJIMA M, NAKAMURA Y, ITO S, et al. Total synthesis of macrocyclic glycosides, clemochinenosides A and B, and berchemolide, by fluorous mixture synthesis[J]. Tetrahedron Lett, 2009, 50(45):6143-6149.
[13] KUANG H X, XIA Y G, YANG B Y, et al. Lignan constituents from Chloranthus japonicus sieb. [J]. Arch Pharm Res, 2009, 32(3):329-334.
[14] NAKANO H, KAWADA N, YOSHIDA M, et al. Isolation and identification of flavonoids accumulated in proanthocyanidin-free barley[J]. Agric Food Chem, 2011, 59(17):9581-9587.
[15] ZHANG H, XU L X, WU P, et al. Flavonoids from the aerial parts of Alpinia officinarum[J]. J Trop Subtrop Bot, 2014, 22(1):89-92.
[16] KATERERE D R, GRAY A I, NASH R J, et al. Phytochemical and antimicrobial investigations of stilbenoids and flavonoids isolated from three species of Combretaceae[J]. Fitoterapia, 2012, 83:932-940.
[17] XIA H J, QIU F, ZHU S, et al. Isolation and identification of ten metabolites of breviscapine in rat urine[J]. Biol Pharm Bull, 2007, 30(7):1308-1316.
[18] KIM J Y, LEE W S, KIM Y S, et al. Isolation of cholinesterase-inhibiting flavonoids from Morus lhou[J]. J Agric Food Chem, 2011, 59:4589-4596.
[19] MALMIR M, GOHARI A R, SAEIDNIA S, et al. A new bioactive monoterpene-flavonoid from Satureja khuzistanica[J]. Fitoterapia, 2015, 105:932-940.
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}
基金
教育部科学技术研究重点资助项目(DF2003078)
{{custom_fund}}