-
1
-
-
0032937593
-
Dihydrodiol dehydrogenases and polycyclic aromatic hydrocarbon activation: Generation of reactive and redox active o-quinones
-
Penning, T. M., Burczynski, M. E., Hung, C. F., McCoull, K. D., Palackal, N. T., and Tsuruda, L. S. (1999) Dihydrodiol dehydrogenases and polycyclic aromatic hydrocarbon activation: generation of reactive and redox active o-quinones. Chem. Res. Toxicol. 12, 1-18.
-
(1999)
Chem. Res. Toxicol.
, vol.12
, pp. 1-18
-
-
Penning, T.M.1
Burczynski, M.E.2
Hung, C.F.3
McCoull, K.D.4
Palackal, N.T.5
Tsuruda, L.S.6
-
2
-
-
84892138934
-
The impact of plant flavonoids on mammalian biology: Implications for immunity, inflammation and cancer
-
Harborne, J. B., Ed., Chapman & Hall, London
-
Middleton, E., and Kandaswami, C. (1994) The impact of plant flavonoids on mammalian biology: implications for immunity, inflammation and cancer. In The flavonoids. Advances in research since 1986 (Harborne, J. B., Ed.) pp 619-652, Chapman & Hall, London.
-
(1994)
The Flavonoids. Advances in Research since 1986
, pp. 619-652
-
-
Middleton, E.1
Kandaswami, C.2
-
3
-
-
0029888128
-
Structure-antioxidant activity relationships of flavonoids and phenolic acids
-
Rice-Evans, C. A., Miller, N. J., and Paganga, G. (1996) Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radical Biol. Med. 20, 933-956.
-
(1996)
Free Radical Biol. Med.
, vol.20
, pp. 933-956
-
-
Rice-Evans, C.A.1
Miller, N.J.2
Paganga, G.3
-
4
-
-
0031656737
-
Functional food science and defence against reactive oxidative species
-
Diplock, A. T., Charleux, J.-L., Crozier-Willi, G., Kok, F. J., Rice-Evans, C., Roberfroid, M., Stahl, W., and Vina-Ribes, J. (1998) Functional food science and defence against reactive oxidative species. Br. J. Nutr. 80, S77-S112.
-
(1998)
Br. J. Nutr.
, vol.80
-
-
Diplock, A.T.1
Charleux, J.-L.2
Crozier-Willi, G.3
Kok, F.J.4
Rice-Evans, C.5
Roberfroid, M.6
Stahl, W.7
Vina-Ribes, J.8
-
5
-
-
0031741669
-
Role of quinoids in estrogen carcinogenesis
-
Bolton, J. L., Pisha, E., Zhang, F., and Qiu, S. (1998) Role of quinoids in estrogen carcinogenesis. Chem. Res. Toxicol. 11, 1113-1127.
-
(1998)
Chem. Res. Toxicol.
, vol.11
, pp. 1113-1127
-
-
Bolton, J.L.1
Pisha, E.2
Zhang, F.3
Qiu, S.4
-
6
-
-
0026727562
-
Polycyclic aromatic hydrocarbon (PAH) ortho-quinone conjugate chemistry: Kinetics of thiol addition to PAH ortho-quinones and structures of thioether adducts of naphthalene-1,2-dione
-
Murty, V. S., and Penning, T. M. (1992) Polycyclic aromatic hydrocarbon (PAH) ortho-quinone conjugate chemistry: kinetics of thiol addition to PAH ortho-quinones and structures of thioether adducts of naphthalene-1,2-dione. Chem.-Biol. Interact. 84, 169-188.
-
(1992)
Chem.-Biol. Interact.
, vol.84
, pp. 169-188
-
-
Murty, V.S.1
Penning, T.M.2
-
7
-
-
0028030658
-
Flavonoids as antioxidants
-
Jovanovic, S. V., Steenken, S., Tosic, M., Marjanovic, B., and Simic, M. G. (1994) Flavonoids as antioxidants. J. Am. Chem. Soc. 116, 4846-4851.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4846-4851
-
-
Jovanovic, S.V.1
Steenken, S.2
Tosic, M.3
Marjanovic, B.4
Simic, M.G.5
-
8
-
-
0018079525
-
Mutagenicity of plant flavonoids: Structural requirements for mutagenic activity in Salmonella typhimurium
-
MacGregor, J. T., and Jurd, L. (1978) Mutagenicity of plant flavonoids: structural requirements for mutagenic activity in Salmonella typhimurium. Mutat. Res. 54, 297-309.
-
(1978)
Mutat. Res.
, vol.54
, pp. 297-309
-
-
MacGregor, J.T.1
Jurd, L.2
-
9
-
-
0029894354
-
17β-Estradiol metabolism by hamster hepatic microsomes: Comparison of catechol estrogen O-methylation with catechol estrogen oxidation and glutathione conjugation
-
Butterworth, M., Lau, S. S., and Monks, T. J. (1996) 17β-Estradiol metabolism by hamster hepatic microsomes: comparison of catechol estrogen O-methylation with catechol estrogen oxidation and glutathione conjugation. Chem. Res. Toxicol. 9, 793-799.
-
(1996)
Chem. Res. Toxicol.
, vol.9
, pp. 793-799
-
-
Butterworth, M.1
Lau, S.S.2
Monks, T.J.3
-
10
-
-
0029949969
-
p-quinone methides are the major decomposition products of catechol estrogen o-quinones
-
Bolton, J. L., and Shen, L. (1996) p-Quinone methides are the major decomposition products of catechol estrogen o-quinones. Carcinogenesis 17, 925-929.
-
(1996)
Carcinogenesis
, vol.17
, pp. 925-929
-
-
Bolton, J.L.1
Shen, L.2
-
11
-
-
0029924611
-
Bioactivation of estrone and its catechol metabolites to quinoid-glutathione conjugates in rat liver microsomes
-
Iverson, S. L., Shen, L., Anlar, N., and Bolton, J. L. (1996) Bioactivation of estrone and its catechol metabolites to quinoid-glutathione conjugates in rat liver microsomes. Chem. Res. Toxicol. 9, 492-499.
-
(1996)
Chem. Res. Toxicol.
, vol.9
, pp. 492-499
-
-
Iverson, S.L.1
Shen, L.2
Anlar, N.3
Bolton, J.L.4
-
12
-
-
0031417558
-
Formation of catechol estrogen glutathione conjugates and γ-glutamyl transpeptidase-dependent nephrotoxicity of 17γ-estradiol in the golden Syrian hamster
-
Butterworth, M., Lau, S. S., and Monks, T. J. (1997) Formation of catechol estrogen glutathione conjugates and γ-glutamyl transpeptidase-dependent nephrotoxicity of 17γ-estradiol in the golden Syrian hamster. Carcinogenesis 18, 561-567.
-
(1997)
Carcinogenesis
, vol.18
, pp. 561-567
-
-
Butterworth, M.1
Lau, S.S.2
Monks, T.J.3
-
13
-
-
0032436645
-
Two-electron electrochemical oxidation of quercetin and kaempferol changes only the flavonoid C-ring
-
Jorgensen, L. V., Cornett, C., Justesen, U., Skibsted, L. H., and Dragsted, L. O. (1998) Two-electron electrochemical oxidation of quercetin and kaempferol changes only the flavonoid C-ring. Free Radical Res. 29, 339-350.
-
(1998)
Free Radical Res.
, vol.29
, pp. 339-350
-
-
Jorgensen, L.V.1
Cornett, C.2
Justesen, U.3
Skibsted, L.H.4
Dragsted, L.O.5
-
14
-
-
0029664866
-
H-1, C-13-NMR and X-ray absorption studies of copper(I) glutathione complexes
-
Corazza, A., Harvey, I., and Sadler, P. J. (1996) H-1, C-13-NMR and X-ray absorption studies of copper(I) glutathione complexes. Eur. J. Biochem. 236, 697-705.
-
(1996)
Eur. J. Biochem.
, vol.236
, pp. 697-705
-
-
Corazza, A.1
Harvey, I.2
Sadler, P.J.3
-
15
-
-
0029001803
-
Quantitative structure activity relationships (QSAR's) based on computer calculated parameters for the overall rate of glutathione S-transferase catalyzed conjugation of a series fluoronitrobenzenes
-
Rietjens, I. M. C. M., Soffers, A. E. M. F., Hooiveld, G., Veeger, C., and Vervoort, J. (1995) Quantitative structure activity relationships (QSAR's) based on computer calculated parameters for the overall rate of glutathione S-transferase catalyzed conjugation of a series fluoronitrobenzenes. Chem. Res. Toxicol. 8, 481-488.
-
(1995)
Chem. Res. Toxicol.
, vol.8
, pp. 481-488
-
-
Rietjens, I.M.C.M.1
Soffers, A.E.M.F.2
Hooiveld, G.3
Veeger, C.4
Vervoort, J.5
-
16
-
-
0029924063
-
Regioselectivity and quantitative structure activity relationships (QSARs) for the conjugation of a series of fluoronitrobenzenes by purified glutathione S-transferases from rats and man
-
Soffers, A. E. M. F., Ploemen, J. H. T. M., Moonen, M., Wobbes, T., Van Ommen, B., Vervoort, J., Van Bladeren, P. J., and Rietjens, I. M. C. M. (1996) Regioselectivity and quantitative structure activity relationships (QSARs) for the conjugation of a series of fluoronitrobenzenes by purified glutathione S-transferases from rats and man. Chem. Res. Toxicol. 9, 638-646.
-
(1996)
Chem. Res. Toxicol.
, vol.9
, pp. 638-646
-
-
Soffers, A.E.M.F.1
Ploemen, J.H.T.M.2
Moonen, M.3
Wobbes, T.4
Van Ommen, B.5
Vervoort, J.6
Van Bladeren, P.J.7
Rietjens, I.M.C.M.8
-
17
-
-
0031040424
-
Mechanism of nucleophilic aromatic substitution of 1-chloro-2,4-dinitrobenzene by glutathione in the gas phase and in solution. Implications for the mode of action of glutathione S-transferase
-
Zheng, Y. J., and Ornstein, R. L. (1997) Mechanism of nucleophilic aromatic substitution of 1-chloro-2,4-dinitrobenzene by glutathione in the gas phase and in solution. Implications for the mode of action of glutathione S-transferase. J. Am. Chem. Soc. 119, 648-655.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 648-655
-
-
Zheng, Y.J.1
Ornstein, R.L.2
-
18
-
-
0030937423
-
Role of active site tyrosine in glutathione S-transferase: Insight from a theoretical study on model systems
-
Zheng, Y. J., and Ornstein, R. L. (1997) Role of active site tyrosine in glutathione S-transferase: insight from a theoretical study on model systems. J. Am. Chem. Soc. 119, 1523-1528.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 1523-1528
-
-
Zheng, Y.J.1
Ornstein, R.L.2
-
19
-
-
0028861909
-
A continuous spectrophotometric method for determining the monophenolase and diphenolase activities of apple polyphenol oxidase
-
Espin, J. C., Morales, M., Varon, R., Tuleda, J., and Garcia-Canovas, F. (1995) A continuous spectrophotometric method for determining the monophenolase and diphenolase activities of apple polyphenol oxidase. Anal. Biochem. 231, 237-246.
-
(1995)
Anal. Biochem.
, vol.231
, pp. 237-246
-
-
Espin, J.C.1
Morales, M.2
Varon, R.3
Tuleda, J.4
Garcia-Canovas, F.5
-
20
-
-
7744236144
-
Multicopper oxidases and oxygenases
-
Solomon, E. I., Sundaram, U. M., and Machonkin, T. E. (1996) Multicopper oxidases and oxygenases. Chem. Rev. 96, 2563-2605.
-
(1996)
Chem. Rev.
, vol.96
, pp. 2563-2605
-
-
Solomon, E.I.1
Sundaram, U.M.2
Machonkin, T.E.3
-
21
-
-
33845378952
-
Substrate analogue binding to the coupled binuclear copper active site in tyrosinase
-
Wilcox, D. E., Porras, A. G., Hwang, Y. T., Lerch, K., Winkler, M. E., and Solomon, E. I. (1985) Substrate analogue binding to the coupled binuclear copper active site in tyrosinase. J. Am. Chem. Soc. 107, 4015-4027.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 4015-4027
-
-
Wilcox, D.E.1
Porras, A.G.2
Hwang, Y.T.3
Lerch, K.4
Winkler, M.E.5
Solomon, E.I.6
-
22
-
-
0029035314
-
Stereoselective catalysis of a retro-Michael reaction by class mu glutathione transferases. Consequences for the internal distribution of products in the active site
-
Chen, J., and Armstrong, R. N. (1995) Stereoselective catalysis of a retro-Michael reaction by class mu glutathione transferases. Consequences for the internal distribution of products in the active site. Chem. Res. Toxicol. 8, 580-585.
-
(1995)
Chem. Res. Toxicol.
, vol.8
, pp. 580-585
-
-
Chen, J.1
Armstrong, R.N.2
-
23
-
-
0022537776
-
Glutathione- and cysteine-mediated cytotoxicity of allyl and benzyl isothiocyanate
-
Bruggeman, I. M., Temmink, J. H. M., and Van Bladeren, P. J. (1986) Glutathione- and cysteine-mediated cytotoxicity of allyl and benzyl isothiocyanate. Toxicol. Appl. Pharmacol. 83, 349-359.
-
(1986)
Toxicol. Appl. Pharmacol.
, vol.83
, pp. 349-359
-
-
Bruggeman, I.M.1
Temmink, J.H.M.2
Van Bladeren, P.J.3
-
24
-
-
0032524470
-
4-Hydroxyanisole: The most suitable monophenolic substrate for determining spectrophotometrically the monophenolase activity of polyphenol oxidase from fruits and vegetables
-
Espin, J. C., Tuleda, J., and Garcia-Canovas, F. (1998) 4-Hydroxyanisole: the most suitable monophenolic substrate for determining spectrophotometrically the monophenolase activity of polyphenol oxidase from fruits and vegetables. Anal. Biochem. 259, 118-126.
-
(1998)
Anal. Biochem.
, vol.259
, pp. 118-126
-
-
Espin, J.C.1
Tuleda, J.2
Garcia-Canovas, F.3
-
25
-
-
0026812465
-
The tomato 66.3k-D polyphenoloxidase gene: Molecular identification and developmental expression
-
Shahar, T., Henning, N., Gutfinger, T., Hareven, D., and Lifschitz, E. (1992) The tomato 66.3k-D polyphenoloxidase gene: molecular identification and developmental expression. Plant Cell 4, 135-147.
-
(1992)
Plant Cell
, vol.4
, pp. 135-147
-
-
Shahar, T.1
Henning, N.2
Gutfinger, T.3
Hareven, D.4
Lifschitz, E.5
-
26
-
-
0345148810
-
Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product
-
Metodiewa, D., Jaiswal, A. K., Cenas, N., Dickancaite, E., and Segura-Aguilar, J. (1999) Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product. Free Radical Biol. Med. 26, 107-116.
-
(1999)
Free Radical Biol. Med.
, vol.26
, pp. 107-116
-
-
Metodiewa, D.1
Jaiswal, A.K.2
Cenas, N.3
Dickancaite, E.4
Segura-Aguilar, J.5
-
27
-
-
0026612119
-
DT-diaphorase and cancer chemotherapy
-
Riley, R. J., and Workman, P. (1992) DT-diaphorase and cancer chemotherapy. Biochem. Pharmacol. 43, 1657-1669.
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 1657-1669
-
-
Riley, R.J.1
Workman, P.2
-
28
-
-
0024498044
-
DT-diaphorase-catalysed reduction of 1,4-naphthoquinone derivatives and glutathionyl-quinone conjugates
-
Buffinton, G. D., Ollinger, K., Brunmark, A., and Cadenas, E. (1989) DT-diaphorase-catalysed reduction of 1,4-naphthoquinone derivatives and glutathionyl-quinone conjugates. Biochem. J. 257, 561-571.
-
(1989)
Biochem. J.
, vol.257
, pp. 561-571
-
-
Buffinton, G.D.1
Ollinger, K.2
Brunmark, A.3
Cadenas, E.4
-
29
-
-
0031910337
-
NAD(P)H:Quinone oxidoreductase 1 reduces the mutagenicity of DNA caused by NADPH:P450 reductase-activated metabolites of benzo[α]pyrene quinones
-
Joseph, P., and Jaiswal, A. K. (1998) NAD(P)H:quinone oxidoreductase 1 reduces the mutagenicity of DNA caused by NADPH:P450 reductase-activated metabolites of benzo[α]pyrene quinones. Br. J. Cancer 77, 709-719.
-
(1998)
Br. J. Cancer
, vol.77
, pp. 709-719
-
-
Joseph, P.1
Jaiswal, A.K.2
|