-
1
-
-
84856068538
-
The role of hormonal therapy in gynecological cancers-current status and future directions
-
Sjoquist, K. M.; Martyn, J.; Edmondson, R. J.; Friedlander, M. L. The role of hormonal therapy in gynecological cancers-current status and future directions Int. J. Gynecol. Cancer 2011, 21, 1328-1333
-
(2011)
Int. J. Gynecol. Cancer
, vol.21
, pp. 1328-1333
-
-
Sjoquist, K.M.1
Martyn, J.2
Edmondson, R.J.3
Friedlander, M.L.4
-
2
-
-
0030006607
-
Synthesis and evaluation of azole-substituted tetrahydronaphthalenes as inhibitors of P450 arom, P450 17, and P450 TxA2
-
Hartmann, R. W.; Frotscher, M.; Ledergerber, D.; Wächter, G. A.; Grün, G. L.; Sergejew, T. F. Synthesis and evaluation of azole-substituted tetrahydronaphthalenes as inhibitors of P450 arom, P450 17, and P450 TxA2 Arch. Pharm. (Weinheim, Ger.) 1996, 329, 251-261
-
(1996)
Arch. Pharm. (Weinheim, Ger.)
, vol.329
, pp. 251-261
-
-
Hartmann, R.W.1
Frotscher, M.2
Ledergerber, D.3
Wächter, G.A.4
Grün, G.L.5
Sergejew, T.F.6
-
3
-
-
28544451936
-
Enantioselective nonsteroidal aromatase inhibitors identified through a multidisciplinary medicinal chemistry approach
-
Cavalli, A.; Bisi, A.; Bertucci, C.; Rosini, C.; Paluszcak, A.; Gobbi, S.; Giorgio, E.; Rampa, A.; Belluti, F.; Piazzi, L.; Valenti, P.; Hartmann, R. W.; Recanatini, M. Enantioselective nonsteroidal aromatase inhibitors identified through a multidisciplinary medicinal chemistry approach J. Med. Chem. 2005, 48, 7282-7289
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7282-7289
-
-
Cavalli, A.1
Bisi, A.2
Bertucci, C.3
Rosini, C.4
Paluszcak, A.5
Gobbi, S.6
Giorgio, E.7
Rampa, A.8
Belluti, F.9
Piazzi, L.10
Valenti, P.11
Hartmann, R.W.12
Recanatini, M.13
-
4
-
-
0038062686
-
Effects of novel 17alpha-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo
-
Haidar, S.; Ehmer, P. B.; Barassin, S.; Batzl-Hartmann, C.; Hartmann, R. W. Effects of novel 17alpha-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo J. Steroid Biochem. Mol. Biol. 2003, 84, 555-562
-
(2003)
J. Steroid Biochem. Mol. Biol.
, vol.84
, pp. 555-562
-
-
Haidar, S.1
Ehmer, P.B.2
Barassin, S.3
Batzl-Hartmann, C.4
Hartmann, R.W.5
-
5
-
-
67349083573
-
Novel CYP17 inhibitors: Synthesis, biological evaluation, structure-activity relationships and modeling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls
-
Hille, U. E.; Hu, Q.; Vock, C.; Negri, M.; Bartels, M.; Müller-Vieira, U.; Lauterbach, T.; Hartmann, R. W. Novel CYP17 inhibitors: synthesis, biological evaluation, structure-activity relationships and modeling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls Eur. J. Med. Chem. 2009, 44, 2765-2775
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2765-2775
-
-
Hille, U.E.1
Hu, Q.2
Vock, C.3
Negri, M.4
Bartels, M.5
Müller-Vieira, U.6
Lauterbach, T.7
Hartmann, R.W.8
-
6
-
-
53549099432
-
Novel aldosterone synthase inhibitors with extended carbocyclic skeleton by a combined ligand-based and structure-based drug design approach
-
Lucas, S; Heim, R; Negri, M; Antes, I; Ries, C; Schewe, K. E.; Bisi, A; Gobbi, S; Hartmann, R. W. Novel aldosterone synthase inhibitors with extended carbocyclic skeleton by a combined ligand-based and structure-based drug design approach J. Med. Chem. 2008, 51, 6138-6149
-
(2008)
J. Med. Chem.
, vol.51
, pp. 6138-6149
-
-
Lucas, S.1
Heim, R.2
Negri, M.3
Antes, I.4
Ries, C.5
Schewe, K.E.6
Bisi, A.7
Gobbi, S.8
Hartmann, R.W.9
-
7
-
-
50249187635
-
Overcoming undesirable CYP1A2 inhibition of pyridylnaphthalene-type aldosterone synthase inhibitors: Influence of heteroaryl derivatization on potency and selectivity
-
Heim, R.; Lucas, S.; Grombein, C. M.; Ries, C.; Schewe, K. E.; Negri, M.; Müller-Vieira, U.; Birk, B.; Hartmann, R. W. Overcoming undesirable CYP1A2 inhibition of pyridylnaphthalene-type aldosterone synthase inhibitors: influence of heteroaryl derivatization on potency and selectivity J. Med. Chem. 2008, 51, 5064-5074
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5064-5074
-
-
Heim, R.1
Lucas, S.2
Grombein, C.M.3
Ries, C.4
Schewe, K.E.5
Negri, M.6
Müller-Vieira, U.7
Birk, B.8
Hartmann, R.W.9
-
8
-
-
58149087304
-
In vivo active aldosterone synthase inhibitors with improved selectivity: Lead optimization providing a series of pyridine substituted 3,4-dihydro-1 H -quinolin-2-one derivatives
-
Lucas, S.; Heim, R.; Ries, C.; Schewe, K. E.; Birk, B.; Hartmann, R. W. In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-1 H -quinolin-2-one derivatives J. Med. Chem. 2008, 51, 8077-8087
-
(2008)
J. Med. Chem.
, vol.51
, pp. 8077-8087
-
-
Lucas, S.1
Heim, R.2
Ries, C.3
Schewe, K.E.4
Birk, B.5
Hartmann, R.W.6
-
9
-
-
79953772535
-
Fine-tuning the selectivity of aldosterone synthase inhibitors: Structure-activity and structure-selectivity insights from studies of heteroaryl substituted 1,2,5,6-tetrahydropyrrolo[3,2,1- ij ]quinolin-4-one derivatives
-
Lucas, S.; Negri, M.; Heim, R.; Zimmer, C.; Hartmann, R. W. Fine-tuning the selectivity of aldosterone synthase inhibitors: structure-activity and structure-selectivity insights from studies of heteroaryl substituted 1,2,5,6-tetrahydropyrrolo[3,2,1- ij ]quinolin-4-one derivatives J. Med. Chem. 2011, 54, 2307-2319
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2307-2319
-
-
Lucas, S.1
Negri, M.2
Heim, R.3
Zimmer, C.4
Hartmann, R.W.5
-
10
-
-
78651515158
-
First selective CYP11B1 inhibitors for the treatment of cortisol-dependent diseases
-
Hille, U. E.; Zimmer, C.; Vock, C. A.; Hartmann, R. W. First selective CYP11B1 inhibitors for the treatment of cortisol-dependent diseases ACS Med. Chem. Lett. 2011, 2, 2-6
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 2-6
-
-
Hille, U.E.1
Zimmer, C.2
Vock, C.A.3
Hartmann, R.W.4
-
11
-
-
80051710067
-
Optimization of the first selective steroid-11β-hydroxylase (CYP11B1) inhibitors for the treatment of cortisol dependent diseases
-
Hille, U. E.; Zimmer, C.; Haupenthal, J.; Hartmann, R. W. Optimization of the first selective steroid-11β-hydroxylase (CYP11B1) inhibitors for the treatment of cortisol dependent diseases ACS Med. Chem. Lett. 2011, 2, 559-564
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 559-564
-
-
Hille, U.E.1
Zimmer, C.2
Haupenthal, J.3
Hartmann, R.W.4
-
12
-
-
0034053626
-
Synthesis of N-substituted piperidine-4-(benzylidene-4-carboxylic acids) and evaluation as inhibitors of steroid-5alpha-reductase type 1 and 2
-
Picard, F.; Baston, E.; Reichert, W.; Hartmann, R. W. Synthesis of N-substituted piperidine-4-(benzylidene-4-carboxylic acids) and evaluation as inhibitors of steroid-5alpha-reductase type 1 and 2 Bioorg. Med. Chem. 2000, 8, 1479-1487
-
(2000)
Bioorg. Med. Chem.
, vol.8
, pp. 1479-1487
-
-
Picard, F.1
Baston, E.2
Reichert, W.3
Hartmann, R.W.4
-
13
-
-
79955776935
-
17β-Hydroxysteroid dehydrogenases (17β-HSD): Novel therapeutic targets, protein structures and recent progress in inhibitor development
-
Marchais-Oberwinkler, S.; Henn, C.; Möller, G.; Klein, T.; Lordon, M.; Negri, M.; Oster, A.; Spadaro, A.; Werth, R.; Xu, K.; Frotscher, M.; Hartmann, R. W.; Adamski, J. 17β-Hydroxysteroid dehydrogenases (17β-HSD): novel therapeutic targets, protein structures and recent progress in inhibitor development J. Steroid Biochem. Mol. Biol. 2011, 125, 66-82
-
(2011)
J. Steroid Biochem. Mol. Biol.
, vol.125
, pp. 66-82
-
-
Marchais-Oberwinkler, S.1
Henn, C.2
Möller, G.3
Klein, T.4
Lordon, M.5
Negri, M.6
Oster, A.7
Spadaro, A.8
Werth, R.9
Xu, K.10
Frotscher, M.11
Hartmann, R.W.12
Adamski, J.13
-
14
-
-
33947596821
-
Expression analysis of the genes involved in estradiol and progesterone action in human ovarian endometriosis
-
Smuc, T.; Pucelj, M. R.; Sinkovec, J.; Husen, B.; Thole, H.; Lanisnik Rizner, T. Expression analysis of the genes involved in estradiol and progesterone action in human ovarian endometriosis Gynecol. Endocrinol. 2007, 23, 105-111
-
(2007)
Gynecol. Endocrinol.
, vol.23
, pp. 105-111
-
-
Smuc, T.1
Pucelj, M.R.2
Sinkovec, J.3
Husen, B.4
Thole, H.5
Lanisnik Rizner, T.6
-
15
-
-
63049119975
-
Selective inhibition of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) reduces estrogen responsive cell growth of T47-D breast cancer cells
-
Kruchten, P.; Werth, R.; Bey, E.; Oster, A.; Marchais-Oberwinkler, S.; Frotscher, M.; Hartmann, R. W. Selective inhibition of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) reduces estrogen responsive cell growth of T47-D breast cancer cells J. Steroid Biochem. Mol. Biol. 2009, 114, 200-206
-
(2009)
J. Steroid Biochem. Mol. Biol.
, vol.114
, pp. 200-206
-
-
Kruchten, P.1
Werth, R.2
Bey, E.3
Oster, A.4
Marchais-Oberwinkler, S.5
Frotscher, M.6
Hartmann, R.W.7
-
16
-
-
33644900197
-
Evaluation of inhibitors for 17beta-hydroxysteroid dehydrogenase type 1 in vivo in immunodeficient mice inoculated with MCF-7 cells stably expressing the recombinant human enzyme
-
Husen, B.; Huhtinen, K.; Poutanen, M.; Kangas, L.; Messinger, J.; Thole, H. Evaluation of inhibitors for 17beta-hydroxysteroid dehydrogenase type 1 in vivo in immunodeficient mice inoculated with MCF-7 cells stably expressing the recombinant human enzyme Mol. Cell. Endocrinol. 2006, 248, 109-113
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 109-113
-
-
Husen, B.1
Huhtinen, K.2
Poutanen, M.3
Kangas, L.4
Messinger, J.5
Thole, H.6
-
17
-
-
40749094550
-
17beta-hydroxysteroid dehydrogenase type 1, and not type 12, is a target for endocrine therapy of hormone-dependent breast cancer
-
Day, J. M.; Foster, P. A.; Tutill, H. J.; Parsons, M. F. C.; Newman, S. P.; Chander, S. K.; Allan, G. M.; Lawrence, H. R.; Vicker, N.; Potter, B. V. L; Reed, M. J.; Purohit, A. 17beta-hydroxysteroid dehydrogenase type 1, and not type 12, is a target for endocrine therapy of hormone-dependent breast cancer Int. J. Cancer 2008, 122, 1931-1940
-
(2008)
Int. J. Cancer
, vol.122
, pp. 1931-1940
-
-
Day, J.M.1
Foster, P.A.2
Tutill, H.J.3
Parsons, M.F.C.4
Newman, S.P.5
Chander, S.K.6
Allan, G.M.7
Lawrence, H.R.8
Vicker, N.9
Potter, B.V.L.10
Reed, M.J.11
Purohit, A.12
-
18
-
-
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. 2009, 19, 6740-6744
-
(2009)
Bioorg. Med. Chem.
, 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
-
19
-
-
70349150178
-
Advances in development of inhibitors of 17beta hydroxysteroid dehydrogenases
-
Poirier, D. Advances in development of inhibitors of 17beta hydroxysteroid dehydrogenases Anti-Cancer Agents Med. Chem. 2009, 9, 642-660
-
(2009)
Anti-Cancer Agents Med. Chem.
, vol.9
, pp. 642-660
-
-
Poirier, D.1
-
20
-
-
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
-
21
-
-
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
-
22
-
-
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
-
23
-
-
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
-
24
-
-
42249099968
-
Novel inhibitors of 17beta-hydroxysteroid dehydrogenase type 1: Templates for design
-
Allan, G. M.; Vicker, N.; Lawrence, H. R.; Tutill, H. J.; Day, J. M.; Huchet, M.; Ferrandis, E.; Reed, M. J.; Purohit, A.; Potter, B. V. L. Novel inhibitors of 17beta-hydroxysteroid dehydrogenase type 1: templates for design Bioorg. Med. Chem. 2008, 16, 4438-4456
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 4438-4456
-
-
Allan, G.M.1
Vicker, N.2
Lawrence, H.R.3
Tutill, H.J.4
Day, J.M.5
Huchet, M.6
Ferrandis, E.7
Reed, M.J.8
Purohit, A.9
Potter, B.V.L.10
-
25
-
-
71049157137
-
Synthesis and biological evaluation of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitors based on a thieno[2,3- d ]pyrimidin-4(3 H)-one core
-
Lilienkampf, A.; Karkola, S.; Alho-Richmond, S.; Koskimies, P.; Johansson, N.; Huhtinen, K.; Vihko, K.; Wähälä, K. Synthesis and biological evaluation of 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitors based on a thieno[2,3- d ]pyrimidin-4(3 H)-one core J. Med. Chem. 2009, 52, 6660-6671
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6660-6671
-
-
Lilienkampf, A.1
Karkola, S.2
Alho-Richmond, S.3
Koskimies, P.4
Johansson, N.5
Huhtinen, K.6
Vihko, K.7
Wähälä, K.8
-
26
-
-
44649100782
-
A 3D QSAR model of 17beta-HSD1 inhibitors based on a thieno[2,3- d ]pyrimidin-4(3 H)-one core applying molecular dynamics simulations and ligand-protein docking
-
Karkola, S.; Lilienkampf, A.; Wähälä, K. A 3D QSAR model of 17beta-HSD1 inhibitors based on a thieno[2,3- d ]pyrimidin-4(3 H)-one core applying molecular dynamics simulations and ligand-protein docking ChemMedChem. 2008, 3, 461-472
-
(2008)
ChemMedChem.
, vol.3
, pp. 461-472
-
-
Karkola, S.1
Lilienkampf, A.2
Wähälä, K.3
-
27
-
-
47749148101
-
Discovery of nonsteroidal 17beta-hydroxysteroid dehydrogenase 1 inhibitors by pharmacophore-based screening of virtual compound libraries
-
Schuster, D.; Nashev, L. G.; Kirchmair, J.; Laggner, C.; Wolber, G.; Langer, T.; Odermatt, A. Discovery of nonsteroidal 17beta-hydroxysteroid dehydrogenase 1 inhibitors by pharmacophore-based screening of virtual compound libraries J. Med. Chem. 2008, 51, 4188-4199
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4188-4199
-
-
Schuster, D.1
Nashev, L.G.2
Kirchmair, J.3
Laggner, C.4
Wolber, G.5
Langer, T.6
Odermatt, A.7
-
28
-
-
60249103689
-
Flavonoids and cinnamic acid derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase type 1
-
Brozic, P.; Kocbek, P.; Sova, M.; Kristl, J.; Martens, S.; Adamski, J.; Gobec, S.; Lanisnik Rizner, T. Flavonoids and cinnamic acid derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase type 1 Mol. Cell. Endocrinol. 2009, 301, 229-234
-
(2009)
Mol. Cell. Endocrinol.
, vol.301
, pp. 229-234
-
-
Brozic, P.1
Kocbek, P.2
Sova, M.3
Kristl, J.4
Martens, S.5
Adamski, J.6
Gobec, S.7
Lanisnik Rizner, T.8
-
29
-
-
78651083688
-
Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1
-
Starčević, S.; Brožič, P.; Turk, S.; Cesar, J.; Lanišnik Rižner, T.; Gobec, S. Synthesis and biological evaluation of (6- and 7-phenyl) coumarin derivatives as selective nonsteroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1 J. Med. Chem. 2011, 54, 248-261
-
(2011)
J. Med. Chem.
, vol.54
, pp. 248-261
-
-
Starčević, S.1
Brožič, P.2
Turk, S.3
Cesar, J.4
Lanišnik Rižner, T.5
Gobec, S.6
-
30
-
-
81255149605
-
Discovery of highly potent, nonsteroidal 17β-hydroxysteroid dehydrogenase type 1 inhibitors by virtual high-throughput screening
-
Starčević, S.; Turk, S.; Brus, B.; Cesar, J.; Lanišnik Rižner, T.; Gobec, S. Discovery of highly potent, nonsteroidal 17β-hydroxysteroid dehydrogenase type 1 inhibitors by virtual high-throughput screening J. Steroid Biochem. Mol. Biol. 2011, 127, 255-261
-
(2011)
J. Steroid Biochem. Mol. Biol.
, vol.127
, pp. 255-261
-
-
Starčević, S.1
Turk, S.2
Brus, B.3
Cesar, J.4
Lanišnik Rižner, T.5
Gobec, S.6
-
31
-
-
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
-
32
-
-
33744738850
-
Induction of endometriosis in the marmoset monkey (Callithrix jacchus)
-
Einspanier, A.; Lieder, K.; Brüns, A.; Husen, B.; Thole, H.; Simon, C. Induction of endometriosis in the marmoset monkey (Callithrix jacchus) Mol. Hum. Reprod. 2006, 12, 291-299
-
(2006)
Mol. Hum. Reprod.
, vol.12
, pp. 291-299
-
-
Einspanier, A.1
Lieder, K.2
Brüns, A.3
Husen, B.4
Thole, H.5
Simon, C.6
-
33
-
-
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
-
34
-
-
79961218004
-
Structural basis for species specific inhibition of 17β- hydroxysteroid dehydrogenase type 1 (17β-HSD1): Computational study and biological validation
-
Klein, T.; Henn, C.; Negri, M.; Frotscher, M. Structural basis for species specific inhibition of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1): computational study and biological validation PLoS One 2011, 6, e22990
-
(2011)
PLoS One
, vol.6
, pp. 22990
-
-
Klein, T.1
Henn, C.2
Negri, M.3
Frotscher, M.4
-
35
-
-
0017819567
-
Synthesis and adrenergic β-blocking activity of some propanolamine derivatives
-
Obase, H.; Tatsuno, H.; Goto, K.; Shigenobu, K.; Kasuya, Y.; Yamada, Y.; Fujii, K.; Yada, S. Synthesis and adrenergic β-blocking activity of some propanolamine derivatives Chem. Pharm. Bull. 1978, 26, 1443-1452
-
(1978)
Chem. Pharm. Bull.
, vol.26
, pp. 1443-1452
-
-
Obase, H.1
Tatsuno, H.2
Goto, K.3
Shigenobu, K.4
Kasuya, Y.5
Yamada, Y.6
Fujii, K.7
Yada, S.8
-
37
-
-
70349089015
-
Synthesis of (S)-imperanene by using allylic substitution
-
Takashima, Y.; Kobayashi, Y. Synthesis of (S)-imperanene by using allylic substitution J. Org. Chem. 2009, 74, 5920-5926
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5920-5926
-
-
Takashima, Y.1
Kobayashi, Y.2
|