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Volumn 43, Issue 1, 2008, Pages 97-107

Identification of lignans by liquid chromatography-electrospray ionization ion-trap mass spectrometry

Author keywords

ESI; Fragmentation; HPLC; Ion trap; Lignan; MS

Indexed keywords

ELECTROSPRAY IONIZATION; FORMALDEHYDE; KETONES; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; SEPARATION;

EID: 39149097864     PISSN: 10765174     EISSN: 10969888     Source Type: Journal    
DOI: 10.1002/jms.1276     Document Type: Article
Times cited : (144)

References (30)
  • 1
    • 0142091113 scopus 로고    scopus 로고
    • Liquid chromatographic-tandem mass spectrometric method for the plant lignan 7-hydroxymatairesinol and its potential metabolites in human plasma
    • Smeds A, Hakala K. Liquid chromatographic-tandem mass spectrometric method for the plant lignan 7-hydroxymatairesinol and its potential metabolites in human plasma. Journal of Chromatography B 2003; 793: 297.
    • (2003) Journal of Chromatography B , vol.793 , pp. 297
    • Smeds, A.1    Hakala, K.2
  • 2
    • 19544377696 scopus 로고    scopus 로고
    • Simultaneous determination of abietine-type diterpenes, flavonolignans and phenolic compounds in compound preparations of Silybum marianum and Salvia miltiorrhiza by HPLC-DAD-ESI MS
    • Zhao Y, Chen B, Yao S. Simultaneous determination of abietine-type diterpenes, flavonolignans and phenolic compounds in compound preparations of Silybum marianum and Salvia miltiorrhiza by HPLC-DAD-ESI MS. Journal of Pharmaceutical and Biomedical Analysis 2005; 38: 564.
    • (2005) Journal of Pharmaceutical and Biomedical Analysis , vol.38 , pp. 564
    • Zhao, Y.1    Chen, B.2    Yao, S.3
  • 4
    • 9144249775 scopus 로고    scopus 로고
    • Structural elucidation and identification of alkaloids in Rhizoma Coptidis by electrospray ionization tandem mass spectrometry
    • Wang D, Liu Z, Gou M, Liu S. Structural elucidation and identification of alkaloids in Rhizoma Coptidis by electrospray ionization tandem mass spectrometry. Journal of Mass Spectrometry 2004; 39: 1356.
    • (2004) Journal of Mass Spectrometry , vol.39 , pp. 1356
    • Wang, D.1    Liu, Z.2    Gou, M.3    Liu, S.4
  • 5
    • 20444380372 scopus 로고    scopus 로고
    • Characterization of phenolic compounds in the chinese herbal drug Tu-Si-Zi by liquid chromatography coupled to electrospray ionization mass spectrometry
    • Ye M, Yan Y, Guo D-A. Characterization of phenolic compounds in the chinese herbal drug Tu-Si-Zi by liquid chromatography coupled to electrospray ionization mass spectrometry. Rapid Communications in Mass Spectrometry 2005; 19: 1469.
    • (2005) Rapid Communications in Mass Spectrometry , vol.19 , pp. 1469
    • Ye, M.1    Yan, Y.2    Guo, D.-A.3
  • 6
    • 0034252330 scopus 로고    scopus 로고
    • HPLC separation of flavonols, flavones and oxidized flavonols with UV-DAD-, electrochemical and ESI-Ion trap MS detection
    • Jungbluth G, Ternes W. HPLC separation of flavonols, flavones and oxidized flavonols with UV-DAD-, electrochemical and ESI-Ion trap MS detection. Fresenius Journal of Analytical Chemistry 2000; 367: 661.
    • (2000) Fresenius Journal of Analytical Chemistry , vol.367 , pp. 661
    • Jungbluth, G.1    Ternes, W.2
  • 7
    • 0033661920 scopus 로고    scopus 로고
    • The identification of dilignols from dehydrogenation mixtures of coniferyl alcohol and apocynol [4-(1-Hydroxyethyl)-2-methoxyphenol] by LC-MS/MS
    • Syrjänen K, Sipilä J, Björk H, Brunow G. The identification of dilignols from dehydrogenation mixtures of coniferyl alcohol and apocynol [4-(1-Hydroxyethyl)-2-methoxyphenol] by LC-MS/MS. Journal of Agricultural and Food Chemistry 2000; 48: 5211.
    • (2000) Journal of Agricultural and Food Chemistry , vol.48 , pp. 5211
    • Syrjänen, K.1    Sipilä, J.2    Björk, H.3    Brunow, G.4
  • 8
    • 0031550286 scopus 로고    scopus 로고
    • Analysis of lignan constituents from Schisandra chinensis by liquid chromatography-electrospray mass spectrometry
    • He X-G, Lian L-Z, Lin L-Z. Analysis of lignan constituents from Schisandra chinensis by liquid chromatography-electrospray mass spectrometry. Journal of Chromatography A 1997; 756: 81.
    • (1997) Journal of Chromatography A , vol.756 , pp. 81
    • He, X.-G.1    Lian, L.-Z.2    Lin, L.-Z.3
  • 10
    • 0342561647 scopus 로고    scopus 로고
    • Saarinen NM, Wärri A, Mäkelä SI, Eckerman C, Reunanen M, Ahotupa M, Salmi SM, Franke AA, Kangas L, Santti R. Hydroxymatairesinol, a novel enterolactone precursor with antitumor properties from coniferous tree (Picea abies). Nutrition and Cancer 2000; 36: 207.
    • Saarinen NM, Wärri A, Mäkelä SI, Eckerman C, Reunanen M, Ahotupa M, Salmi SM, Franke AA, Kangas L, Santti R. Hydroxymatairesinol, a novel enterolactone precursor with antitumor properties from coniferous tree (Picea abies). Nutrition and Cancer 2000; 36: 207.
  • 12
    • 23844529912 scopus 로고    scopus 로고
    • Lignans in treatment of cancer and other diseases
    • Lee K-H, Xiao Z. Lignans in treatment of cancer and other diseases. Phytochemistry Reviews 2003; 2: 341.
    • (2003) Phytochemistry Reviews , vol.2 , pp. 341
    • Lee, K.-H.1    Xiao, Z.2
  • 13
    • 3242802726 scopus 로고    scopus 로고
    • Optimization of a liquid chromatography-tandem mass spectrometry method for quantification of the plant lignans secoisolariciresinol, matairesinol, lariciresinol, and pinoresinol in food
    • Milder IEJ, Arts ICW, Venema DP, Lasaroms JJP, Wähälä K, Hollman PCH. Optimization of a liquid chromatography-tandem mass spectrometry method for quantification of the plant lignans secoisolariciresinol, matairesinol, lariciresinol, and pinoresinol in food. Journal of Agricultural and Food Chemistry 2004; 52: 4643.
    • (2004) Journal of Agricultural and Food Chemistry , vol.52 , pp. 4643
    • Milder, I.E.J.1    Arts, I.C.W.2    Venema, D.P.3    Lasaroms, J.J.P.4    Wähälä, K.5    Hollman, P.C.H.6
  • 16
    • 0035982101 scopus 로고    scopus 로고
    • Synthetic transformation of hydroxymatairesinol from Norway pruce (Picea abies) to 7-hydroxysecoisolariciresinol, (+)-lariciresinol and (+)-cyclolariciresinol
    • Eklund P, Sillanpää R, Sjöholm R. Synthetic transformation of hydroxymatairesinol from Norway pruce (Picea abies) to 7-hydroxysecoisolariciresinol, (+)-lariciresinol and (+)-cyclolariciresinol. Journal of the Chemical Society, Perkin Transactions 1 2002; 19: 1906.
    • (2002) Journal of the Chemical Society, Perkin Transactions , vol.1 , Issue.19 , pp. 1906
    • Eklund, P.1    Sillanpää, R.2    Sjöholm, R.3
  • 17
    • 0037669298 scopus 로고    scopus 로고
    • Synthesis of (-)-matairesinol, (-)-enterolactone, and (-)-enterodiol from the natural lignan hydroxymatairesinol
    • Eklund P, Lindholm A, Mikkola J-P, Smeds A, Lehtilä R, Sjöholm R. Synthesis of (-)-matairesinol, (-)-enterolactone, and (-)-enterodiol from the natural lignan hydroxymatairesinol. Organic Letters 2003; 5: 491.
    • (2003) Organic Letters , vol.5 , pp. 491
    • Eklund, P.1    Lindholm, A.2    Mikkola, J.-P.3    Smeds, A.4    Lehtilä, R.5    Sjöholm, R.6
  • 18
    • 0037835778 scopus 로고    scopus 로고
    • Oxidative transformation of the natural lignan hydroxymatairesinol with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone
    • Eklund P, Sjöholm R. Oxidative transformation of the natural lignan hydroxymatairesinol with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. Tetrahedron 2003; 59: 4515.
    • (2003) Tetrahedron , vol.59 , pp. 4515
    • Eklund, P.1    Sjöholm, R.2
  • 19
    • 3042668774 scopus 로고    scopus 로고
    • A new lariciresinol-type butyrolactone lignan derived from hydroxymatairesinol and its identification in spruce wood
    • Eklund P, Willför S, Smeds A, Sundell F, Sjöholm R. A new lariciresinol-type butyrolactone lignan derived from hydroxymatairesinol and its identification in spruce wood. Journal of Natural Products 2004; 67: 927.
    • (2004) Journal of Natural Products , vol.67 , pp. 927
    • Eklund, P.1    Willför, S.2    Smeds, A.3    Sundell, F.4    Sjöholm, R.5
  • 20
    • 21844452443 scopus 로고    scopus 로고
    • Bioactive phenolic substances in industrially important tree species. Part 4: Identification of two new 7-hydroxy divanillyl bytyrolactol lignans in some spruce, fir and pine species
    • Willför S, Eklund P, Sjöholm R, Reunanen M, Sillanpää R, von Shoultz S, Hemming J, Nisula L, Holmbom B. Bioactive phenolic substances in industrially important tree species. Part 4: identification of two new 7-hydroxy divanillyl bytyrolactol lignans in some spruce, fir and pine species. Holzforschung 2005; 59: 413.
    • (2005) Holzforschung , vol.59 , pp. 413
    • Willför, S.1    Eklund, P.2    Sjöholm, R.3    Reunanen, M.4    Sillanpää, R.5    von Shoultz, S.6    Hemming, J.7    Nisula, L.8    Holmbom, B.9
  • 22
    • 0141661668 scopus 로고    scopus 로고
    • α,β-Dibenzyl-γ-butyrolactone lignan alcohols: Total synthesis of (±)-7′-hydroxyenterolactone, (±)-7′- hydroxymatairesinol and (±)-8-hydroxyenterolactone
    • Mäkelä TH, Wähälä KT, Hase TA. α,β-Dibenzyl-γ-butyrolactone lignan alcohols: total synthesis of (±)-7′-hydroxyenterolactone, (±)-7′- hydroxymatairesinol and (±)-8-hydroxyenterolactone. Steroids 2000; 65: 437.
    • (2000) Steroids , vol.65 , pp. 437
    • Mäkelä, T.H.1    Wähälä, K.T.2    Hase, T.A.3
  • 23
    • 0000955599 scopus 로고
    • A simple method for the synthesis of lignan skeletons. Syntheses of (±) -parabenzlactone and (±) -hinokinin
    • Asano Y, Kamikawa T, Tororoyama T. A simple method for the synthesis of lignan skeletons. Syntheses of (±) -parabenzlactone and (±) -hinokinin. Bulletin of the Chemical Society of Japan 1976; 49: 3232.
    • (1976) Bulletin of the Chemical Society of Japan , vol.49 , pp. 3232
    • Asano, Y.1    Kamikawa, T.2    Tororoyama, T.3
  • 24
    • 39149104164 scopus 로고    scopus 로고
    • Erdtman H. Constitution of resin phenols and their biogenetic connections. I. Pinoresinol. Preliminary communication. Svensk Kemisk Tidskrift 1934; 46: 229.
    • Erdtman H. Constitution of resin phenols and their biogenetic connections. I. Pinoresinol. Preliminary communication. Svensk Kemisk Tidskrift 1934; 46: 229.
  • 27
    • 1142303819 scopus 로고    scopus 로고
    • Mass spectrometry in the structural analysis of flavonoids
    • Cuyckens F, Claeys M. Mass spectrometry in the structural analysis of flavonoids. Journal of Mass Spectrometry 2004; 39: 1.
    • (2004) Journal of Mass Spectrometry , vol.39 , pp. 1
    • Cuyckens, F.1    Claeys, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.