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Volumn 37, Issue 10, 2002, Pages 1013-1018

Synthesis of 9,9,9-trideutero-1,4-dihydroxynonane mercapturic acid (d3-DHN-MA), a useful internal standard for DHN-MA urinalysis

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CARBONYLATION; ESTERS; FATTY ACIDS; LITHIUM COMPOUNDS; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 0036818951     PISSN: 00244201     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11745-006-0994-z     Document Type: Article
Times cited : (1)

References (16)
  • 1
    • 0025814980 scopus 로고
    • Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde and related aldehydes
    • Esterbauer, H., Zollner, H., and Schaur, R.J. (1991) Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde and related aldehydes, Free Radic. Biol. Med. 11, 81-128.
    • (1991) Free Radic. Biol. Med. , vol.11 , pp. 81-128
    • Esterbauer, H.1    Zollner, H.2    Schaur, R.J.3
  • 2
    • 0034456018 scopus 로고    scopus 로고
    • 4-Hydroxynonenal in the pathomechanisms of oxidative stress
    • Poli, G., and Schaur, R.J. (2000) 4-Hydroxynonenal in the pathomechanisms of oxidative stress, Life 50, 315-321.
    • (2000) Life , vol.50 , pp. 315-321
    • Poli, G.1    Schaur, R.J.2
  • 3
    • 0035877699 scopus 로고    scopus 로고
    • Two distinct pathways of formation of 4-hydroxynonenal, mechanisms of nonenzymatic transformation of the 9- and 13-hydroperoxides of linoleic acid to 4-hydroxyalkenals
    • Schneider, C., Tallman, K.A., Porter, N.A., and Brash, A.R. (2001) Two distinct pathways of formation of 4-hydroxynonenal. mechanisms of nonenzymatic transformation of the 9- and 13-hydroperoxides of linoleic acid to 4-hydroxyalkenals, J. Biol. Chem. 276, 20831-20838.
    • (2001) J. Biol. Chem. , vol.276 , pp. 20831-20838
    • Schneider, C.1    Tallman, K.A.2    Porter, N.A.3    Brash, A.R.4
  • 4
    • 0025697262 scopus 로고
    • Malondialdehyde and thiobarbituric acid-reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury
    • Janero, D.R. (1990) Malondialdehyde and thiobarbituric acid-reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury, Free Radic. Biol. Med. 9, 515-540.
    • (1990) Free Radic. Biol. Med. , vol.9 , pp. 515-540
    • Janero, D.R.1
  • 5
    • 0028797410 scopus 로고
    • Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat
    • Alary, J., Bravais, F., Cravedi, J.P., Debrauwer, L., Rao, D., and Bories, G. (1995) Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat, Chem. Res. Toxicol. 8, 34-39.
    • (1995) Chem. Res. Toxicol. , vol.8 , pp. 34-39
    • Alary, J.1    Bravais, F.2    Cravedi, J.P.3    Debrauwer, L.4    Rao, D.5    Bories, G.6
  • 6
    • 0031906914 scopus 로고    scopus 로고
    • 1,4-Dihydroxynonene mercapturic acid, the major end metabolite of exogenous 4-Hydroxy-2-nonenal, is a physiological component of rat and human urine
    • Alary, J., Debrauwer, L., Fernandez, Y., Cravedi, J.P., Rao, D., and Bories, G. (1998) 1,4-Dihydroxynonene mercapturic acid, the major end metabolite of exogenous 4-Hydroxy-2-nonenal, is a physiological component of rat and human urine, Chem. Res. Toxicol. 11, 130-135.
    • (1998) Chem. Res. Toxicol. , vol.11 , pp. 130-135
    • Alary, J.1    Debrauwer, L.2    Fernandez, Y.3    Cravedi, J.P.4    Rao, D.5    Bories, G.6
  • 7
    • 0032731288 scopus 로고    scopus 로고
    • Analysis in the rat of 4-hydroxynonenal metabolites excreted in bile: Evidence of enterohepatic circulation of these byproducts of lipid peroxidation
    • Laurent, A., Alary, J., Debrauwer, L., and Cravedi, J.P. (1999) Analysis in the Rat of 4-hydroxynonenal metabolites excreted in bile: Evidence of enterohepatic circulation of these byproducts of lipid peroxidation, Chem. Res. Toxicol. 12, 887-894.
    • (1999) Chem. Res. Toxicol. , vol.12 , pp. 887-894
    • Laurent, A.1    Alary, J.2    Debrauwer, L.3    Cravedi, J.P.4
  • 8
    • 0032873271 scopus 로고    scopus 로고
    • Glutathione conjugation of 4-hydroxy-trans-2,3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes
    • Boon, P.J.M., Marinho, H.S., Oosting, R., and Mulder, G.J. (1999) Glutathione conjugation of 4-hydroxy-trans-2,3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes, Toxicol. Appl. Pharmacol. 159, 214-223.
    • (1999) Toxicol. Appl. Pharmacol. , vol.159 , pp. 214-223
    • Boon, P.J.M.1    Marinho, H.S.2    Oosting, R.3    Mulder, G.J.4
  • 9
    • 0542418919 scopus 로고
    • Facile synthesis of 4-hydroxy-(e)-2-alkenoic esters from aldehydes
    • Tanikaga, R., Nozaki, Y., Tamura, T., and Kaji, A. (1983) Facile synthesis of 4-hydroxy-(e)-2-alkenoic esters from aldehydes, Synthesis, 134-135.
    • (1983) Synthesis , pp. 134-135
    • Tanikaga, R.1    Nozaki, Y.2    Tamura, T.3    Kaji, A.4
  • 10
    • 0033607651 scopus 로고    scopus 로고
    • The synthesis of 14-membered macrocyclic ethers
    • Clyne, D.S., and Weiler, L. (1999) The synthesis of 14-membered macrocyclic ethers, Tetrahedron 55, 13659-13682.
    • (1999) Tetrahedron , vol.55 , pp. 13659-13682
    • Clyne, D.S.1    Weiler, L.2
  • 11
    • 0001118854 scopus 로고
    • Action of aldehydes on normal and malignant cells. III. Synthesis of homologous 4-hydroxy-2-alkenals
    • Esterbauer, H., and Weger, W. (1967) Action of aldehydes on normal and malignant cells. III. Synthesis of homologous 4-hydroxy-2-alkenals, Monatsh. Chem. 98, 1994-2000.
    • (1967) Monatsh. Chem. , vol.98 , pp. 1994-2000
    • Esterbauer, H.1    Weger, W.2
  • 14
    • 0026629921 scopus 로고
    • Synthesis of a γ-azetidinyl-β-hydroxy-α-amino acid derivative, a key intermediate for the synthesis of mugineic acid
    • Matsuura, F., Hamada, Y., and Shioiri, T. (1992) Synthesis of a γ-azetidinyl-β-hydroxy-α-amino acid derivative, a key intermediate for the synthesis of mugineic acid, Tetrahedron: Asymmetry 3, 1069-1074.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 1069-1074
    • Matsuura, F.1    Hamada, Y.2    Shioiri, T.3
  • 16
    • 0003608528 scopus 로고
    • Aldrich, Milwaukee, WI, Spectra 423A (3-mercapto-2-butanol) and 1282B (N-acetyl-L-cysteine)
    • 1H FT NMR Spectra, Edition I, Volume I, Aldrich, Milwaukee, WI, Spectra 423A (3-mercapto-2-butanol) and 1282B (N-acetyl-L-cysteine). Netlink: www.sigma-aldrich.com
    • (1993) 1H FT NMR Spectra, Edition I , vol.1
    • Pouchert, C.J.1    Behnke, J.2


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