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Volumn 24, Issue 4-5, 2003, Pages 149-159

Basic aspects of the biochemical reactivity of 4-hydroxynonenal

Author keywords

4 Hydroxynonenal; Michael addition; Reaction mechanisms; Schiff base formation

Indexed keywords

4 HYDROXYNONENAL; CYSTEINE; HISTIDINE; LYSINE; SCHIFF BASE;

EID: 0043172509     PISSN: 00982997     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0098-2997(03)00009-8     Document Type: Conference Paper
Times cited : (298)

References (20)
  • 1
    • 14444270605 scopus 로고    scopus 로고
    • 2,3-Epoxy-4-hydroxynonenal, a potential lipid peroxidation product for etheno adduct formation, is not a substrate of human epoxide hydrolase
    • Chen H.J.C., Gonzalez F.J., Shou M.G., Chung F.L. 2,3-Epoxy-4-hydroxynonenal, a potential lipid peroxidation product for etheno adduct formation, is not a substrate of human epoxide hydrolase. Carcinogenesis. 19:1998;939-943.
    • (1998) Carcinogenesis , vol.19 , pp. 939-943
    • Chen, H.J.C.1    Gonzalez, F.J.2    Shou, M.G.3    Chung, F.L.4
  • 4
    • 0035798606 scopus 로고    scopus 로고
    • Antioxidative function and substrate-specificity of NAD(P)H-dependent alkenal/one oxidoreductase a new role for leukotriene B-4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase
    • Dick R.A., Kwak M.K., Sutter T.R., Kensler T.W. Antioxidative function and substrate-specificity of NAD(P)H-dependent alkenal/one oxidoreductase a new role for leukotriene B-4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase. J. Biol. Chem. 276:2001;40803-40810.
    • (2001) J. Biol. Chem. , vol.276 , pp. 40803-40810
    • Dick, R.A.1    Kwak, M.K.2    Sutter, T.R.3    Kensler, T.W.4
  • 6
    • 0034904237 scopus 로고    scopus 로고
    • Effect of 4-hydroxy-2(E)-nonenal on soybean lipoxygenase-1
    • Gardner H.W., Deighton N. Effect of 4-hydroxy-2(E)-nonenal on soybean lipoxygenase-1. Lipids. 36:2001;623-628.
    • (2001) Lipids , vol.36 , pp. 623-628
    • Gardner, H.W.1    Deighton, N.2
  • 7
    • 0027410529 scopus 로고
    • Oxygenation of (3Z)-nonenal to (2E)-4-hydroxy-2-nonenal in the broad bean (Vicia faba L.)
    • Gardner H.W., Hamberg M. Oxygenation of (3Z)-nonenal to (2E)-4-hydroxy-2-nonenal in the broad bean (Vicia faba L.). J. Biol. Chem. 268:1993;6971-6977.
    • (1993) J. Biol. Chem. , vol.268 , pp. 6971-6977
    • Gardner, H.W.1    Hamberg, M.2
  • 9
    • 85012049777 scopus 로고    scopus 로고
    • (S)-preferential cytotoxicity of 4-hydroxy-2(E)-nonenal enantiomers in rat clone 9 cells
    • Hiratsuka A., Saito H., Watabe T. (S)-preferential cytotoxicity of 4-hydroxy-2(E)-nonenal enantiomers in rat clone 9 cells. Toxicology. 164:2001;199.
    • (2001) Toxicology , vol.164 , pp. 199
    • Hiratsuka, A.1    Saito, H.2    Watabe, T.3
  • 13
    • 0034456018 scopus 로고    scopus 로고
    • 4-Hydroxynonenal in the Pathomechanisms of Oxidative Stress. IUBMB
    • Poli G., Schaur R.J. 4-Hydroxynonenal in the Pathomechanisms of Oxidative Stress. IUBMB. Life. 50:2000;315-321.
    • (2000) Life , vol.50 , pp. 315-321
    • Poli, G.1    Schaur, R.J.2
  • 14
    • 0034935945 scopus 로고    scopus 로고
    • Experimental Studies on the Mechanism of Phospholipase-C Activation by the Lipid-Peroxidation Products 4-Hydroxynonenal and 2-Nonenal
    • Rossi M.A., Dimauro C., Dianzani M.U. Experimental Studies on the Mechanism of Phospholipase-C Activation by the Lipid-Peroxidation Products 4-Hydroxynonenal and 2-Nonenal. Int. J. Tissue React. 23:2001;45-50.
    • (2001) Int. J. Tissue React. , vol.23 , pp. 45-50
    • Rossi, M.A.1    Dimauro, C.2    Dianzani, M.U.3
  • 15
    • 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., Brash A.R. 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. 276:2001;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
  • 16
    • 0030746621 scopus 로고    scopus 로고
    • The lipid-peroxidation product, 4-hydroxy-2-trans-nonenal, alters the conformation of cortical synaptosomal membrane-proteins
    • Subramaniam R., Roediger F., Jordan B., Mattson M.P., Keller J.N., Waeg G., Butterfield D.A. The lipid-peroxidation product, 4-hydroxy-2-trans-nonenal, alters the conformation of cortical synaptosomal membrane-proteins. J. Neurochem. 69:1997;1161-1169.
    • (1997) J. Neurochem. , vol.69 , pp. 1161-1169
    • Subramaniam, R.1    Roediger, F.2    Jordan, B.3    Mattson, M.P.4    Keller, J.N.5    Waeg, G.6    Butterfield, D.A.7
  • 17
    • 0035969833 scopus 로고    scopus 로고
    • Selective protection by stable tranfected human Aldh3A1 (but not human Aldh1A1) against toxicity of aliphatic-aldehydes in V79 cells
    • Townsend A.J., Leonekabler S., Haynes R.L., Wu Y.H., Szweda L., Bunting K.D. Selective protection by stable tranfected human Aldh3A1 (but not human Aldh1A1) against toxicity of aliphatic-aldehydes in V79 cells. Chem.-Biol. Interact. 130:2001;261-273.
    • (2001) Chem.-Biol. Interact. , vol.130 , pp. 261-273
    • Townsend, A.J.1    Leonekabler, S.2    Haynes, R.L.3    Wu, Y.H.4    Szweda, L.5    Bunting, K.D.6
  • 18
    • 0035964580 scopus 로고    scopus 로고
    • Detection of 1,N-2-propanodeoxyguanosine adducts of trans-4-hydroxy-2-nonenal after gavage of trans-4-hydroxy-2-nonenal or induction of lipid-peroxidation with carbon-tetrachloride in F344 rats
    • Wacker M., Wanek P., Eder E. Detection of 1,N-2-propanodeoxyguanosine adducts of trans-4-hydroxy-2-nonenal after gavage of trans-4-hydroxy-2-nonenal or induction of lipid-peroxidation with carbon-tetrachloride in F344 rats. Chem.-Biol. Interact. 137:2001;269-283.
    • (2001) Chem.-Biol. Interact. , vol.137 , pp. 269-283
    • Wacker, M.1    Wanek, P.2    Eder, E.3
  • 19
    • 0033529896 scopus 로고    scopus 로고
    • Independent synthesis, solution behavior, and studies on the mechanism of formation of a primary amine-derived fluorophore representing cross-linking of proteins by (E)-4-hydroxy-2-nonenal
    • Xu G.Z., Liu Y., Sayre L.M. Independent synthesis, solution behavior, and studies on the mechanism of formation of a primary amine-derived fluorophore representing cross-linking of proteins by (E)-4-hydroxy-2-nonenal. J. Org. Chem. 64:1999;5732-5745.
    • (1999) J. Org. Chem. , vol.64 , pp. 5732-5745
    • Xu, G.Z.1    Liu, Y.2    Sayre, L.M.3
  • 20
    • 0032901632 scopus 로고    scopus 로고
    • Ability of carnosine and other skeletal-muscle components to quench unsaturated aldehydic lipid oxidation-products
    • Zhou S.Y., Decker E.A. Ability of carnosine and other skeletal-muscle components to quench unsaturated aldehydic lipid oxidation-products. J. Agric. Food Chem. 47:1999;51-55.
    • (1999) J. Agric. Food Chem. , vol.47 , pp. 51-55
    • Zhou, S.Y.1    Decker, E.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.