-
1
-
-
0027225486
-
Expression cloning and characterization of human 17 beta-hydroxysteroid dehydrogenase type 2, a microsomal enzyme possessing 20 alpha-hydroxysteroid dehydrogenase activity
-
Wu, L.; Einstein, M.; Geissler, W. M.; Chan, H. K.; Elliston, K. O.; Andersson, S. Expression cloning and characterization of human 17 beta-hydroxysteroid dehydrogenase type 2, a microsomal enzyme possessing 20 alpha-hydroxysteroid dehydrogenase activity J. Biol. Chem. 1993, 268, 12964-12969
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 12964-12969
-
-
Wu, L.1
Einstein, M.2
Geissler, W.M.3
Chan, H.K.4
Elliston, K.O.5
Andersson, S.6
-
2
-
-
0033623260
-
3β-Hydroxysteroid dehydrogenase/Δ5→4-isomerase activity associated with the human 17β-hydroxysteroid dehydrogenase type 2 isoform
-
Suzuki, T.; Sasano, H.; Andersson, S.; Mason, J. I. 3β- Hydroxysteroid dehydrogenase/Δ5→4-isomerase activity associated with the human 17β-hydroxysteroid dehydrogenase type 2 isoform J. Clin. Endocrinol. Metab. 2000, 85, 3669-3672
-
(2000)
J. Clin. Endocrinol. Metab.
, vol.85
, pp. 3669-3672
-
-
Suzuki, T.1
Sasano, H.2
Andersson, S.3
Mason, J.I.4
-
3
-
-
0036359415
-
Tissue culture models for studies of hormone and vitamin action in bone cells
-
Bodine, P. V. N.; Komm, B. S. Tissue culture models for studies of hormone and vitamin action in bone cells Vitam. Horm. 2002, 64, 101-151
-
(2002)
Vitam. Horm.
, vol.64
, pp. 101-151
-
-
Bodine, P.V.N.1
Komm, B.S.2
-
4
-
-
42649091112
-
Androgens and bone
-
Vanderschueren, D.; Gaytant, J.; Boonen, S.; Venken, K. Androgens and bone Curr. Opin. Endocrinol., Diabetes Obes. 2008, 15, 250-254
-
(2008)
Curr. Opin. Endocrinol., Diabetes Obes.
, vol.15
, pp. 250-254
-
-
Vanderschueren, D.1
Gaytant, J.2
Boonen, S.3
Venken, K.4
-
5
-
-
2942736921
-
Androgens and bone
-
Vanderschueren, D.; Vandenput, L.; Boonen, S.; Lindberg, M. K.; Bouillon, R.; Ohlsson, C. Androgens and bone Endocr. Rev. 2004, 25, 389-425
-
(2004)
Endocr. Rev.
, vol.25
, pp. 389-425
-
-
Vanderschueren, D.1
Vandenput, L.2
Boonen, S.3
Lindberg, M.K.4
Bouillon, R.5
Ohlsson, C.6
-
6
-
-
0034063389
-
Mortality and institutionalization following hip fracture
-
Cree, M.; Soskolne, C. L.; Belseck, E.; Hornig, J.; McElhaney, J. E.; Brant, R.; Suarez-Almazor, M. Mortality and institutionalization following hip fracture J. Am. Geriatr. Soc. 2000, 48, 283-288
-
(2000)
J. Am. Geriatr. Soc.
, vol.48
, pp. 283-288
-
-
Cree, M.1
Soskolne, C.L.2
Belseck, E.3
Hornig, J.4
McElhaney, J.E.5
Brant, R.6
Suarez-Almazor, M.7
-
7
-
-
33646404613
-
Effects of third-generation aromatase inhibitors on bone
-
McCloskey, E. Effects of third-generation aromatase inhibitors on bone Eur. J. Cancer 2006, 42, 1044-1051
-
(2006)
Eur. J. Cancer
, vol.42
, pp. 1044-1051
-
-
McCloskey, E.1
-
8
-
-
0036185685
-
Antiresorptive treatment of postmenopausal osteoporosis: Comparison of study designs and outcomes in large clinical trials with fracture as an endpoint
-
Marcus, R.; Wong, M.; Heath, H., 3rd; Stock, J. L. Antiresorptive treatment of postmenopausal osteoporosis: comparison of study designs and outcomes in large clinical trials with fracture as an endpoint Endocr. Rev. 2002, 23, 16-37
-
(2002)
Endocr. Rev.
, vol.23
, pp. 16-37
-
-
Marcus, R.1
Wong, M.2
Heath III, H.3
Stock, J.L.4
-
9
-
-
0034739277
-
Alendronate for the treatment of osteoporosis in men
-
Orwoll, E.; Ettinger, M.; Weiss, S.; Miller, P.; Kendler, D.; Graham, J.; Adami, S.; Weber, K.; Lorenc, R.; Pietschmann, P.; Vandormael, K.; Lombardi, A. Alendronate for the treatment of osteoporosis in men N. Engl. J. Med. 2000, 343, 604-610
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 604-610
-
-
Orwoll, E.1
Ettinger, M.2
Weiss, S.3
Miller, P.4
Kendler, D.5
Graham, J.6
Adami, S.7
Weber, K.8
Lorenc, R.9
Pietschmann, P.10
Vandormael, K.11
Lombardi, A.12
-
10
-
-
33644616548
-
Efficacy of risedronate in men with primary and secondary osteoporosis: Results of a 1-year study
-
Ringe, J. D.; Faber, H.; Farahmand, P.; Dorst, A. Efficacy of risedronate in men with primary and secondary osteoporosis: results of a 1-year study Rheumatol. Int. 2006, 26, 427-31
-
(2006)
Rheumatol. Int.
, vol.26
, pp. 427-31
-
-
Ringe, J.D.1
Faber, H.2
Farahmand, P.3
Dorst, A.4
-
11
-
-
0033581212
-
Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: Results from a 3-year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators
-
Ettinger, B.; Black, D. M.; Mitlak, B. H.; Knickerbocker, R. K.; Nickelsen, T.; Genant, H. K.; Christiansen, C.; Delmas, P. D.; Zanchetta, J. R.; Stakkestad, J.; Glüer, C. C.; Krueger, K.; Cohen, F. J.; Eckert, S.; Ensrud, K. E.; Avioli, L. V.; Lips, P.; Cummings, S. R. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators JAMA, J. Am. Med. Assoc. 1999, 282, 637-645
-
(1999)
JAMA, J. Am. Med. Assoc.
, vol.282
, pp. 637-645
-
-
Ettinger, B.1
Black, D.M.2
Mitlak, B.H.3
Knickerbocker, R.K.4
Nickelsen, T.5
Genant, H.K.6
Christiansen, C.7
Delmas, P.D.8
Zanchetta, J.R.9
Stakkestad, J.10
Glüer, C.C.11
Krueger, K.12
Cohen, F.J.13
Eckert, S.14
Ensrud, K.E.15
Avioli, L.V.16
Lips, P.17
Cummings, S.R.18
-
12
-
-
0027360512
-
The effect of postmenopausal estrogen therapy on bone density in elderly women
-
Felson, D. T.; Zhang, Y.; Hannan, M. T.; Kiel, D. P.; Wilson, P. W.; Anderson, J. J. The effect of postmenopausal estrogen therapy on bone density in elderly women N. Engl. J. Med. 1993, 329, 1141-1146
-
(1993)
N. Engl. J. Med.
, vol.329
, pp. 1141-1146
-
-
Felson, D.T.1
Zhang, Y.2
Hannan, M.T.3
Kiel, D.P.4
Wilson, P.W.5
Anderson, J.J.6
-
13
-
-
0037070255
-
Hormone replacement therapy in relation to breast cancer
-
Chen, C.-L.; Weiss, N. S.; Newcomb, P.; Barlow, W.; White, E. Hormone replacement therapy in relation to breast cancer JAMA, J. Am. Med. Assoc. 2002, 287, 734-741
-
(2002)
JAMA, J. Am. Med. Assoc.
, vol.287
, pp. 734-741
-
-
Chen, C.-L.1
Weiss, N.S.2
Newcomb, P.3
Barlow, W.4
White, E.5
-
14
-
-
0031058448
-
Risk of endometrial cancer in relation to use of oestrogen combined with cyclic progestagen therapy in postmenopausal women
-
Beresford, S. A.; Weiss, N. S.; Voigt, L. F.; McKnight, B. Risk of endometrial cancer in relation to use of oestrogen combined with cyclic progestagen therapy in postmenopausal women Lancet 1997, 349, 458-61
-
(1997)
Lancet
, vol.349
, pp. 458-61
-
-
Beresford, S.A.1
Weiss, N.S.2
Voigt, L.F.3
McKnight, B.4
-
15
-
-
0028809308
-
Hormone replacement therapy and endometrial cancer risk: A meta-analysis
-
Grady, D.; Gebretsadik, T.; Kerlikowske, K.; Ernster, V.; Petitti, D. Hormone replacement therapy and endometrial cancer risk: a meta-analysis Obstet. Gynecol. 1995, 85, 304-313
-
(1995)
Obstet. Gynecol.
, vol.85
, pp. 304-313
-
-
Grady, D.1
Gebretsadik, T.2
Kerlikowske, K.3
Ernster, V.4
Petitti, D.5
-
16
-
-
0032176301
-
17Beta-hydroxysteroid dehydrogenases in human bone cells
-
Dong, Y.; Qiu, Q. Q.; Debear, J.; Lathrop, W. F.; Bertolini, D. R.; Tamburini, P. P. 17Beta-hydroxysteroid dehydrogenases in human bone cells J. Bone Miner. Res. 1998, 13, 1539-1546
-
(1998)
J. Bone Miner. Res.
, vol.13
, pp. 1539-1546
-
-
Dong, Y.1
Qiu, Q.Q.2
Debear, J.3
Lathrop, W.F.4
Bertolini, D.R.5
Tamburini, P.P.6
-
17
-
-
0035931120
-
Distribution of 17beta-hydroxysteroid dehydrogenases in human osteoblast-like cells
-
Feix, M.; Wolf, L.; Schweikert, H. U. Distribution of 17beta-hydroxysteroid dehydrogenases in human osteoblast-like cells Mol. Cell. Endocrinol. 2001, 171, 163-164
-
(2001)
Mol. Cell. Endocrinol.
, vol.171
, pp. 163-164
-
-
Feix, M.1
Wolf, L.2
Schweikert, H.U.3
-
18
-
-
0031801531
-
Characterization of aromatase and 17 beta-hydroxysteroid dehydrogenase expression in rat osteoblastic cells
-
Eyre, L. J.; Bland, R.; Bujalska, I. J.; Sheppard, M. C.; Stewart, P. M.; Hewison, M. Characterization of aromatase and 17 beta-hydroxysteroid dehydrogenase expression in rat osteoblastic cells J. Bone Miner. Res. 1998, 13, 996-1004
-
(1998)
J. Bone Miner. Res.
, vol.13
, pp. 996-1004
-
-
Eyre, L.J.1
Bland, R.2
Bujalska, I.J.3
Sheppard, M.C.4
Stewart, P.M.5
Hewison, M.6
-
19
-
-
13144277564
-
Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
-
van Grunsven, E G; van Berkel, E.; Ijlst, L.; Vreken, P.; de Klerk, J. B.; Adamski, J.; Lemonde, H.; Clayton, P. T.; Cuebas, D. A.; Wanders, R. J. Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 2128-2133
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 2128-2133
-
-
Van Grunsven, E.G.1
Van Berkel, E.2
Ijlst, L.3
Vreken, P.4
De Klerk, J.B.5
Adamski, J.6
Lemonde, H.7
Clayton, P.T.8
Cuebas, D.A.9
Wanders, R.J.10
-
20
-
-
0021884506
-
17 beta-Hydroxysteroid and 20 alpha-hydroxysteroid dehydrogenase activities of human placental microsomes: Kinetic evidence for two enzymes differing in substrate specificity
-
Blomquist, C. H.; Lindemann, N. J.; Hakanson, E. Y. 17 beta-Hydroxysteroid and 20 alpha-hydroxysteroid dehydrogenase activities of human placental microsomes: kinetic evidence for two enzymes differing in substrate specificity Arch. Biochem. Biophys. 1985, 239, 206-215
-
(1985)
Arch. Biochem. Biophys.
, vol.239
, pp. 206-215
-
-
Blomquist, C.H.1
Lindemann, N.J.2
Hakanson, E.Y.3
-
21
-
-
3042574084
-
Inhibition of type 2 17β-hydroxysteroid dehydrogenase by estradiol derivatives bearing a lactone on the D-ring: Structure-activity relationships
-
Bydal, P.; Auger, S.; Poirier, D. Inhibition of type 2 17β-hydroxysteroid dehydrogenase by estradiol derivatives bearing a lactone on the D-ring: structure-activity relationships Steroids 2004, 69, 325-342
-
(2004)
Steroids
, vol.69
, pp. 325-342
-
-
Bydal, P.1
Auger, S.2
Poirier, D.3
-
22
-
-
0035931325
-
Inhibitors of type II 17beta-hydroxysteroid dehydrogenase
-
Poirier, D.; Bydal, P.; Tremblay, M. R.; Sam, K. M.; Luu-The, V. Inhibitors of type II 17beta-hydroxysteroid dehydrogenase Mol. Cell. Endocrinol. 2001, 171, 119-128
-
(2001)
Mol. Cell. Endocrinol.
, vol.171
, pp. 119-128
-
-
Poirier, D.1
Bydal, P.2
Tremblay, M.R.3
Sam, K.M.4
Luu-The, V.5
-
23
-
-
0028822046
-
Steroidal spiro-gamma-lactones that inhibit 17 beta-hydroxysteroid dehydrogenase activity in human placental microsomes
-
Sam, K. M.; Auger, S.; Luu-The, V.; Poirier, D. Steroidal spiro-gamma-lactones that inhibit 17 beta-hydroxysteroid dehydrogenase activity in human placental microsomes J. Med. Chem. 1995, 38, 4518-4528
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4518-4528
-
-
Sam, K.M.1
Auger, S.2
Luu-The, V.3
Poirier, D.4
-
24
-
-
0033007678
-
Spironolactone-related inhibitors of type II 17beta-hydroxysteroid dehydrogenase: Chemical synthesis, receptor binding affinities, and proliferative/antiproliferative activities
-
Tremblay, M. R.; Luu-The, V.; Leblanc, G.; Noël, P.; Breton, E.; Labrie, F.; Poirier, D. Spironolactone-related inhibitors of type II 17beta-hydroxysteroid dehydrogenase: chemical synthesis, receptor binding affinities, and proliferative/antiproliferative activities Bioorg. Med. Chem. 1999, 7, 1013-1023
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 1013-1023
-
-
Tremblay, M.R.1
Luu-The, V.2
Leblanc, G.3
Noël, P.4
Breton, E.5
Labrie, F.6
Poirier, D.7
-
25
-
-
13444310940
-
4,5-Disubstituted cis-pyrrolidinones as inhibitors of 17β-hydroxysteroid dehydrogenase II. Part 1: Synthetic approach
-
Cook, J. H.; Barzya, J.; Brennan, C.; Lowe, D.; Wang, Y.; Redman, A.; Scott, W. J.; Wood, J. E. 4,5-Disubstituted cis-pyrrolidinones as inhibitors of 17β-hydroxysteroid dehydrogenase II. Part 1: Synthetic approach Tetrahedron Lett. 2005, 46, 1525-1528
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1525-1528
-
-
Cook, J.H.1
Barzya, J.2
Brennan, C.3
Lowe, D.4
Wang, Y.5
Redman, A.6
Scott, W.J.7
Wood, J.E.8
-
26
-
-
19944363836
-
4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 2. SAR
-
Gunn, D.; Akuche, C.; Baryza, J.; Blue, M.-L.; Brennan, C.; Campbell, A.-M.; Choi, S.; Cook, J.; Conrad, P.; Dixon, B.; Dumas, J.; Ehrlich, P.; Gane, T.; Joe, T.; Johnson, J.; Jordan, J.; Kramss, R.; Liu, P.; Levy, J.; Lowe, D.; McAlexander, I.; Natero, R.; Redman, A. M.; Scott, W.; Seng, T.; Sibley, R.; Wang, M.; Wang, Y.; Wood, J.; Zhang, Z. 4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 2. SAR Bioorg. Med. Chem. Lett. 2005, 15, 3053-3057
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 3053-3057
-
-
Gunn, D.1
Akuche, C.2
Baryza, J.3
Blue, M.-L.4
Brennan, C.5
Campbell, A.-M.6
Choi, S.7
Cook, J.8
Conrad, P.9
Dixon, B.10
Dumas, J.11
Ehrlich, P.12
Gane, T.13
Joe, T.14
Johnson, J.15
Jordan, J.16
Kramss, R.17
Liu, P.18
Levy, J.19
Lowe, D.20
McAlexander, I.21
Natero, R.22
Redman, A.M.23
Scott, W.24
Seng, T.25
Sibley, R.26
Wang, M.27
Wang, Y.28
Wood, J.29
Zhang, Z.30
more..
-
27
-
-
33746843579
-
4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 3. Identification of lead candidate
-
Wood, J.; Bagi, C. M.; Akuche, C.; Bacchiocchi, A.; Baryza, J.; Blue, M.-L.; Brennan, C.; Campbell, A.-M.; Choi, S.; Cook, J. H.; Conrad, P.; Dixon, B. R.; Ehrlich, P. P.; Gane, T.; Gunn, D.; Joe, T.; Johnson, J. S.; Jordan, J.; Kramss, R.; Liu, P.; Levy, J.; Lowe, D. B.; McAlexander, I.; Natero, R.; Redman, A. M.; Scott, W. J.; Town, C.; Wang, M.; Wang, Y.; Zhang, Z. 4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 3. Identification of lead candidate Bioorg. Med. Chem. Lett. 2006, 16, 4965-4968
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 4965-4968
-
-
Wood, J.1
Bagi, C.M.2
Akuche, C.3
Bacchiocchi, A.4
Baryza, J.5
Blue, M.-L.6
Brennan, C.7
Campbell, A.-M.8
Choi, S.9
Cook, J.H.10
Conrad, P.11
Dixon, B.R.12
Ehrlich, P.P.13
Gane, T.14
Gunn, D.15
Joe, T.16
Johnson, J.S.17
Jordan, J.18
Kramss, R.19
Liu, P.20
Levy, J.21
Lowe, D.B.22
McAlexander, I.23
Natero, R.24
Redman, A.M.25
Scott, W.J.26
Town, C.27
Wang, M.28
Wang, Y.29
Zhang, Z.30
more..
-
28
-
-
78651480234
-
17β-HSD2 inhibitors for the treatment of osteoporosis: Identification of a promising scaffold
-
Wetzel, M.; Marchais-Oberwinkler, S.; Hartmann, R. W. 17β-HSD2 inhibitors for the treatment of osteoporosis: identification of a promising scaffold Bioorg. Med. Chem. 2011, 19, 807-815
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 807-815
-
-
Wetzel, M.1
Marchais-Oberwinkler, S.2
Hartmann, R.W.3
-
29
-
-
80455140547
-
Introduction of an electron withdrawing group on the hydroxyphenylnaphthol scaffold improves the potency of 17β-hydroxysteroid dehydrogenase type 2 (17β-HSD2) inhibitors
-
Wetzel, M.; Marchais-Oberwinkler, S.; Perspicace, E.; Möller, G.; Adamski, J.; Hartmann, R. W. Introduction of an electron withdrawing group on the hydroxyphenylnaphthol scaffold improves the potency of 17β- hydroxysteroid dehydrogenase type 2 (17β-HSD2) inhibitors J. Med. Chem. 2011, 54, 7547-7557
-
(2011)
J. Med. Chem.
, vol.54
, pp. 7547-7557
-
-
Wetzel, M.1
Marchais-Oberwinkler, S.2
Perspicace, E.3
Möller, G.4
Adamski, J.5
Hartmann, R.W.6
-
30
-
-
84855799481
-
Discovery of a new class of bicyclic substituted hydroxyphenylmethanones as 17β-hydroxysteroid dehydrogenase type 2 (17β-HSD2) inhibitors for the treatment of osteoporosis
-
Wetzel, M.; Gargano, E. M.; Hinsberger, S.; Marchais-Oberwinkler, S.; Hartmann, R. W. Discovery of a new class of bicyclic substituted hydroxyphenylmethanones as 17β-hydroxysteroid dehydrogenase type 2 (17β-HSD2) inhibitors for the treatment of osteoporosis Eur. J. Med. Chem. 2012, 47, 1-17
-
(2012)
Eur. J. Med. Chem.
, vol.47
, pp. 1-17
-
-
Wetzel, M.1
Gargano, E.M.2
Hinsberger, S.3
Marchais-Oberwinkler, S.4
Hartmann, R.W.5
-
31
-
-
84864575078
-
Synthesis and biological evaluation of phenyl substituted 1 H -1,2,4-triazoles as non-steroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 2
-
Al-Soud, Y. A.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Synthesis and biological evaluation of phenyl substituted 1 H -1,2,4-triazoles as non-steroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 2 Arch. Pharm. 2012, 345, 610-621
-
(2012)
Arch. Pharm.
, vol.345
, pp. 610-621
-
-
Al-Soud, Y.A.1
Marchais-Oberwinkler, S.2
Frotscher, M.3
Hartmann, R.W.4
-
32
-
-
80955166115
-
Triazole ring-opening leads to the discovery of potent nonsteroidal 17β-hydroxysteroid dehydrogenase type 2 inhibitors
-
Xu, K.; Al-Soud, Y. A.; Wetzel, M.; Hartmann, R. W.; Marchais- Oberwinkler, S. Triazole ring-opening leads to the discovery of potent nonsteroidal 17β-hydroxysteroid dehydrogenase type 2 inhibitors Eur. J. Med. Chem. 2011, 46, 5978-5990
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 5978-5990
-
-
Xu, K.1
Al-Soud, Y.A.2
Wetzel, M.3
Hartmann, R.W.4
Marchais-Oberwinkler, S.5
-
33
-
-
56749178091
-
Effect of 17beta-hydroxysteroid dehydrogenase type 2 inhibitor on bone strength in ovariectomized cynomolgus monkeys
-
Bagi, C. M.; Wood, J.; Wilkie, D.; Dixon, B. Effect of 17beta-hydroxysteroid dehydrogenase type 2 inhibitor on bone strength in ovariectomized cynomolgus monkeys J. Musculoskeletal Neuronal Interact. 2008, 8, 267-280
-
(2008)
J. Musculoskeletal Neuronal Interact.
, vol.8
, pp. 267-280
-
-
Bagi, C.M.1
Wood, J.2
Wilkie, D.3
Dixon, B.4
-
34
-
-
41849117998
-
Design, synthesis, and biological evaluation of (hydroxyphenyl) naphthalene and -quinoline derivatives: Potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) for the treatment of estrogen-dependent diseases
-
Frotscher, M.; Ziegler, E.; Marchais-Oberwinkler, S.; Kruchten, P.; Neugebauer, A.; Fetzer, L.; Scherer, C.; Müller-Vieira, U.; Messinger, J.; Thole, H.; Hartmann, R. W. Design, synthesis, and biological evaluation of (hydroxyphenyl)naphthalene and -quinoline derivatives: potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) for the treatment of estrogen-dependent diseases J. Med. Chem. 2008, 51, 2158-2169
-
(2008)
J. Med. Chem.
, vol.51
, pp. 2158-2169
-
-
Frotscher, M.1
Ziegler, E.2
Marchais-Oberwinkler, S.3
Kruchten, P.4
Neugebauer, A.5
Fetzer, L.6
Scherer, C.7
Müller-Vieira, U.8
Messinger, J.9
Thole, H.10
Hartmann, R.W.11
-
35
-
-
49449087479
-
Substituted 6-phenyl-2-naphthols. Potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1): Design, synthesis, biological evaluation, and pharmacokinetics
-
Marchais-Oberwinkler, S.; Kruchten, P.; Frotscher, M.; Ziegler, E.; Neugebauer, A.; Bhoga, U.; Bey, E.; Müller-Vieira, U.; Messinger, J.; Thole, H.; Hartmann, R. W. Substituted 6-phenyl-2-naphthols. Potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1): design, synthesis, biological evaluation, and pharmacokinetics J. Med. Chem. 2008, 51, 4685-4698
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4685-4698
-
-
Marchais-Oberwinkler, S.1
Kruchten, P.2
Frotscher, M.3
Ziegler, E.4
Neugebauer, A.5
Bhoga, U.6
Bey, E.7
Müller-Vieira, U.8
Messinger, J.9
Thole, H.10
Hartmann, R.W.11
-
36
-
-
78751651034
-
New drug-like hydroxyphenylnaphthol steroidomimetics as potent and selective 17β-hydroxysteroid dehydrogenase type 1 inhibitors for the treatment of estrogen-dependent diseases
-
Marchais-Oberwinkler, S.; Wetzel, M.; Ziegler, E.; Kruchten, P.; Werth, R.; Henn, C.; Hartmann, R. W.; Frotscher, M. New drug-like hydroxyphenylnaphthol steroidomimetics as potent and selective 17β-hydroxysteroid dehydrogenase type 1 inhibitors for the treatment of estrogen-dependent diseases J. Med. Chem. 2011, 54, 534-547
-
(2011)
J. Med. Chem.
, vol.54
, pp. 534-547
-
-
Marchais-Oberwinkler, S.1
Wetzel, M.2
Ziegler, E.3
Kruchten, P.4
Werth, R.5
Henn, C.6
Hartmann, R.W.7
Frotscher, M.8
-
37
-
-
44649139243
-
Design, synthesis and biological evaluation of bis(hydroxyphenyl) azoles as potent and selective non-steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) for the treatment of estrogen-dependent diseases
-
Bey, E.; Marchais-Oberwinkler, S.; Kruchten, P.; Frotscher, M.; Werth, R.; Oster, A.; Algül, O.; Neugebauer, A.; Hartmann, R. W. Design, synthesis and biological evaluation of bis(hydroxyphenyl) azoles as potent and selective non-steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) for the treatment of estrogen-dependent diseases Bioorg. Med. Chem. 2008, 16, 6423-6435
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 6423-6435
-
-
Bey, E.1
Marchais-Oberwinkler, S.2
Kruchten, P.3
Frotscher, M.4
Werth, R.5
Oster, A.6
Algül, O.7
Neugebauer, A.8
Hartmann, R.W.9
-
38
-
-
56249114885
-
Design, synthesis, biological evaluation and pharmacokinetics of bis(hydroxyphenyl) substituted azoles, thiophenes, benzenes, and aza-benzenes as potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1)
-
Bey, E.; Marchais-Oberwinkler, S.; Werth, R.; Negri, M.; Al-Soud, Y. A.; Kruchten, P.; Oster, A.; Frotscher, M.; Birk, B.; Hartmann, R. W. Design, synthesis, biological evaluation and pharmacokinetics of bis(hydroxyphenyl) substituted azoles, thiophenes, benzenes, and aza-benzenes as potent and selective nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) J. Med. Chem. 2008, 51, 6725-6739
-
(2008)
J. Med. Chem.
, vol.51
, pp. 6725-6739
-
-
Bey, E.1
Marchais-Oberwinkler, S.2
Werth, R.3
Negri, M.4
Al-Soud, Y.A.5
Kruchten, P.6
Oster, A.7
Frotscher, M.8
Birk, B.9
Hartmann, R.W.10
-
39
-
-
71049173249
-
New insights into the SAR and binding modes of bis(hydroxyphenyl) thiophenes and -benzenes: Influence of additional substituents on 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitory activity and selectivity
-
Bey, E.; Marchais-Oberwinkler, S.; Negri, M.; Kruchten, P.; Oster, A.; Klein, T.; Spadaro, A.; Werth, R.; Frotscher, M.; Birk, B.; Hartmann, R. W. New insights into the SAR and binding modes of bis(hydroxyphenyl)thiophenes and -benzenes: influence of additional substituents on 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitory activity and selectivity J. Med. Chem. 2009, 52, 6724-6743
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6724-6743
-
-
Bey, E.1
Marchais-Oberwinkler, S.2
Negri, M.3
Kruchten, P.4
Oster, A.5
Klein, T.6
Spadaro, A.7
Werth, R.8
Frotscher, M.9
Birk, B.10
Hartmann, R.W.11
-
40
-
-
77953131205
-
Novel estrone mimetics with high 17beta-HSD1 inhibitory activity
-
Oster, A.; Klein, T.; Werth, R.; Kruchten, P.; Bey, E.; Negri, M.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Novel estrone mimetics with high 17beta-HSD1 inhibitory activity Bioorg. Med. Chem. 2010, 18, 3494-3505
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3494-3505
-
-
Oster, A.1
Klein, T.2
Werth, R.3
Kruchten, P.4
Bey, E.5
Negri, M.6
Marchais-Oberwinkler, S.7
Frotscher, M.8
Hartmann, R.W.9
-
41
-
-
78649513552
-
Bicyclic substituted hydroxyphenylmethanones as novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) for the treatment of estrogen-dependent diseases
-
Oster, A.; Hinsberger, S.; Werth, R.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Bicyclic substituted hydroxyphenylmethanones as novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) for the treatment of estrogen-dependent diseases J. Med. Chem. 2010, 53, 8176-8186
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8176-8186
-
-
Oster, A.1
Hinsberger, S.2
Werth, R.3
Marchais-Oberwinkler, S.4
Frotscher, M.5
Hartmann, R.W.6
-
42
-
-
79952092998
-
Bicyclic substituted hydroxyphenylmethanone type inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17 β-HSD1): The role of the bicyclic moiety
-
Oster, A.; Klein, T.; Henn, C.; Werth, R.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Bicyclic substituted hydroxyphenylmethanone type inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17 β-HSD1): the role of the bicyclic moiety ChemMedChem 2011, 6, 476-487
-
(2011)
ChemMedChem
, vol.6
, pp. 476-487
-
-
Oster, A.1
Klein, T.2
Henn, C.3
Werth, R.4
Marchais-Oberwinkler, S.5
Frotscher, M.6
Hartmann, R.W.7
-
43
-
-
84855398790
-
Hydroxybenzothiazoles as new nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1)
-
Spadaro, A.; Negri, M.; Marchais-Oberwinkler, S.; Bey, E.; Frotscher, M. Hydroxybenzothiazoles as new nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) PLoS One 2012, 7, e29252
-
(2012)
PLoS One
, vol.7
, pp. 29252
-
-
Spadaro, A.1
Negri, M.2
Marchais-Oberwinkler, S.3
Bey, E.4
Frotscher, M.5
-
44
-
-
84858032721
-
Optimization of hydroxybenzothiazoles as novel potent and selective inhibitors of 17β-HSD1
-
Spadaro, A.; Frotscher, M.; Hartmann, R. W. Optimization of hydroxybenzothiazoles as novel potent and selective inhibitors of 17β-HSD1 J. Med. Chem. 2012, 55, 2469-2473
-
(2012)
J. Med. Chem.
, vol.55
, pp. 2469-2473
-
-
Spadaro, A.1
Frotscher, M.2
Hartmann, R.W.3
-
45
-
-
84859791222
-
Lead optimization of 17β-HSD1 inhibitors of the (hydroxyphenyl) naphthol sulfonamide type for the treatment of endometriosis
-
Henn, C.; Einspanier, A.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Lead optimization of 17β-HSD1 inhibitors of the (hydroxyphenyl)naphthol sulfonamide type for the treatment of endometriosis J. Med. Chem. 2012, 55, 3307-3318
-
(2012)
J. Med. Chem.
, vol.55
, pp. 3307-3318
-
-
Henn, C.1
Einspanier, A.2
Marchais-Oberwinkler, S.3
Frotscher, M.4
Hartmann, R.W.5
-
46
-
-
0036831679
-
A concerted, rational design of type 1 17beta-hydroxysteroid dehydrogenase inhibitors: Estradiol-adenosine hybrids with high affinity
-
Qiu, W.; Campbell, R. L.; Gangloff, A.; Dupuis, P.; Boivin, R. P.; Tremblay, M. R.; Poirier, D.; Lin, S.-X. A concerted, rational design of type 1 17beta-hydroxysteroid dehydrogenase inhibitors: estradiol-adenosine hybrids with high affinity FASEB J. 2002, 16, 1829-1831
-
(2002)
FASEB J.
, vol.16
, pp. 1829-1831
-
-
Qiu, W.1
Campbell, R.L.2
Gangloff, A.3
Dupuis, P.4
Boivin, R.P.5
Tremblay, M.R.6
Poirier, D.7
Lin, S.-X.8
-
47
-
-
60349085495
-
Development of a biological screening system for the evaluation of highly active and selective 17beta-HSD1-inhibitors as potential therapeutic agents
-
Kruchten, P.; Werth, R.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Development of a biological screening system for the evaluation of highly active and selective 17beta-HSD1-inhibitors as potential therapeutic agents Mol. Cell. Endocrinol. 2009, 301, 154-157
-
(2009)
Mol. Cell. Endocrinol.
, vol.301
, pp. 154-157
-
-
Kruchten, P.1
Werth, R.2
Marchais-Oberwinkler, S.3
Frotscher, M.4
Hartmann, R.W.5
-
48
-
-
80054910315
-
Computational investigation of the binding mode of bis(hydroxylphenyl) arenes in 17β-HSD1: Molecular dynamics simulations, MM-PBSA free energy calculations, and molecular electrostatic potential maps
-
Negri, M.; Recanatini, M.; Hartmann, R. W. Computational investigation of the binding mode of bis(hydroxylphenyl)arenes in 17β-HSD1: molecular dynamics simulations, MM-PBSA free energy calculations, and molecular electrostatic potential maps J. Comput.-Aided Mol. Des. 2011, 25, 795-811
-
(2011)
J. Comput.-Aided Mol. Des.
, vol.25
, pp. 795-811
-
-
Negri, M.1
Recanatini, M.2
Hartmann, R.W.3
-
49
-
-
18144382577
-
2,5-Diphenylfuran-based pure antiestrogens with selectivity for the estrogen receptor alpha
-
Zimmermann, J.; Liebl, R.; von Angerer, E. 2,5-Diphenylfuran-based pure antiestrogens with selectivity for the estrogen receptor alpha J. Steroid Biochem. Mol. Biol. 2005, 94, 57-66
-
(2005)
J. Steroid Biochem. Mol. Biol.
, vol.94
, pp. 57-66
-
-
Zimmermann, J.1
Liebl, R.2
Von Angerer, E.3
-
50
-
-
79957731848
-
Identification of chemically diverse, novel inhibitors of 17β-hydroxysteroid dehydrogenase type 3 and 5 by pharmacophore-based virtual screening
-
Schuster, D.; Kowalik, D.; Kirchmair, J.; Laggner, C.; Markt, P.; Aebischer-Gumy, C.; Ströhle, F.; Möller, G.; Wolber, G.; Wilckens, T.; Langer, T.; Odermatt, A.; Adamski, J. Identification of chemically diverse, novel inhibitors of 17β-hydroxysteroid dehydrogenase type 3 and 5 by pharmacophore-based virtual screening J. Steroid Biochem. Mol. Biol. 2011, 125, 148-161
-
(2011)
J. Steroid Biochem. Mol. Biol.
, vol.125
, pp. 148-161
-
-
Schuster, D.1
Kowalik, D.2
Kirchmair, J.3
Laggner, C.4
Markt, P.5
Aebischer-Gumy, C.6
Ströhle, F.7
Möller, G.8
Wolber, G.9
Wilckens, T.10
Langer, T.11
Odermatt, A.12
Adamski, J.13
-
51
-
-
71749120228
-
Structure-based design, synthesis and in vitro characterization of potent 17beta-hydroxysteroid dehydrogenase type 1 inhibitors based on 2-substitutions of estrone and d -homo-estrone
-
Möller, G.; Deluca, D.; Gege, C.; Rosinus, A.; Kowalik, D.; Peters, O.; Droescher, P.; Elger, W.; Adamski, J.; Hillisch, A. Structure-based design, synthesis and in vitro characterization of potent 17beta-hydroxysteroid dehydrogenase type 1 inhibitors based on 2-substitutions of estrone and d -homo-estrone Bioorg. Med. Chem. Lett. 2009, 19, 6740-6744
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6740-6744
-
-
Möller, G.1
Deluca, D.2
Gege, C.3
Rosinus, A.4
Kowalik, D.5
Peters, O.6
Droescher, P.7
Elger, W.8
Adamski, J.9
Hillisch, A.10
-
52
-
-
79953235168
-
Crystal structures of 11β-hydroxysteroid dehydrogenase type 1 and their use in drug discovery
-
Thomas, M. P.; Potter, B. V. L Crystal structures of 11β- hydroxysteroid dehydrogenase type 1 and their use in drug discovery Future Med. Chem. 2011, 3, 367-390
-
(2011)
Future Med. Chem.
, vol.3
, pp. 367-390
-
-
Thomas, M.P.1
Potter, B.V.L.2
-
53
-
-
0030059256
-
Unusual evolution of 11beta- and 17beta-hydroxysteroid and retinol dehydrogenases
-
Baker, M. E. Unusual evolution of 11beta- and 17beta-hydroxysteroid and retinol dehydrogenases BioEssays 1996, 18, 63-70
-
(1996)
BioEssays
, vol.18
, pp. 63-70
-
-
Baker, M.E.1
-
54
-
-
79957758271
-
Characterization of activity and binding mode of glycyrrhetinic acid derivatives inhibiting 11β-hydroxysteroid dehydrogenase type 2
-
Kratschmar, D. V.; Vuorinen, A.; Da Cunha, T.; Wolber, G.; Classen-Houben, D.; Doblhoff, O.; Schuster, D.; Odermatt, A. Characterization of activity and binding mode of glycyrrhetinic acid derivatives inhibiting 11β-hydroxysteroid dehydrogenase type 2 J. Steroid Biochem. Mol. Biol. 2011, 125, 129-142
-
(2011)
J. Steroid Biochem. Mol. Biol.
, vol.125
, pp. 129-142
-
-
Kratschmar, D.V.1
Vuorinen, A.2
Da Cunha, T.3
Wolber, G.4
Classen-Houben, D.5
Doblhoff, O.6
Schuster, D.7
Odermatt, A.8
-
55
-
-
84863207913
-
Inflammatory regulation of glucocorticoid metabolism in mesenchymal stromal cells
-
Ahasan, M. M.; Hardy, R.; Jones, C.; Kaur, K.; Nanus, D.; Juarez, M.; Morgan, S. A.; Hassan-Smith, Z.; Bénézech, C.; Caamaño, J. H.; Hewison, M.; Lavery, G.; Rabbitt, E. H.; Clark, A. R.; Filer, A.; Buckley, C. D.; Raza, K.; Stewart, P. M.; Cooper, M. S. Inflammatory regulation of glucocorticoid metabolism in mesenchymal stromal cells Arthritis Rheum. 2012, 64, 2404-2413
-
(2012)
Arthritis Rheum.
, vol.64
, pp. 2404-2413
-
-
Ahasan, M.M.1
Hardy, R.2
Jones, C.3
Kaur, K.4
Nanus, D.5
Juarez, M.6
Morgan, S.A.7
Hassan-Smith, Z.8
Bénézech, C.9
Caamaño, J.H.10
Hewison, M.11
Lavery, G.12
Rabbitt, E.H.13
Clark, A.R.14
Filer, A.15
Buckley, C.D.16
Raza, K.17
Stewart, P.M.18
Cooper, M.S.19
-
56
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Delivery Rev. 2001, 46, 3-26
-
(2001)
Adv. Drug Delivery Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
57
-
-
0022445670
-
Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability
-
Denizot, F.; Lang, R. Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability J. Immunol. Methods 1986, 89, 271-277
-
(1986)
J. Immunol. Methods
, vol.89
, pp. 271-277
-
-
Denizot, F.1
Lang, R.2
-
58
-
-
23844496476
-
Mouse models in skeletal physiology and osteoporosis: Experiences and data on 14839 cases from the Hamburg Mouse Archives
-
Pogoda, P.; Priemel, M.; Schilling, A.; Gebauer, M.; Catalá- Lehnenf, P.; Barvencik, F.; Beil, F.; Münch, C.; Rupprecht, M.; Müldner, C.; Rueger, J.; Schinke, T.; Amling, M.; Pogoda, P.; Priemel, M.; Schilling, A.; Gebauer, M.; Catalá-Lehnen, P.; Barvencik, F.; Beil, F.; Munch, C.; Rupprecht, M.; Miildner, C.; Rueger, J.; Schinke, T.; Amling, M. Mouse models in skeletal physiology and osteoporosis: experiences and data on 14839 cases from the Hamburg Mouse Archives J. Bone Miner. Metab. 2005, 23, 97-102
-
(2005)
J. Bone Miner. Metab.
, vol.23
, pp. 97-102
-
-
Pogoda, P.1
Priemel, M.2
Schilling, A.3
Gebauer, M.4
Catalá-Lehnenf, P.5
Barvencik, F.6
Beil, F.7
Münch, C.8
Rupprecht, M.9
Müldner, C.10
Rueger, J.11
Schinke, T.12
Amling, M.13
Pogoda, P.14
Priemel, M.15
Schilling, A.16
Gebauer, M.17
Catalá-Lehnen, P.18
Barvencik, F.19
Beil, F.20
Munch, C.21
Rupprecht, M.22
Miildner, C.23
Rueger, J.24
Schinke, T.25
Amling, M.26
more..
-
59
-
-
84872362392
-
Mouse Models for the Study of Fracture Healing and Bone Regeneration
-
Duque, G. Watanabe, K. Springer: London
-
Joerg, H.; Holstein, P. G. Mouse Models for the Study of Fracture Healing and Bone Regeneration. In Osteoporosis Research: Animal Models; Duque, G.; Watanabe, K., Eds.; Springer: London, 2011; pp 175-191.
-
(2011)
Osteoporosis Research: Animal Models
, pp. 175-191
-
-
Joerg, H.1
Holstein, P.G.2
-
60
-
-
0027425436
-
Crystallization and preliminary X-ray diffraction analysis of the complex of human placental 17 beta-hydroxysteroid dehydrogenase with NADP
-
Zhu, D. W.; Lee, X.; Breton, R.; Ghosh, D.; Pangborn, W.; Daux, W. L.; Lin, S. X. Crystallization and preliminary X-ray diffraction analysis of the complex of human placental 17 beta-hydroxysteroid dehydrogenase with NADP J. Mol. Biol. 1993, 234, 242-244
-
(1993)
J. Mol. Biol.
, vol.234
, pp. 242-244
-
-
Zhu, D.W.1
Lee, X.2
Breton, R.3
Ghosh, D.4
Pangborn, W.5
Daux, W.L.6
Lin, S.X.7
-
61
-
-
33750593096
-
Aging reduces the efficacy of estrogen substitution to attenuate cardiac hypertrophy in female spontaneously hypertensive rats
-
Jazbutyte, V.; Hu, K.; Kruchten, P.; Bey, E.; Maier, S. K. G.; Fritzemeier, K.-H.; Prelle, K.; Hegele-Hartung, C.; Hartmann, R. W.; Neyses, L.; Ertl, G.; Pelzer, T. Aging reduces the efficacy of estrogen substitution to attenuate cardiac hypertrophy in female spontaneously hypertensive rats Hypertension 2006, 48, 579-586
-
(2006)
Hypertension
, vol.48
, pp. 579-586
-
-
Jazbutyte, V.1
Hu, K.2
Kruchten, P.3
Bey, E.4
Maier, S.K.G.5
Fritzemeier, K.-H.6
Prelle, K.7
Hegele-Hartung, C.8
Hartmann, R.W.9
Neyses, L.10
Ertl, G.11
Pelzer, T.12
-
62
-
-
0033214482
-
The N-terminal anchor sequences of 11beta-hydroxysteroid dehydrogenases determine their orientation in the endoplasmic reticulum membrane
-
Odermatt, A.; Arnold, P.; Stauffer, A.; Frey, B. M.; Frey, F. J. The N-terminal anchor sequences of 11beta-hydroxysteroid dehydrogenases determine their orientation in the endoplasmic reticulum membrane J. Biol. Chem. 1999, 274, 28762-28770
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 28762-28770
-
-
Odermatt, A.1
Arnold, P.2
Stauffer, A.3
Frey, B.M.4
Frey, F.J.5
-
63
-
-
0026737624
-
Subunit identity of the dimeric 17 beta-hydroxysteroid dehydrogenase from human placenta
-
Lin, S. X.; Yang, F.; Jin, J. Z.; Breton, R.; Zhu, D. W.; Luu-The, V.; Labrie, F. Subunit identity of the dimeric 17 beta-hydroxysteroid dehydrogenase from human placenta J. Biol. Chem. 1992, 267, 16182-16187
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 16182-16187
-
-
Lin, S.X.1
Yang, F.2
Jin, J.Z.3
Breton, R.4
Zhu, D.W.5
Luu-The, V.6
Labrie, F.7
-
64
-
-
0031841053
-
C16 and C17 derivatives of estradiol as inhibitors of 17 beta-hydroxysteroid dehydrogenase type 1: Chemical synthesis and structure-activity relationships
-
Sam, K. M.; Boivin, R. P.; Tremblay, M. R.; Auger, S.; Poirier, D. C16 and C17 derivatives of estradiol as inhibitors of 17 beta-hydroxysteroid dehydrogenase type 1: chemical synthesis and structure-activity relationships Drug Des. Discovery 1998, 15, 157-180
-
(1998)
Drug Des. Discovery
, vol.15
, pp. 157-180
-
-
Sam, K.M.1
Boivin, R.P.2
Tremblay, M.R.3
Auger, S.4
Poirier, D.5
-
65
-
-
33644889618
-
17Beta-hydroxysteroid dehydrogenase type 1 and type 2: Association between mRNA expression and activity in cell lines
-
Day, J. M.; Tutill, H. J.; Newman, S. P.; Purohit, A.; Lawrence, H. R.; Vicker, N.; Potter, B. V. L; Reed, M. J. 17Beta-hydroxysteroid dehydrogenase type 1 and type 2: association between mRNA expression and activity in cell lines Mol. Cell. Endocrinol. 2006, 248, 246-249
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 246-249
-
-
Day, J.M.1
Tutill, H.J.2
Newman, S.P.3
Purohit, A.4
Lawrence, H.R.5
Vicker, N.6
Potter, B.V.L.7
Reed, M.J.8
|