Ellagic acid rhamnosides from the stem bark of Eucalyptus globulus

被引:67
作者
Kim, JP
Lee, IK
Yun, BS
Chung, SH
Shim, GS
Koshino, H
Yoo, ID
机构
[1] Korea Res Inst Biosci & Biotechnol, Taejon 305600, South Korea
[2] Hansol Inst Sci & Technol, Kyungki Do 472850, South Korea
[3] RIKEN, Inst Phys & Chem Res, Wako, Saitama 3510198, Japan
关键词
Eucalyptus globulus; myrtaceae; stem bark; ellagic acid rhamnosides; antioxidant activity;
D O I
10.1016/S0031-9422(01)00146-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Four ellagic acid rhamnosides were isolated from the stem bark of Eucalyptus globulus. Their structures have been established on the basis of the analysis of their H-1 NMR. C-13 NMR. HMBC, IR and MS spectral data. The HMBC data of these compounds were most useful for their structure determinations, with these bring determined to be 3-O-methylellagic acid 3 ' -O-alpha -rhamnopyranoside, 3-O-methylellagic acid 3 ' -O-alpha -3 " -O-acetylrhamnopyranoside, 3-O-methylellagic acid 3 ' -O-alpha -2 " -O-acetylrhamnopyranosidc. 3-O-methylellagic acid 3 ' -O-a-4 " -O-acetylrhamnopyranoside, respectively. Their antioxidant activities were evaluated by measuring the inhibition of lipid pel oxidation using rat liver microsomes. with IC50 values of 10.0 14.0 mug/ml. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:587 / 591
页数:5
相关论文
共 24 条
  • [1] ISOLATION AND CHARACTERIZATION OF EUGLOBALS FROM EUCALYPTUS-GLOBULUS LABILL BY PREPARATIVE REVERSED-PHASE LIQUID-CHROMATOGRAPHY
    AMANO, T
    KOMIYA, T
    HORI, M
    GOTO, M
    KOZUKA, M
    SAWADA, T
    [J]. JOURNAL OF CHROMATOGRAPHY, 1981, 208 (02): : 347 - 355
  • [2] Barr A, 1993, TRADITIONAL ABORIGIN
  • [3] CROW WD, 1977, TETRAHEDRON LETT, P1073
  • [4] Elliot W.R., 1984, ENCY AUSTR PLANTS SU, V4
  • [5] REARRANGEMENT REACTIONS OF AROMADENDRANE DERIVATIVES - THE SYNTHESIS OF (+)-MAALIOL, STARTING FROM NATURAL (+)-AROMADENDRENE-IV
    GIJSEN, HJM
    WIJNBERG, JBPA
    VANRAVENSWAAY, C
    DEGROOT, A
    [J]. TETRAHEDRON, 1994, 50 (16) : 4733 - 4744
  • [6] THE SYNTHESIS OF (-)-KESSANE, STARTING FROM NATURAL (+)-AROMADENDRENE .2.
    GIJSEN, HJM
    WIJNBERG, JBPA
    STORK, GA
    DEGROOT, A
    [J]. TETRAHEDRON, 1991, 47 (25) : 4409 - 4416
  • [7] THE SYNTHESIS OF MONOHYDROXY AND DIHYDROXY AROMADENDRANE SESQUITERPENES, STARTING FROM NATURAL (+)-AROMADENDRENE .3.
    GIJSEN, HJM
    WIJNBERG, JBPA
    STORK, GA
    DEGROOT, A
    DEWAARD, MA
    VANNISTELROOY, JGM
    [J]. TETRAHEDRON, 1992, 48 (12) : 2465 - 2476
  • [8] THE CONVERSION OF NATURAL (+)-AROMADENDRENE INTO CHIRAL SYNTHONS .1.
    GIJSEN, HJM
    KANAI, K
    STORK, GA
    WIJNBERG, JBPA
    ORRU, RVA
    SEELEN, CGJM
    VANDERKERK, SM
    DEGROOT, A
    [J]. TETRAHEDRON, 1990, 46 (20) : 7237 - 7246
  • [9] Inoscavin A, a new free radical scavenger from the mushroom Inonotus xeranticus
    Kim, JP
    Yun, BS
    Shim, YK
    Yoo, ID
    [J]. TETRAHEDRON LETTERS, 1999, 40 (36) : 6643 - 6644
  • [10] Sesquiterpene O-naphthoquinones from the root bark of Ulmus davidiana
    Kim, JP
    Kim, WG
    Koshino, H
    Jung, J
    Yoo, ID
    [J]. PHYTOCHEMISTRY, 1996, 43 (02) : 425 - 430