-
1
-
-
0023179020
-
Structure-activity relationships of dietary indoles: A proposed mechanism of action as modifiers of xenobiotic metabolism
-
Bradfield, C. A., and Bjeldanes, L. F. (1987) Structure-activity relationships of dietary indoles: a proposed mechanism of action as modifiers of xenobiotic metabolism. J. Toxicol. Environ. Health 21, 311-323.
-
(1987)
J. Toxicol. Environ. Health
, vol.21
, pp. 311-323
-
-
Bradfield, C.A.1
Bjeldanes, L.F.2
-
2
-
-
0026591316
-
Oligomerization of indole-3-carbinol in aqueous acid
-
Grose, K. R., and Bjeldanes, L. F. (1992) Oligomerization of indole-3-carbinol in aqueous acid. Chem. Res. Toxicol. 5, 188-193.
-
(1992)
Chem. Res. Toxicol.
, vol.5
, pp. 188-193
-
-
Grose, K.R.1
Bjeldanes, L.F.2
-
3
-
-
0029123884
-
Mechanisms of tumor modulation by indole-3-carbinol: Disposition and excretion in male Fischer 344 rats
-
Stresser, D. M., Williams, D. E., Griffin, D. A., and Bailey, G. S. (1995) Mechanisms of tumor modulation by indole-3-carbinol: disposition and excretion in male Fischer 344 rats. Drug Metab. Dispos. 23, 965-975.
-
(1995)
Drug Metab. Dispos.
, vol.23
, pp. 965-975
-
-
Stresser, D.M.1
Williams, D.E.2
Griffin, D.A.3
Bailey, G.S.4
-
4
-
-
0018137952
-
Inhibition of polycyclic hydrocarbon-induced neoplasia by naturally occurring indoles
-
Wattenberg, L. W., and Loub, W. D. (1978) Inhibition of polycyclic hydrocarbon-induced neoplasia by naturally occurring indoles. Cancer Res. 38, 1410-1413.
-
(1978)
Cancer Res.
, vol.38
, pp. 1410-1413
-
-
Wattenberg, L.W.1
Loub, W.D.2
-
5
-
-
0031715037
-
Aryl hydrocarbon receptor-mediated antiestrogenic and antitumorigenic activity of diindolylmethane
-
Chen, I., McDougal, A., Wang, F., and Safe, S. (1998) Aryl hydrocarbon receptor-mediated antiestrogenic and antitumorigenic activity of diindolylmethane. Carcinogenesis 19, 1631-1639.
-
(1998)
Carcinogenesis
, vol.19
, pp. 1631-1639
-
-
Chen, I.1
McDougal, A.2
Wang, F.3
Safe, S.4
-
6
-
-
0038418500
-
Plant-derived 3,3′-diindolylmethane is a strong androgen antagonist in human prostate cancer cells
-
Le, H. T., Schaldach, C. M., Firestone, G. L., and Bjeldanes, L. F. (2003) Plant-derived 3,3′-diindolylmethane is a strong androgen antagonist in human prostate cancer cells. J. Biol. Chem. 278, 21136-21145.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 21136-21145
-
-
Le, H.T.1
Schaldach, C.M.2
Firestone, G.L.3
Bjeldanes, L.F.4
-
7
-
-
0034662488
-
Ligand-independent activation of estrogen receptor function by 3,3′-diindolylmethane in human breast cancer cells
-
Riby, J. E., Chang, G. H. F., Firestone, G. L., and Bjeldanes, L. F. (2000) Ligand-independent activation of estrogen receptor function by 3,3′-diindolylmethane in human breast cancer cells. Biochem. Pharmacol. 60, 167-177.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 167-177
-
-
Riby, J.E.1
Chang, G.H.F.2
Firestone, G.L.3
Bjeldanes, L.F.4
-
8
-
-
0035984590
-
3,3′-Diindolylmethane (DIM) induces a G1 cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21WAF1/CIP1 expression
-
Hong, C., Kim, H.-A., Firestone, G. L., and Bjeldanes, L. F. (2002) 3,3′-Diindolylmethane (DIM) induces a G1 cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21WAF1/CIP1 expression. Carcinogenesis 23, 1297-1305.
-
(2002)
Carcinogenesis
, vol.23
, pp. 1297-1305
-
-
Hong, C.1
Kim, H.-A.2
Firestone, G.L.3
Bjeldanes, L.F.4
-
9
-
-
0035161486
-
Cytostatic effects of 3,3′-diindolylmethane in human endometrial cancer cells result from an estrogen receptor-mediated increase in transforming growth factor-alpha expression
-
Leong H., Firestone G. L., and Bjeldanes L. F. (2001) Cytostatic effects of 3,3′-diindolylmethane in human endometrial cancer cells result from an estrogen receptor-mediated increase in transforming growth factor-alpha expression. Carcinogenesis 22, 1809-1817.
-
(2001)
Carcinogenesis
, vol.22
, pp. 1809-1817
-
-
Leong, H.1
Firestone, G.L.2
Bjeldanes, L.F.3
-
10
-
-
0030297325
-
3,3-Diindolylmethane induces apoptosis in human cancer cells
-
Ge, X., Yannai, S., Rennert, G., Gruener, N., and Fares, F. A. (1996) 3,3-Diindolylmethane induces apoptosis in human cancer cells. Biochem. Biophys. Res. Commun. 228, 153-158.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.228
, pp. 153-158
-
-
Ge, X.1
Yannai, S.2
Rennert, G.3
Gruener, N.4
Fares, F.A.5
-
11
-
-
0037087501
-
Bcl-2 family-mediated apoptotic effects of 3,3′-diindolylmethane (DIM) in human breast cancer cells
-
Hong, C., Firestone, G. L., and Bjeldanes, L. F. (2002) Bcl-2 family-mediated apoptotic effects of 3,3′-diindolylmethane (DIM) in human breast cancer cells. Biochem. Pharmacol. 63, 1085-1097.
-
(2002)
Biochem. Pharmacol.
, vol.63
, pp. 1085-1097
-
-
Hong, C.1
Firestone, G.L.2
Bjeldanes, L.F.3
-
12
-
-
0035241872
-
3,3′-Diindolylmethane, a major condensation product of indole-3-carbinol, is a potent estrogen in the rainbow trout
-
Shilling, A. D., Carlson, D. B., Katchamart, S., and Williams, D. E. (2001) 3,3′-Diindolylmethane, a major condensation product of indole-3-carbinol, is a potent estrogen in the rainbow trout. Toxicol. Appl. Pharmacol. 170, 191-200.
-
(2001)
Toxicol. Appl. Pharmacol.
, vol.170
, pp. 191-200
-
-
Shilling, A.D.1
Carlson, D.B.2
Katchamart, S.3
Williams, D.E.4
-
13
-
-
0029348265
-
The anticarcinogen 3,3′-diindolylmethane is an inhibitor of cytochrome P-450
-
Stresser, D. M., Bjeldanes, L. F., Bailey, G. S., and Williams, D. E. (1995) The anticarcinogen 3,3′-diindolylmethane is an inhibitor of cytochrome P-450. J. Biochem. Toxicol. 10, 191-201.
-
(1995)
J. Biochem. Toxicol.
, vol.10
, pp. 191-201
-
-
Stresser, D.M.1
Bjeldanes, L.F.2
Bailey, G.S.3
Williams, D.E.4
-
14
-
-
0035527478
-
Quantitative determination of 3,3′-diindolylmethane in urine of individuals receiving indole-3-carbinol
-
Sepkovic, D. W., Bradlow, H. L., and Bell, M. (2001) Quantitative determination of 3,3′-diindolylmethane in urine of individuals receiving indole-3-carbinol. Nutr. Cancer 41, 57-63.
-
(2001)
Nutr. Cancer
, vol.41
, pp. 57-63
-
-
Sepkovic, D.W.1
Bradlow, H.L.2
Bell, M.3
-
15
-
-
0036170855
-
Fate of indole-3-carbinol in cultured human breast tumor cells
-
Staub, R. E., Feng, C., Onisko, B., Bailey, G. S., Firestone, G. L., and Bjeldanes, L. F. (2002) Fate of indole-3-carbinol in cultured human breast tumor cells. Chem. Res. Toxicol. 15, 101-109.
-
(2002)
Chem. Res. Toxicol.
, vol.15
, pp. 101-109
-
-
Staub, R.E.1
Feng, C.2
Onisko, B.3
Bailey, G.S.4
Firestone, G.L.5
Bjeldanes, L.F.6
-
16
-
-
0000311595
-
The hydrogenolysis of 3-hydroxymethylindole and other indole derivatives with lithium aluminum hydride
-
Leete, E., and Marion, L. (1953) The hydrogenolysis of 3-hydroxymethylindole and other indole derivatives with lithium aluminum hydride. Can. J. Chem. 31, 775-784.
-
(1953)
Can. J. Chem.
, vol.31
, pp. 775-784
-
-
Leete, E.1
Marion, L.2
-
17
-
-
0034325177
-
Spectroscopy and photophysics of 1-phenylisatin and oxindole
-
Bangal, P. R., and Chakravorti, S. (2000) Spectroscopy and photophysics of 1-phenylisatin and oxindole. Opt. Mater. (Amsterdam) 15, 131-141.
-
(2000)
Opt. Mater. (Amsterdam)
, vol.15
, pp. 131-141
-
-
Bangal, P.R.1
Chakravorti, S.2
-
18
-
-
0027964479
-
Localization of 5-lipoxygenase to the nucleus of unstimulated rat basophilic leukemia cells
-
Brock, T. G., Paine, R., III, and Peters-Golden, M. (1994) Localization of 5-lipoxygenase to the nucleus of unstimulated rat basophilic leukemia cells. J. Biol. Chem. 35, 22059-22066.
-
(1994)
J. Biol. Chem.
, vol.35
, pp. 22059-22066
-
-
Brock, T.G.1
Paine III, R.2
Peters-Golden, M.3
-
19
-
-
0026046412
-
Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: Comparisons with 2,3,7,8- tetrachlorodibenzo-p-dioxin
-
Bjeldanes L. F., Kim J. Y., Grose K. R., Bartholomew J. C., and Bradfield C. A. (1991) Aromatic hydrocarbon responsiveness-receptor agonists generated from indole-3-carbinol in vitro and in vivo: comparisons with 2,3,7,8-tetrachlorodibenzo-p-dioxin. Proc. Natl. Acad. Sci. U.S.A. 88, 9543-9547.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 9543-9547
-
-
Bjeldanes, L.F.1
Kim, J.Y.2
Grose, K.R.3
Bartholomew, J.C.4
Bradfield, C.A.5
-
20
-
-
0033750995
-
Quercetin and resveratrol potently reduce estrogen sulfotransferase activity in normal human mammary epithelial cells
-
Otake, Y., Nolan, A. L., Walle, K., and Walle, T. (2000) Quercetin and resveratrol potently reduce estrogen sulfotransferase activity in normal human mammary epithelial cells. J. Steroid Biochem. Mol. Biol. 73, 265-270.
-
(2000)
J. Steroid Biochem. Mol. Biol.
, vol.73
, pp. 265-270
-
-
Otake, Y.1
Nolan, A.L.2
Walle, K.3
Walle, T.4
-
21
-
-
0036155381
-
Flavonoids inhibit genetic toxicity produced by carcinogens in cells expressing CYP1A2 and CYP1A1
-
Lautraite, S., Musonda, A. C., Doehmer, J., Edwards, G. O., and Chipman, J. K. (2002) Flavonoids inhibit genetic toxicity produced by carcinogens in cells expressing CYP1A2 and CYP1A1. Mutagenesis 17, 45-53.
-
(2002)
Mutagenesis
, vol.17
, pp. 45-53
-
-
Lautraite, S.1
Musonda, A.C.2
Doehmer, J.3
Edwards, G.O.4
Chipman, J.K.5
-
22
-
-
0035192944
-
Differential inhibition and inactivation of human CYP1 enzymes by trans-resveratrol: Evidence for mechanism-based inactivation of CYP1A2
-
Chang T. K., Chen J., and Lee W. B. (2001) Differential inhibition and inactivation of human CYP1 enzymes by trans-resveratrol: evidence for mechanism-based inactivation of CYP1A2. J. Pharmacol. Exp. Ther. 299, 874-882.
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.299
, pp. 874-882
-
-
Chang, T.K.1
Chen, J.2
Lee, W.B.3
-
23
-
-
0031854435
-
Evidence supporting the formation of 2,3-epoxy-3-methylindoline: A reactive intermediate of the pneumotoxin 3-methyl-indole
-
Skordos, K. W., Skiles, G. L., Laycock, J. D., Lanza, D. L., and Yost, G. S. (1998) Evidence supporting the formation of 2,3-epoxy-3-methylindoline: a reactive intermediate of the pneumotoxin 3-methyl-indole. Chem. Res. Toxicol. 11, 741-749.
-
(1998)
Chem. Res. Toxicol.
, vol.11
, pp. 741-749
-
-
Skordos, K.W.1
Skiles, G.L.2
Laycock, J.D.3
Lanza, D.L.4
Yost, G.S.5
-
24
-
-
0032853327
-
Identification of phase I metabolites of 3-methylindole produced by pig liver microsomes
-
Diaz, G. J., Skordos, K. W., Yost, G. S., and Squires, E. J. (1999) Identification of phase I metabolites of 3-methylindole produced by pig liver microsomes. Drug Metab. Dispos. 27, 1150-1156.
-
(1999)
Drug Metab. Dispos.
, vol.27
, pp. 1150-1156
-
-
Diaz, G.J.1
Skordos, K.W.2
Yost, G.S.3
Squires, E.J.4
-
25
-
-
0027423549
-
Identification of goat and mouse urinary metabolites of the pneumotoxin, 3-methylindole
-
Smith, D. J., Skiles, G. L., Appleton, M. L., Carlson, J. R., and Yost, G. S. (1993) Identification of goat and mouse urinary metabolites of the pneumotoxin, 3-methylindole. Xenobiotica 23, 1025-1044.
-
(1993)
Xenobiotica
, vol.23
, pp. 1025-1044
-
-
Smith, D.J.1
Skiles, G.L.2
Appleton, M.L.3
Carlson, J.R.4
Yost, G.S.5
-
26
-
-
0038171278
-
Phase II in vitro metabolism of 3-methylindole metabolites in porcine liver
-
Diaz, G. J., and Squires, E. J. (2003) Phase II in vitro metabolism of 3-methylindole metabolites in porcine liver. Xenobiotica 33, 485-498.
-
(2003)
Xenobiotica
, vol.33
, pp. 485-498
-
-
Diaz, G.J.1
Squires, E.J.2
-
27
-
-
0012918014
-
Identification of selected metabolites of skatole in plasma and urine from pigs
-
Baek, C., Hansen-Moller, J., Friis, C., Cornett, C., and Hansen, S. H. (1997) Identification of selected metabolites of skatole in plasma and urine from pigs. J. Agric. Food Chem. 45, 2332-2340.
-
(1997)
J. Agric. Food Chem.
, vol.45
, pp. 2332-2340
-
-
Baek, C.1
Hansen-Moller, J.2
Friis, C.3
Cornett, C.4
Hansen, S.H.5
-
28
-
-
0018569630
-
The metabolism and disposition of 3-methylindole in goats
-
Hammond, A. C., Carlson, J. R., and Willett, J. D. (1979) The metabolism and disposition of 3-methylindole in goats. Life Sci. 25, 1301-1306.
-
(1979)
Life Sci.
, vol.25
, pp. 1301-1306
-
-
Hammond, A.C.1
Carlson, J.R.2
Willett, J.D.3
-
29
-
-
0024413262
-
Isolation and identification of 3-hydroxy-3-methyloxindole, the major murine metabolite of 3-methylindole
-
Skiles, G. L., Adams, J. D., Jr., and Yost, G. S. (1989) Isolation and identification of 3-hydroxy-3-methyloxindole, the major murine metabolite of 3-methylindole. Chem. Res. Toxicol. 2, 254-259.
-
(1989)
Chem. Res. Toxicol.
, vol.2
, pp. 254-259
-
-
Skiles, G.L.1
Adams Jr., J.D.2
Yost, G.S.3
-
30
-
-
0000719920
-
13C NMR study of the prototropic equilibria of 2-indolinone
-
13C NMR study of the prototropic equilibria of 2-indolinone. J. Mol. Struct. 160, 319-325.
-
(1987)
J. Mol. Struct.
, vol.160
, pp. 319-325
-
-
Dobrowolski, P.1
Stefaniak, L.2
-
31
-
-
0025696935
-
Reduction of the membrane fluidity of human breast cancer cells by tamoxifen and 17beta-estradiol
-
Clarke, R., van den Berg, H. W., and Murphy, R. F. (1990) Reduction of the membrane fluidity of human breast cancer cells by tamoxifen and 17beta-estradiol. J. Natl. Cancer Inst. 82, 1702-1705.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1702-1705
-
-
Clarke, R.1
Van Den Berg, H.W.2
Murphy, R.F.3
-
32
-
-
0028331217
-
Tamoxifen: New membrane-mediated mechanisms of action and therapeutic advances
-
Wiseman, H. (1994) Tamoxifen: new membrane-mediated mechanisms of action and therapeutic advances. Trends Pharmacol. Sci. 15, 83-89.
-
(1994)
Trends Pharmacol. Sci.
, vol.15
, pp. 83-89
-
-
Wiseman, H.1
-
33
-
-
0033922250
-
Inhibition of mitochondrial proton F0F1-ATPase/ATP synthase by polyphenolic phytochemicals
-
Zheng, J., and Ramirez, V. D. (2000) Inhibition of mitochondrial proton F0F1-ATPase/ATP synthase by polyphenolic phytochemicals. Br. J. Pharmacol. 130, 1115-1123.
-
(2000)
Br. J. Pharmacol.
, vol.130
, pp. 1115-1123
-
-
Zheng, J.1
Ramirez, V.D.2
-
34
-
-
2442476238
-
Anticarcinogenic and antioxidant activity of diindolylmethane derivatives
-
Benabadji, S. H., Wen, R., Zheng, J., Dong, X., and Yuan, S. (2004) Anticarcinogenic and antioxidant activity of diindolylmethane derivatives. Acta Pharmacol. Sin. 25, 666-671.
-
(2004)
Acta Pharmacol. Sin.
, vol.25
, pp. 666-671
-
-
Benabadji, S.H.1
Wen, R.2
Zheng, J.3
Dong, X.4
Yuan, S.5
-
35
-
-
3342896766
-
Protection of tamoxifen against oxidation of mitochondrial thiols and NAD(P)H underlying the permeability transition induced by prooxidants
-
Cardoso, C. M. P., Almeida, L. M., and Custodio, J. B. A. (2004) Protection of tamoxifen against oxidation of mitochondrial thiols and NAD(P)H underlying the permeability transition induced by prooxidants. Chem.-Biol Interact. 148, 149-161.
-
(2004)
Chem.-Biol Interact.
, vol.148
, pp. 149-161
-
-
Cardoso, C.M.P.1
Almeida, L.M.2
Custodio, J.B.A.3
-
36
-
-
0028318442
-
Tamoxifen and hydroxytamoxifen as intramembranous inhibitors of lipid peroxidation. Evidence for peroxyl radical scavenging activity
-
Custodio, J. B. A., Dinis, T. C. P., Almeida, L. M., and Madeira, V. M. C. (1994) Tamoxifen and hydroxytamoxifen as intramembranous inhibitors of lipid peroxidation. Evidence for peroxyl radical scavenging activity. Biochem. Pharmacol. 47, 1989-1998.
-
(1994)
Biochem. Pharmacol.
, vol.47
, pp. 1989-1998
-
-
Custodio, J.B.A.1
Dinis, T.C.P.2
Almeida, L.M.3
Madeira, V.M.C.4
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