-
1
-
-
0037125379
-
Risks and benefits of estrogen plus progestin in healthy postmenopausal women: Principal results from the Womens Health Initiative randomized controlled trial
-
Writing Group for the Womens Health Initiative Investigators
-
Writing Group for the Womens Health Initiative Investigators. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Womens Health Initiative randomized controlled trial JAMA, J. Am. Med. Assoc. 2002, 288, 321-323
-
(2002)
JAMA, J. Am. Med. Assoc.
, vol.288
, pp. 321-323
-
-
-
2
-
-
0037830132
-
Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women
-
Chlebowski, R. T.; Hendrix, S. L.; Langer, R. D.; Stefanick, M. L.; Gass, M.; Lane, D.; Rodabough, R. J.; Gilligan, M. A.; Cyr, M. G.; Thomson, C. A.; Khandekar, J.; Petrovitch, H.; McTiernan, A. Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women JAMA, J. Am. Med. Assoc. 2003, 289, 3243-3253
-
(2003)
JAMA, J. Am. Med. Assoc.
, vol.289
, pp. 3243-3253
-
-
Chlebowski, R.T.1
Hendrix, S.L.2
Langer, R.D.3
Stefanick, M.L.4
Gass, M.5
Lane, D.6
Rodabough, R.J.7
Gilligan, M.A.8
Cyr, M.G.9
Thomson, C.A.10
Khandekar, J.11
Petrovitch, H.12
McTiernan, A.13
-
3
-
-
33645232747
-
The risk of breast, endometrial and ovarian cancer in users of hormonal preparations. MiniReview
-
Bernstein, L. The risk of breast, endometrial and ovarian cancer in users of hormonal preparations. MiniReview Basic Clin. Pharmacol. Toxicol. 2006, 98, 288-296
-
(2006)
Basic Clin. Pharmacol. Toxicol.
, vol.98
, pp. 288-296
-
-
Bernstein, L.1
-
4
-
-
0003509335
-
-
Oxford University Press: Oxford, U.K
-
Parkin, D. M.; Whelan, S. L.; Ferlay, J.; Raymond, L.; Young, J. Cancer Incidence in Five Continents; Oxford University Press: Oxford, U.K., 1997.
-
(1997)
Cancer Incidence in Five Continents
-
-
Parkin, D.M.1
Whelan, S.L.2
Ferlay, J.3
Raymond, L.4
Young, J.5
-
5
-
-
0035984006
-
Estrogen: Physiology, pharmacology, and formulations for replacement therapy
-
Ruggiero, R. J.; Likis, F. E. Estrogen: physiology, pharmacology, and formulations for replacement therapy J. Midwifery Womens Health 2002, 47, 130-138
-
(2002)
J. Midwifery Womens Health
, vol.47
, pp. 130-138
-
-
Ruggiero, R.J.1
Likis, F.E.2
-
6
-
-
2542449166
-
Hormone replacement therapy for the primary prevention of chronic diseases: Recommendation statement from the Canadian Task Force on Preventive Health Care
-
Canadian Task Force on Preventive Health Care
-
Wathen, C. N.; Feig, D. S.; Feightner, J. W.; Abramson, B. L.; Cheung, A. M.; Canadian Task Force on Preventive Health Care. Hormone replacement therapy for the primary prevention of chronic diseases: recommendation statement from the Canadian Task Force on Preventive Health Care Can. Med. Assoc. J. 2004, 170, 1535-1537
-
(2004)
Can. Med. Assoc. J.
, vol.170
, pp. 1535-1537
-
-
Wathen, C.N.1
Feig, D.S.2
Feightner, J.W.3
Abramson, B.L.4
Cheung, A.M.5
-
7
-
-
0346599193
-
National use of post-menopausal hormone therapy: Annual trends and response to recent evidence
-
Hersh, A. L.; Stefanick, M. L.; Stafford, R. S. National use of post-menopausal hormone therapy: annual trends and response to recent evidence JAMA, J. Am. Med. Assoc. 2004, 291, 47-53
-
(2004)
JAMA, J. Am. Med. Assoc.
, vol.291
, pp. 47-53
-
-
Hersh, A.L.1
Stefanick, M.L.2
Stafford, R.S.3
-
8
-
-
33746847720
-
Catechol estrogen quinones as initiators of breast and other human cancers
-
Cavalieri, E.; Chakravarti, D.; Guttenplan, J.; Hart, E.; Ingle, J.; Jankowiak, R.; Muti, P.; Rogan, E.; Russo, J.; Santen, R.; Sutter, T. Catechol estrogen quinones as initiators of breast and other human cancers Biophys. Acta, Rev. Cancer 2006, 1766, 63-78
-
(2006)
Biophys. Acta, Rev. Cancer
, vol.1766
, pp. 63-78
-
-
Cavalieri, E.1
Chakravarti, D.2
Guttenplan, J.3
Hart, E.4
Ingle, J.5
Jankowiak, R.6
Muti, P.7
Rogan, E.8
Russo, J.9
Santen, R.10
Sutter, T.11
-
9
-
-
0343144815
-
Mechanism of cytochrome P450-catalyzed aromatic hydroxylation of estrogens
-
Sarabia, S. F.; Zhu, B. T.; Kurosawa, T.; Tohma, M.; Liehr, J. G. Mechanism of cytochrome P450-catalyzed aromatic hydroxylation of estrogens Chem. Res. Toxicol. 1997, 10, 767-771
-
(1997)
Chem. Res. Toxicol.
, vol.10
, pp. 767-771
-
-
Sarabia, S.F.1
Zhu, B.T.2
Kurosawa, T.3
Tohma, M.4
Liehr, J.G.5
-
10
-
-
0032973129
-
The major metabolite of equilin, 4-hydroxyequilin, autoxidizes to an o -quinone which isomerizes to the potent cytotoxin 4-hydroxyequilenin-o-quinone
-
Zhang, F.; Chen, Y.; Pisha, E.; Shen, I.; Xioong, Y.; van Breemen, R. B.; Bolton, J. L. The major metabolite of equilin, 4-hydroxyequilin, autoxidizes to an o -quinone which isomerizes to the potent cytotoxin 4-hydroxyequilenin-o- quinone Chem. Res. Toxicol. 1999, 12, 204-213
-
(1999)
Chem. Res. Toxicol.
, vol.12
, pp. 204-213
-
-
Zhang, F.1
Chen, Y.2
Pisha, E.3
Shen, I.4
Xioong, Y.5
Van Breemen, R.B.6
Bolton, J.L.7
-
11
-
-
0036680017
-
Quinoids, quinoid radicals, and phenoxyl radicals from estrogens and antiestrogens: Role in carcinogenesis?
-
Bolton, J. L. Quinoids, quinoid radicals, and phenoxyl radicals from estrogens and antiestrogens: role in carcinogenesis? Toxicology 2002, 177, 55-65
-
(2002)
Toxicology
, vol.177
, pp. 55-65
-
-
Bolton, J.L.1
-
12
-
-
0036231082
-
Oxidative DNA damage induced by equine estrogen metabolites: Role of estrogen receptor
-
Liu, X.; Yao, J.; Pisha, E.; Yang, Y.; Hua, Y.; van Breemen, R. B.; Bolton, J. L. Oxidative DNA damage induced by equine estrogen metabolites: role of estrogen receptor Chem. Res. Toxicol. 2002, 15, 512-519
-
(2002)
Chem. Res. Toxicol.
, vol.15
, pp. 512-519
-
-
Liu, X.1
Yao, J.2
Pisha, E.3
Yang, Y.4
Hua, Y.5
Van Breemen, R.B.6
Bolton, J.L.7
-
13
-
-
10744226193
-
Effect of halogenated substituents on the metabolism and estrogenic effects of the equine estrogen, equilenin
-
Liu, X.; Zhang, F.; Liu, H.; Burdette, J. E.; Li, Y.; Cassia, R. O.; Pisha, M; Yao, J.; van Breemen, R. B; Swanson, S. M.; Bolton, J. L. Effect of halogenated substituents on the metabolism and estrogenic effects of the equine estrogen, equilenin Chem. Res. Toxicol. 2003, 16, 741-749
-
(2003)
Chem. Res. Toxicol.
, vol.16
, pp. 741-749
-
-
Liu, X.1
Zhang, F.2
Liu, H.3
Burdette, J.E.4
Li, Y.5
Cassia, R.O.6
Pisha, M.7
Yao, J.8
Van Breemen, R.B.9
Swanson, S.M.10
Bolton, J.L.11
-
14
-
-
3242703146
-
Oxidation of raloxifene to potential toxic quinoids: Formation of a di-quinone methide and o -quinones
-
Yu, L.; Liu, H.; Li, W.; Zhang, F.; Luckie, C.; van Breemen, R. B.; Thatcher, G. R. J.; Bolton, J. L. Oxidation of raloxifene to potential toxic quinoids: formation of a di-quinone methide and o -quinones Chem. Res. Toxicol. 2004, 17, 879-888
-
(2004)
Chem. Res. Toxicol.
, vol.17
, pp. 879-888
-
-
Yu, L.1
Liu, H.2
Li, W.3
Zhang, F.4
Luckie, C.5
Van Breemen, R.B.6
Thatcher, G.R.J.7
Bolton, J.L.8
-
15
-
-
0036236626
-
Initiation of cancer and other diseases by catechol ortho-quinones: A unifying mechanism
-
Cavalieri, E. L.; Rogan, E. G.; Chakravarti, D. Initiation of cancer and other diseases by catechol ortho-quinones: a unifying mechanism Cell. Mol. Life Sci. 2002, 59, 665-681
-
(2002)
Cell. Mol. Life Sci.
, vol.59
, pp. 665-681
-
-
Cavalieri, E.L.1
Rogan, E.G.2
Chakravarti, D.3
-
16
-
-
1242274631
-
The Role of Endogenous Catechol Quinones in the Initiation of Cancer and Neurodegenerative Diseases
-
DOI 10.1016/S0076-6879(04)82017-2
-
Cavalieri, E.; Rogan, E.; Chakravarti, D. The role of endogenous catechol quinones in the initiation of cancer and neurodegenerative diseases Methods Enzymol. 2004, 382B (Quinones and Quinone Enzymes) 293-319 (Pubitemid 38240797)
-
(2004)
Methods in Enzymology
, vol.382
, pp. 293-319
-
-
Cavalieri, E.1
Rogan, E.2
Chakravarti, D.3
-
17
-
-
31844450313
-
The greater reactivity of estradiol-3,4-quinone vs. estradiol-2,3-quinone with DNA in the formation of depurinating adducts: Implications for tumor-initiating activity
-
Zahid, M.; Kohli, E.; Saeed, M.; Rogan, E.; Cavalieri, E. The greater reactivity of estradiol-3,4-quinone vs. estradiol-2,3-quinone with DNA in the formation of depurinating adducts: implications for tumor-initiating activity Chem. Res. Toxicol. 2006, 19, 164-172
-
(2006)
Chem. Res. Toxicol.
, vol.19
, pp. 164-172
-
-
Zahid, M.1
Kohli, E.2
Saeed, M.3
Rogan, E.4
Cavalieri, E.5
-
18
-
-
0035022732
-
Genotoxicity of the steroidal oestrogens oestrone and oestradiol: Possible mechanism of uterine and mammary cancer development
-
Liehr, J. G. Genotoxicity of the steroidal oestrogens oestrone and oestradiol: possible mechanism of uterine and mammary cancer development Hum. Reprod. Update 2001, 10, 273-281
-
(2001)
Hum. Reprod. Update
, vol.10
, pp. 273-281
-
-
Liehr, J.G.1
-
19
-
-
0041837376
-
Development of novel antioxidants: Design, synthesis, and reactivity
-
Hussain, H. H.; Babic, G.; Durst, T.; Wright, J. S.; Flueraru, M.; Chichirau, A.; Chepelev, L. L. Development of novel antioxidants: design, synthesis, and reactivity J. Org. Chem. 2003, 68, 7023-7032
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7023-7032
-
-
Hussain, H.H.1
Babic, G.2
Durst, T.3
Wright, J.S.4
Flueraru, M.5
Chichirau, A.6
Chepelev, L.L.7
-
20
-
-
11344289617
-
Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: The connection between extracellular autoxidation and molecular electronic structure
-
Chichirau, A.; Flueraru, M.; Chepelev, L. L.; Wright, J. S.; Willmore, William, G.; Durst, T.; Hussain, H. H.; Charron, M. Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: the connection between extracellular autoxidation and molecular electronic structure Free Radical Biol. Med. 2005, 38, 344-355
-
(2005)
Free Radical Biol. Med.
, vol.38
, pp. 344-355
-
-
Chichirau, A.1
Flueraru, M.2
Chepelev, L.L.3
Wright, J.S.4
Willmore William, G.5
Durst, T.6
Hussain, H.H.7
Charron, M.8
-
21
-
-
27544509498
-
Cytotoxicity and cytoprotective activity in naphthalenediols depends on their tendency to form naphthoquinones
-
Flueraru, M.; Chichirau, A.; Chepelev, L. L.; Willmore, W. G.; Durst, T.; Charron, M.; Barclay, L. R. C.; Wright, J. S. Cytotoxicity and cytoprotective activity in naphthalenediols depends on their tendency to form naphthoquinones Free Radical Biol. Med. 2005, 39, 1368-1377
-
(2005)
Free Radical Biol. Med.
, vol.39
, pp. 1368-1377
-
-
Flueraru, M.1
Chichirau, A.2
Chepelev, L.L.3
Willmore, W.G.4
Durst, T.5
Charron, M.6
Barclay, L.R.C.7
Wright, J.S.8
-
22
-
-
33748987658
-
Cytotoxicity and cytoprotective activity of naphthalenediols in rat cortical neurons
-
Flueraru, M.; So, R.; Willmore, W. G.; Poulter, M. O.; Durst, T.; Charron, M.; Wright, J. S. Cytotoxicity and cytoprotective activity of naphthalenediols in rat cortical neurons Chem. Res. Toxicol. 2006, 19, 1221-1227
-
(2006)
Chem. Res. Toxicol.
, vol.19
, pp. 1221-1227
-
-
Flueraru, M.1
So, R.2
Willmore, W.G.3
Poulter, M.O.4
Durst, T.5
Charron, M.6
Wright, J.S.7
-
23
-
-
0026040838
-
Molecular mechanisms of quinone cytotoxicity
-
OBrien, P. J. Molecular mechanisms of quinone cytotoxicity Chem.-Biol. Interact. 1991, 80, 1-41
-
(1991)
Chem.-Biol. Interact.
, vol.80
, pp. 1-41
-
-
Obrien, P.J.1
-
24
-
-
25444521979
-
Tyrosinase-catalyzed oxidation of 17beta estradiol: Structure elucidation of the products formed beyond catechol estrogen quinones
-
Pezzella, A.; Lista, L.; Napolitano, A; dIschia, M. Tyrosinase-catalyzed oxidation of 17beta estradiol: structure elucidation of the products formed beyond catechol estrogen quinones Chem. Res. Toxicol. 2005, 18, 1413-1419
-
(2005)
Chem. Res. Toxicol.
, vol.18
, pp. 1413-1419
-
-
Pezzella, A.1
Lista, L.2
Napolitano, A.3
Dischia, M.4
-
25
-
-
77950996693
-
1,4-Naphthoquinones as inducers of oxidative damage and stress signaling in aCaT human keratinocytes
-
Klaus, V.; Hartmann, T.; Gambini, G.; Graf, P.; Stahl, W.; Hartwig, A.; Klotz, L. A. 1,4-Naphthoquinones as inducers of oxidative damage and stress signaling in aCaT human keratinocytes Arch. Biochem. Biophys. 2010, 496, 93-100
-
(2010)
Arch. Biochem. Biophys.
, vol.496
, pp. 93-100
-
-
Klaus, V.1
Hartmann, T.2
Gambini, G.3
Graf, P.4
Stahl, W.5
Hartwig, A.6
Klotz, L.A.7
-
26
-
-
0031039888
-
Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors and α and β
-
DOI 10.1210/en.138.3.863
-
Kuiper, G. G. J.; Carlsson, B.; Grandien, K.; Enmark, E.; Haggblad, J.; Nilsson, S.; Gustafsson, J. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors α and β Endocrinology 1997, 138, 863-870 (Pubitemid 27089735)
-
(1997)
Endocrinology
, vol.138
, Issue.3
, pp. 863-870
-
-
Kuiper, G.G.J.M.1
Carlsson, B.2
Grandien, K.3
Enmark, E.4
Haggblad, J.5
Nilsson, S.6
Gustafsson, J.-A.7
-
27
-
-
0031733298
-
Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β
-
Kuiper, G. G. J.; Lemmen, J. G.; Carlsson, B.; Corton, J. C.; Safe, S. H.; van der Saag, P. T.; van der Burg, B.; Gustafsson, J. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β Endocrinology 1998, 139, 4252-4263
-
(1998)
Endocrinology
, vol.139
, pp. 4252-4263
-
-
Kuiper, G.G.J.1
Lemmen, J.G.2
Carlsson, B.3
Corton, J.C.4
Safe, S.H.5
Van Der Saag, P.T.6
Van Der Burg, B.7
Gustafsson, J.8
-
28
-
-
33751542905
-
International Union of Pharmacology. LXIV. Estrogen receptors
-
Dahlman-Wright, K.; Cavailles, V.; Fuqua, S. K.; Jordan, V. C.; Katzenellenbogen, J. A.; Korach, K. S.; Maggi, A.; Muramatsu, M.; Parker, M. G.; Gustafsson, J.-A. International Union of Pharmacology. LXIV. Estrogen receptors Pharmacol. Rev. 2006, 58, 773-781
-
(2006)
Pharmacol. Rev.
, vol.58
, pp. 773-781
-
-
Dahlman-Wright, K.1
Cavailles, V.2
Fuqua, S.K.3
Jordan, V.C.4
Katzenellenbogen, J.A.5
Korach, K.S.6
Maggi, A.7
Muramatsu, M.8
Parker, M.G.9
Gustafsson, J.-A.10
-
29
-
-
0033117680
-
Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens
-
Fink, B. E.; Mortenson, D. S.; Stauffer, S. R.; Aron, Z. D.; Katzenellenbogen, J. A. Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens Chem. Biol. 1999, 6, 205-219
-
(1999)
Chem. Biol.
, vol.6
, pp. 205-219
-
-
Fink, B.E.1
Mortenson, D.S.2
Stauffer, S.R.3
Aron, Z.D.4
Katzenellenbogen, J.A.5
-
30
-
-
13944255737
-
Indazole estrogens: Highly selective ligands for the estrogen receptor β
-
De Angelis, M. D.; Stossi, F.; Carlson, K. E.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Indazole estrogens: highly selective ligands for the estrogen receptor β J. Med. Chem. 2005, 48, 1132-1144
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1132-1144
-
-
De Angelis, M.D.1
Stossi, F.2
Carlson, K.E.3
Katzenellenbogen, B.S.4
Katzenellenbogen, J.A.5
-
31
-
-
15444377440
-
Binding thermodynamics as a tool to investigate the mechanisms of drug-receptor interactions: Thermodynamics of cytoplasmic steroid/nuclear receptors in comparison with membrane receptors
-
Gilli, P.; Gilli, G.; Borea, P. A.; Varani, K.; Scatturin, A.; Dalpiaz, A. Binding thermodynamics as a tool to investigate the mechanisms of drug-receptor interactions: thermodynamics of cytoplasmic steroid/nuclear receptors in comparison with membrane receptors J. Med. Chem. 2005, 48, 2026-2035
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2026-2035
-
-
Gilli, P.1
Gilli, G.2
Borea, P.A.3
Varani, K.4
Scatturin, A.5
Dalpiaz, A.6
-
32
-
-
0031059270
-
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
-
Anstead, G. M.; Carlson, K. E.; Katzenellenbogen, J. A. The estradiol pharmacophore: ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site Steroids 1997, 62, 268-303
-
(1997)
Steroids
, vol.62
, pp. 268-303
-
-
Anstead, G.M.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
-
33
-
-
0031040614
-
Different residues of the human estrogen receptor are involved in the recognition of structurally diverse estrogens and antiestrogens
-
Ekena, K.; Weis, K. E.; Katzenellenbogen, J. A.; Katzenellenbogen, B. S. Different residues of the human estrogen receptor are involved in the recognition of structurally diverse estrogens and antiestrogens J. Biol. Chem. 1997, 272, 5069-5075
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 5069-5075
-
-
Ekena, K.1
Weis, K.E.2
Katzenellenbogen, J.A.3
Katzenellenbogen, B.S.4
-
34
-
-
0030734795
-
Altered ligand binding properties and enhanced stability of a constitutively active estrogen receptor: Evidence that an open pocket conformation is required for ligand interaction
-
Carlson, K. E.; Choi, I.; Gee, A.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Altered ligand binding properties and enhanced stability of a constitutively active estrogen receptor: evidence that an open pocket conformation is required for ligand interaction Biochemistry 1997, 36, 14897-14905
-
(1997)
Biochemistry
, vol.36
, pp. 14897-14905
-
-
Carlson, K.E.1
Choi, I.2
Gee, A.3
Katzenellenbogen, B.S.4
Katzenellenbogen, J.A.5
-
35
-
-
13944255737
-
Indazole estrogens: Highly selective ligands for the estrogen receptor beta
-
De Angelis, M.; Stossi, F.; Carlson, K. A.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Indazole estrogens: highly selective ligands for the estrogen receptor beta J. Med. Chem. 2005, 48, 1132-1144
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1132-1144
-
-
De Angelis, M.1
Stossi, F.2
Carlson, K.A.3
Katzenellenbogen, B.S.4
Katzenellenbogen, J.A.5
-
36
-
-
0034727853
-
Pyrazole ligands: Structure-affinity/activity relationships and estrogen receptor-alpha-selective agonists
-
Stauffer, S. R.; Coletta, C. J.; Tedesco, R.; Nishiguchi, G.; Carlson, K.; Sun, J.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Pyrazole ligands: structure-affinity/activity relationships and estrogen receptor-alpha-selective agonists J. Med. Chem. 2000, 43, 4934-4947
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4934-4947
-
-
Stauffer, S.R.1
Coletta, C.J.2
Tedesco, R.3
Nishiguchi, G.4
Carlson, K.5
Sun, J.6
Katzenellenbogen, B.S.7
Katzenellenbogen, J.A.8
-
37
-
-
0034500470
-
Estrogen receptors: Selective ligands, partners, and distinctive pharmacology
-
discussion 194-195
-
Katzenellenbogen, B. S.; Montano, M. M.; Ediger, T. R.; Sun, J.; Ekena, K.; Lazennec, G.; Martini, P. G.; McInerney, E. M.; Delage-Mourroux, R.; Weis, K.; Katzenellenbogen, J. A. Estrogen receptors: selective ligands, partners, and distinctive pharmacology Recent Prog. Horm. Res. 2000, 55, 163-193; discussion 194-195
-
(2000)
Recent Prog. Horm. Res.
, vol.55
, pp. 163-193
-
-
Katzenellenbogen, B.S.1
Montano, M.M.2
Ediger, T.R.3
Sun, J.4
Ekena, K.5
Lazennec, G.6
Martini, P.G.7
McInerney, E.M.8
Delage-Mourroux, R.9
Weis, K.10
Katzenellenbogen, J.A.11
-
38
-
-
0004752110
-
Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-alpha or estrogen receptor-beta
-
Sun, J.; Meyers, M. J.; Fink, B. E.; Rajendran, R.; Katzenellenbogen, J. A.; Katzenellenbogen, B. S. Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-alpha or estrogen receptor-beta Endocrinology 1999, 140, 800-804
-
(1999)
Endocrinology
, vol.140
, pp. 800-804
-
-
Sun, J.1
Meyers, M.J.2
Fink, B.E.3
Rajendran, R.4
Katzenellenbogen, J.A.5
Katzenellenbogen, B.S.6
-
39
-
-
0035068096
-
The estrogen receptor: A structure-based approach to the design of new specific hormone-receptor combinations
-
Tedesco, R.; Thomas, J. A.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. The estrogen receptor: a structure-based approach to the design of new specific hormone-receptor combinations Chem. Biol. 2001, 8, 277-287
-
(2001)
Chem. Biol.
, vol.8
, pp. 277-287
-
-
Tedesco, R.1
Thomas, J.A.2
Katzenellenbogen, B.S.3
Katzenellenbogen, J.A.4
-
40
-
-
0036177151
-
Antagonists selective for estrogen receptor alpha
-
Sun, J.; Huang, Y. R.; Harrington, W. R.; Sheng, S.; Katzenellenbogen, J. A.; Katzenellenbogen, B. S. Antagonists selective for estrogen receptor alpha Endocrinology 2002, 143, 941-947
-
(2002)
Endocrinology
, vol.143
, pp. 941-947
-
-
Sun, J.1
Huang, Y.R.2
Harrington, W.R.3
Sheng, S.4
Katzenellenbogen, J.A.5
Katzenellenbogen, B.S.6
-
41
-
-
59649129757
-
Deconstructing estradiol: Removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists
-
Asim, M.; El-Safiti, M.; Qian, Y.; Choueiri, C.; Salari, S.; Cheng, J.; Shadnia, H.; Bal, M.; Pratt, M. A. C.; Carlson, K. E.; Katzenellenbogen, J. A.; Wright, J. S.; Durst, T. Deconstructing estradiol: removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists Bioorg. Med. Chem. Lett. 2009, 19, 1250-1253
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 1250-1253
-
-
Asim, M.1
El-Safiti, M.2
Qian, Y.3
Choueiri, C.4
Salari, S.5
Cheng, J.6
Shadnia, H.7
Bal, M.8
Pratt, M.A.C.9
Carlson, K.E.10
Katzenellenbogen, J.A.11
Wright, J.S.12
Durst, T.13
-
42
-
-
59649129757
-
Deconstructing estradiol: Removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists
-
(Erratum to document cited in CA150:423383)
-
Asim, M.; El-Salfiti, M.; Qian, Y.; Choueiri, C.; Salari, S.; Cheng, J.; Shadnia, H.; Bal, M.; Pratt, M. A C.; Carlson, K. E.; Katzenellenbogen, J. A.; Wright, J. S.; Durst, T. Deconstructing estradiol: removal of B-ring generates compounds which are potent and subtype-selective estrogen receptor agonists Bioorg. Med. Chem. Lett. 2009, 19, 2605 (Erratum to document cited in CA150:423383)
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2605
-
-
Asim, M.1
El-Salfiti, M.2
Qian, Y.3
Choueiri, C.4
Salari, S.5
Cheng, J.6
Shadnia, H.7
Bal, M.8
Pratt, M.A.C.9
Carlson, K.E.10
Katzenellenbogen, J.A.11
Wright, J.S.12
Durst, T.13
-
44
-
-
0016721419
-
Studies in antifertility agents. 8. Seco steroids. 2. 5,6-Secoestradiol and some related compounds
-
Bindra, J. S.; Neyyarapally, A. T.; Gupta, R. C.; Kamboj, V. P.; Anand, N. Studies in antifertility agents. 8. Seco steroids. 2. 5,6-Secoestradiol and some related compounds J. Med. Chem. 1975, 18, 921-925
-
(1975)
J. Med. Chem.
, vol.18
, pp. 921-925
-
-
Bindra, J.S.1
Neyyarapally, A.T.2
Gupta, R.C.3
Kamboj, V.P.4
Anand, N.5
-
45
-
-
0015605094
-
Antifertility agents. Synthesis of dialkylaminoethoxy derivatives of 3-alkyl-2,3-diphenylpropiophenones
-
Neyyarapally, A. T.; Gupta, R. C.; Srivastava, S. C.; Bindra, J. SS.; Groveer, P. K.; Setty, B. S.; Anand, N. Antifertility agents. Synthesis of dialkylaminoethoxy derivatives of 3-alkyl-2,3-diphenylpropiophenones Indian J. Chem. 1973, 11, 325-329
-
(1973)
Indian J. Chem.
, vol.11
, pp. 325-329
-
-
Neyyarapally, A.T.1
Gupta, R.C.2
Srivastava, S.C.3
Bindra, J.S.S.4
Groveer, P.K.5
Setty, B.S.6
Anand, N.7
-
46
-
-
71049135731
-
Synthesis and antitumor activities of 3-modified 2-methoxyestradiol analogs
-
Suwandi, L. S.; Agoston, G. E.; Shah, J. H.; Hanson, A. D.; Zhan, X. H.; LaVallee, T. M.; Treston, A. M. Synthesis and antitumor activities of 3-modified 2-methoxyestradiol analogs Bioorg. Med. Chem. Lett. 2009, 19, 6459-6462
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6459-6462
-
-
Suwandi, L.S.1
Agoston, G.E.2
Shah, J.H.3
Hanson, A.D.4
Zhan, X.H.5
Lavallee, T.M.6
Treston, A.M.7
-
47
-
-
71049183916
-
Synthesis, antiproliferative, and pharmacokinetic properties of 3- and 17-double-modified analogs of 2-methoxyestradiol
-
Agoston, G. E.; Shah, J. H.; Suwandi, L.; Hanson, A. D.; Zhan, X.; LaVallee, T. M.; Pribluda, V.; Treston, A. M. Synthesis, antiproliferative, and pharmacokinetic properties of 3- and 17-double-modified analogs of 2-methoxyestradiol Bioorg. Med. Chem. Lett. 2009, 19, 6241-6244
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6241-6244
-
-
Agoston, G.E.1
Shah, J.H.2
Suwandi, L.3
Hanson, A.D.4
Zhan, X.5
Lavallee, T.M.6
Pribluda, V.7
Treston, A.M.8
-
48
-
-
71749116055
-
Synthesis of 2- and 17-substituted estrone analogs and their antiproliferative structure-activity relationships compared to 2-methoxyestradiol
-
Shah, J. H.; Agoston, G. E.; Suwandi, L.; Hunsucker, K.; Pribluda, V.; Zhan, X. H.; Swartz, G. M.; La Vallee, T. M.; Treston, A. M. Synthesis of 2- and 17-substituted estrone analogs and their antiproliferative structure-activity relationships compared to 2-methoxyestradiol Bioorg. Med. Chem. 2009, 17, 7344-7352
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7344-7352
-
-
Shah, J.H.1
Agoston, G.E.2
Suwandi, L.3
Hunsucker, K.4
Pribluda, V.5
Zhan, X.H.6
Swartz, G.M.7
La Vallee, T.M.8
Treston, A.M.9
-
49
-
-
78751675901
-
-
PCT Int. Appl. PCT/US2003/002728
-
Agoston, G. E.; Shah, J. H.; Hunsucker, K. A.; Treston, A. M.; Pribluda, V. S. Nonsteroidal Analogs of 2-Methoxyestradiol for the Treatment of Diseases Characterized by Undesirable Angiogenesis, Proliferative Activity, or Cell Mitosis. PCT Int. Appl. PCT/US2003/002728, 2003.
-
(2003)
Nonsteroidal Analogs of 2-Methoxyestradiol for the Treatment of Diseases Characterized by Undesirable Angiogenesis, Proliferative Activity, or Cell Mitosis
-
-
Agoston, G.E.1
Shah, J.H.2
Hunsucker, K.A.3
Treston, A.M.4
Pribluda, V.S.5
-
50
-
-
78751675901
-
-
PCT Int. Appl. PCT/US2003/002917
-
Agoston, G. E.; Shah, J. H.; Hunsucker, K. A.; Treston, A. M.; Pribluda, V. S. Nonsteroidal Analogs of 2-Methoxyestradiol for Treatment of Diseases Characterized by Undesirable Angiogenesis and Proliferative Activity. PCT Int. Appl. PCT/US2003/002917, 2003.
-
(2003)
Nonsteroidal Analogs of 2-Methoxyestradiol for Treatment of Diseases Characterized by Undesirable Angiogenesis and Proliferative Activity
-
-
Agoston, G.E.1
Shah, J.H.2
Hunsucker, K.A.3
Treston, A.M.4
Pribluda, V.S.5
-
51
-
-
78751654088
-
-
note
-
There is no specific reference for this statement, but it is an assumption that has been shared by many workers in the field of estrogen modeling because of the subnanomolar binding affinity of estradiol for ERα (J. A. Katzenellenbogen, personal communication).
-
-
-
-
52
-
-
0036828135
-
Characterization of the biological roles of the estrogen receptors, ERalpha and ERbeta, in estrogen target tissues in vivo through the use of an ERalpha-selective ligand
-
Harris, H. A.; Katzenellenbogen, J. A.; Katzenellenbogen, B. S. Characterization of the biological roles of the estrogen receptors, ERalpha and ERbeta, in estrogen target tissues in vivo through the use of an ERalpha-selective ligand Endocrinology 2002, 143, 4172-4177
-
(2002)
Endocrinology
, vol.143
, pp. 4172-4177
-
-
Harris, H.A.1
Katzenellenbogen, J.A.2
Katzenellenbogen, B.S.3
-
53
-
-
0037245578
-
Estrogenic diazenes: Heterocyclic non-steroidal estrogens of unusual structure with selectivity for estrogen receptor subtypes
-
Ghosh, U.; Ganessunker, D.; Sattigeri, V. J.; Carlson, K. E.; Mortensen, D. J.; Katzenellenbogen, B. S.; Katzenellenbogen, J. A. Estrogenic diazenes: heterocyclic non-steroidal estrogens of unusual structure with selectivity for estrogen receptor subtypes Bioorg. Med. Chem. 2003, 11, 629-657
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 629-657
-
-
Ghosh, U.1
Ganessunker, D.2
Sattigeri, V.J.3
Carlson, K.E.4
Mortensen, D.J.5
Katzenellenbogen, B.S.6
Katzenellenbogen, J.A.7
-
54
-
-
78751670756
-
-
An erratum containing this correction was sent to the editor of BioOrganic and Medicinal Chemistry Letters in August, 2010
-
An erratum containing this correction was sent to the editor of BioOrganic and Medicinal Chemistry Letters in August, 2010.
-
-
-
-
55
-
-
0016691895
-
Total syntheses of optically active 19-nor steroids. (+)-Estr-4-ene-3,17- dione and (+)-13.beta.-ethylgon-4-ene-3,17-dione
-
Micheli, R. A.; Hajos, Z. G.; Cohen, N.; Parrish, D. R.; Portland, L. A.; Sciamanna, W.; Scott, M. A.; Wehrli, P. A. Total syntheses of optically active 19-nor steroids. (+)-Estr-4-ene-3,17-dione and (+)-13.beta.-ethylgon-4-ene-3,17- dione J. Org. Chem. 1975, 40, 675-681
-
(1975)
J. Org. Chem.
, vol.40
, pp. 675-681
-
-
Micheli, R.A.1
Hajos, Z.G.2
Cohen, N.3
Parrish, D.R.4
Portland, L.A.5
Sciamanna, W.6
Scott, M.A.7
Wehrli, P.A.8
-
56
-
-
0002262097
-
(+)-(7aS)-2,3,7,7a-Tetrahydro-7a-methyl-1 H -indene-1,5-(6 H)-dione (1 H -indene-1,5(6 H)-dione, 2,3,7,7a-tetrahydro-7a-methyl-, (S)-)
-
Hajos, Z. G.; Parrish, D. R. (+)-(7aS)-2,3,7,7a-Tetrahydro-7a-methyl-1 H -indene-1,5-(6 H)-dione (1 H -indene-1,5(6 H)-dione, 2,3,7,7a-tetrahydro-7a- methyl-, (S)-) Org. Synth. 1985, 63, 26-36
-
(1985)
Org. Synth.
, vol.63
, pp. 26-36
-
-
Hajos, Z.G.1
Parrish, D.R.2
-
57
-
-
0001075632
-
A general method fpr the selective reduction of ketones in the presence of enones
-
Ward, D. E.; Rhee, C. K.; Zoghaib, W. M. A general method fpr the selective reduction of ketones in the presence of enones Tetrahedron Lett. 1988, 29, 517-520
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 517-520
-
-
Ward, D.E.1
Rhee, C.K.2
Zoghaib, W.M.3
-
58
-
-
0001586773
-
Effects of solvation on the enthalpies of reaction of tert -butoxyl radicals with phenol and on the calculated O-H bond strength in phenol
-
Wayner, D. D. M.; Lusztyk, E.; Page, D.; Ingold, K. U.; Mulder, P.; Larhoven, L. J. J.; Aldrich, H. S. Effects of solvation on the enthalpies of reaction of tert -butoxyl radicals with phenol and on the calculated O-H bond strength in phenol J. Am. Chem. Soc. 1995, 117, 8737-8744
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 8737-8744
-
-
Wayner, D.D.M.1
Lusztyk, E.2
Page, D.3
Ingold, K.U.4
Mulder, P.5
Larhoven, L.J.J.6
Aldrich, H.S.7
-
59
-
-
0001107787
-
Theoretical study of X-H bond energetics (X = C,N,O,S): Application to substituent effects, gas phase acidities and redox potentials
-
DiLabio, G. A.; Pratt, D. A.; LoFaro, A. D.; Wright, J. S. Theoretical study of X-H bond energetics (X = C,N,O,S): application to substituent effects, gas phase acidities and redox potentials J. Phys. Chem. A 1999, 103, 1653-1661
-
(1999)
J. Phys. Chem. A
, vol.103
, pp. 1653-1661
-
-
Dilabio, G.A.1
Pratt, D.A.2
Lofaro, A.D.3
Wright, J.S.4
-
60
-
-
0035857407
-
Predicting the activity of phenolic antioxidants
-
Wright, J. S.; Johnson, E. R.; DiLabio, G. A. Predicting the activity of phenolic antioxidants J. Am. Chem. Soc. 2001, 123, 1173-1183
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 1173-1183
-
-
Wright, J.S.1
Johnson, E.R.2
Dilabio, G.A.3
-
61
-
-
47049124324
-
Understanding the toxicity of phenols: Using quantitative structure-activity relationship and enthalpy changes to discriminate between possible mechanisms
-
Shadnia, H.; Wright, J. S. Understanding the toxicity of phenols: using quantitative structure-activity relationship and enthalpy changes to discriminate between possible mechanisms Chem. Res. Toxicol. 2008, 21, 1197-1204
-
(2008)
Chem. Res. Toxicol.
, vol.21
, pp. 1197-1204
-
-
Shadnia, H.1
Wright, J.S.2
-
62
-
-
49049110055
-
Computational modeling of substituent effects on phenol toxicity
-
Wright, J. S.; Shadnia, H. Computational modeling of substituent effects on phenol toxicity Chem. Res. Toxicol. 2008, 21, 1426-1431
-
(2008)
Chem. Res. Toxicol.
, vol.21
, pp. 1426-1431
-
-
Wright, J.S.1
Shadnia, H.2
-
63
-
-
0026548738
-
The metabolism of 2- and 4-fluoro-17β-estradiol in the rat and its implications for estrogen carcinogenesis
-
Morgan, P.; Maggs, J. L.; Bulman-Page, P. C.; Hussain, F.; Park, B. K. The metabolism of 2- and 4-fluoro-17β-estradiol in the rat and its implications for estrogen carcinogenesis Biochem. Pharmacol. 1992, 43, 985-994
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 985-994
-
-
Morgan, P.1
Maggs, J.L.2
Bulman-Page, P.C.3
Hussain, F.4
Park, B.K.5
-
64
-
-
0020631150
-
2-Fluoroestradiol. Separation of estrogenicity from carcinogenicity
-
Liehr, J. G. 2-Fluoroestradiol. Separation of estrogenicity from carcinogenicity Mol. Pharmacol. 1983, 23, 278-281
-
(1983)
Mol. Pharmacol.
, vol.23
, pp. 278-281
-
-
Liehr, J.G.1
-
65
-
-
2942586818
-
Quantitative structure-toxicity relationships by accelerated cytotoxicity mechanism screening
-
Siraki, A. G.; Chevaldina, T.; Moridani, M. Y.; OBrien, P. J. Quantitative structure-toxicity relationships by accelerated cytotoxicity mechanism screening Curr. Opin. Drug Discovery Dev. 2004, 7 (1) 118-125
-
(2004)
Curr. Opin. Drug Discovery Dev.
, vol.7
, Issue.1
, pp. 118-125
-
-
Siraki, A.G.1
Chevaldina, T.2
Moridani, M.Y.3
Obrien, P.J.4
-
66
-
-
78751665347
-
-
The PDB file for 1GWR.pdb can be downloaded from
-
The PDB file for 1GWR.pdb can be downloaded from www.rcsb.org.
-
-
-
-
67
-
-
0037077233
-
Interaction of transcriptional intermediary factor 2 nuclear receptor box peptides with the coactivator binding site of estrogen receptor alpha
-
Warnmark, A.; Treuter, E.; Gustafsson, J. A.; Hubbard, R. E.; Brzozowski, A. M.; Pike, A. C. W. Interaction of transcriptional intermediary factor 2 nuclear receptor box peptides with the coactivator binding site of estrogen receptor alpha J. Biol. Chem. 2001, 277, 21862-21868
-
(2001)
J. Biol. Chem.
, vol.277
, pp. 21862-21868
-
-
Warnmark, A.1
Treuter, E.2
Gustafsson, J.A.3
Hubbard, R.E.4
Brzozowski, A.M.5
Pike, A.C.W.6
-
68
-
-
0031733298
-
Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β
-
Kuiper, G. G. J. M.; Lemmen, J. G.; Carlsson, B.; Corton, J. C.; Safe, S. H.; Van Der Saag, P. T.; Van Der Burg, B.; Gustafsson, J. A. Interaction of estrogenic chemicals and phytoestrogens with estrogen receptor β Endocrinology 1998, 139, 4252-4263
-
(1998)
Endocrinology
, vol.139
, pp. 4252-4263
-
-
Kuiper, G.G.J.M.1
Lemmen, J.G.2
Carlsson, B.3
Corton, J.C.4
Safe, S.H.5
Van Der Saag, P.T.6
Van Der Burg, B.7
Gustafsson, J.A.8
-
69
-
-
0031040254
-
Cooperativity and dimerization of recombinant human estrogen receptor hormone-binding domain
-
Brandt, M. E.; Vickery, L. E. Cooperativity and dimerization of recombinant human estrogen receptor hormone-binding domain J. Biol. Chem. 1997, 272, 4843-4849
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 4843-4849
-
-
Brandt, M.E.1
Vickery, L.E.2
-
70
-
-
0027322696
-
Hormone- and DNA-binding mechanisms of the recombinant human estrogen receptor
-
Obourn, J. D.; Koszewski, N. J.; Notides, A. C. Hormone- and DNA-binding mechanisms of the recombinant human estrogen receptor Biochemistry 1993, 32, 6229-6236
-
(1993)
Biochemistry
, vol.32
, pp. 6229-6236
-
-
Obourn, J.D.1
Koszewski, N.J.2
Notides, A.C.3
-
71
-
-
71849084143
-
Capacity of type i and II ligands to confer to estrogen receptor alpha an appropriate conformation for the recruitment of coactivators containing a LxxLL motif - Relationship with the regulation of receptor level and ERE-dependent transcription in MCF-7 cells
-
Bourgoin-Voillard, S.; Gallo, D.; Laïos, I.; Cleeren, A.; El Bali, L.; Jacquot, Y.; Nonclercq, D.; Laurent, G.; Tabet, J. C.; Leclercq, G. Capacity of type I and II ligands to confer to estrogen receptor alpha an appropriate conformation for the recruitment of coactivators containing a LxxLL motif - Relationship with the regulation of receptor level and ERE-dependent transcription in MCF-7 cells Biochem. Pharmacol. 2010, 79, 746-757
-
(2010)
Biochem. Pharmacol.
, vol.79
, pp. 746-757
-
-
Bourgoin-Voillard, S.1
Gallo, D.2
Laïos, I.3
Cleeren, A.4
El Bali, L.5
Jacquot, Y.6
Nonclercq, D.7
Laurent, G.8
Tabet, J.C.9
Leclercq, G.10
-
72
-
-
0037422460
-
Quantitative structure toxicity relationships for phenols in isolated rat hepatocytes
-
Moridani, M. Y.; Siraki, A.; OBrien, P. J. Quantitative structure toxicity relationships for phenols in isolated rat hepatocytes Chem.-Biol. Interact. 2003, 145 (2) 213-223
-
(2003)
Chem.-Biol. Interact.
, vol.145
, Issue.2
, pp. 213-223
-
-
Moridani, M.Y.1
Siraki, A.2
Obrien, P.J.3
-
73
-
-
5144232262
-
Proline-catalyzed asymmetric aldol reactions of tetrahydro-4 H -thiopyran-4-one with aldehydes
-
Ward, D. E.; Jheengut, V. Proline-catalyzed asymmetric aldol reactions of tetrahydro-4 H -thiopyran-4-one with aldehydes Tetradehron Lett. 2004, 45, 8347-8350
-
(2004)
Tetradehron Lett.
, vol.45
, pp. 8347-8350
-
-
Ward, D.E.1
Jheengut, V.2
|