메뉴 건너뛰기




Volumn 62, Issue 13, 2014, Pages 2837-2844

Antioxidant capacity of 1-deoxy-d-erythro-hexo-2,3-diulose and d-arabino-hexo-2-ulose

Author keywords

1 deoxy d erythro hexo 2,3 diulose; 1 deoxyglucosone; antioxidant capacity; d arabino hexo 2 ulose; d glucosone; EPR spectroscopy; Folin Ciocalteu assay; Maillard reaction; maltol; reductone; reductone ether; TEAC assay; weighted average antioxidant capacity

Indexed keywords

ANTIOXIDANTS; CHEMICAL REACTIONS; GLYCOSYLATION; PARAMAGNETIC RESONANCE; ELECTRON SPIN RESONANCE SPECTROSCOPY; MAGNETIC RESONANCE; REACTION INTERMEDIATES;

EID: 84897535261     PISSN: 00218561     EISSN: 15205118     Source Type: Journal    
DOI: 10.1021/jf404322r     Document Type: Article
Times cited : (24)

References (26)
  • 1
    • 33947448299 scopus 로고
    • Chemistry of browning reactions in model systems
    • Hodge, J. E. Chemistry of browning reactions in model systems J. Agric. Food Chem. 1953, 1, 928-943
    • (1953) J. Agric. Food Chem. , vol.1 , pp. 928-943
    • Hodge, J.E.1
  • 2
    • 0000916315 scopus 로고
    • Action des acides aminés sur les sucres; Formation des mélanoïdines par voie méthodique
    • Maillard, L.-C. Action des acides aminés sur les sucres; formation des mélanoïdines par voie méthodique C. R. Acad. Sci. 1912, 154, 66-68
    • (1912) C. R. Acad. Sci. , vol.154 , pp. 66-68
    • Maillard, L.-C.1
  • 3
    • 0000407561 scopus 로고
    • Die Maillard-Reaktion in Lebensmitteln und im menschlichen Körper - Neue Ergebnisse zu Chemie, Biochemie und Medizin
    • Ledl, F.; Schleicher, E. Die Maillard-Reaktion in Lebensmitteln und im menschlichen Körper-neue Ergebnisse zu Chemie, Biochemie und Medizin Angew. Chem. 1990, 102, 597-626
    • (1990) Angew. Chem. , vol.102 , pp. 597-626
    • Ledl, F.1    Schleicher, E.2
  • 4
    • 70349314616 scopus 로고    scopus 로고
    • Degradation of glucose: Reinvestigation of reactive α-dicarbonyl compounds
    • Gobert, J.; Glomb, M. A. Degradation of glucose: reinvestigation of reactive α-dicarbonyl compounds J. Agric. Food Chem. 2009, 57, 8591-8597
    • (2009) J. Agric. Food Chem. , vol.57 , pp. 8591-8597
    • Gobert, J.1    Glomb, M.A.2
  • 5
    • 0026413087 scopus 로고
    • Autoxidative degradation of Amadori compounds in the presence of copper ion
    • Kawakshi, S.; Tsunehiro, J.; Uchida, K. Autoxidative degradation of Amadori compounds in the presence of copper ion Carbohydr. Res. 1991, 211, 167-171
    • (1991) Carbohydr. Res. , vol.211 , pp. 167-171
    • Kawakshi, S.1    Tsunehiro, J.2    Uchida, K.3
  • 7
    • 19444385711 scopus 로고    scopus 로고
    • Antioxidant activity of water-soluble Maillard reaction products
    • Yilmaz, Y.; Toledo, R. Antioxidant activity of water-soluble Maillard reaction products Food Chem. 2004, 93, 273-278
    • (2004) Food Chem. , vol.93 , pp. 273-278
    • Yilmaz, Y.1    Toledo, R.2
  • 8
    • 0037041912 scopus 로고    scopus 로고
    • Antiradical efficiency of Maillard reaction mixtures in a hydrophilic media
    • Morales, F. J.; Babbel, M.-J. Antiradical efficiency of Maillard reaction mixtures in a hydrophilic media J. Agric. Food Chem. 2002, 50, 2788-2792
    • (2002) J. Agric. Food Chem. , vol.50 , pp. 2788-2792
    • Morales, F.J.1    Babbel, M.-J.2
  • 9
    • 0347834082 scopus 로고
    • Formation of reducing substances in the Maillard reaction between d -glucose and γ-aminobutyric acid
    • Ninomiya, M.; Matsuzaki, T.; Shigematsu, H. Formation of reducing substances in the Maillard reaction between d -glucose and γ-aminobutyric acid Biosci., Biotechnol., Biochem. 1992, 56 (5) 806-807
    • (1992) Biosci., Biotechnol., Biochem. , vol.56 , Issue.5 , pp. 806-807
    • Ninomiya, M.1    Matsuzaki, T.2    Shigematsu, H.3
  • 12
    • 0011428996 scopus 로고
    • Formation of pyrrolinone reductones by heating hexoses with amino acids
    • Ledl, F.; Fritsch, G. Formation of pyrrolinone reductones by heating hexoses with amino acids Z. Lebensm.-Unters. -Forsch. 1984, 178 (1) 41-44
    • (1984) Z. Lebensm.-Unters. -Forsch. , vol.178 , Issue.1 , pp. 41-44
    • Ledl, F.1    Fritsch, G.2
  • 14
    • 77952181445 scopus 로고    scopus 로고
    • Oxygen-dependent fragmentation reactions during the degradation of 1-deoxy- d - Erythro -hexo-2,3-diulose
    • Voigt, M.; Smuda, M.; Pfahler, C.; Glomb, M. A. Oxygen-dependent fragmentation reactions during the degradation of 1-deoxy- d-erythro -hexo-2,3-diulose J. Agric. Food Chem. 2010, 58, 5685-5691
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 5685-5691
    • Voigt, M.1    Smuda, M.2    Pfahler, C.3    Glomb, M.A.4
  • 15
    • 56149107352 scopus 로고    scopus 로고
    • Comparative antioxidant capacities of phenolic compounds by various tests
    • Tabart, J.; Kevers, C.; Pincemail, J.; Defraigne, J.-O.; Dommes, J. Comparative antioxidant capacities of phenolic compounds by various tests Food Chem. 2009, 113, 1226-1233
    • (2009) Food Chem. , vol.113 , pp. 1226-1233
    • Tabart, J.1    Kevers, C.2    Pincemail, J.3    Defraigne, J.-O.4    Dommes, J.5
  • 16
    • 77954881171 scopus 로고    scopus 로고
    • Investigation of reactive α-dicarbonyl compounds generated from the Maillard reactions of l-methionine with reducing sugars via their stable quinoxaline derivates
    • Pfeifer, Y. V.; Kroh, L. W. Investigation of reactive α-dicarbonyl compounds generated from the Maillard reactions of l-methionine with reducing sugars via their stable quinoxaline derivates J. Agric. Food Chem. 2010, 58, 8293-8299
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 8293-8299
    • Pfeifer, Y.V.1    Kroh, L.W.2
  • 17
    • 0034680714 scopus 로고    scopus 로고
    • Synthesis of 1-deoxy- d - Erythro -hexo-2,3-diulose, a major hexose Maillard intermediate
    • Glomb, M. A.; Pfahler, Ch. Synthesis of 1-deoxy- d-erythro -hexo-2,3-diulose, a major hexose Maillard intermediate Carbohydr. Res. 2000, 329, 515-523
    • (2000) Carbohydr. Res. , vol.329 , pp. 515-523
    • Glomb, M.A.1    Pfahler, Ch.2
  • 18
    • 78049270042 scopus 로고    scopus 로고
    • 3-Deoxygalactosone, a "new" 1,2-dicarbonyl compound in milk products
    • Hellwig, M.; Degen, J.; Henle, Th. 3-Deoxygalactosone, a "new" 1,2-dicarbonyl compound in milk products J. Agric. Food Chem. 2010, 58, 10752-10760
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 10752-10760
    • Hellwig, M.1    Degen, J.2    Henle, Th.3
  • 19
    • 36148943196 scopus 로고    scopus 로고
    • Determination of glyceraldehyde formed in glucose degradation and glycation
    • Usui, T.; Yoshino, M.; Watanabe, H.; Hayase, F. Determination of glyceraldehyde formed in glucose degradation and glycation Biosci., Biotechnol., Biochem. 2007, 71 (9) 2162-2168
    • (2007) Biosci., Biotechnol., Biochem. , vol.71 , Issue.9 , pp. 2162-2168
    • Usui, T.1    Yoshino, M.2    Watanabe, H.3    Hayase, F.4
  • 20
    • 27144510592 scopus 로고    scopus 로고
    • Electron spin resonance - A spectroscopic method for determining the antioxidant activity
    • Rohn, S.; Kroh, L. W. Electron spin resonance-a spectroscopic method for determining the antioxidant activity Mol. Nutr. Food Res. 2005, 49, 898-907
    • (2005) Mol. Nutr. Food Res. , vol.49 , pp. 898-907
    • Rohn, S.1    Kroh, L.W.2
  • 21
    • 0033805608 scopus 로고    scopus 로고
    • The problem of using one-dimensional methods to evaluate multifunctional food and biological antioxidants
    • Frankel, E. N.; Meyer, A. S. The problem of using one-dimensional methods to evaluate multifunctional food and biological antioxidants J. Sci. Food Agric. 2000, 80, 1925-1941
    • (2000) J. Sci. Food Agric. , vol.80 , pp. 1925-1941
    • Frankel, E.N.1    Meyer, A.S.2
  • 22
    • 84868578801 scopus 로고    scopus 로고
    • Milieu dependence of isomeric composition of 1-deoxy- d - Erythro -hexo-2,3-diulose in aqueous solution determined by high-resolution NMR spectroscopy
    • Kaufmann, M.; Haase, P. T.; Mügge, C.; Kroh, L. W. Milieu dependence of isomeric composition of 1-deoxy- d-erythro -hexo-2,3-diulose in aqueous solution determined by high-resolution NMR spectroscopy Carbohydr. Res. 2012, 364, 15-21
    • (2012) Carbohydr. Res. , vol.364 , pp. 15-21
    • Kaufmann, M.1    Haase, P.T.2    Mügge, C.3    Kroh, L.W.4
  • 23
    • 0037184280 scopus 로고    scopus 로고
    • Enzymatic synthesis of d -glucosone 6-phosphate (d - Arabino -hexos-2-ulose 6-(dihydrogen phosphate)) and NMR analysis of isomeric forms
    • Freimund, S.; Baldes, L.; Huwig, A.; Giffhorn, F. Enzymatic synthesis of d -glucosone 6-phosphate (d-arabino -hexos-2-ulose 6-(dihydrogen phosphate)) and NMR analysis of isomeric forms Carbohydr. Res. 2002, 337, 1585-1587
    • (2002) Carbohydr. Res. , vol.337 , pp. 1585-1587
    • Freimund, S.1    Baldes, L.2    Huwig, A.3    Giffhorn, F.4
  • 24
    • 84887122962 scopus 로고    scopus 로고
    • Milieu dependence of isomeric composition of d - Arabino -hexo-2-ulose in aqueous solution determined by high-resolution NMR spectroscopy
    • Kaufmann, M.; Haase, P. T.; Mügge, C.; Kroh, L. W. Milieu dependence of isomeric composition of d-arabino -hexo-2-ulose in aqueous solution determined by high-resolution NMR spectroscopy J. Agric. Food Chem. 2013, 61 (43) 10220-10224
    • (2013) J. Agric. Food Chem. , vol.61 , Issue.43 , pp. 10220-10224
    • Kaufmann, M.1    Haase, P.T.2    Mügge, C.3    Kroh, L.W.4
  • 25
    • 67149138148 scopus 로고    scopus 로고
    • Reactivity of 1-desoxy- d - Erythro -hexo-2,3-diulose: A key intermediate in the Maillard chemistry of hexoses
    • Voigt, M.; Glomb, M. A. Reactivity of 1-desoxy- d-erythro -hexo-2,3-diulose: a key intermediate in the Maillard chemistry of hexoses J. Agric. Food Chem. 2009, 57, 4765-4770
    • (2009) J. Agric. Food Chem. , vol.57 , pp. 4765-4770
    • Voigt, M.1    Glomb, M.A.2
  • 26
    • 0001696723 scopus 로고    scopus 로고
    • On the role of 2,3-dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-one in the Maillard Rreaction
    • Kim, M.-O.; Baltes, W. On the role of 2,3-dihydro-3,5-dihydroxy-6-methyl- 4(H)-pyran-4-one in the Maillard Rreaction J. Agric. Food Chem. 1996, 44, 282-289
    • (1996) J. Agric. Food Chem. , vol.44 , pp. 282-289
    • Kim, M.-O.1    Baltes, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.