Identification of shikonin and its ester derivatives from the roots of Echium italicum L.

被引:49
作者
Albreht, Alen [1 ]
Vovk, Irena [1 ]
Simonovska, Breda [1 ]
Srbinoska, Marija [2 ]
机构
[1] Natl Inst Chem, Food Chem Lab, SI-1000 Ljubljana, Slovenia
[2] Tobacco Inst, Dept Chem Tobacco, MK-7500 Prilep, Macedonia
关键词
Echium italicum L; Shikonin; Naphthoquinones; Synthesis; HPLC-VIS; HPLC-MS; TLC; NMR; PERFORMANCE LIQUID-CHROMATOGRAPHY; LITHOSPERMUM-ERYTHRORHIZON; NAPHTHOQUINONE DERIVATIVES; ALKANNA-TINCTORIA; ISOHEXENYLNAPHTHAZARINS; CULTURES; NAPHTHAQUINONES; POLYMERIZATION; SPECTROMETRY; ENANTIOMERS;
D O I
10.1016/j.chroma.2009.01.098
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nine shikonin pigments: shikonin (S), acetylshikonin (AS), propionylshikonin (PS), isobutyrylshikonin (IBS), tiglylshikonin (TS), 3,3-dimethylacrylshikonin (DAS), angelylshikonin (ANS), 2-methyl-n-butyrylshikonin (MBS) and isovalerylshikonin (IVS) were identified in the root epidermis of Echium italicum L. for the first time. A new thin-layer chromatographic (TLC) method for the separation of enantiomers alkannin and shikonin proved only shikonin after saponification of the root extract, and was afterwards esterified with the corresponding acyl chloride to acquire seven standard compounds (all except ANS). The developed isocratic high-peformance liquid chromatographic (HPLC) methods with VIS and mass spectrometry (MS) detection, allowed for the first time simultaneous separation of all nine compounds with similar structures including positional and geometric isomers in a short time. Structures of the main five compounds (AS, IBS, ANS, MBS, IVS) isolated from the extract by a new semi-preparative HPLC on C18 have additionally been confirmed by H-1 and C-13 nuclear magnetic resonance spectra, which were reported for AS and MBS for the first time. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3156 / 3162
页数:7
相关论文
共 40 条
  • [1] Afzal M., 1996, AGR BIOL CHEM TOKYO, V50, P1651
  • [2] Analysis of alkannin derivatives from Alkanna species by high-performance liquid chromatography/photodiode array/mass spectrometry
    Assimopoulou, A. N.
    Karapanagiotis, I.
    Vasiliou, A.
    Kokkini, S.
    Papageorgiou, V. P.
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2006, 20 (12) : 1359 - 1374
  • [3] Study on the enantiomeric ratio of the pharmaceutical substances alkannin and shikonin
    Assimopoulou, AN
    Papageorgiou, VP
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2004, 18 (10) : 791 - 799
  • [4] Study on isohexenylnaphthazarins polymerization in alkaline media
    Assimopoulou, AN
    Papageorgiou, VP
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2004, 18 (08) : 508 - 522
  • [5] Study on polymerization of the pharmaceutical substances isohexenylnaphthazarins
    Assimopoulou, AN
    Papageorgiou, VP
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2004, 18 (08) : 492 - 500
  • [6] Quantitative determination of naphthaquinones of Arnebia densiflora (Nordm.) Ledeb. by an improved high-performance liquid chromatographic method
    Bozan, B
    Baser, KHC
    Kara, S
    [J]. JOURNAL OF CHROMATOGRAPHY A, 1997, 782 (01) : 133 - 136
  • [7] Cell-specific production and antimicrobial activity of naphthoquinones in roots of Lithospermum erythrorhizon
    Brigham, LA
    Michaels, PJ
    Flores, HE
    [J]. PLANT PHYSIOLOGY, 1999, 119 (02) : 417 - 428
  • [8] Shikonin production by p-fluorophenylalanine resistant cells of Lithospermum erythrorhizon
    Bulgakov, VP
    Kozyrenko, MM
    Fedoreyev, SA
    Mischenko, NP
    Denisenko, VA
    Zvereva, LV
    Pokushalova, TV
    Zhuravlev, YN
    [J]. FITOTERAPIA, 2001, 72 (04) : 394 - 401
  • [9] A new EGFR inhibitor induces apoptosis in colon cancer cells
    Calonghi, N.
    Pagnotta, E.
    Parolin, C.
    Mangano, C.
    Bolognesi, M. L.
    Melchiorre, C.
    Masotti, L.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 354 (02) : 409 - 413
  • [10] CHAISUKSANT R, 1995, PHARMAZIE, V50, P363