-
1
-
-
33644891865
-
Novel, potent inhibitors of 17beta-hydroxysteroid dehydrogenase type 1
-
Allan G.M., Bubert C., Vicker N., Smith A., Tutill H.J., Purohit A., Reed M.J., and Potter B.V. Novel, potent inhibitors of 17beta-hydroxysteroid dehydrogenase type 1. Mol. Cell. Endocrinol. 248 1-2 (2006) 204-207
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, Issue.1-2
, pp. 204-207
-
-
Allan, G.M.1
Bubert, C.2
Vicker, N.3
Smith, A.4
Tutill, H.J.5
Purohit, A.6
Reed, M.J.7
Potter, B.V.8
-
2
-
-
33244477418
-
Modification of estrone at the 6, 16, and 17 positions: novel potent inhibitors of 17beta-hydroxysteroid dehydrogenase type 1
-
Allan G.M., Lawrence H.R., Cornet J., Bubert C., Fischer D.S., Vicker N., Smith A., Tutill H.J., Purohit A., Day J.M., Mahon M.F., Reed M.J., and Potter B.V. Modification of estrone at the 6, 16, and 17 positions: novel potent inhibitors of 17beta-hydroxysteroid dehydrogenase type 1. J. Med. Chem. 49 4 (2006) 1325-1345
-
(2006)
J. Med. Chem.
, vol.49
, Issue.4
, pp. 1325-1345
-
-
Allan, G.M.1
Lawrence, H.R.2
Cornet, J.3
Bubert, C.4
Fischer, D.S.5
Vicker, N.6
Smith, A.7
Tutill, H.J.8
Purohit, A.9
Day, J.M.10
Mahon, M.F.11
Reed, M.J.12
Potter, B.V.13
-
3
-
-
0033954256
-
The Protein Data Bank
-
PDB ID: 17 beta HSD1: 1A27, 1BHS, 1DHT, 1EQU, 1FDS, 1FDS, 1FDT, 1FDU, 1FDV, 1FDW, 1I5R, 1IOL, 1QYV, 1QYW, 1QYX, 3DHE, ER: '1A52', '1ERE', '1ERR', '1G50',' 1GWQ', '1GWR', '1HJ1', '1L2J', '1NDE', '1PCG', '1QKM', '1QKN', '1QKT', '1QKU', '1R5K', '1S9P', '1S9Q', '1SJ0', '1U3Q', '1U3R', '1U3S', '1U9E', '1UOM', '1X76', '1X78', '1X7B', '1X7E', '1X7J', '1X7R', '1XP1', '1XP6', '1XP9', '1XPC', '1XQC', '1YIM', '1YIN', '1YY4', '1YYE', '1ZAF', '2AYR', '3ERD', '3ERT'
-
Bermann H.M., Westbrook J., Feng Z., Gilliland G., Bhat T.N., Weissig H., Shindyalov I.N., and Bourne P.E. The Protein Data Bank. Nucleic Acids Res. 28 (2000) 235-242 PDB ID: 17 beta HSD1: 1A27, 1BHS, 1DHT, 1EQU, 1FDS, 1FDS, 1FDT, 1FDU, 1FDV, 1FDW, 1I5R, 1IOL, 1QYV, 1QYW, 1QYX, 3DHE, ER: '1A52', '1ERE', '1ERR', '1G50',' 1GWQ', '1GWR', '1HJ1', '1L2J', '1NDE', '1PCG', '1QKM', '1QKN', '1QKT', '1QKU', '1R5K', '1S9P', '1S9Q', '1SJ0', '1U3Q', '1U3R', '1U3S', '1U9E', '1UOM', '1X76', '1X78', '1X7B', '1X7E', '1X7J', '1X7R', '1XP1', '1XP6', '1XP9', '1XPC', '1XQC', '1YIM', '1YIN', '1YY4', '1YYE', '1ZAF', '2AYR', '3ERD', '3ERT'
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 235-242
-
-
Bermann, H.M.1
Westbrook, J.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
Weissig, H.6
Shindyalov, I.N.7
Bourne, P.E.8
-
4
-
-
0027996582
-
An oxy-cope rearrangement approach to C(15) α-alkylated derivatives of estradiol
-
Bojack G., and Künzer H. An oxy-cope rearrangement approach to C(15) α-alkylated derivatives of estradiol. Tetrahedron Lett. 35 48 (1994) 9025-9026
-
(1994)
Tetrahedron Lett.
, vol.35
, Issue.48
, pp. 9025-9026
-
-
Bojack, G.1
Künzer, H.2
-
5
-
-
0030586820
-
The structure of a complex of human 17beta-hydroxysteroid dehydrogenase with estradiol and NADP+ identifies two principal targets for the design of inhibitors
-
Breton R., Housset D., Mazza C., and Fontecilla-Camps J.C. The structure of a complex of human 17beta-hydroxysteroid dehydrogenase with estradiol and NADP+ identifies two principal targets for the design of inhibitors. Structure 4 8 (1996) 905-915
-
(1996)
Structure
, vol.4
, Issue.8
, pp. 905-915
-
-
Breton, R.1
Housset, D.2
Mazza, C.3
Fontecilla-Camps, J.C.4
-
6
-
-
39049103081
-
Inhibitors of 17beta-hydroxysteroid dehydrogenase type 1
-
Brozic P., Lanisnik Rizner T., and Gobec S. Inhibitors of 17beta-hydroxysteroid dehydrogenase type 1. Curr. Med. Chem. 15 2 (2008) 137-150
-
(2008)
Curr. Med. Chem.
, vol.15
, Issue.2
, pp. 137-150
-
-
Brozic, P.1
Lanisnik Rizner, T.2
Gobec, S.3
-
7
-
-
17744371434
-
Phytochemical glyceollins, isolated from soy, mediate antihormonal effects through estrogen receptor alpha and beta
-
Burow M.E., Boue S.M., Collins-Burow B.M., Melnik L.I., Duong B.N., Carter-Wientjes C.H., Li S., Wiese T.E., Cleveland T.E., and McLachlan J.A. Phytochemical glyceollins, isolated from soy, mediate antihormonal effects through estrogen receptor alpha and beta. J. Clin. Endocrinol. Metab. 86 4 (2001) 1750-1758
-
(2001)
J. Clin. Endocrinol. Metab.
, vol.86
, Issue.4
, pp. 1750-1758
-
-
Burow, M.E.1
Boue, S.M.2
Collins-Burow, B.M.3
Melnik, L.I.4
Duong, B.N.5
Carter-Wientjes, C.H.6
Li, S.7
Wiese, T.E.8
Cleveland, T.E.9
McLachlan, J.A.10
-
8
-
-
0038183247
-
The synthesis of C-15 β-substituted 1,3,5(10)-estratrienes I
-
Cantrall E.W., Littell R., and Bernstein S. The synthesis of C-15 β-substituted 1,3,5(10)-estratrienes I. J. Org. Chem. 29 (1964) 64
-
(1964)
J. Org. Chem.
, vol.29
, pp. 64
-
-
Cantrall, E.W.1
Littell, R.2
Bernstein, S.3
-
9
-
-
0037507933
-
The synthesis of C-15 β-substituted 1,3,5(10)-estratrienes II
-
Cantrall E.W., Littell R., and Bernstein S. The synthesis of C-15 β-substituted 1,3,5(10)-estratrienes II. J. Org. Chem. 29 (1964) 214
-
(1964)
J. Org. Chem.
, vol.29
, pp. 214
-
-
Cantrall, E.W.1
Littell, R.2
Bernstein, S.3
-
10
-
-
15244352525
-
17Beta-hydroxysteroid dehydrogenases involved in local oestrogen synthesis have prognostic significance in breast cancer
-
Gunnarsson C., Hellqvist E., and Stal O. 17Beta-hydroxysteroid dehydrogenases involved in local oestrogen synthesis have prognostic significance in breast cancer. Br. J. Cancer 92 3 (2005) 547-552
-
(2005)
Br. J. Cancer
, vol.92
, Issue.3
, pp. 547-552
-
-
Gunnarsson, C.1
Hellqvist, E.2
Stal, O.3
-
11
-
-
43049108105
-
Amplification of HSD17B1 has prognostic significance in postmenopausal breast cancer
-
Gunnarsson C., Jerevall P.L., Hammar K., Olsson B., Nordenskjöld B., Jansson A., and Stål O. Amplification of HSD17B1 has prognostic significance in postmenopausal breast cancer. Breast Cancer Res. Treat. 108 1 (2008) 35-41
-
(2008)
Breast Cancer Res. Treat.
, vol.108
, Issue.1
, pp. 35-41
-
-
Gunnarsson, C.1
Jerevall, P.L.2
Hammar, K.3
Olsson, B.4
Nordenskjöld, B.5
Jansson, A.6
Stål, O.7
-
12
-
-
60249086156
-
-
Hirvelä, L., Johansson, N., Koskimies, P., Pentikäinen, O.T., Nyrönen, T., Salminen, T.A., Johnson, M.S., 2005. Novel compounds and their use in therapy, WO2005032527
-
Hirvelä, L., Johansson, N., Koskimies, P., Pentikäinen, O.T., Nyrönen, T., Salminen, T.A., Johnson, M.S., 2005. Novel compounds and their use in therapy, WO2005032527
-
-
-
-
13
-
-
33751240474
-
Human hydroxysteroid (17-beta) dehydrogenase 1 expression enhances estrogen sensitivity of MCF-7 breast cancer cell xenografts
-
Husen B., Huhtinen K., Saloniemi T., Messinger J., Thole H.H., and Poutanen M. Human hydroxysteroid (17-beta) dehydrogenase 1 expression enhances estrogen sensitivity of MCF-7 breast cancer cell xenografts. Endocrinology 147 11 (2006) 5333-5339
-
(2006)
Endocrinology
, vol.147
, Issue.11
, pp. 5333-5339
-
-
Husen, B.1
Huhtinen, K.2
Saloniemi, T.3
Messinger, J.4
Thole, H.H.5
Poutanen, M.6
-
14
-
-
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., and 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. 248 1-2 (2006) 109-113
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, Issue.1-2
, pp. 109-113
-
-
Husen, B.1
Huhtinen, K.2
Poutanen, M.3
Kangas, L.4
Messinger, J.5
Thole, H.6
-
15
-
-
8744310782
-
Increased expression of type I 17beta-hydroxysteroid dehydrogenase enhances in situ production of estradiol in uterine leiomyoma
-
Kasai T., Shozu M., Murakami K., Segawa T., Shinohara K., Nomura K., and Inoue M. Increased expression of type I 17beta-hydroxysteroid dehydrogenase enhances in situ production of estradiol in uterine leiomyoma. J. Clin. Endocrinol. Metab. 89 11 (2004) 5661-5668
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, Issue.11
, pp. 5661-5668
-
-
Kasai, T.1
Shozu, M.2
Murakami, K.3
Segawa, T.4
Shinohara, K.5
Nomura, K.6
Inoue, M.7
-
16
-
-
41349097890
-
Homo- and heterogeneous Ru-base metathesis catalysts in cross metathesis of 15.allylestrone-towards 17β-hydroxysteroid dehydrogenase type 1 inhibitors
-
Kirschning A., Harmrolfs K., Mennecke K., Messinger J., Schön U., and Grela K. Homo- and heterogeneous Ru-base metathesis catalysts in cross metathesis of 15.allylestrone-towards 17β-hydroxysteroid dehydrogenase type 1 inhibitors. Tetrahedron Lett. 49 (2008) 3019-3022
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3019-3022
-
-
Kirschning, A.1
Harmrolfs, K.2
Mennecke, K.3
Messinger, J.4
Schön, U.5
Grela, K.6
-
17
-
-
0003068163
-
The immature rat uterus in the assay of estrogenic substances, a comparison of estradiol, estrone and estriol
-
Lauson H.D., Heller C.G., Golden J.B., and Severinghaus E.L. The immature rat uterus in the assay of estrogenic substances, a comparison of estradiol, estrone and estriol. Endocrinology 24 (1939) 35-44
-
(1939)
Endocrinology
, vol.24
, pp. 35-44
-
-
Lauson, H.D.1
Heller, C.G.2
Golden, J.B.3
Severinghaus, E.L.4
-
18
-
-
19944426826
-
BODIL: a molecular modeling environment for structure-function analysis and drug design
-
Lehtonen J.V., Still D.J., Rantanen V.V., Ekholm J., Björklund D., Iftikhar Z., Huhtala M., Repo S., Jussila A., Jaakkola J., Pentikäinen O., Nyrönen T., Salminen T., Gyllenberg M., and Johnson M. BODIL: a molecular modeling environment for structure-function analysis and drug design. J. Comput. Aided Mol. Des. 18 6 (2004) 401-419
-
(2004)
J. Comput. Aided Mol. Des.
, vol.18
, Issue.6
, pp. 401-419
-
-
Lehtonen, J.V.1
Still, D.J.2
Rantanen, V.V.3
Ekholm, J.4
Björklund, D.5
Iftikhar, Z.6
Huhtala, M.7
Repo, S.8
Jussila, A.9
Jaakkola, J.10
Pentikäinen, O.11
Nyrönen, T.12
Salminen, T.13
Gyllenberg, M.14
Johnson, M.15
-
19
-
-
0037151061
-
Purification, reconstitution, and steady-state kinetics of the trans-membrane 17 beta-hydroxysteroid dehydrogenase 2
-
Lu M.L., Huang Y.W., and Lin S.X. Purification, reconstitution, and steady-state kinetics of the trans-membrane 17 beta-hydroxysteroid dehydrogenase 2. J. Biol. Chem. 277 25 (2002) 22123-22130
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.25
, pp. 22123-22130
-
-
Lu, M.L.1
Huang, Y.W.2
Lin, S.X.3
-
20
-
-
0029593494
-
Characteristics of human types 1,2 and 3 17 beta-hydroxysteroid dehydrogenase activities: oxidation/reduction and inhibition
-
Luu-The V., Zhang Y., Poirier D., and Labrie F. Characteristics of human types 1,2 and 3 17 beta-hydroxysteroid dehydrogenase activities: oxidation/reduction and inhibition. J. Steroid Biochem. Mol. Biol. 5 5-6 (1995) 581-587
-
(1995)
J. Steroid Biochem. Mol. Biol.
, vol.5
, Issue.5-6
, pp. 581-587
-
-
Luu-The, V.1
Zhang, Y.2
Poirier, D.3
Labrie, F.4
-
21
-
-
0345345251
-
The chemistry of estrin. VI. The ring structure of crystalline trihydroxy- and ketohydroxyestrin
-
Marrian G.F., and Haslewood G.A.D. The chemistry of estrin. VI. The ring structure of crystalline trihydroxy- and ketohydroxyestrin. J. Soc. Chem. Ind. Trans. 51 (1932) 277
-
(1932)
J. Soc. Chem. Ind. Trans.
, vol.51
, pp. 277
-
-
Marrian, G.F.1
Haslewood, G.A.D.2
-
22
-
-
0026587358
-
Distribution of 17 beta-hydroxysteroid dehydrogenase gene expression and activity in rat and human tissues
-
Martel C., Rhéaume E., Takahashi M., Trudel C., Couët J., Luu-The V., Simard J., and Labrie F. Distribution of 17 beta-hydroxysteroid dehydrogenase gene expression and activity in rat and human tissues. J. Steroid Biochem. Mol. Biol. 41 3-8 (1992) 597-603
-
(1992)
J. Steroid Biochem. Mol. Biol.
, vol.41
, Issue.3-8
, pp. 597-603
-
-
Martel, C.1
Rhéaume, E.2
Takahashi, M.3
Trudel, C.4
Couët, J.5
Luu-The, V.6
Simard, J.7
Labrie, F.8
-
23
-
-
60249090199
-
-
Messinger, J., Thole, H.H., Husen, B., Van Steen, B.J., Schneider, G., Hulshoff, J.B.E., Koskimies, P., Johansson, N., Adamski, J. 2005. Novel 17β-hydroxysteroid dehydrogenase type I inhibitors, WO05047303.
-
Messinger, J., Thole, H.H., Husen, B., Van Steen, B.J., Schneider, G., Hulshoff, J.B.E., Koskimies, P., Johansson, N., Adamski, J. 2005. Novel 17β-hydroxysteroid dehydrogenase type I inhibitors, WO05047303.
-
-
-
-
24
-
-
33644899920
-
New inhibitors of 17β-hydroxysteroid dehydrogenase type 1
-
Messinger J., Hirvelä L., Husen B., Kangas L., Koskimies P., Pentikäiinen O., Saarenketo P., and Thole H. New inhibitors of 17β-hydroxysteroid dehydrogenase type 1. Mol. Cell. Endocrinol. 248 (2006) 192-198
-
(2006)
Mol. Cell. Endocrinol.
, vol.248
, pp. 192-198
-
-
Messinger, J.1
Hirvelä, L.2
Husen, B.3
Kangas, L.4
Koskimies, P.5
Pentikäiinen, O.6
Saarenketo, P.7
Thole, H.8
-
25
-
-
0029670229
-
Human 17 beta-hydroxysteroid dehydrogenase type 1 and type 2 isoenzymes have opposite activities in cultured cells and characteristic cell- and tissue-specific expression
-
Miettinen M.M., Mustonen M.V., Poutanen M.H., Isomaa V.V., and Vihko R.K. Human 17 beta-hydroxysteroid dehydrogenase type 1 and type 2 isoenzymes have opposite activities in cultured cells and characteristic cell- and tissue-specific expression. Biochem. J. 314 (1996) 839-845
-
(1996)
Biochem. J.
, vol.314
, pp. 839-845
-
-
Miettinen, M.M.1
Mustonen, M.V.2
Poutanen, M.H.3
Isomaa, V.V.4
Vihko, R.K.5
-
26
-
-
0030272290
-
Synthesis and evaluation of estradiol derivatives with 16 alpha-(bromoalkylamide), 16 alpha-(bromoalkyl) or 16 alpha-(bromoalkynyl) side chain as inhibitors of 17 beta-hydroxysteroid dehydrogenase type 1 without estrogenic activity
-
Pelletier J.D., and Poirier D. Synthesis and evaluation of estradiol derivatives with 16 alpha-(bromoalkylamide), 16 alpha-(bromoalkyl) or 16 alpha-(bromoalkynyl) side chain as inhibitors of 17 beta-hydroxysteroid dehydrogenase type 1 without estrogenic activity. Bioorg. Med. Chem. 4 10 (1996) 1617-1628
-
(1996)
Bioorg. Med. Chem.
, vol.4
, Issue.10
, pp. 1617-1628
-
-
Pelletier, J.D.1
Poirier, D.2
-
27
-
-
0029998812
-
17β-Hydroxysteroid dehydrogenase: inhibitors and inhibitor design
-
Penning T.M. 17β-Hydroxysteroid dehydrogenase: inhibitors and inhibitor design. Endocr. Relat. Cancer 3 (1996) 41-56
-
(1996)
Endocr. Relat. Cancer
, vol.3
, pp. 41-56
-
-
Penning, T.M.1
-
28
-
-
0025948753
-
Synthesis of 17β-estradiol derivatives with N-butyl,N-methyl alkylamide side chain at position 15
-
Poirier D., Mérand Y., and Labrie F. Synthesis of 17β-estradiol derivatives with N-butyl,N-methyl alkylamide side chain at position 15. Tetrahedron 47 37 (1991) 7751-7766
-
(1991)
Tetrahedron
, vol.47
, Issue.37
, pp. 7751-7766
-
-
Poirier, D.1
Mérand, Y.2
Labrie, F.3
-
29
-
-
0030571293
-
D-ring alkylamine derivatives of estradiol: effect on er-binding affinity and antiestrogenic activity
-
Poirier D., Mérand Y., Labrie C., and Labrie F. D-ring alkylamine derivatives of estradiol: effect on er-binding affinity and antiestrogenic activity. Bioorg. Med. Chem. Lett. 6 21 (1996) 2537-2542
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, Issue.21
, pp. 2537-2542
-
-
Poirier, D.1
Mérand, Y.2
Labrie, C.3
Labrie, F.4
-
30
-
-
0037277521
-
Inhibitors of 17 beta-hydroxysteroid dehydrogenases
-
Poirier D. Inhibitors of 17 beta-hydroxysteroid dehydrogenases. Curr. Med. Chem. 10 6 (2003) 453-477
-
(2003)
Curr. Med. Chem.
, vol.10
, Issue.6
, pp. 453-477
-
-
Poirier, D.1
-
31
-
-
0029817523
-
Aromatase and 17 beta-hydroxysteroid dehydrogenase type 1 in human breast carcinoma
-
Sasano H., Frost A.R., Saitoh R., Harada N., Poutanen M., Vihko R., Bulun S.E., Silverberg S.G., and Nagura H. Aromatase and 17 beta-hydroxysteroid dehydrogenase type 1 in human breast carcinoma. J. Clin. Endocrinol. Metab. 81 11 (1996) 4042-4046
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, Issue.11
, pp. 4042-4046
-
-
Sasano, H.1
Frost, A.R.2
Saitoh, R.3
Harada, N.4
Poutanen, M.5
Vihko, R.6
Bulun, S.E.7
Silverberg, S.G.8
Nagura, H.9
-
32
-
-
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., and Rizner T.L. Expression analysis of the genes involved in estradiol and progesterone action in human ovarian endometriosis. Gynecol. Endocrinol. 23 2 (2007) 105-111
-
(2007)
Gynecol. Endocrinol.
, vol.23
, Issue.2
, pp. 105-111
-
-
Smuc, T.1
Pucelj, M.R.2
Sinkovec, J.3
Husen, B.4
Thole, H.5
Rizner, T.L.6
-
33
-
-
0032568527
-
Crystallographic comparison of the estrogen and progesterone receptor's ligand binding domains
-
Tanenbaum D.M., Wang Y., Williams S.P., and Sigler P.B. Crystallographic comparison of the estrogen and progesterone receptor's ligand binding domains. Proc. Natl. Acad. Sci. USA 95 11 (1998) 5998-6003
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, Issue.11
, pp. 5998-6003
-
-
Tanenbaum, D.M.1
Wang, Y.2
Williams, S.P.3
Sigler, P.B.4
-
34
-
-
20844442945
-
Association between endometriosis and genetic polymorphisms of the estradiol-synthesizing enzyme genes HSD17B1 and CYP19
-
Tsuchiya M., Nakao H., Katoh T., Sasaki H., Hiroshima M., Tanaka T., Matsunaga T., Hanaoka T., Tsugane S., and Ikenoue T. Association between endometriosis and genetic polymorphisms of the estradiol-synthesizing enzyme genes HSD17B1 and CYP19. Hum. Reprod. 20 4 (2005) 974-978
-
(2005)
Hum. Reprod.
, vol.20
, Issue.4
, pp. 974-978
-
-
Tsuchiya, M.1
Nakao, H.2
Katoh, T.3
Sasaki, H.4
Hiroshima, M.5
Tanaka, T.6
Matsunaga, T.7
Hanaoka, T.8
Tsugane, S.9
Ikenoue, T.10
|