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Volumn 166, Issue , 2015, Pages 397-406

Acylated anthocyanins from sprouts of Raphanus sativus cv. Sango: Isolation, structure elucidation and antioxidant activity

Author keywords

Anthocyanins; Mass spectrometry; NMR; Peroxyl radicals; Phenolic acids; Radish sprouts

Indexed keywords

ACYLATION; ANTIOXIDANTS; LINOLEIC ACID; MASS SPECTROMETRY; MICELLES; NUCLEAR MAGNETIC RESONANCE; RATE CONSTANTS;

EID: 84903843495     PISSN: 03088146     EISSN: 18737072     Source Type: Journal    
DOI: 10.1016/j.foodchem.2014.06.056     Document Type: Article
Times cited : (54)

References (32)
  • 2
    • 84860735634 scopus 로고    scopus 로고
    • The reaction of sulfenic acids with peroxyl radicals: Insights into the radical-trapping antioxidant activity of plant-derived thiosulfinates
    • R. Amorati, P.T. Lynett, L. Valgimigli, and D.A. Pratt The reaction of sulfenic acids with peroxyl radicals: insights into the radical-trapping antioxidant activity of plant-derived thiosulfinates Chemistry - A European Journal 18 2012 6370 6379
    • (2012) Chemistry - A European Journal , vol.18 , pp. 6370-6379
    • Amorati, R.1    Lynett, P.T.2    Valgimigli, L.3    Pratt, D.A.4
  • 4
    • 79955383526 scopus 로고    scopus 로고
    • Kinetic and thermodynamic aspects of the chain-breaking antioxidant activity of ascorbic acid derivatives in non-aqueous media
    • R. Amorati, G.F. Pedulli, and L. Valgimigli Kinetic and thermodynamic aspects of the chain-breaking antioxidant activity of ascorbic acid derivatives in non-aqueous media Organic & Biomolecular Chemistry 9 2011 3792 3800
    • (2011) Organic & Biomolecular Chemistry , vol.9 , pp. 3792-3800
    • Amorati, R.1    Pedulli, G.F.2    Valgimigli, L.3
  • 5
    • 84861878152 scopus 로고    scopus 로고
    • Modulation of the antioxidant activity of phenols by non-covalent interactions
    • R. Amorati, and L. Valgimigli Modulation of the antioxidant activity of phenols by non-covalent interactions Organic & Biomolecular Chemistry 10 2012 4147 4158
    • (2012) Organic & Biomolecular Chemistry , vol.10 , pp. 4147-4158
    • Amorati, R.1    Valgimigli, L.2
  • 6
    • 84885116424 scopus 로고    scopus 로고
    • 5-S-Lipoylhydroxytyrosol, a multidefense antioxidant featuring a solvent-tunable peroxyl radical-scavenging 3-thio-1,2-dihydroxybenzene motif
    • R. Amorati, L. Valgimigli, L. Panzella, A. Napolitano, and M. d'Ischia 5-S-Lipoylhydroxytyrosol, a multidefense antioxidant featuring a solvent-tunable peroxyl radical-scavenging 3-thio-1,2-dihydroxybenzene motif Journal of Organic Chemistry 78 2013 9857 9864
    • (2013) Journal of Organic Chemistry , vol.78 , pp. 9857-9864
    • Amorati, R.1    Valgimigli, L.2    Panzella, L.3    Napolitano, A.4    D'Ischia, M.5
  • 7
    • 39149119265 scopus 로고    scopus 로고
    • Characterisation of anthocyanins in red cabbage using high resolution liquid chromatography coupled with photodiode array detection and electrospray ionization-linear ion trap mass spectrometry
    • P. Arapitsas, P.J.R. Sjoeberg, and C. Turner Characterisation of anthocyanins in red cabbage using high resolution liquid chromatography coupled with photodiode array detection and electrospray ionization-linear ion trap mass spectrometry Food Chemistry 109 2008 219 226
    • (2008) Food Chemistry , vol.109 , pp. 219-226
    • Arapitsas, P.1    Sjoeberg, P.J.R.2    Turner, C.3
  • 8
    • 0031696562 scopus 로고    scopus 로고
    • -succinyl-β-glucopyranoside) and other anthocyanins from Phragmites australis
    • DOI 10.1016/S0031-9422(98)00064-8, PII S0031942298000648
    • T. Fossen, and ∅.M. Andersen Cyanidin 3-O-(6″-succinyl- β-glucopyranoside) and other anthocyanins from Phragmites australis Phytochemistry 49 1998 1065 1068 (Pubitemid 28457641)
    • (1998) Phytochemistry , vol.49 , Issue.4 , pp. 1065-1068
    • Fossen, T.1    Andersen, O.M.2
  • 9
    • 0001759538 scopus 로고    scopus 로고
    • Flavonids, coumarins, and cinnamic acids as antioxidants in a micellar system. Structure-activity relationship
    • M.C. Foti, M. Piattelli, M.T. Baratta, and G. Ruberto Flavonoids, coumarins, and cinnamic acids as antioxidants in a micellar system. Structure-activity relationship Journal of Agriculture and Food Chemistry 44 1996 497 501 (Pubitemid 126469456)
    • (1996) Journal of Agricultural and Food Chemistry , vol.44 , Issue.2 , pp. 497-501
    • Foti, M.1    Piattelli, M.2    Baratta, M.T.3    Ruberto, G.4
  • 10
    • 69749115870 scopus 로고    scopus 로고
    • A density functional study of antioxidant properties on anthocyanidins
    • R. Guzmán, C. Santiago, and M. Sánchez A density functional study of antioxidant properties on anthocyanidins Journal of Molecular Structure 935 2009 110 114
    • (2009) Journal of Molecular Structure , vol.935 , pp. 110-114
    • Guzmán, R.1    Santiago, C.2    Sánchez, M.3
  • 11
    • 78049482434 scopus 로고    scopus 로고
    • Anthocyanins of fruits and vegetables - Their occurrence, analysis and role in human nutrition
    • M. Horbowicz, R. Kosson, A. Grzesiuk, and H. Debski Anthocyanins of fruits and vegetables - Their occurrence, analysis and role in human nutrition Vegetable Crops Research Bulletin 68 2008 5 22
    • (2008) Vegetable Crops Research Bulletin , vol.68 , pp. 5-22
    • Horbowicz, M.1    Kosson, R.2    Grzesiuk, A.3    Debski, H.4
  • 12
    • 0001492556 scopus 로고
    • Structure of three diacylated anthocyanins isolated from red cabbage, Brassica oleracea
    • E. Idaka, H. Yamakita, T. Ogawa, T. Kondo, M. Yamamoto, and T. Goto Structure of three diacylated anthocyanins isolated from red cabbage, Brassica oleracea Chemistry Letters 1987 1213 1216
    • (1987) Chemistry Letters , pp. 1213-1216
    • Idaka, E.1    Yamakita, H.2    Ogawa, T.3    Kondo, T.4    Yamamoto, M.5    Goto, T.6
  • 13
    • 84883668245 scopus 로고    scopus 로고
    • Quantitative studies on structure-ORAC relationships of anthocyanins from eggplant and radish using 3D-QSAR
    • P. Jing, S. Zhao, S. Ruan, Z. Sui, L. Chen, and L. Jiang et al. Quantitative studies on structure-ORAC relationships of anthocyanins from eggplant and radish using 3D-QSAR Food Chemistry 145 2014 365 371
    • (2014) Food Chemistry , vol.145 , pp. 365-371
    • Jing, P.1    Zhao, S.2    Ruan, S.3    Sui, Z.4    Chen, L.5    Jiang, L.6
  • 20
    • 84858296206 scopus 로고    scopus 로고
    • Identification and analysis of isothiocyanates and new acylated anthocyanins in the juice of Raphanus sativus cv. Sango sprouts
    • R. Matera, S. Gabbanini, G.R. De Nicola, R. Iori, G. Petrillo, and L. Valgimigli Identification and analysis of isothiocyanates and new acylated anthocyanins in the juice of Raphanus sativus cv. Sango sprouts Food Chemistry 133 2012 563 572
    • (2012) Food Chemistry , vol.133 , pp. 563-572
    • Matera, R.1    Gabbanini, S.2    De Nicola, G.R.3    Iori, R.4    Petrillo, G.5    Valgimigli, L.6
  • 21
    • 33947220223 scopus 로고    scopus 로고
    • Anthocyanin from the rhizome of Raphanus sativus, and change in the composition during maturation
    • M. Mori, S. Nakagawa, M. Maeschima, S. Niiura, and K. Yoshida Anthocyanin from the rhizome of Raphanus sativus, and change in the composition during maturation Heterocycles 69 2006 239 251
    • (2006) Heterocycles , vol.69 , pp. 239-251
    • Mori, M.1    Nakagawa, S.2    Maeschima, M.3    Niiura, S.4    Yoshida, K.5
  • 22
    • 0037052317 scopus 로고    scopus 로고
    • Acylated anthocyanins from red radish (Raphanus sativus L.)
    • DOI 10.1016/S0031-9422(02)00063-8, PII S0031942202000638
    • T. Otsuki, H. Matsufuji, M. Takeda, M. Toyoda, and Y. Goda Acylated anthocyanins from red radish (Raphanus sativus L.) Phytochemistry 60 2002 79 87 (Pubitemid 34516843)
    • (2002) Phytochemistry , vol.60 , Issue.1 , pp. 79-87
    • Otsuki, T.1    Matsufuji, H.2    Takeda, M.3    Toyoda, M.4    Goda, Y.5
  • 24
    • 15244352099 scopus 로고    scopus 로고
    • Review of methods to determine chain-breaking antioxidant activity in food
    • DOI 10.1016/j.foodchem.2004.08.004
    • V. Roginsky, and E.A. Lissi Review of methods to determine chain-breaking antioxidant activity in food Food Chemistry 92 2005 235 254 (Pubitemid 40387587)
    • (2005) Food Chemistry , vol.92 , Issue.2 , pp. 235-254
    • Roginsky, V.1    Lissi, E.A.2
  • 25
    • 57049154634 scopus 로고    scopus 로고
    • Tetra-acylated cyanidin 3-sophoroside-5-glucosides from the flowers of Iberis umbellata L. (Cruciferae)
    • N. Saito, F. Tatsuzawa, E. Suenaga, K. Toki, K. Shinoda, and A. Shigihara et al. Tetra-acylated cyanidin 3-sophoroside-5-glucosides from the flowers of Iberis umbellata L. (Cruciferae) Phytochemistry 69 2008 3139 3150
    • (2008) Phytochemistry , vol.69 , pp. 3139-3150
    • Saito, N.1    Tatsuzawa, F.2    Suenaga, E.3    Toki, K.4    Shinoda, K.5    Shigihara, A.6
  • 27
    • 0038737420 scopus 로고    scopus 로고
    • New Acylated Anthocyanins from Brassica campestris var. Chinensis
    • M. Suzuki, T. Nagata, and N. Terahara New acylated anthocyanins from Brassica campestris var. chinensis Bioscience, Biotechnology, and Biochemistry 61 1997 1929 1930 (Pubitemid 127471794)
    • (1997) Bioscience, Biotechnology and Biochemistry , vol.61 , Issue.11 , pp. 1929-1930
    • Suzuki, M.1    Nagata, T.2    Terahara, N.3
  • 31
    • 84860725826 scopus 로고    scopus 로고
    • Antioxidants in chemistry and biology
    • C. Chatgilialoglu, A. Studer, John Wiley & Sons Chirchester (UK)
    • L. Valgimigli, and D.A. Pratt Antioxidants in chemistry and biology C. Chatgilialoglu, A. Studer, Encyclopedia of radicals in chemistry, biology and materials Vol. 3 2012 John Wiley & Sons Chirchester (UK) 1623 1678
    • (2012) Encyclopedia of Radicals in Chemistry, Biology and Materials , vol.3 VOL. , pp. 1623-1678
    • Valgimigli, L.1    Pratt, D.A.2
  • 32
    • 84877096056 scopus 로고    scopus 로고
    • Comparison of the activities of hydrophilic anthocyanins and lipophilic tocols in black rice bran against lipid oxidation
    • X. Zhang, Y. Shen, W. Prinyawiwatkul, J.M. King, and Z. Xu Comparison of the activities of hydrophilic anthocyanins and lipophilic tocols in black rice bran against lipid oxidation Food Chemistry 141 2013 111 116
    • (2013) Food Chemistry , vol.141 , pp. 111-116
    • Zhang, X.1    Shen, Y.2    Prinyawiwatkul, W.3    King, J.M.4    Xu, Z.5


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