-
1
-
-
65449169237
-
Vertebrate sex steroid receptors: Evolution, ligands, and neurodistribution
-
G. Guerriero Vertebrate sex steroid receptors: evolution, ligands, and neurodistribution Annals of the New York Academy of Sciences 1163 2009 154 168
-
(2009)
Annals of the New York Academy of Sciences
, vol.1163
, pp. 154-168
-
-
Guerriero, G.1
-
2
-
-
61349180173
-
Role of steroid hormone coregulators in health and disease
-
M.K. Thakur, and V. Paramanik Role of steroid hormone coregulators in health and disease Hormone Research 71 2009 194 200
-
(2009)
Hormone Research
, vol.71
, pp. 194-200
-
-
Thakur, M.K.1
Paramanik, V.2
-
3
-
-
0031059270
-
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
-
DOI 10.1016/S0039-128X(96)00242-5, PII S0039128X96002425
-
G.M. Anstead, K.E. Carlson, and J.A. Katzenellenbogen The estradiol pharmacophore: ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site Steroids 62 1997 268 303 (Pubitemid 27114399)
-
(1997)
Steroids
, vol.62
, Issue.3
, pp. 268-303
-
-
Anstead, G.M.1
Carlson, K.E.2
Katzenellenbogen, J.A.3
-
4
-
-
58849157644
-
Structural characteristics of anabolic androgenic steroids contributing to binding to the androgen receptor and to their anabolic and androgenic activities. Applied modifications in the steroidal structure
-
A.G. Fragkaki, Y.S. Angelis, M. Koupparis, A. Tsantili-Kakoulidou, G. Kokotos, and C. Georgakopoulos Structural characteristics of anabolic androgenic steroids contributing to binding to the androgen receptor and to their anabolic and androgenic activities. Applied modifications in the steroidal structure Steroids 74 2009 172 197
-
(2009)
Steroids
, vol.74
, pp. 172-197
-
-
Fragkaki, A.G.1
Angelis, Y.S.2
Koupparis, M.3
Tsantili-Kakoulidou, A.4
Kokotos, G.5
Georgakopoulos, C.6
-
5
-
-
0346366920
-
The significance of the 20-carbonyl group of progesterone in steroid receptor binding: A molecular dynamics and structure-based ligand design study
-
DOI 10.1016/j.steroids.2003.08.009
-
A. Hillisch, J. von Langen, B. Menzenbach, P. Droescher, G. Kaufmann, B. Schneider, and W. Elger The significance of the 20-carbonyl group of progesterone in steroid receptor binding: a molecular dynamics and structure-based ligand design study Steroids 68 2003 869 878 (Pubitemid 37532411)
-
(2003)
Steroids
, vol.68
, Issue.10-13
, pp. 869-878
-
-
Hillisch, A.1
Von Langen, J.2
Menzenbach, B.3
Droescher, P.4
Kaufmann, G.5
Schneider, B.6
Elger, W.7
-
6
-
-
77957689777
-
Hormone-dependent cancers: New approaches to identification of potential diagnostic and/or therapeutic biomarkers
-
A.C. Herington, L.K. Chopin, P. Jeffery, L. de Amorim, T. Veveris-Lowe, L. Bui, and J.A. Clements Hormone-dependent cancers: new approaches to identification of potential diagnostic and/or therapeutic biomarkers Asia-Pacific Journal of Molecular Biology and Biotechnology 18 2010 63 66
-
(2010)
Asia-Pacific Journal of Molecular Biology and Biotechnology
, vol.18
, pp. 63-66
-
-
Herington, A.C.1
Chopin, L.K.2
Jeffery, P.3
De Amorim, L.4
Veveris-Lowe, T.5
Bui, L.6
Clements, J.A.7
-
8
-
-
0029658503
-
Inhibition of steroid C(17(20)) lyase with C-17-heteroaryl steroids
-
DOI 10.1016/0968-0896(96)00135-6
-
J.P. Burkhart, C.A. Gates, M.E. Laughlin, R.J. Resvick, and N.P. Peet Inhibition of steroid C17(20) lyase with C-17-heteroaryl steroids Bioorganic and Medicinal Chemistry 4 1996 1411 1420 (Pubitemid 26319992)
-
(1996)
Bioorganic and Medicinal Chemistry
, vol.4
, Issue.9
, pp. 1411-1420
-
-
Burkhart, J.P.1
Gates, C.A.2
Laughlin, M.E.3
Resvick, R.J.4
Peet, N.P.5
-
9
-
-
70350574648
-
17,20-lyase
-
17,20-lyase Steroids 74 2009 1025 1032
-
(2009)
Steroids
, vol.74
, pp. 1025-1032
-
-
Ondré, D.1
Wölfling, J.2
Tóth, I.3
Szécsi, M.4
Julesz, J.5
Schneider, G.6
-
11
-
-
77950516746
-
17,20-lyase
-
17,20-lyase Steroids 75 2010 450 456
-
(2010)
Steroids
, vol.75
, pp. 450-456
-
-
Iványi, Z.1
Wölfling, J.2
Görbe, T.3
Szécsi, M.4
Wittmann, T.5
Schneider, G.6
-
12
-
-
0034106931
-
Aromatase inhibitors and their application in breast cancer treatment
-
DOI 10.1016/S0039-128X(99)00104-X, PII S0039128X9900104X
-
A.M.H. Brodie, and V.C.O. Njar Aromatase inhibitors and their application in breast cancer treatment Steroids 65 2000 171 179 (Pubitemid 30129250)
-
(2000)
Steroids
, vol.65
, Issue.4
, pp. 171-179
-
-
Brodie, A.M.H.1
Njar, V.C.O.2
-
13
-
-
79952572567
-
Synthesis of some novel androstanes as potential aromatase inhibitors
-
M.R. Yadav, P.M. Sabale, R. Giridhar, C. Zimmer, J. Haupenthal, and R.W. Hartmann Synthesis of some novel androstanes as potential aromatase inhibitors Steroids 76 2011 464 470
-
(2011)
Steroids
, vol.76
, pp. 464-470
-
-
Yadav, M.R.1
Sabale, P.M.2
Giridhar, R.3
Zimmer, C.4
Haupenthal, J.5
Hartmann, R.W.6
-
14
-
-
0028987866
-
Tamoxifen: Toxicities and drug resistance during the treatment and prevention of breast cancer
-
V.C. Jordan Tamoxifen: toxicities and drug resistance during the treatment and prevention of breast cancer Annual Review of Pharmacology and Toxicology 35 1995 195 211
-
(1995)
Annual Review of Pharmacology and Toxicology
, vol.35
, pp. 195-211
-
-
Jordan, V.C.1
-
15
-
-
0034528890
-
2-Methoxyestradiol: An endogenous antiangiogenic and antiproliferative drug candidate
-
DOI 10.1023/A:1026543018478
-
V.S. Pribluda, E.R. Gubish, T.M. LaVallee, A. Treston, G.M. Swartz, and J.S. Green 2-Methoxyestradiol: an endogenous antiangiogenic and antiproliferative drug candidate Cancer and Metastasis Reviews 19 2000 173 179 (Pubitemid 32004707)
-
(2000)
Cancer and Metastasis Reviews
, vol.19
, Issue.1-2
, pp. 173-179
-
-
Pribluda, V.S.1
Gubish Jr., E.R.2
LaVallee, T.M.3
Treston, A.4
Swartz, G.M.5
Green, S.J.6
-
16
-
-
0034812089
-
2-Methoxyestradiol induces G2/M arrest and apoptosis in prostate cancer
-
DOI 10.1006/bbrc.2001.5320
-
L.R. Quadan, C.M. Perez-Stable, C. Anderson, G. D'lppolito, A. Herron, G.A. Howard, and A.B. Roos 2-Methoxyestradiol induces G2/M arrest and apoptosis in prostate cancer Biochemical and Biophysical Research Communications 285 2001 1259 1266 (Pubitemid 32912919)
-
(2001)
Biochemical and Biophysical Research Communications
, vol.285
, Issue.5
, pp. 1259-1266
-
-
Qadan, L.R.1
Perez-Stable, C.M.2
Anderson, C.3
D'Ippolito, G.4
Herron, A.5
Howard, G.A.6
Roos, B.A.7
-
17
-
-
0030949341
-
2-Methoxyestradiol, an endogenous estrogen metabolite, induces apoptosis in endothelial cells and inhibits angiogenesis: Possible role for stress- activated protein kinase signaling pathway and Fas expression
-
T.-L. Yue, X. Wang, C.S. Louden, S. Gupta, K. Pillarisetti, J.-L. Gu, T.K. Hart, P.G. Lysko, and Z.G. Feuerstein 2-Methoxyestradiol, an endogenous estrogen metabolite, induces apoptosis in endothelial cells and inhibits angiogenesis: possible role for stress-activated protein kinase signaling pathway and Fas expression Molecular Pharmacology 51 1997 951 962 (Pubitemid 27249128)
-
(1997)
Molecular Pharmacology
, vol.51
, Issue.6
, pp. 951-962
-
-
Yue, T.-L.1
Wang, X.2
Louden, C.S.3
Gupta, S.4
Pillarisetti, K.5
Gu, J.-L.6
Hart, T.K.7
Lysko, P.G.8
Feuerstein, G.Z.9
-
18
-
-
5644252022
-
Breast cancer risk during HRT: Influence of estradiol metabolites on breast cancer and endothelial cell proliferation
-
DOI 10.1016/j.maturitas.2004.02.004, PII S0378512204000933
-
H. Seeger, F.-U. Deuringer, D. Wallwiener, and A.O. Mueck Breast cancer risk during HRT: influence of estradiol metabolites on breast cancer and endothelial cell proliferation Maturitas 49 2004 235 240 (Pubitemid 39370791)
-
(2004)
Maturitas
, vol.49
, Issue.3
, pp. 235-240
-
-
Seeger, H.1
Deuringer, F.-U.2
Wallwiener, D.3
Mueck, A.O.4
-
19
-
-
77954311612
-
2-Methoxyestradiol - Biology and mechanism of action
-
A.O. Mueck, and H. Seeger 2-Methoxyestradiol - biology and mechanism of action Steroids 75 2010 625 631
-
(2010)
Steroids
, vol.75
, pp. 625-631
-
-
Mueck, A.O.1
Seeger, H.2
-
20
-
-
79952812631
-
Influence of estradiol analogue on cell growth, morphology and death in esophageal carcinoma cells
-
T. Mqoco, S. Marais, and A. Joubert Influence of estradiol analogue on cell growth, morphology and death in esophageal carcinoma cells Biocell 34 2010 113 120
-
(2010)
Biocell
, vol.34
, pp. 113-120
-
-
Mqoco, T.1
Marais, S.2
Joubert, A.3
-
21
-
-
0034837267
-
Angiogenetic and anti-angiogenetic effects of estradiol and its metabolites
-
A.O. Mueck, C. Lippert, H. Seeger, and D. Wallwiener Angiogenetic and antiangiogenetic effects of estradiol and its metabolites Journal of Clinical and Basic Cardiology 4 2001 153 155 (Pubitemid 32822411)
-
(2001)
Journal of Clinical and Basic Cardiology
, vol.4
, Issue.2
, pp. 153-155
-
-
Mueck, A.O.1
Seeger, H.2
Lippert, C.3
Wallwiener, D.4
-
22
-
-
0036645421
-
2-Methoxyestradiol inhibits proliferation and induces apoptosis independently of estrogen receptors α and β
-
T.M. LaVallee, X.H. Zhan, C.J. Herbstritt, E.C. Kough, S.J. Green, and S.V. Pribluda 2-Methoxyestradiol inhibits proliferation and induces apoptosis independently of estrogen receptors α and β Cancer Research 62 2002 3691 3697 (Pubitemid 34728848)
-
(2002)
Cancer Research
, vol.62
, Issue.13
, pp. 3691-3697
-
-
LaVallee, T.M.1
Zhan, X.H.2
Herbstritt, C.J.3
Kough, E.C.4
Green, S.J.5
Pribluda, V.S.6
-
23
-
-
0037320432
-
2-methoxyestradiol, a promising anticancer agent
-
DOI 10.1592/phco.23.2.165.32088
-
N.J. Lakhani, M.A. Sarkar, J. Venitz, and D.W. Figg 2-Methoxyestradiol, a promising anticancer agent Pharmacotherapy 23 2003 165 172 (Pubitemid 36197457)
-
(2003)
Pharmacotherapy
, vol.23
, Issue.2
, pp. 165-172
-
-
Lakhani, N.J.1
Sarkar, M.A.2
Venitz, J.3
Figg, W.D.4
-
24
-
-
79960445267
-
Synthesis of novel steroidal 17α-triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro
-
É. Frank, J. Molnár, I. Zupkó, Z. Kádár, and J. Wölfling Synthesis of novel steroidal 17α-triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro Steroids 76 2011 1141 1148
-
(2011)
Steroids
, vol.76
, pp. 1141-1148
-
-
Frank, É.1
Molnár, J.2
Zupkó, I.3
Kádár, Z.4
Wölfling, J.5
-
25
-
-
0037333882
-
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
-
DOI 10.1016/S0039-128X(02)00181-2
-
J. Wölfling, E. Mernyák, É. Frank, G. Falkay, Á. Márki, R. Minorics, and Gy Schneider Synthesis and receptor-binding examinations of the normal and 13-epi-d-homoestrones and their 3-methyl ethers Steroids 68 2003 277 288 (Pubitemid 36298791)
-
(2003)
Steroids
, vol.68
, Issue.3
, pp. 277-288
-
-
Wolfling, J.1
Mernyak, E.2
Frank, E.3
Falkay, G.4
Marki, A.5
Minorics, R.6
Schneider, G.7
-
26
-
-
34249824594
-
2-induced intramolecular 1,3-dipolar cycloaddition
-
DOI 10.1055/s-2007-977452
-
2-induced intramolecular 1,3-dipolar cycloaddition Synlett 2007 1311 1313 (Pubitemid 46846498)
-
(2007)
Synlett
, Issue.8
, pp. 1311-1313
-
-
Frank, E.1
Kardos, Z.2
Wolfling, J.3
Schneider, G.4
-
27
-
-
34547204029
-
Characterization of in vitro and in vivo metabolic pathways of the investigational anticancer agent, 2-methoxyestradiol
-
DOI 10.1002/jps.20837
-
N.J. Lakhani, A. Sparreboom, X. Xu, T.D. Veenstra, J. Venitz, W.L. Dahut, and W.D. Figg Characterization of in vitro and in vivo metabolic pathways of the investigational anticancer agent, 2-methoxyestradiol Journal of Pharmaceutical Sciences 96 2007 1821 1831 (Pubitemid 47122958)
-
(2007)
Journal of Pharmaceutical Sciences
, vol.96
, Issue.7
, pp. 1821-1831
-
-
Lakhani, N.J.1
Sparreboom, A.2
Xu, X.3
Veenstra, T.D.4
Venitz, J.5
Dahut, W.L.6
Figg, W.D.7
-
28
-
-
0033918981
-
Synthesis of B-ring homologated estradiol analogues that modulate tubulin polymerization and microtubule stability
-
DOI 10.1021/jm0001119
-
Z. Wang, D. Yang, A.K. Mohanakrishnan, P.E. Fanwick, P. Nampoothiri, E. Hamel, and M. Cushman Synthesis of B-ring homologated estradiol analogues that modulate tubulin polymerization and microtubule stability Journal of Medicinal Chemistry 43 2000 2419 2429 (Pubitemid 30431941)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.12
, pp. 2419-2429
-
-
Wang, Z.1
Yang, D.2
Mohanakrishnan, A.K.3
Fanwick, P.E.4
Nampoothiri, P.5
Hamel, E.6
Cushman, M.7
-
29
-
-
0036890130
-
Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs
-
DOI 10.1016/S0039-128X(02)00066-1, PII S0039128X02000661
-
P.N. Rao, J.W. Cessac, T.L. Tinley, and S.L. Mooberry Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs Steroids 67 2002 1079 1089 (Pubitemid 35341726)
-
(2002)
Steroids
, vol.67
, Issue.13-14
, pp. 1079-1089
-
-
Rao, P.N.1
Cessac, J.W.2
Tinley, T.L.3
Mooberry, S.L.4
-
30
-
-
0036890192
-
A new, practical synthesis of 2-methoxyestradiols
-
DOI 10.1016/S0039-128X(02)00065-X, PII S0039128X0200065X
-
P.N. Rao, and J.W. Cessac A new, practical synthesis of 2-methoxyestradiols Steroids 67 2002 1065 1070 (Pubitemid 35341724)
-
(2002)
Steroids
, vol.67
, Issue.13-14
, pp. 1065-1070
-
-
Rao, P.N.1
Cessac, J.W.2
-
31
-
-
37649021764
-
Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs. Part III
-
P.N. Rao, J.W. Cessac, J.W. Boyd, A.D. Hanson, and J. Shah Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs. Part III Steroids 73 2008 171 183
-
(2008)
Steroids
, vol.73
, pp. 171-183
-
-
Rao, P.N.1
Cessac, J.W.2
Boyd, J.W.3
Hanson, A.D.4
Shah, J.5
-
32
-
-
71749116055
-
Synthesis of 2- and 17-substituted estrone analogs and their antiproliferative structure-activity relationships compared to 2-methoxyestradiol
-
J.H. Shah, G.E. Agoston, L. Suwandi, K. Hunsucker, V. Pribluda, X.H. Zhan, G.M. Swartz, T.M. LaVallee, and A.M. Treston Synthesis of 2- and 17-substituted estrone analogs and their antiproliferative structure-activity relationships compared to 2-methoxyestradiol Bioorganic and Medicinal Chemistry 17 2009 7344 7352
-
(2009)
Bioorganic and Medicinal Chemistry
, vol.17
, pp. 7344-7352
-
-
Shah, J.H.1
Agoston, G.E.2
Suwandi, L.3
Hunsucker, K.4
Pribluda, V.5
Zhan, X.H.6
Swartz, G.M.7
Lavallee, T.M.8
Treston, A.M.9
-
33
-
-
37649021764
-
Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs. Part II
-
P.N. Rao, J.W. Cessac, J.W. Boyd, A.D. Hanson, and J. Shah Synthesis and antimitotic activity of novel 2-methoxyestradiol analogs. Part II Steroids 73 2008 158 170
-
(2008)
Steroids
, vol.73
, pp. 158-170
-
-
Rao, P.N.1
Cessac, J.W.2
Boyd, J.W.3
Hanson, A.D.4
Shah, J.5
-
34
-
-
71049135731
-
Synthesis and antitumor activities of 3-modified 2-methoxyestradiol analogs
-
L.S. Suwandi, G.E. Agoston, J.H. Shah, A.D. Hanson, X.H. Zhan, T.M. LaVallee, and A.M. Treston Synthesis and antitumor activities of 3-modified 2-methoxyestradiol analogs Bioorganic and Medicinal Chemistry Letters 19 2009 6459 6462
-
(2009)
Bioorganic and Medicinal Chemistry Letters
, vol.19
, pp. 6459-6462
-
-
Suwandi, L.S.1
Agoston, G.E.2
Shah, J.H.3
Hanson, A.D.4
Zhan, X.H.5
Lavallee, T.M.6
Treston, A.M.7
-
35
-
-
71049183916
-
Synthesis, antiproliferative, and pharmacokinetic properties of 3- and 17-double-modified analogs of 2-methoxyestradiol
-
G.E. Agoston, J.H. Shah, L. Suwandi, A.D. Hanson, X. Zhan, T.M. LaVallee, V. Pribluda, and A.M. Treston Synthesis, antiproliferative, and pharmacokinetic properties of 3- and 17-double-modified analogs of 2-methoxyestradiol Bioorganic and Medicinal Chemistry Letters 19 2009 6241 6244
-
(2009)
Bioorganic and Medicinal Chemistry Letters
, vol.19
, pp. 6241-6244
-
-
Agoston, G.E.1
Shah, J.H.2
Suwandi, L.3
Hanson, A.D.4
Zhan, X.5
Lavallee, T.M.6
Pribluda, V.7
Treston, A.M.8
-
36
-
-
41649119942
-
Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents
-
DOI 10.1021/jm701319c
-
M.P. Leese, F.L. Jourdan, K. Gaukroger, M.F. Mahon, S.P. Newman, and P.A. Foster Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents Journal of Medicinal Chemistry 51 2008 1295 1308 (Pubitemid 351480390)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.5
, pp. 1295-1308
-
-
Leese, M.P.1
Jourdan, F.L.2
Gaukroger, K.3
Mahon, M.F.4
Newman, S.P.5
Foster, P.A.6
Stengel, C.7
Regis-Lydi, S.8
Ferrandis, E.9
Di Fiore, A.10
De Simone, G.11
Supuran, C.T.12
Purohit, A.13
Reed, M.J.14
Potter, B.V.L.15
-
37
-
-
34548498111
-
3,17-Disubstituted 2-alkylestra-1,3,5(10)-trien-3-ol derivatives: Synthesis, in vitro and in vivo anticancer activity
-
DOI 10.1021/jm070405v
-
C. Bubert, M.P. Leese, M.F. Mahon, E. Ferrandis, S. Regis-Lydi, P.G. Kasprzyk, and S.P. Newman 3,17-Disubstituted 2-alkylestra-1,3,5(10)trien-3-ol derivatives: synthesis, in vitro and in vivo anticancer activity Journal of Medicinal Chemistry 50 2007 4431 4443 (Pubitemid 47378840)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.18
, pp. 4431-4443
-
-
Bubert, C.1
Leese, M.P.2
Mahon, M.F.3
Ferrandis, E.4
Regis-Lydi, S.5
Kasprzyk, P.G.6
Newman, S.P.7
Ho, Y.T.8
Purohit, A.9
Reed, M.J.10
Potter, B.V.L.11
-
38
-
-
77950564911
-
Synthesis, antitubulin, and antiproliferative SAR of analogues of 2-methoxyestradiol-3,17-O,O-bis-sulfamate
-
F. Jourdan, M.P. Leese, W. Dohle, E. Hamel, E. Ferrandis, and S.P. Newman Synthesis, antitubulin, and antiproliferative SAR of analogues of 2-methoxyestradiol-3,17-O,O-bis-sulfamate Journal of Medicinal Chemistry 53 2010 2942 2951
-
(2010)
Journal of Medicinal Chemistry
, vol.53
, pp. 2942-2951
-
-
Jourdan, F.1
Leese, M.P.2
Dohle, W.3
Hamel, E.4
Ferrandis, E.5
Newman, S.P.6
-
39
-
-
35348890352
-
Synthesis and structure-activity relationships of 16-modified analogs of 2-methoxyestradiol
-
DOI 10.1016/j.bmc.2007.09.011, PII S0968089607007882
-
G.E. Agoston, J.H. Shah, T.M. LaVallee, X. Zhan, V.S. Pribluda, and A.M. Treston Synthesis and structure-activity relationships of modified analogs of 2-methoxyestradiol Bioorganic and Medicinal Chemistry 15 2007 7524 7537 (Pubitemid 47575931)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.24
, pp. 7524-7537
-
-
Agoston, G.E.1
Shah, J.H.2
LaVallee, T.M.3
Zhan, X.4
Pribluda, V.S.5
Treston, A.M.6
-
40
-
-
12644312578
-
Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride
-
A.J. Mancuso, S.-L. Huang, and D. Swern Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride Journal of Organic Chemistry 43 1978 2480 2482
-
(1978)
Journal of Organic Chemistry
, vol.43
, pp. 2480-2482
-
-
Mancuso, A.J.1
Huang, S.-L.2
Swern, D.3
-
41
-
-
4744371076
-
Effects of altering the electronics of 2-methoxyestradiol on cell proliferation, on cytotoxicity in human cancer cell cultures, and on tubulin polymerization
-
DOI 10.1021/jm049647a
-
A.B. Edsall, A.K. Mohanakrishnan, D. Yand, P.E. Fanwick, E. Hamel, A.D. Hanson, G.E. Agoston, and M. Cushman Effects of altering the electronics of 2-methoxyestradiol on cell proliferation, on cytotoxicity in human cancer cell cultures, and on tubulin polymerization Journal of Medicinal Chemistry 47 2004 5126 5139 (Pubitemid 39314910)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.21
, pp. 5126-5139
-
-
Edsall, A.B.1
Mohanakrishnan, A.K.2
Yang, D.3
Fanwick, P.E.4
Hamel, E.5
Hanson, A.D.6
Agoston, G.E.7
Cushman, M.8
-
42
-
-
80053564266
-
Synthesis of 2-substituted 17β-hydroxy/17-methylene estratrienes and their in vitro cytotoxicity in human cancer cell cultures
-
G. Panchapakesan, V. Dhayalan, N.D. Moorthy, N. Saranya, and A.K. Mohanakrishnan Synthesis of 2-substituted 17β-hydroxy/17-methylene estratrienes and their in vitro cytotoxicity in human cancer cell cultures Steroids 76 2011 1491 1504
-
(2011)
Steroids
, vol.76
, pp. 1491-1504
-
-
Panchapakesan, G.1
Dhayalan, V.2
Moorthy, N.D.3
Saranya, N.4
Mohanakrishnan, A.K.5
-
43
-
-
77955920545
-
Stereoselective synthesis of some methyl-substituted steroid hormones and their in vitro cytotoxic activity against human gastric cancer cell line MGC-803
-
C. Li, W. Qiu, Z. Yang, J. Luo, F. Yang, M. Liu, J. Xie, and J. Tang Stereoselective synthesis of some methyl-substituted steroid hormones and their in vitro cytotoxic activity against human gastric cancer cell line MGC-803 Steroids 75 2010 859 869
-
(2010)
Steroids
, vol.75
, pp. 859-869
-
-
Li, C.1
Qiu, W.2
Yang, Z.3
Luo, J.4
Yang, F.5
Liu, M.6
Xie, J.7
Tang, J.8
-
44
-
-
84864421108
-
Antiproliferative effect of normal and 13-epi-d-homoestrone and their 3-methyl ethers on human reproductive cancer cell lines
-
R. Minorics, N. Bózsity, J. Wölfling, E. Mernyák, Gy. Schneider, Á. Márki, G. Falkay, I. Ocsovszki, and I. Zupkó Antiproliferative effect of normal and 13-epi-d-homoestrone and their 3-methyl ethers on human reproductive cancer cell lines Journal of Steroid Biochemistry 132 2012 168 175
-
(2012)
Journal of Steroid Biochemistry
, vol.132
, pp. 168-175
-
-
Minorics, R.1
Bózsity, N.2
Wölfling, J.3
Mernyák, E.4
Schneider, Gy.5
Márki, Á.6
Falkay, G.7
Ocsovszki, I.8
Zupkó, I.9
-
45
-
-
83655201154
-
Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation - Ring-closing metathesis - Dihydroxylation sequence
-
T. Saloranta, I. Zupkó, J. Rahkila, Gy. Schneider, J. Wölfling, and R. Leino Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation - ring-closing metathesis - dihydroxylation sequence Steroids 77 2012 110 117
-
(2012)
Steroids
, vol.77
, pp. 110-117
-
-
Saloranta, T.1
Zupkó, I.2
Rahkila, J.3
Schneider, Gy.4
Wölfling, J.5
Leino, R.6
-
46
-
-
0037211772
-
Anti-proliferative action of endogenous dehydroepiandrosterone metabolites on human cancer cell lines
-
DOI 10.1016/S0039-128X(02)00117-4, PII S0039128X02001174
-
S. Yoshida, A. Honda, Y. Matsuzaki, S. Fukushima, N. Tanaka, A. Takagiwa, Y. Fujimoto, H. Miyazaki, and G. Salen Anti-proliferative action of endogenous dehydroepiandrosterone metabolites on human cancer cell lines Steroids 68 2003 73 83 (Pubitemid 35418305)
-
(2003)
Steroids
, vol.68
, Issue.1
, pp. 73-83
-
-
Yoshida, S.1
Honda, A.2
Matsuzaki, Y.3
Fukushima, S.4
Tanaka, N.5
Takagiwa, A.6
Fujimoto, Y.7
Miyazaki, H.8
Salen, G.9
-
47
-
-
33748596879
-
Dehydroepiandrosterone and its derivatives: Potentially novel anti-proliferative and chemopreventive agents
-
DOI 10.2174/138161206778194015
-
Y. Matsuzaki, and A. Honda Dehydroepiandrosterone and its derivatives: potentially novel anti-proliferative and chemopreventive agents Current Pharmaceutical Design 12 2006 3411 3421 (Pubitemid 44375466)
-
(2006)
Current Pharmaceutical Design
, vol.12
, Issue.26
, pp. 3411-3421
-
-
Matsuzaki, Y.1
Honda, A.2
-
48
-
-
80052337216
-
Synthesis, antiproliferative activity, acute toxicity and assessment of the antiandrogenic activities of new androstane derivatives
-
N. Dhingra, T.R. Bhardwaj, N. Mehta, T. Muklopadhyay, A. Kumar, and M. Kumar Synthesis, antiproliferative activity, acute toxicity and assessment of the antiandrogenic activities of new androstane derivatives Archives of Pharmacal Research 34 2011 1055 1063
-
(2011)
Archives of Pharmacal Research
, vol.34
, pp. 1055-1063
-
-
Dhingra, N.1
Bhardwaj, T.R.2
Mehta, N.3
Muklopadhyay, T.4
Kumar, A.5
Kumar, M.6
-
49
-
-
70049100740
-
Synthesis and antitumor activity of new d-seco and d-homo androstane derivatives
-
E.A. Djurendić, M.P. Zaviš, M.N. Sakač, J.J. Čanadi, V.V. Kojić, G.M. Bogdanović, and K.M. Penov Gaši Synthesis and antitumor activity of new d-seco and d-homo androstane derivatives Steroids 74 2009 983 988
-
(2009)
Steroids
, vol.74
, pp. 983-988
-
-
Djurendić, E.A.1
Zaviš, M.P.2
Sakač, M.N.3
Čanadi, J.J.4
Kojić, V.V.5
Bogdanović, G.M.6
Penov Gaši, K.M.7
-
50
-
-
84886720226
-
Inhibition of aromatase: Insight from recent studies
-
R.J. Santen Inhibition of aromatase: insight from recent studies Steroids 72 2007 31 40
-
(2007)
Steroids
, vol.72
, pp. 31-40
-
-
Santen, R.J.1
-
51
-
-
18844443185
-
Aromatase inhibitors in the treatment of breast cancer
-
DOI 10.1210/er.2004-0015
-
R.W. Brueggemeier, J.C. Hackett, and E.S. Diaz-Cruz Aromatase inhibitors in the treatment of breast cancer Endocrine Reviews 26 2005 331 345 (Pubitemid 40686647)
-
(2005)
Endocrine Reviews
, vol.26
, Issue.3
, pp. 331-345
-
-
Brueggemeier, R.W.1
Hackett, J.C.2
Diaz-Cruz, E.S.3
-
52
-
-
0026765043
-
Conformational analysis of the aromatase inhibitor 3-ethyl-3(4-pyridyl) piperidine-2,6-dione (Rogletimide) and discovery of potent 5-alkyl derivatives
-
R. McCague, and M.G. Rowlands Conformational analysis of the aromatase inhibitor 3-ethyl-3(4-pyridyl)piperidine-2,6-dione (Rogletimide) and discovery of potent 5-alkyl derivatives Journal of Medicinal Chemistry 35 1992 3699 3704
-
(1992)
Journal of Medicinal Chemistry
, vol.35
, pp. 3699-3704
-
-
McCague, R.1
Rowlands, M.G.2
-
53
-
-
33846020540
-
Synthesis and biological evaluation of some 17-picolyl and 17-picolinylidene androst-5-ene derivatives
-
DOI 10.1016/j.steroids.2006.10.002, PII S0039128X06002121
-
K.M.P. Gaši, M.D.D. Brenesel, E.A. Djurendić, M.N. Sakač, J.J. Daljev, T. Armbruster, S. Andrić, D.M. Sladić, T.T. Božić, I.N. Novaković, and Z.D. Juranić Synthesis and biological evaluation of some 17-picolyl and 17-picolinylidene androst-5-ene derivatives Steroids 72 2007 31 40 (Pubitemid 46049816)
-
(2007)
Steroids
, vol.72
, Issue.1
, pp. 31-40
-
-
Gasi, K.M.P.1
Brenesel, M.Dj.D.2
Djurendic, E.A.3
Sakac, M.N.4
Canadi, J.J.5
Daljev, J.J.6
Armbruster, T.7
Andric, S.8
Sladic, D.M.9
Bozic, T.T.10
Novakovic, I.T.11
Juranic, Z.D.12
-
54
-
-
37049028370
-
Synthesis of some epoxy and/or N-oxy 17-picolyl and 17-picolinylidene- androst-5-ene derivatives and evaluation of their biological activity
-
DOI 10.1016/j.steroids.2007.09.005, PII S0039128X0700178X
-
E. Djurendić, J. Daljev, M. Sakač, J. Čanadi, S.J. Šanta, S. Andrić, O. Klisurić, V. Kojić, G. Bogdavović, M. Djurendić-Brenesel, S. Novaković, and K.P. Gaši Synthesis of some epoxy and/or N-oxy 17-picolyl and 17-picolinylidene-androst-5-ene derivatives and evaluation of their biological activity Steroids 73 2008 129 138 (Pubitemid 350245673)
-
(2008)
Steroids
, vol.73
, Issue.1
, pp. 129-138
-
-
Djurendic, E.1
Daljev, J.2
Sakac, M.3
Canadi, J.4
Santa, S.J.5
Andric, S.6
Klisuric, O.7
Kojic, V.8
Bogdanovic, G.9
Djurendic-Brenesel, M.10
Novakovic, S.11
Gasi, K.P.12
-
55
-
-
3242844094
-
Partial syntheses of 21,27-bisnordemissidine from epiandrosterone and dehydroepiandrosterone acetates. Crystal and molecular structure of 21,27-bisnordemissidine hydrobromide
-
D. Miljković, K. Gaši, M. Kindjer, S. Stanković, and B. Ribar Partial syntheses of 21,27-bisnordemissidine from epiandrosterone and dehydroepiandrosterone acetates. Crystal and molecular structure of 21,27-bisnordemissidine hydrobromide Croatica Chemica Acta 58 1985 721 736
-
(1985)
Croatica Chemica Acta
, vol.58
, pp. 721-736
-
-
Miljković, D.1
Gaši, K.2
Kindjer, M.3
Stanković, S.4
Ribar, B.5
-
56
-
-
0008749598
-
3β-Acetoxy-17-picolinylidene-5-androstene-16-one: The key intermediate in 21,27-bisnorsolanidine synthesis
-
D. Miljković, and K. Gaši 3β-Acetoxy-17- picolinylidene-5-androstene-16-one: the key intermediate in 21,27- bisnorsolanidine synthesis Bulletin de la Société Chimique Beograd 46 1981 263 268
-
(1981)
Bulletin de la Société Chimique Beograd
, vol.46
, pp. 263-268
-
-
Miljković, D.1
Gaši, K.2
-
58
-
-
78049306126
-
Intramolecular approach to some new D-ring-fused steroidal isoxazolidines by 1,3-dipolar cycloaddition: Synthesis, theoretical and in vitro pharmacological studies
-
É. Frank, Z. Mucsi, M. Szécsi, I. Zupkó, J. Wölfling, and Gy. Schneider Intramolecular approach to some new D-ring-fused steroidal isoxazolidines by 1,3-dipolar cycloaddition: synthesis, theoretical and in vitro pharmacological studies New Journal of Chemistry 34 2010 2671 2681
-
(2010)
New Journal of Chemistry
, vol.34
, pp. 2671-2681
-
-
Frank, É.1
Mucsi, Z.2
Szécsi, M.3
Zupkó, I.4
Wölfling, J.5
Schneider, Gy.6
-
59
-
-
11844255741
-
Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates
-
DOI 10.1021/ja0471525
-
F. Himo, T. Lowell, R. Hilgraf, V.V. Rostovtsev, L. Noodleman, K.B. Sharpless, and V.V. Fokin Copper(I)-catalyzed synthesis of azoles, DFT study predicts unprecedented reactivity and intermediates Journal of the American Chemical Society 127 2005 210 216 (Pubitemid 40094384)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.1
, pp. 210-216
-
-
Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovtsev, V.V.4
Noodleman, L.5
Sharpless, K.B.6
Fokin, V.V.7
-
60
-
-
84865445982
-
Synthesis, characterization and biological evaluation of some novel 17-isoxazoles in the estrone series
-
D. Kovács, Z. Kádár, G. Mótyán, Gy. Schneider, J. Wölfling, I. Zupkó, and É. Frank Synthesis, characterization and biological evaluation of some novel 17-isoxazoles in the estrone series Steroids 77 2012 1075 1085
-
(2012)
Steroids
, vol.77
, pp. 1075-1085
-
-
Kovács, D.1
Kádár, Z.2
Mótyán, G.3
Schneider, Gy.4
Wölfling, J.5
Zupkó, I.6
Frank, É.7
-
61
-
-
0031782188
-
Steroidal isoxazoles, isoxazolines and isoxazolidines
-
Ch Camoutsis, and S. Nikolaroupoulos Steroidal isoxazoles, isoxazolines and isoxazolidines Journal of Heterocyclic Chemistry 35 1998 731 759 (Pubitemid 28436517)
-
(1998)
Journal of Heterocyclic Chemistry
, vol.35
, Issue.4
, pp. 731-759
-
-
Camoutsis, Ch.1
Nikolaropoulos, S.2
-
62
-
-
77955918647
-
Studies on novel D-ring substituted steroidal pyrazolines as potential anticancer agents
-
A.H. Banday, B.P. Mir, I.H. Lone, K.A. Suri, and H.M.S. Kumar Studies on novel D-ring substituted steroidal pyrazolines as potential anticancer agents Steroids 75 2010 805 809
-
(2010)
Steroids
, vol.75
, pp. 805-809
-
-
Banday, A.H.1
Mir, B.P.2
Lone, I.H.3
Suri, K.A.4
Kumar, H.M.S.5
-
63
-
-
84858337486
-
Synthesis of D-ring-substituted (5′R)- and (5′S)-17β- pyrazolinylandrostene epimers and comparison of their potent anticancer activities
-
Z. Iványi, N. Szabó, J. Huber, J. Wölfling, I. Zupkó, M. Szécsi, and Gy. Schneider Synthesis of D-ring-substituted (5′R)- and (5′S)-17β-pyrazolinylandrostene epimers and comparison of their potent anticancer activities Steroids 77 2012 566 574
-
(2012)
Steroids
, vol.77
, pp. 566-574
-
-
Iványi, Z.1
Szabó, N.2
Huber, J.3
Wölfling, J.4
Zupkó, I.5
Szécsi, M.6
Schneider, Gy.7
-
64
-
-
43049118945
-
Chemical synthesis of 2β-amino-5α-androstane-3α, 17β-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
-
DOI 10.1016/j.bmc.2008.03.031, PII S0968089608002393
-
D. Thibeault, J. Roy, P. DeRoy, and D. Poirier Chemical synthesis of 2β-amino-5α-androstane-3α,17β-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells Bioorganic and Medicinal Chemistry 16 2008 5062 5077 (Pubitemid 351625881)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.9
, pp. 5062-5077
-
-
Thibeault, D.1
Roy, J.2
DeRoy, P.3
Poirier, D.4
-
65
-
-
80051573783
-
Libraries of 2β-(N-substituted piperazino)-5α-androstane- 3α,17β-diols: Chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes
-
J. Roy, R. Maltais, H. Jegham, and D. Poirier Libraries of 2β-(N-substituted piperazino)-5α-androstane-3α,17β-diols: chemical synthesis and cytotoxic effects on human leukemia HL-60 cells and on normal lymphocytes Molecular Diversity 15 2011 317 339
-
(2011)
Molecular Diversity
, vol.15
, pp. 317-339
-
-
Roy, J.1
Maltais, R.2
Jegham, H.3
Poirier, D.4
-
66
-
-
2442596190
-
Glycoalkaloids and metabolites inhibit the growth of human colon (HT29) and liver (HepG2) cancer cells
-
K.R. Lee, N. Kozukue, J.S. Han, J.H. Park, E.Y. Chang, E.J. Baek, J.S. Chang, and M. Friedman Glycoalkaloids and metabolites inhibit the growth of human colon (HT29) and liver (HepG2) cancer cells Journal of Agricultural and Food Chemistry 52 2004 2832 2839
-
(2004)
Journal of Agricultural and Food Chemistry
, vol.52
, pp. 2832-2839
-
-
Lee, K.R.1
Kozukue, N.2
Han, J.S.3
Park, J.H.4
Chang, E.Y.5
Baek, E.J.6
Chang, J.S.7
Friedman, M.8
-
67
-
-
0035015140
-
Inhibitory effect of steroidal alkaloids on drug transport and multidrug resistance in human cancer cells
-
Y. Lavie, T. Harel-Orbital, W. Gaffield, and M. Liscovitch Inhibitory effect of steroidal alkaloids on drug transport and multidrug resistance in human cancer cells Anticancer Research 21 2001 1189 1194 (Pubitemid 32494229)
-
(2001)
Anticancer Research
, vol.21
, Issue.2 A
, pp. 1189-1194
-
-
Lavie, Y.1
Harel-Orbital, T.2
Gaffield, W.3
Liscovitch, M.4
-
69
-
-
78650509902
-
Antiproliferaive effects of some novel synthetic solanidine analogs on HL-60 human leukemia cells in vitro
-
R. Minorics, T. Szekeres, G. Krupitza, P. Saiko, B. Giessrigl, J. Wölfling, É. Frank, and I. Zupkó Antiproliferaive effects of some novel synthetic solanidine analogs on HL-60 human leukemia cells in vitro Steroids 76 2011 156 162
-
(2011)
Steroids
, vol.76
, pp. 156-162
-
-
Minorics, R.1
Szekeres, T.2
Krupitza, G.3
Saiko, P.4
Giessrigl, B.5
Wölfling, J.6
Frank, É.7
Zupkó, I.8
-
70
-
-
0023018014
-
1-antihistamine and mast cell stabilizing properties
-
DOI 10.1021/jm00161a022
-
D.R. Buckle, C.J. Rockell, H. Smith, and B.A. Spicer Piperazinylalkoxy[1] benzopyrano[2,3-d]-1,2,3-triazol-9(1H)-ones with combined H1-antihistamine and mast cell stabilizing properties Journal of Medicinal Chemistry 29 1986 2262 2267 (Pubitemid 17182304)
-
(1986)
Journal of Medicinal Chemistry
, vol.29
, Issue.11
, pp. 2262-2267
-
-
Buckle, D.R.1
Rockell, C.J.M.2
Smith, H.3
Spicer, B.A.4
-
71
-
-
0028063421
-
1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-β-D- ribofuranosyl]- 3'-spiro-5''-(4''-amino-1'',2''-oxathiole 2'',2''-dioxide) (TSAO) analogues: Synthesis and anti-HIV-1 activity
-
DOI 10.1021/jm00050a015
-
R. Alvarez, S. Velazquez, A. San-Felix, S. Aquaro, E. De Clercq, and C.F. Perno 1,2,3-Triazole-[2′,5′-bis-O-(tertbutyldimethylsilyl)-beta-d- ribofuranosyl]-3′-spiro-5″-(4″-amino-1″, 2″-oxathiole 2″,2″-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity Journal of Medicinal Chemistry 37 1994 4185 4194 (Pubitemid 24379707)
-
(1994)
Journal of Medicinal Chemistry
, vol.37
, Issue.24
, pp. 4185-4194
-
-
Alvarez, R.1
Velazquez, S.2
San-Felix, A.3
Aquaro, S.4
De Clercq, E.5
Perno -, C.F.6
Karlsson, A.7
Balzarini, J.8
Camarasa, M.J.9
-
72
-
-
0030593886
-
16 steroids; inhibitors of 17α-hydroxylase/17, 20-lyase (17α-lyase)
-
DOI 10.1016/S0960-894X(96)00512-4, PII S0960894X96005124
-
16 steroids; inhibitions of 17α-hydroxylase/17,20-lyase (17α-lyase) Bioorganic and Medicinal Chemistry Letters 6 1996 2777 2782 (Pubitemid 26387265)
-
(1996)
Bioorganic and Medicinal Chemistry Letters
, vol.6
, Issue.22
, pp. 2777-2782
-
-
Njar, V.C.O.1
Klus, G.T.2
Brodie, A.M.H.3
-
73
-
-
0037099395
-
A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
DOI 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
-
V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B. Sharpless A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective ligation of azides and terminal alkynes Angewandte Chemie International Edition 41 2002 2596 2599 (Pubitemid 34803480)
-
(2002)
Angewandte Chemie - International Edition
, vol.41
, Issue.14
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
74
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
-
DOI 10.1021/jo011148j
-
C.W. Tornøe, C. Christensen, and M. Meldal Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides Journal of Organic Chemistry 67 2002 3057 3064 (Pubitemid 34457265)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.9
, pp. 3057-3064
-
-
Tornoe, C.W.1
Christensen, C.2
Meldal, M.3
-
75
-
-
51049094897
-
Cu(I)-catalyzed azide-alkyne cycloaddition
-
M. Meldal, and C.W. Tornøe Cu(I)-catalyzed azide-alkyne cycloaddition Chemical Reviews 108 2008 2952 3015
-
(2008)
Chemical Reviews
, vol.108
, pp. 2952-3015
-
-
Meldal, M.1
Tornøe, C.W.2
-
76
-
-
77955926541
-
D-ring substituted 1,2,3-triazolyl 20-keto pregnanes as potential anticancer agents: Synthesis and biological evaluation
-
A.H. Banday, S.A. Shameem, B.D. Gupta, and H.M.S. Kumar D-ring substituted 1,2,3-triazolyl 20-keto pregnanes as potential anticancer agents: synthesis and biological evaluation Steroids 75 2010 801 804
-
(2010)
Steroids
, vol.75
, pp. 801-804
-
-
Banday, A.H.1
Shameem, S.A.2
Gupta, B.D.3
Kumar, H.M.S.4
-
77
-
-
79959627028
-
Synthesis and in vitro antiproliferative activity of novel androst-5-ene triazolyl and tetrazolyl derivatives
-
Z. Kádár, D. Kovács, É. Frank, Gy. Schneider, J. Huber, I. Zupkó, T. Bartók, and J. Wölfling Synthesis and in vitro antiproliferative activity of novel androst-5-ene triazolyl and tetrazolyl derivatives Molecules 16 2011 4786 4806
-
(2011)
Molecules
, vol.16
, pp. 4786-4806
-
-
Kádár, Z.1
Kovács, D.2
Frank, É.3
Schneider, Gy.4
Huber, J.5
Zupkó, I.6
Bartók, T.7
Wölfling, J.8
-
78
-
-
33744966628
-
A new solvent system for efficient synthesis of 1,2,3-triazoles
-
DOI 10.1016/j.tetlet.2006.05.079, PII S0040403906010045
-
B.Y. Lee, S.R. Park, H.B. Jeon, and K.S. Kim A new solvent system for efficient synthesis of 1,2,3-triazoles Tetrahedron Letters 47 2006 5105 5109 (Pubitemid 43867620)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.29
, pp. 5105-5109
-
-
Lee, B.-Y.1
Park, S.R.2
Jeon, H.B.3
Kim, K.S.4
-
79
-
-
84857031226
-
A facile "click" approach to novel 15β-triazolyl-5α- androstane derivatives and an evaluation of their antiproliferative activities in vitro
-
Z. Kádár, J. Molnár, Gy. Schneider, I. Zupkó, and É. Frank A facile "click" approach to novel 15β-triazolyl-5α-androstane derivatives and an evaluation of their antiproliferative activities in vitro Bioorganic and Medicinal Chemistry 20 2012 1396 1402
-
(2012)
Bioorganic and Medicinal Chemistry
, vol.20
, pp. 1396-1402
-
-
Kádár, Z.1
Molnár, J.2
Schneider, Gy.3
Zupkó, I.4
Frank, É.5
-
80
-
-
0007203421
-
Addition of azoimide to unsaturated ketones in the steroid series. Synthesis of N-(17β-hydroxy-3-oxo-5α-androstan-15β-yl)- succinamoic acid and its evaluation as hapten for dihydrotestosterone immunoanalysis
-
I. Cherny, V. Pouzar, O. Lapcik, and R. Hampl Addition of azoimide to unsaturated ketones in the steroid series - synthesis of (oxy-3-oxo-5α- androstan-15β-yl)succinamoic acid and its evaluation as hapten for dihydrotestosterone immuno analysis Collection of Czechoslovak Chemical Communications 62 1997 1931 1939 (Pubitemid 127405273)
-
(1997)
Collection of Czechoslovak Chemical Communications
, vol.62
, Issue.12
, pp. 1931-1939
-
-
Cerny, I.1
Pouzar, V.2
Lapcik, O.3
Hampl, R.4
-
81
-
-
81255128918
-
Efficient approach to novel 1α-triazolyl-5α-androstane derivatives as potent antiproliferative agents
-
Z. Kádár, Á. Baji, I. Zupkó, T. Bartók, J. Wölfling, and É. Frank Efficient approach to novel 1α-triazolyl-5α-androstane derivatives as potent antiproliferative agents Organic & Biomolecular Chemistry 9 2011 8051 8057
-
(2011)
Organic & Biomolecular Chemistry
, vol.9
, pp. 8051-8057
-
-
Kádár, Z.1
Baji, Á.2
Zupkó, I.3
Bartók, T.4
Wölfling, J.5
Frank, É.6
|