-
1
-
-
0023913120
-
The steroid and thyroid hormone receptor superfamily
-
Evans, R. M. The steroid and thyroid hormone receptor superfamily. Science 1988, 240, 889-895.
-
(1988)
Science
, vol.240
, pp. 889-895
-
-
Evans, R.M.1
-
2
-
-
0028283503
-
Molecular mechanisms of action of steroid/thyroid receptor superfamily members
-
Tsai, M.-J.; O'Malley, B. W. Molecular mechanisms of action of steroid/thyroid receptor superfamily members. Annu. Rev. Biochem. 1994, 63, 451-486.
-
(1994)
Annu. Rev. Biochem.
, vol.63
, pp. 451-486
-
-
Tsai, M.-J.1
O'Malley, B.W.2
-
4
-
-
0035986071
-
The estrogen receptor: More than the average transcription factor
-
Hart, L. L.; Davie, J. R. The estrogen receptor: more than the average transcription factor. Biochem. Cell Biol. 2002, 80, 335-341.
-
(2002)
Biochem. Cell Biol.
, vol.80
, pp. 335-341
-
-
Hart, L.L.1
Davie, J.R.2
-
5
-
-
0034735850
-
A structural biologist's view of the oestrogen receptor
-
Pike, A. C. W.; Brzozowski, A. M.; Hubbard, R. E. A structural biologist's view of the oestrogen receptor. J. Steroid Biochem. Mol. Biol. 2000, 74, 261-268.
-
(2000)
J. Steroid Biochem. Mol. Biol.
, vol.74
, pp. 261-268
-
-
Pike, A.C.W.1
Brzozowski, A.M.2
Hubbard, R.E.3
-
6
-
-
0034735859
-
Molecular mechanisms of estrogen action: Selectve ligands and receptor pharmacology
-
Katzenellenbogen, B. S.; Choi, I.; Delage-Mourroux, R.; Ediger, T. R.; Martini, P. G. V.; Montano, M.; Sun, J.; Weis, K.; Katzenellenbogen, J. A. Molecular mechanisms of estrogen action: selectve ligands and receptor pharmacology. J. Steroid Biochem. Mol. Biol. 2000, 74, 279-285.
-
(2000)
J. Steroid Biochem. Mol. Biol.
, vol.74
, pp. 279-285
-
-
Katzenellenbogen, B.S.1
Choi, I.2
Delage-Mourroux, R.3
Ediger, T.R.4
Martini, P.G.V.5
Montano, M.6
Sun, J.7
Weis, K.8
Katzenellenbogen, J.A.9
-
7
-
-
0029127132
-
Cellular mechanisms which distinguish between hormone- and antihormone-activated estrogen receptor
-
McDonnell, D. P.; Dana, S. L.; Hoener, P. A.; Lieberman, B. A.; Imhof, M. O.; Stein, R. B. Cellular mechanisms which distinguish between hormone- and antihormone-activated estrogen receptor. Ann. N.Y. Acad. Sci. 2001, 949, 121-137.
-
(2001)
Ann. N.Y. Acad. Sci.
, vol.949
, pp. 121-137
-
-
McDonnell, D.P.1
Dana, S.L.2
Hoener, P.A.3
Lieberman, B.A.4
Imhof, M.O.5
Stein, R.B.6
-
8
-
-
0033775525
-
Molecular mechanisms of selective estrogen receptor modulator (SERM) action
-
Dutertre, M.; Smith, C. L. Molecular mechanisms of selective estrogen receptor modulator (SERM) action. J. Pharmacol. Exp. Ther. 2000, 295, 431-437.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.295
, pp. 431-437
-
-
Dutertre, M.1
Smith, C.L.2
-
9
-
-
0033641674
-
Mechanism of action of estrogens and selective estrogen receptor modulators
-
Krishnan, V.; Heath, H.; Bryant, H. U. Mechanism of action of estrogens and selective estrogen receptor modulators. Vitam. Horm. 2001, 60, 123-147.
-
(2001)
Vitam. Horm.
, vol.60
, pp. 123-147
-
-
Krishnan, V.1
Heath, H.2
Bryant, H.U.3
-
10
-
-
0035680322
-
Structure-function relationships in estrogen receptors and the characterization of novel selective estrogen receptor modulators with unique pharmacological profiles
-
Katzenellenbogen, B. S.; Sun, J.; Harrington, W. R.; Kraichely, D. M.; Ganessunker, D.; Katzenellenbogen, J. A. Structure-function relationships in estrogen receptors and the characterization of novel selective estrogen receptor modulators with unique pharmacological profiles. Ann. N.Y. Acad. Sci. 2001, 949, 6-15.
-
(2001)
Ann. N.Y. Acad. Sci.
, vol.949
, pp. 6-15
-
-
Katzenellenbogen, B.S.1
Sun, J.2
Harrington, W.R.3
Kraichely, D.M.4
Ganessunker, D.5
Katzenellenbogen, J.A.6
-
11
-
-
0036225994
-
Molecular forms of the estrogen receptor in breast cancer
-
Leclercq, G. Molecular forms of the estrogen receptor in breast cancer. J. Steroid Biochem. Mol. Biol. 2002, 80, 259-272.
-
(2002)
J. Steroid Biochem. Mol. Biol.
, vol.80
, pp. 259-272
-
-
Leclercq, G.1
-
12
-
-
0035222516
-
Drug discovery and the intracellular receptor family
-
Miner, J. N.; Tyree, C. M. Drug discovery and the intracellular receptor family. Vitam. Horm. 2001, 62, 253-280.
-
(2001)
Vitam. Horm.
, vol.62
, pp. 253-280
-
-
Miner, J.N.1
Tyree, C.M.2
-
13
-
-
0036094708
-
Transcription factors and neoplasia: Vistas in novel drug design
-
Karamouzis, M. V.; Gorgoulis, V. G.; Papavassiliou, A. G. Transcription factors and neoplasia: vistas in novel drug design. Clin. Cancer Res. 2002, 8, 949-961.
-
(2002)
Clin. Cancer Res.
, vol.8
, pp. 949-961
-
-
Karamouzis, M.V.1
Gorgoulis, V.G.2
Papavassiliou, A.G.3
-
14
-
-
0031039798
-
The novel anti-estrogen iodoxifene inhibits the growth of human cancer xenografts and reduces the frequency of acquired anti-estrogen resistance
-
Johnston, S. R. D.; Riddle, S.; Haynes, B. P.; Hern, R. A.; Smith, I. E.; Jarman, M.; Dowsett, M. The novel anti-estrogen iodoxifene inhibits the growth of human cancer xenografts and reduces the frequency of acquired anti-estrogen resistance. Br. J. Cancer 1997, 75, 804-809.
-
(1997)
Br. J. Cancer
, vol.75
, pp. 804-809
-
-
Johnston, S.R.D.1
Riddle, S.2
Haynes, B.P.3
Hern, R.A.4
Smith, I.E.5
Jarman, M.6
Dowsett, M.7
-
15
-
-
0021201213
-
Anti-estrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4- hydroxyphenyl)benzo[b]-thien-2-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride LY 156758, a remarkably effective estrogen antagonist with only minimal intrinsic activity
-
Jones, C. D.; Jevnikar, M. G.; Pike, A. J.; Peters, M. K.; Black, L. J.; Falcone, J. F.; Clemens, J. A. Anti-estrogens. 2. Structure-activity studies in a series of 3-aroyl-2-arylbenzo[b]thiophene derivatives leading to [6-hydroxy-2-(4-hydroxyphenyl)benzo[b]-thien-2-yl][4-[2-(1-piperidinyl)ethoxy] phenyl]methanone hydrochloride LY 156758, a remarkably effective estrogen antagonist with only minimal intrinsic activity. J. Med. Chem. 1984, 27, 1057-1066.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 1057-1066
-
-
Jones, C.D.1
Jevnikar, M.G.2
Pike, A.J.3
Peters, M.K.4
Black, L.J.5
Falcone, J.F.6
Clemens, J.A.7
-
16
-
-
0003630405
-
Discovery and synthesis of [6-hydroxy-3-[4-[2-(1-piperidinyl)-ethoxy] phenoxy]-2-(4-hydroxyphenyl)]benzo[b]thiophene: A novel, highly potent, selective estrogen receptor modulator
-
Palkowitz, A. D.; Glasebrook, A. L.; Thrasher, K. J.; Hauser, K. L.; Short, L. L.; Phillips, D. L.; Muehl, B. S.; Sato, M.; Shetler, P. K.; Cullinan, G. L.; Pell, T. R.; Bryant, H. U. Discovery and synthesis of [6-hydroxy-3-[4-[2-(1-piperidinyl)-ethoxy]phenoxy]-2-(4-hydroxyphenyl)]benzo[b] thiophene: a novel, highly potent, selective estrogen receptor modulator. J. Med. Chem. 1997, 40, 1407-1416.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1407-1416
-
-
Palkowitz, A.D.1
Glasebrook, A.L.2
Thrasher, K.J.3
Hauser, K.L.4
Short, L.L.5
Phillips, D.L.6
Muehl, B.S.7
Sato, M.8
Shetler, P.K.9
Cullinan, G.L.10
Pell, T.R.11
Bryant, H.U.12
-
17
-
-
0033051859
-
EM-652 (SCH 57068), a third generation SERM acting as a pure anti-estrogen in the mammary gland and endometrium
-
LaBrie, F.; LaBrie, C.; Belanger, A.; Simard, J.; Gauthier, S.; Luu-The, V.; Merand, Y.; Giguere, V.; Candas, B.; Luo, S.; Martel, C.; Singh, S. M.; Fournier, M.; Coquet, A.; Richard, V.; Charbonneau, R.; Charpanet, G.; Tremblay, A.; Cusan, L.; Villeux, R. EM-652 (SCH 57068), a third generation SERM acting as a pure anti-estrogen in the mammary gland and endometrium. J. Steroid Biochem. Mol. Biol. 1999, 69, 51-84.
-
(1999)
J. Steroid Biochem. Mol. Biol.
, vol.69
, pp. 51-84
-
-
LaBrie, F.1
LaBrie, C.2
Belanger, A.3
Simard, J.4
Gauthier, S.5
Luu-The, V.6
Merand, Y.7
Giguere, V.8
Candas, B.9
Luo, S.10
Martel, C.11
Singh, S.M.12
Fournier, M.13
Coquet, A.14
Richard, V.15
Charbonneau, R.16
Charpanet, G.17
Tremblay, A.18
Cusan, L.19
Villeux, R.20
more..
-
18
-
-
0034787326
-
A new anti-estrogen, 2-(4-hydroxy-phenyl)-3-methyl-1-[4-(2-piperidin-2- yl-ethoxy-)benzyl]-1H-indol-5-ol hydrochloride (ERA-923), inhibits the growth of tamoxifen-sensitive and -resistant tumors and is devoid of uterotrophic effects in mice and rats
-
Greenberger, L. M.; Annablr, T.; Collins, K. I.; Komm, B. S.; Lyttle, C. R.; Miller, C. P.; Satyaswaroop, P. G.; Zhang, Y.; Frost, P. A new anti-estrogen, 2-(4-hydroxy-phenyl)-3-methyl-1-[4-(2-piperidin-2-yl-ethoxy-) benzyl]-1H-indol-5-ol hydrochloride (ERA-923), inhibits the growth of tamoxifen-sensitive and -resistant tumors and is devoid of uterotrophic effects in mice and rats. Clin. Cancer Res. 2001, 7, 3166-3177.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 3166-3177
-
-
Greenberger, L.M.1
Annablr, T.2
Collins, K.I.3
Komm, B.S.4
Lyttle, C.R.5
Miller, C.P.6
Satyaswaroop, P.G.7
Zhang, Y.8
Frost, P.9
-
19
-
-
0035203757
-
Ethyl side-chain modifications in novel flexible anti-estrogens-design, synthesis and biological efficacy in assay against the MCF-7 breast tumor cell line
-
Meegan, M. J.; Hughes, R. B.; Lloyd, D. G.; Williams, D. C.; Zisterer, D. M. Ethyl side-chain modifications in novel flexible anti-estrogens-design, synthesis and biological efficacy in assay against the MCF-7 breast tumor cell line. Anti-Cancer Drug Des. 2001, 16, 57-69.
-
(2001)
Anti-Cancer Drug Des.
, vol.16
, pp. 57-69
-
-
Meegan, M.J.1
Hughes, R.B.2
Lloyd, D.G.3
Williams, D.C.4
Zisterer, D.M.5
-
20
-
-
0035904877
-
Activity of a tamoxifen-raloxifene hybrid ligand for estrogen receptors at an AP-1 site
-
Weatherman, R. V.; Carroll, D. C.; Scanlan, T. S. Activity of a tamoxifen-raloxifene hybrid ligand for estrogen receptors at an AP-1 site. Bioorg. Med. Chem. Lett. 2001, 11, 3129-3131.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 3129-3131
-
-
Weatherman, R.V.1
Carroll, D.C.2
Scanlan, T.S.3
-
21
-
-
0032581614
-
Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP 336156, a diaryltetrahydronaphthalene
-
Rosati, R. L.; Da Silva, J.; Cameron, K. O.; Thompson, D. D.; Ke, H. Z.; Toler, S. M.; Brown, T. A.; Pan, L. C.; Ebbinghaus, C. F.; Reinhold, A. R.; Elliott, N. C.; Newhouse, B. N.; Tjoa, C. M.; Sweetnam, P. M.; Cole, M. J.; Arriola, M. W.; Gauthier, J. W.; Crawford, D. T.; Nickerson, D. F.; Pine, C. M.; Qi, H.; Simmons, H. A.; Tkalcevic, G. T. Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP 336156, a diaryltetrahydronaphthalene. J. Med. Chem. 1998, 41, 2928-2931.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2928-2931
-
-
Rosati, R.L.1
Da Silva, J.2
Cameron, K.O.3
Thompson, D.D.4
Ke, H.Z.5
Toler, S.M.6
Brown, T.A.7
Pan, L.C.8
Ebbinghaus, C.F.9
Reinhold, A.R.10
Elliott, N.C.11
Newhouse, B.N.12
Tjoa, C.M.13
Sweetnam, P.M.14
Cole, M.J.15
Arriola, M.W.16
Gauthier, J.W.17
Crawford, D.T.18
Nickerson, D.F.19
Pine, C.M.20
Qi, H.21
Simmons, H.A.22
Tkalcevic, G.T.23
more..
-
22
-
-
0036132053
-
Synthesis and pharmacological evaluation of novel cis-3,4-diaryl- hydroxychromanes as high affinity partial agonists for the estrogen receptor
-
Bury, P. S.; Christiansen, L. B.; Jacobsen, P.; Jorgensen, A. S.; Kanstrup, A.; Naerum, L.; Bain, S.; Fledelius, C.; Gissel, B.; Hansen, B. S.; Korsgaard, N.; Thorpe, S. M.; Wasserman, K. Synthesis and pharmacological evaluation of novel cis-3,4-diaryl-hydroxychromanes as high affinity partial agonists for the estrogen receptor. Bioorg. Med. Chem. 2002, 10, 125-145.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 125-145
-
-
Bury, P.S.1
Christiansen, L.B.2
Jacobsen, P.3
Jorgensen, A.S.4
Kanstrup, A.5
Naerum, L.6
Bain, S.7
Fledelius, C.8
Gissel, B.9
Hansen, B.S.10
Korsgaard, N.11
Thorpe, S.M.12
Wasserman, K.13
-
23
-
-
0034989904
-
Control of the estrogen-like action of tamoxifen-estrogen receptor complex by the surface amino acid at position 351
-
Levenson, A. S.; MacGregor-Schafer, J. I.; Bentrm, D. J.; Pease, K. M.; Jordan, V. C. Control of the estrogen-like action of tamoxifen-estrogen receptor complex by the surface amino acid at position 351. J. Steroid Biochem. Mol. Biol. 2001, 76, 61-70.
-
(2001)
J. Steroid Biochem. Mol. Biol.
, vol.76
, pp. 61-70
-
-
Levenson, A.S.1
MacGregor-Schafer, J.I.2
Bentrm, D.J.3
Pease, K.M.4
Jordan, V.C.5
-
24
-
-
0035884114
-
Molecular classification of estrogens
-
Jordan, V. C.; MacGregor-Schafer, J.; Levenson, A. S.; Liu, H.; Pease, K. M.; Simons, L. A.; Zapf, J. W. Molecular classification of estrogens. Cancer Res. 2001, 61, 6619-6623.
-
(2001)
Cancer Res.
, vol.61
, pp. 6619-6623
-
-
Jordan, V.C.1
MacGregor-Schafer, J.2
Levenson, A.S.3
Liu, H.4
Pease, K.M.5
Simons, L.A.6
Zapf, J.W.7
-
25
-
-
0025945627
-
Structure-activity relationships of estrogenic ligands. Synthesis and evaluation of (17α,20E/Z)-21-halogenated-19-norpregna-1,3,5(10),20- tetraene-3,17β-diols
-
Napolitano, E.; Fiaschi, R.; Hanson, R. N. Structure-activity relationships of estrogenic ligands. Synthesis and evaluation of (17α,20E/Z)-21-halogenated-19-norpregna-1,3,5(10),20-tetraene-3, 17β-diols. J. Med. Chem. 1991, 34, 2754-2759.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2754-2759
-
-
Napolitano, E.1
Fiaschi, R.2
Hanson, R.N.3
-
26
-
-
0029891668
-
Synthesis and estrogen receptor binding of (17α,20E)- and (17α,20Z)-21-phenylthio- and phenylseleno-19-norpregna-1,3,5(10),20- tetraene-3,17β-diols
-
Napolitano, E.; Fiaschi, R.; Herman, L. W.; Hanson, R. N. Synthesis and estrogen receptor binding of (17α,20E)- and (17α,20Z)-21-phenylthio- and phenylseleno-19-norpregna-1,3,5(10),20-tetraene-3,17β-diols. Steroids 1996, 61, 384-387.
-
(1996)
Steroids
, vol.61
, pp. 384-387
-
-
Napolitano, E.1
Fiaschi, R.2
Herman, L.W.3
Hanson, R.N.4
-
27
-
-
0030474378
-
Stereochemical probes for the estrogen receptor: Synthesis and receptor binding of (17α,20E/Z)-21-phenyl-19-norpregna-1,3,5(10),20-tetraene-3, 17β-diols
-
Hanson, R. N.; Herman, L. W.; Fiaschi, R.; Napolitano, E. Stereochemical probes for the estrogen receptor: Synthesis and receptor binding of (17α,20E/Z)-21-phenyl-19-norpregna-1,3,5(10),20-tetraene-3,17β-diols. Steroids 1996, 61, 718-722.
-
(1996)
Steroids
, vol.61
, pp. 718-722
-
-
Hanson, R.N.1
Herman, L.W.2
Fiaschi, R.3
Napolitano, E.4
-
28
-
-
0031850313
-
Novel high affinity steroidal estrogenic ligands: Synthesis and receptor binding of 11β-vinyl-17α-E/Z-phenylselenovinyl estradiols
-
Hanson, R. N.; Napolitano, E.; Fiaschi, R. Novel high affinity steroidal estrogenic ligands: Synthesis and receptor binding of 11β-vinyl-17α- E/Z-phenylselenovinyl estradiols. Steroids 1998, 63, 479-483.
-
(1998)
Steroids
, vol.63
, pp. 479-483
-
-
Hanson, R.N.1
Napolitano, E.2
Fiaschi, R.3
-
29
-
-
0032547897
-
Synthesis and evaluation of 11β-substituted-21-chloro/iodo- (17α,20E/Z)-19-norpregna-1,3,5(10),20-tetraene-3,17β-diols: High affinity ligands for the estrogen receptor
-
Hanson, R. N.; Napolitano, E.; Fiaschi, R. Synthesis and evaluation of 11β-substituted-21-chloro/iodo-(17α,20E/Z)-19-norpregna-1,3,5(10), 20-tetraene-3,17β-diols: High affinity ligands for the estrogen receptor. J. Med. Chem. 1998, 41, 4686-4692.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4686-4692
-
-
Hanson, R.N.1
Napolitano, E.2
Fiaschi, R.3
-
30
-
-
0034735863
-
From ligand to response: Generating diversity in nuclear coregulator function
-
McKenna, N. J.; O'Malley, B. W. From ligand to response: generating diversity in nuclear coregulator function. J. Steroid Biochem. Mol. Biol. 2000, 74, 351-356.
-
(2000)
J. Steroid Biochem. Mol. Biol.
, vol.74
, pp. 351-356
-
-
McKenna, N.J.1
O'Malley, B.W.2
-
31
-
-
0035300412
-
Circumventing tamoxifen resistance in breast cancers using antiestrogens that induce unique conformational changes in the estrogen receptor
-
Connor, C. E.; Norris, J. D.; Broadwater, G.; Willson, T. M.; Gottardis, M. M.; Dewhirst, M. W.; McDonnell, D. P. Circumventing tamoxifen resistance in breast cancers using antiestrogens that induce unique conformational changes in the estrogen receptor. Cancer Res. 2001, 61, 2917-2922.
-
(2001)
Cancer Res.
, vol.61
, pp. 2917-2922
-
-
Connor, C.E.1
Norris, J.D.2
Broadwater, G.3
Willson, T.M.4
Gottardis, M.M.5
Dewhirst, M.W.6
McDonnell, D.P.7
-
32
-
-
0036327965
-
Identification and characterization of novel estrogen receptor-β-sparing antiprogestins
-
Sathya, G.; Jansen, M. S.; Nagel, S. C.; Cook, C. E.; McDonnell, D. P. Identification and characterization of novel estrogen receptor-β-sparing antiprogestins. Endocrinology 2002, 143, 3071-3082.
-
(2002)
Endocrinology
, vol.143
, pp. 3071-3082
-
-
Sathya, G.1
Jansen, M.S.2
Nagel, S.C.3
Cook, C.E.4
McDonnell, D.P.5
-
33
-
-
0035328727
-
Silencing and reactivation of the selective estrogen receptor modulator-estrogen receptor α complex
-
Liu, H.; Lee, E.-S.; De Los Reyes, A.; Zapf, J. W.; Jordan, V. C. Silencing and reactivation of the selective estrogen receptor modulator-estrogen receptor α complex. Cancer Res. 2001, 61, 3632-3639.
-
(2001)
Cancer Res.
, vol.61
, pp. 3632-3639
-
-
Liu, H.1
Lee, E.-S.2
De Los Reyes, A.3
Zapf, J.W.4
Jordan, V.C.5
-
34
-
-
0036682426
-
Gene expression profiles with activation of the estrogen receptor á-selective estrogen receptor modulator complex in breast cancer cells expressing wild-type estrogen receptor
-
Levenson, A. S.; Svoboda, K. M.; Pease, K. M.; Kaiser, S. A.; Chen, B.; Simons, L. A.; Jovanovic, B. D.; Dyck, P. A.; Jordan, V. C. Gene expression profiles with activation of the estrogen receptor á-selective estrogen receptor modulator complex in breast cancer cells expressing wild-type estrogen receptor. Cancer Res. 2002, 62, 4419-4426.
-
(2002)
Cancer Res.
, vol.62
, pp. 4419-4426
-
-
Levenson, A.S.1
Svoboda, K.M.2
Pease, K.M.3
Kaiser, S.A.4
Chen, B.5
Simons, L.A.6
Jovanovic, B.D.7
Dyck, P.A.8
Jordan, V.C.9
-
35
-
-
0037328806
-
Evaluation of 17a-(trifluoromethylphenyl)vinyl estradiols as novel estrogen receptor ligands
-
Hanson, R. N.; Lee, C. Y.; Friel, C. J.; DeSombre, E. R.; Hughes, A. Evaluation of 17a-(trifluoromethylphenyl)vinyl estradiols as novel estrogen receptor ligands. Steroids 2003, 68, 143-148.
-
(2003)
Steroids
, vol.68
, pp. 143-148
-
-
Hanson, R.N.1
Lee, C.Y.2
Friel, C.J.3
DeSombre, E.R.4
Hughes, A.5
-
36
-
-
0038798622
-
Synthesis and evaluation of (17α,20E)-21-(4-substituted-phenyl)-19- norpregna-1,3,5(10),20-tetraene-3,17/3-diols as probes for the estrogen receptor-α (ERα) hormone binding domain
-
Hanson, R. N.; Lee, C. Y.; Friel, C. J.; Dilis, R.; DeSombre, E. R.; Hughes, A. Synthesis and evaluation of (17α,20E)-21-(4-substituted-phenyl) -19-norpregna-1,3,5(10),20-tetraene-3,17/3-diols as probes for the estrogen receptor-α (ERα) hormone binding domain. J. Med. Chem. 2003, 46, 2865-2876.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2865-2876
-
-
Hanson, R.N.1
Lee, C.Y.2
Friel, C.J.3
Dilis, R.4
DeSombre, E.R.5
Hughes, A.6
-
37
-
-
0010043534
-
Synthesis and characterization and reactivity of 2-functionalized vinylstannanes
-
Lebl, T.; Holecek, J.; Dymal, M.; Steinborn, D. Synthesis and characterization and reactivity of 2-functionalized vinylstannanes. J. Organomet. Chem. 2001, 625, 86-94.
-
(2001)
J. Organomet. Chem.
, vol.625
, pp. 86-94
-
-
Lebl, T.1
Holecek, J.2
Dymal, M.3
Steinborn, D.4
-
38
-
-
0026458098
-
Preparation of Z-vinylstannanes via hydrozirconation of stannylacetylenes
-
Lipshutz, B. H.; Keil, R.; Barton, J. C. Preparation of Z-vinylstannanes via hydrozirconation of stannylacetylenes. Tetrahedron Lett. 1992, 33, 5861-5864.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 5861-5864
-
-
Lipshutz, B.H.1
Keil, R.2
Barton, J.C.3
-
39
-
-
0029058098
-
Molecular characterization by mass spectrometry of the human estrogen receptor ligand-binding domain expressed in Escherichia coli
-
Sielstad, D. A.; Carlson, K. E.; Katzenellenbogen, J. A.; Kushner, P. J.; Greene, G. L. Molecular characterization by mass spectrometry of the human estrogen receptor ligand-binding domain expressed in Escherichia coli. Mol. Endocrinol. 1993, 9, 647-658.
-
(1993)
Mol. Endocrinol.
, vol.9
, pp. 647-658
-
-
Sielstad, D.A.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
Kushner, P.J.4
Greene, G.L.5
-
40
-
-
0023924825
-
Estrogen receptor binding affinity and uterotrophic activity of triphenylhaloethylenes
-
DeSombre, E. R.; Mease, R. C.; Sanghavi, J.; Singh, T.; Seevers, R. H.; Hughes, A. Estrogen receptor binding affinity and uterotrophic activity of triphenylhaloethylenes. J. Steroid Biochem. 1988, 29, 583-590.
-
(1988)
J. Steroid Biochem.
, vol.29
, pp. 583-590
-
-
DeSombre, E.R.1
Mease, R.C.2
Sanghavi, J.3
Singh, T.4
Seevers, R.H.5
Hughes, A.6
-
41
-
-
0000814012
-
Receptor binding as a tool in the development of new bioactive steroids
-
Ariens, E. J., Ed.; Academic Press: New York
-
Raynaud, J. P.; Ojasoo, T.; Bouton, M. M.; Philibert, D. Receptor binding as a tool in the development of new bioactive steroids. In Drug Design; Ariens, E. J., Ed.; Academic Press: New York, 1979; Vol. VIII, pp 169-214.
-
(1979)
Drug Design
, vol.8
, pp. 169-214
-
-
Raynaud, J.P.1
Ojasoo, T.2
Bouton, M.M.3
Philibert, D.4
-
42
-
-
0034956939
-
Overexpression, purificiation and crystal structure of native ER alpha LBD
-
Eiler, S.; Gangloff, M.; Duclaud, S.; Moras, D.; Ruff, M. Overexpression, purificiation and crystal structure of native ER alpha LBD. Protein Expression Purif. 2001, 20, 165.
-
(2001)
Protein Expression Purif.
, vol.20
, pp. 165
-
-
Eiler, S.1
Gangloff, M.2
Duclaud, S.3
Moras, D.4
Ruff, M.5
-
43
-
-
0033549832
-
The first general method for Stille cross-couplings of aryl chlorides
-
Littke, A. F.; Fu, G. C. The first general method for Stille cross-couplings of aryl chlorides. Angew. Chem., Int. Ed. 1999, 38, 2411-2416.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 2411-2416
-
-
Littke, A.F.1
Fu, G.C.2
-
44
-
-
0037112673
-
Palladium-catalyzed coupling reactions of aryl chlorides
-
Littke, A. F.; Fu, G. C. Palladium-catalyzed coupling reactions of aryl chlorides. Angew. Chem., Int. Ed. 2002, 41, 4176-4211.
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4176-4211
-
-
Littke, A.F.1
Fu, G.C.2
-
45
-
-
0141963219
-
Full-length estrogen receptor α and its ligand-binding domain adopt different conformations upon ligand binding
-
Bapat, A. R.; Frail, D. E. Full-length estrogen receptor α and its ligand-binding domain adopt different conformations upon ligand binding. J. Steroid Biochem. Mol. Biol. 2003, 86, 143-149.
-
(2003)
J. Steroid Biochem. Mol. Biol.
, vol.86
, pp. 143-149
-
-
Bapat, A.R.1
Frail, D.E.2
-
46
-
-
0032554879
-
Three-dimensional models of estrogen receptor ligand binding domain complexes, based on related crystal structures and mutational and structure-activity relationships
-
Wurtz, J.-M.; Egner, U.; Heinrich, N.; Moras, D.; Mueller-Fahrnow, A. Three-dimensional models of estrogen receptor ligand binding domain complexes, based on related crystal structures and mutational and structure-activity relationships. J. Med. Chem. 1998, 41, 1803-1814.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1803-1814
-
-
Wurtz, J.-M.1
Egner, U.2
Heinrich, N.3
Moras, D.4
Mueller-Fahrnow, A.5
-
47
-
-
0033949276
-
Receptor-based 3-D QSAR analysis of estrogen receptor ligands-merging the accuracy of receptor-based alignments with the computational efficiency of ligand-based methods
-
Sippl, W. Receptor-based 3-D QSAR analysis of estrogen receptor ligands-merging the accuracy of receptor-based alignments with the computational efficiency of ligand-based methods. J. Comput.-Aided Mol. Des. 2000, 14, 559-572.
-
(2000)
J. Comput.-Aided Mol. Des.
, vol.14
, pp. 559-572
-
-
Sippl, W.1
-
48
-
-
0034793546
-
Different ligands-different receptor conformations: Modeling of the hERα-LBD in complexes with agonists and antagonists
-
Egner, U.; Heinrich, N.; Ruff, M.; Gangloff, M.; Mueller-Fahrnow, A.; Wurtz, J.-M. Different ligands-different receptor conformations: modeling of the hERα-LBD in complexes with agonists and antagonists. Med. Res. Rev. 2001, 21, 523-539.
-
(2001)
Med. Res. Rev.
, vol.21
, pp. 523-539
-
-
Egner, U.1
Heinrich, N.2
Ruff, M.3
Gangloff, M.4
Mueller-Fahrnow, A.5
Wurtz, J.-M.6
-
49
-
-
0242577782
-
CoMFA and docking study of novel estrogen receptor subtype selective ligands
-
Wolohan, P.; Reichert, D. E. CoMFA and docking study of novel estrogen receptor subtype selective ligands. J. Comput.-Aided Mol. Des. 2003, 17, 313-328.
-
(2003)
J. Comput.-Aided Mol. Des.
, vol.17
, pp. 313-328
-
-
Wolohan, P.1
Reichert, D.E.2
-
50
-
-
0038798604
-
Nuclear hormone receptor targeted virtual screening
-
Schipira, M.; Abagyan, R.; Totrov, M. Nuclear hormone receptor targeted virtual screening. J. Med. Chem. 2003, 46, 3045-3059.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3045-3059
-
-
Schipira, M.1
Abagyan, R.2
Totrov, M.3
-
51
-
-
0842304419
-
Prediction of ligand binding affinity and orientation of xenoestrogens to the estrogen receptor by molecular dynamics simulations and the linear interaction energy method
-
in press
-
van Lipzig, M. M. H.; ter Laak, A. M.; Jongejan, A.; Vermeulen, N. P. E.; Wamelink, M.; Geerke, D.; Meerman, J. H. N. Prediction of ligand binding affinity and orientation of xenoestrogens to the estrogen receptor by molecular dynamics simulations and the linear interaction energy method. J. Med. Chem., in press.
-
J. Med. Chem.
-
-
Van Lipzig, M.M.H.1
Ter Laak, A.M.2
Jongejan, A.3
Vermeulen, N.P.E.4
Wamelink, M.5
Geerke, D.6
Meerman, J.H.N.7
-
52
-
-
0035203984
-
Homology modeling of the estrogen receptor subtype β (ERβ) and calculation of ligand binding affinities
-
DeLisle, R. K.; Yu, S.-J.; Nair A. C.; Welsh, W. J. Homology modeling of the estrogen receptor subtype β (ERβ) and calculation of ligand binding affinities. J. Mol. Graphics Modell. 2001, 20, 155-167.
-
(2001)
J. Mol. Graphics Modell.
, vol.20
, pp. 155-167
-
-
DeLisle, R.K.1
Yu, S.-J.2
Nair, A.C.3
Welsh, W.J.4
-
54
-
-
21244506263
-
Structure-function relationships in the estrogen receptors and the characterization of novel selective estrogen receptor modulators with unique pharmacological profiles
-
submitted
-
Katzenellenbogen, B. S.; Sun, J.; Harrington, W. R.; Kraichely, D. M.; Ganessunker, D.; Katzenellenbogen, J. A. Structure-function relationships in the estrogen receptors and the characterization of novel selective estrogen receptor modulators with unique pharmacological profiles. Ann. N. Y. Acad. Sci., submitted.
-
Ann. N. Y. Acad. Sci.
-
-
Katzenellenbogen, B.S.1
Sun, J.2
Harrington, W.R.3
Kraichely, D.M.4
Ganessunker, D.5
Katzenellenbogen, J.A.6
-
56
-
-
0032567678
-
A computational study of the resistance of HIV-1 aspartic protease to inhibitors ABT-538 and VX-478 and design of new analogues
-
Nair, A. C.; Miertus, S.; Tossi, A.; Romeo, D. A computational study of the resistance of HIV-1 aspartic protease to inhibitors ABT-538 and VX-478 and design of new analogues. Biochem. Biophys. Res. Commun. 1998, 242, 545-551.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.242
, pp. 545-551
-
-
Nair, A.C.1
Miertus, S.2
Tossi, A.3
Romeo, D.4
|