-
1
-
-
0034947164
-
Catechin metabolism: Glutathione conjugate formation catalysed by tyrosinase, peroxidase, and cytochrome P450
-
Moridani M.Y., Scobie H., O'Brien P.J. Catechin metabolism: glutathione conjugate formation catalysed by tyrosinase, peroxidase, and cytochrome P450. Chem. Res. Toxicol. 14:2001;841-848.
-
(2001)
Chem. Res. Toxicol.
, vol.14
, pp. 841-848
-
-
Moridani, M.Y.1
Scobie, H.2
O'Brien, P.J.3
-
2
-
-
0034772876
-
Caffeic acid, chlorogenic acid, and dihydrocaffeic acid metabolism: Glutathione conjugate formation
-
Moridani M.Y., Scobie H., Jamshidzadeh A., Salehi P., O'Brien P.J. Caffeic acid, chlorogenic acid, and dihydrocaffeic acid metabolism: glutathione conjugate formation. Drug Metab. Dispos. 29:2001;1432-1439.
-
(2001)
Drug Metab. Dispos.
, vol.29
, pp. 1432-1439
-
-
Moridani, M.Y.1
Scobie, H.2
Jamshidzadeh, A.3
Salehi, P.4
O'Brien, P.J.5
-
3
-
-
84987350912
-
Measurement of chlorogenic acid and flavonol glycosides in apple juice by a chromatographic-fluorometric method
-
Buren J.V., Vos L.D., Pilnik W. Measurement of chlorogenic acid and flavonol glycosides in apple juice by a chromatographic-fluorometric method. J. Food Sci. 38:1973;656-658.
-
(1973)
J. Food Sci.
, vol.38
, pp. 656-658
-
-
Buren, J.V.1
Vos, L.D.2
Pilnik, W.3
-
4
-
-
0016806440
-
Possible carcinogenic effects of coffee constituents
-
Challis B.C., Barlett C.D. Possible carcinogenic effects of coffee constituents. Nature. 254:1975;532-533.
-
(1975)
Nature
, vol.254
, pp. 532-533
-
-
Challis, B.C.1
Barlett, C.D.2
-
5
-
-
0031038440
-
Quercetin protects cutaneous tissue-associated cell types including sensory neurons from oxidative stress induced by glutathione depletion: Cooperative effects of ascorbic acid
-
Skaper S.D., Fabris M., Ferrari V., Dalle Carbonare M., Leon A. Quercetin protects cutaneous tissue-associated cell types including sensory neurons from oxidative stress induced by glutathione depletion: cooperative effects of ascorbic acid. Free Radic. Biol. Med. 22:1997;669-678.
-
(1997)
Free Radic. Biol. Med.
, vol.22
, pp. 669-678
-
-
Skaper, S.D.1
Fabris, M.2
Ferrari, V.3
Dalle Carbonare, M.4
Leon, A.5
-
6
-
-
0030825875
-
Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes
-
Duthie S.J., Collins A.R., Duthie G.G., Dobson V.L. Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes. Mutat. Res. 393:1997;223-231.
-
(1997)
Mutat. Res.
, vol.393
, pp. 223-231
-
-
Duthie, S.J.1
Collins, A.R.2
Duthie, G.G.3
Dobson, V.L.4
-
7
-
-
0029888128
-
Structure-antioxidant activity relationships of flavonoids and phenolic acids
-
Rice-Evans C.A., Miller N.J., Paganga G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radic. Biol. Med. 20:1996;933-956.
-
(1996)
Free Radic. Biol. Med.
, vol.20
, pp. 933-956
-
-
Rice-Evans, C.A.1
Miller, N.J.2
Paganga, G.3
-
8
-
-
0024431747
-
Inhibitory effects of the tyrosine kinase inhibitor genistein on mammalian DNA topoisomerase II
-
Markovits J., Linassier C., Fosse P., Couprie J., Pierre J., Jacquemin-Sablon A., Saucier J.M., Le Pecq J.B., Larsen A.K. Inhibitory effects of the tyrosine kinase inhibitor genistein on mammalian DNA topoisomerase II. Cancer Res. 49:1989;5111-5117.
-
(1989)
Cancer Res.
, vol.49
, pp. 5111-5117
-
-
Markovits, J.1
Linassier, C.2
Fosse, P.3
Couprie, J.4
Pierre, J.5
Jacquemin-Sablon, A.6
Saucier, J.M.7
Le Pecq, J.B.8
Larsen, A.K.9
-
9
-
-
0032547015
-
Green tea epigallocatechin gallate shows a pronounced growth inhibitory effect on cancerous cells but not on their normal counterparts
-
Chen Z.P., Schell J.B., Ho C.T., Chen K.Y. Green tea epigallocatechin gallate shows a pronounced growth inhibitory effect on cancerous cells but not on their normal counterparts. Cancer Lett. 129:1998;173-179.
-
(1998)
Cancer Lett.
, vol.129
, pp. 173-179
-
-
Chen, Z.P.1
Schell, J.B.2
Ho, C.T.3
Chen, K.Y.4
-
10
-
-
0021348497
-
Caffeic acid is a selective inhibitor for leukotriene biosynthesis
-
Koshihara Y., Neichi T., Murota S., Lao A., Fujimoto Y., Tatsuno T. Caffeic acid is a selective inhibitor for leukotriene biosynthesis. Biochim. Biophys. Acta. 17:1984;92-97.
-
(1984)
Biochim. Biophys. Acta
, vol.17
, pp. 92-97
-
-
Koshihara, Y.1
Neichi, T.2
Murota, S.3
Lao, A.4
Fujimoto, Y.5
Tatsuno, T.6
-
11
-
-
0027240013
-
Inhibition of 4-nitroquinoline-1-oxide-induced rat tongue carcinogenesis by the naturally occurring plant phenolics caffeic, ellagic, chlorogenic and ferulic acids
-
Tanaka T., Kojima T., Kawamori T., Wang A., Suzui M., Okamoto K., Mori H. Inhibition of 4-nitroquinoline-1-oxide-induced rat tongue carcinogenesis by the naturally occurring plant phenolics caffeic, ellagic, chlorogenic and ferulic acids. Carcinogenesis. 14:1993;1321-1325.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1321-1325
-
-
Tanaka, T.1
Kojima, T.2
Kawamori, T.3
Wang, A.4
Suzui, M.5
Okamoto, K.6
Mori, H.7
-
12
-
-
0027215866
-
Chemoprevention of diethylnitrosamine-induced hepatocarcinogenesis by a simple phenolic acid protocatechuic acid in rats
-
Tanaka T., Kojima T., Kawamori T., Yoshimi N., Mori H. Chemoprevention of diethylnitrosamine-induced hepatocarcinogenesis by a simple phenolic acid protocatechuic acid in rats. Cancer Res. 15:1993;2775-2779.
-
(1993)
Cancer Res.
, vol.15
, pp. 2775-2779
-
-
Tanaka, T.1
Kojima, T.2
Kawamori, T.3
Yoshimi, N.4
Mori, H.5
-
13
-
-
0026594634
-
Activities of flavonoids for the cleavage of DNA in the presence of Cu(II): Correlation with generation of active oxygen species
-
Said Ahmad M., Fazal F., Rahman A., Hadi S.M., Parish J.H. Activities of flavonoids for the cleavage of DNA in the presence of Cu(II): correlation with generation of active oxygen species. Carcinogenesis. 13:1992;605-608.
-
(1992)
Carcinogenesis
, vol.13
, pp. 605-608
-
-
Said Ahmad, M.1
Fazal, F.2
Rahman, A.3
Hadi, S.M.4
Parish, J.H.5
-
14
-
-
0027104640
-
The glutathione conjugates of tert-butyl hydroquinone as potent redox cycling agents and possible reactive agents underlying the toxicity of butylated hydroxyanisole
-
van Ommen B., Koster A., Verhagen H., van Bladeren P.J. The glutathione conjugates of tert-butyl hydroquinone as potent redox cycling agents and possible reactive agents underlying the toxicity of butylated hydroxyanisole. Biochem. Biophys. Res. Commun. 189:1992;309-314.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.189
, pp. 309-314
-
-
Van Ommen, B.1
Koster, A.2
Verhagen, H.3
Van Bladeren, P.J.4
-
15
-
-
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., Dragsted L.O. Two-electron electrochemical oxidation of quercetin and kaempferol changes only the flavonoid C-ring. Free Radic. Res. 29:1998;339-350.
-
(1998)
Free Radic. Res.
, vol.29
, pp. 339-350
-
-
Jorgensen, L.V.1
Cornett, C.2
Justesen, U.3
Skibsted, L.H.4
Dragsted, L.O.5
-
16
-
-
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., Segura-Aguilar J. Quercetin may act as a cytotoxic prooxidant after its metabolic activation to semiquinone and quinoidal product. Free Radic. Biol. Med. 26:1999;107-116.
-
(1999)
Free Radic. Biol. Med.
, vol.26
, pp. 107-116
-
-
Metodiewa, D.1
Jaiswal, A.K.2
Cenas, N.3
Dickancaite, E.4
Segura-Aguilar, J.5
-
17
-
-
0031886669
-
Structure-activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers
-
Cos P., Ying L., Calomme M., Hu J.P., Cimanga K., Van Poel B., Pieters L., Vlietinck A.J., Vanden Berghe D. Structure-activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers. J. Nat. Prod. 61:1998;71-76.
-
(1998)
J. Nat. Prod.
, vol.61
, pp. 71-76
-
-
Cos, P.1
Ying, L.2
Calomme, M.3
Hu, J.P.4
Cimanga, K.5
Van Poel, B.6
Pieters, L.7
Vlietinck, A.J.8
Vanden Berghe, D.9
-
18
-
-
0035865879
-
Peroxidative metabolism of apigenin and naringenin versus luteolin and quercetin: Glutathione oxidation and conjugation
-
Galati G., Moridani M.Y., Chan T.S., O'Brien P.J. Peroxidative metabolism of apigenin and naringenin versus luteolin and quercetin: glutathione oxidation and conjugation. Free Radic. Biol. Med. 15:2001;370-382.
-
(2001)
Free Radic. Biol. Med.
, vol.15
, pp. 370-382
-
-
Galati, G.1
Moridani, M.Y.2
Chan, T.S.3
O'Brien, P.J.4
-
19
-
-
0029921813
-
Structural aspects of antioxidant activity of flavonoids
-
van Acker S.A., van den Berg D.J., Tromp M.N., Griffioen D.H., van Bennekom W.P., van der Vijgh W.J., Bast A. Structural aspects of antioxidant activity of flavonoids. Free Radic. Biol. Med. 20:1996;331-342.
-
(1996)
Free Radic. Biol. Med.
, vol.20
, pp. 331-342
-
-
Van Acker, S.A.1
Van den Berg, D.J.2
Tromp, M.N.3
Griffioen, D.H.4
Van Bennekom, W.P.5
Van der Vijgh, W.J.6
Bast, A.7
-
20
-
-
0034519306
-
Cancer chemoprevention and apoptosis mechanisms induced by dietary polyphenolics
-
Galati G., Teng S., Moridani M.Y., Chan T.S., O'Brien P.J. Cancer chemoprevention and apoptosis mechanisms induced by dietary polyphenolics. Drug Met. Drug Interact. 17:2000;311-349.
-
(2000)
Drug Met. Drug Interact.
, vol.17
, pp. 311-349
-
-
Galati, G.1
Teng, S.2
Moridani, M.Y.3
Chan, T.S.4
O'Brien, P.J.5
-
21
-
-
0037139351
-
Comparative quantitative structure toxicity relationships for flavonoids evaluated in isolated rat hepatocytes and HeLa tumor cells
-
Moridani M.Y., Galati G., O'Brien P.J. Comparative quantitative structure toxicity relationships for flavonoids evaluated in isolated rat hepatocytes and HeLa tumor cells. Chem.-Biol. Interac. 20:2002;251-264.
-
(2002)
Chem.-Biol. Interac.
, vol.20
, pp. 251-264
-
-
Moridani, M.Y.1
Galati, G.2
O'Brien, P.J.3
-
22
-
-
0042027108
-
On the toxicity of phenols to fast growing cells. A QSAR model for a radical-based toxicity
-
C.D. Selassie, A.J. Shusterman, S. Kapur, R.P. Verma, L. Zhang, C. Hansch, On the toxicity of phenols to fast growing cells. A QSAR model for a radical-based toxicity, J. Chem. Soc. Perkin Trans. II (1999) 2729-2733.
-
(1999)
J. Chem. Soc. Perkin Trans. II
, pp. 2729-2733
-
-
Selassie, C.D.1
Shusterman, A.J.2
Kapur, S.3
Verma, R.P.4
Zhang, L.5
Hansch, C.6
-
24
-
-
0028679436
-
Predicting modes of toxic action from chemical structure: An overview
-
Bradbury S.P. Predicting modes of toxic action from chemical structure: an overview. SAR QSAR Environ. Res. 2:1994;89-104.
-
(1994)
SAR QSAR Environ. Res.
, vol.2
, pp. 89-104
-
-
Bradbury, S.P.1
-
25
-
-
0014874208
-
On the parabolic relationship between drug potency and hydrophobicity
-
McFarland J.W. On the parabolic relationship between drug potency and hydrophobicity. J. Med. Chem. 13:1970;1192-1196.
-
(1970)
J. Med. Chem.
, vol.13
, pp. 1192-1196
-
-
McFarland, J.W.1
-
28
-
-
0015239908
-
Effects of ring substituents on the activity of phenols as inhibitors and uncouplers of mitochondrial respiration
-
Stockdale M., Selwyn M.J. Effects of ring substituents on the activity of phenols as inhibitors and uncouplers of mitochondrial respiration. Eur. J. Biochem. 21:1971;565-574.
-
(1971)
Eur. J. Biochem.
, vol.21
, pp. 565-574
-
-
Stockdale, M.1
Selwyn, M.J.2
-
29
-
-
0025318548
-
Quantitative analysis of uncoupling activity of substituted phenols with a physicochemical substituent and molecular parameters
-
Miyoshi H., Tsujishita H., Tokutake N., Fujita T. Quantitative analysis of uncoupling activity of substituted phenols with a physicochemical substituent and molecular parameters. Biochim. Biophys. Acta. 1016:1990;99-106.
-
(1990)
Biochim. Biophys. Acta
, vol.1016
, pp. 99-106
-
-
Miyoshi, H.1
Tsujishita, H.2
Tokutake, N.3
Fujita, T.4
-
30
-
-
0023654643
-
Quantitative relationship between protonophoric and uncoupling activities of substituted phenols
-
Miyoshi H., Nishioka T., Fujita T. Quantitative relationship between protonophoric and uncoupling activities of substituted phenols. Biochim. Biophys. Acta. 891:1987;194-204.
-
(1987)
Biochim. Biophys. Acta
, vol.891
, pp. 194-204
-
-
Miyoshi, H.1
Nishioka, T.2
Fujita, T.3
-
31
-
-
0344806276
-
Prooxidant toxicity of polyphenolic antioxidants to HL-60 cells: Description of quantitative structure-activity relationships
-
Sergediene E., Jonsson K., Szymusiak H., Tyrakowska B., Rietjens I.M., Cenas N. Prooxidant toxicity of polyphenolic antioxidants to HL-60 cells: description of quantitative structure-activity relationships. FEBS Lett. 462:1999;392-396.
-
(1999)
FEBS Lett.
, vol.462
, pp. 392-396
-
-
Sergediene, E.1
Jonsson, K.2
Szymusiak, H.3
Tyrakowska, B.4
Rietjens, I.M.5
Cenas, N.6
-
32
-
-
0034659106
-
Comparative QSAR evidence for a free-radical mechanism of phenol-induced toxicity
-
Hansch C., McKarns S.C., Smith C.J., Doolittle D.J. Comparative QSAR evidence for a free-radical mechanism of phenol-induced toxicity. Chem.-Biol. Interact. 127:2000;61-72.
-
(2000)
Chem.-Biol. Interact.
, vol.127
, pp. 61-72
-
-
Hansch, C.1
McKarns, S.C.2
Smith, C.J.3
Doolittle, D.J.4
-
33
-
-
0037420966
-
Metabolic activation of 3-hydroxyanisole by isloated rat hepatocytes
-
M.Y. Moridani, S.S. Cheon, S. Khan, P.J. O'Brien, Metabolic activation of 3-hydroxyanisole by isloated rat hepatocytes, Chem. Biol. Interact. 142 (2003) 317-333.
-
(2003)
Chem. Biol. Interact.
, vol.142
, pp. 317-333
-
-
Moridani, M.Y.1
Cheon, S.S.2
Khan, S.3
O'Brien, P.J.4
-
34
-
-
0027092534
-
The enzymatic formation and chemical reactivity of quinone methides correlate with alkylphenol-induced toxicity in rat hepatocytes
-
Bolton J.L., Valerio L.G. Jr, Thompson J.A. The enzymatic formation and chemical reactivity of quinone methides correlate with alkylphenol-induced toxicity in rat hepatocytes. Chem. Res. Toxicol. 5:1992;816-822.
-
(1992)
Chem. Res. Toxicol.
, vol.5
, pp. 816-822
-
-
Bolton, J.L.1
Valerio L.G., Jr.2
Thompson, J.A.3
-
35
-
-
0028831731
-
Quinone methide formation from para isomers of methylphenol (cresol), ethylphenol, and isopropylphenol: Relationship to toxicity
-
Thompson D.C., Perera K., London R. Quinone methide formation from para isomers of methylphenol (cresol), ethylphenol, and isopropylphenol: relationship to toxicity. Chem. Res. Toxicol. 8:1995;55-60.
-
(1995)
Chem. Res. Toxicol.
, vol.8
, pp. 55-60
-
-
Thompson, D.C.1
Perera, K.2
London, R.3
|