檵木水溶性化学成分研究

杨郁, 徐锐, 李长伟, 任凤霞, 赵毅民, 张杨

中国药学杂志 ›› 2022, Vol. 57 ›› Issue (11) : 886-889.

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中国药学杂志 ›› 2022, Vol. 57 ›› Issue (11) : 886-889. DOI: 10.11669/cpj.2022.11.004
论著

檵木水溶性化学成分研究

  • 杨郁, 徐锐, 李长伟, 任凤霞, 赵毅民, 张杨*
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Water-soluble Constituents from Leaves of Loropetalum chinense

  • YANG Yu, XU Rui, LI Chang-wei, REN Feng-xia, ZHAO Yi-min, ZHANG Yang*
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摘要

目的 研究檵木水溶性化学成分。方法 采用大孔树脂、硅胶、凝胶、制备高效液相等色谱技术进行分离,根据波谱数据对化合物进行结构鉴定。结果 从檵木叶中分离得到10个化合物,分别鉴定为(6S,9R)-roseoside(1),rhododendrin(2),epirhododendrin(3),(1S,2R,4S,5S)(-)-Angelicoidenol 2-O-β-D-glucopyranoside(4),dihydroalangionoside A(5),(Z)-3-hexenyl β-primeveroside(6),benzyl β-primeveroside(7),(Z)-3-hexenyl O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside(8),rhododendrol 4'-O-β-D-glucopyranoside(9),3-(4-hydroxyphenol)propyl β-D-glucopyranoside(10)。结论 化合物1~7,9,10均首次从该属植物中分离得到。

Abstract

OBJECTIVE To study the water-soluble chemical constituents in the leaves of Loropetalum chinense. METHODS The chemical constituents were isolated by macroporous resin, ODS column, silica gel column, Sephadex LH-20 and preparative HPLC. Their structures were identified on the basis of spectral data analysis. RESULTS Ten compounds were isolated from L.chinense leaves and identified as(6S,9R)-roseoside(1), rhododendrin(2), epirhododendrin(3), (1S,2R,4S,5S)(-)-angelicoidenol 2-O-β-D-glucopyranoside(4), dihydroalangionoside A(5),(Z)-3-hexenyl β-primeveroside(6), benzyl β-primeveroside(7),(Z)-3-hexenyl O-α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside(8), rhododendrol 4'-O-β-D-glucopyranoside(9), and 3-(4-hydroxyphenol)propyl β-D-glucopyranoside(10). CONCLUSION Compounds 1-7, 9, and 10 are isolated from this genus for the first time.

关键词

檵木 / 单萜糖苷 / 苯酚糖苷 / 己烯醇糖苷

Key words

Loropetalum chinense / monoterpenoid glucosides / phenolic glucoside / hexenol glucoside

引用本文

导出引用
杨郁, 徐锐, 李长伟, 任凤霞, 赵毅民, 张杨. 檵木水溶性化学成分研究[J]. 中国药学杂志, 2022, 57(11): 886-889 https://doi.org/10.11669/cpj.2022.11.004
YANG Yu, XU Rui, LI Chang-wei, REN Feng-xia, ZHAO Yi-min, ZHANG Yang. Water-soluble Constituents from Leaves of Loropetalum chinense[J]. Chinese Pharmaceutical Journal, 2022, 57(11): 886-889 https://doi.org/10.11669/cpj.2022.11.004
中图分类号: R284.1   

参考文献

[1] LI J,BOGLE A L,KLEIN A S. Phylogenetic relationships in the Hamamelidaceae:Evidence from the nucleotide sequences of the plastid gene matK[J].Plant Syst Evol,1999,218(3):205-219.
[2] XIAO L,YUE Y Z,CHEN J Y,et al. Research progress of active pharmaceutical ingredients and pharmacological action of Loropetalum Chinense var. Rubrum[J].Hunan Agric Sci(湖南农业科学),2017,126(6):119-121.
[3] WANG G,LIU J S,LI H Y,et al. Chemical constituents of Loropetalum chinense[J].Nat Prod Res Dev(天然产物研究与开发),2011,23(2):267-269.
[4] ZHANG Y,REN F X,YANG Y,et al. Chemical constituents and biological activities of Loropetalum chinense and Loropetalum chinense var. rubrum:research advances[J].J Int Pharm Res(国际药学研究杂志),2014,41(3):307-312.
[5] YANG Y,YU N J,ZHANG Y,et al. Study on chemical constituents from leaves of Loropetalum chinense[J].Chin Pharm J(中国药学杂志), 2015,50(3):205-208.
[6] ZHANG W G,ZHANG C,LI M L,et al. Phytochemical and chemotaxonomic study on Loropetalum chinense(R. Br.) Oliv[J]. Biochem Syst Ecol, 2018,81:80-82.
[7] ZHANG Y,REN F X,YANG Y,et al. Loropetalum chinense extract comprising quinic acid,glucoside compounds and their medical application:China,CN105287659[P]. 2016-06-23.
[8] LIU H H,YU Y M,ZHANG T,et al. Chemical constituents from Asplenium unilaterale[J]. Chin Pharm J(中国药学杂志),2017,52(2):100-104.
[9] PAN F F,LUNDGREN L N. Rhododendrol glycosides and phenyl glucosides from inner bark of Betulapubescens[J]. Phytochemistry,1994,36(1):79-83.
[10] FUCHINO H,KONISHI S,SATOH T,et al. Chemical evaluation of Betula species in Japan. Ⅱ. Constituents of Betulaplatyphylla var. japonica[J]. Chem Pharm Bull,1996,44(5):1033-1038.
[11] KERSTIN S S.(1S,2R,4S,5S)-Angelicoidenol-2-O-β-D-glucopyranoside-a moose deterrent compound in scots pine(Pinussylvestris L.)[J]. J Chem Ecol,1992,18(11):2025-2039.
[12] OTSUKA H,KAMADA K,OGIMI C,et al. Alangionosides A and B,ionol glycosides from leaves of Alangium premnifolium[J]. Phytochemistry,1994,35(5):1331-1334.
[13] NISHIKITANI M,WANG D M,KUBOTA K,et al.(Z)-3-Hexenyl and trans-linalool 3,7-oxide β-primeveroside isolated as aroma precursors from leaves of a green tea cultivar[J].Biosci Biotechnol Biochem,1999,69(9):1631-1633.
[14] KAWAHARA E,FUJII M,KATO K,et al. Chemoenzymatic synthesis of naturally occurring benzyl 6-O-glycosyl-β-D-glucopyranoside[J]. Chem Pharm Bull,2005,53(8):1058-1061.
[15] YANG D,JIA X H,XIE H H. Heptylvicianoside and methyl caramboside from sour star fruit[J].Nat Prod Res,2019, 33(8):1233-1236.
[16] FUCHINO H,SATOH T,HIDA J,et al. Chemical evaluation of Betula species in Japan. Ⅵ. constituents of Betulaschmidtii[J]. Chem Pharm Bull,1998,46(6):1051-1053.
[17] HAN C,HUANG Z J,ZHENG C,et al. Nitric oxide donating anilinopyrimidines: Synthesis and biological evaluation as EGFR inhibitors[J]. Eur J Med Chem,2013,66:82-90.
[18] ONO M,YASUDA S,SHIONO Y,et al. A new hemiterpene glycoside from the ripe tomatoes[J]. Nat Prod Res,2015,29(3):262-267.
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