-
1
-
-
0016272566
-
The involvement of human placental microsomal cytochrome P-450 in aromatization
-
Thompson Jr. E.A., and Siiteri P.K. The involvement of human placental microsomal cytochrome P-450 in aromatization. J Biol Chem 249 (1974) 5373-5378
-
(1974)
J Biol Chem
, vol.249
, pp. 5373-5378
-
-
Thompson Jr., E.A.1
Siiteri, P.K.2
-
2
-
-
0023180688
-
Purification and characterization of human placental aromatase cytochrome P-450
-
Kellis Jr. J., and Vickery L.E. Purification and characterization of human placental aromatase cytochrome P-450. J Biol Chem 262 (1987) 4413-4420
-
(1987)
J Biol Chem
, vol.262
, pp. 4413-4420
-
-
Kellis Jr., J.1
Vickery, L.E.2
-
3
-
-
0025872595
-
Purification of human placental aromatase cytochrome P-450 with monoclonal antibody and its characterization
-
Yoshida N., and Osawa Y. Purification of human placental aromatase cytochrome P-450 with monoclonal antibody and its characterization. Biochemistry 30 (1991) 3003-3010
-
(1991)
Biochemistry
, vol.30
, pp. 3003-3010
-
-
Yoshida, N.1
Osawa, Y.2
-
4
-
-
0000636448
-
Conversion of 19-hydroxy-4-androstene-3,17-dione to estrone by endocrine tissue
-
Meyer A.S. Conversion of 19-hydroxy-4-androstene-3,17-dione to estrone by endocrine tissue. Biochim Biophys Acta 17 (1995) 441-442
-
(1995)
Biochim Biophys Acta
, vol.17
, pp. 441-442
-
-
Meyer, A.S.1
-
6
-
-
0001689527
-
1H]-3β-hydroxy-androst-5-en-17-one by human placental aromatase
-
1H]-3β-hydroxy-androst-5-en-17-one by human placental aromatase. J Am Chem Soc 108 (1986) 1847-1852
-
(1986)
J Am Chem Soc
, vol.108
, pp. 1847-1852
-
-
Caspi, E.1
Arunachalam, Y.2
Nelson, P.A.3
-
7
-
-
0020073188
-
Mechanistic studies on C-19 demethylation in oestrogen biosynthesis
-
Akhtar M., Calder M.R., Corina D.L., and Wright J.N. Mechanistic studies on C-19 demethylation in oestrogen biosynthesis. Biochem J 201 (1982) 569-580
-
(1982)
Biochem J
, vol.201
, pp. 569-580
-
-
Akhtar, M.1
Calder, M.R.2
Corina, D.L.3
Wright, J.N.4
-
9
-
-
0024502595
-
Dissociation of 19-hydroxy-, 19-oxo-, and aromatizing activities in human placental microsomes through the use of suicide substrate to aromatase
-
Bednarski P.J., and Nelson S.D. Dissociation of 19-hydroxy-, 19-oxo-, and aromatizing activities in human placental microsomes through the use of suicide substrate to aromatase. J Steroid Biochem 32 (1989) 309-316
-
(1989)
J Steroid Biochem
, vol.32
, pp. 309-316
-
-
Bednarski, P.J.1
Nelson, S.D.2
-
11
-
-
0025284640
-
2H]-androgens into oestrogens by human placental aromatase
-
2H]-androgens into oestrogens by human placental aromatase. Biochem J 268 (1990) 553-561
-
(1990)
Biochem J
, vol.268
, pp. 553-561
-
-
Cole, P.A.1
Robinson, C.H.2
-
12
-
-
0027997441
-
Aromatase inhibitors in the treatment of breast cancer
-
Brodie A.M.H. Aromatase inhibitors in the treatment of breast cancer. J Steroid Biochem Mol Biol 49 (1994) 281-287
-
(1994)
J Steroid Biochem Mol Biol
, vol.49
, pp. 281-287
-
-
Brodie, A.M.H.1
-
13
-
-
0034991842
-
Recent advances in the clinical application of aromatase inhibitors
-
Harper-Wynne C., and Dowsett M. Recent advances in the clinical application of aromatase inhibitors. J Steroid Biochem Mol Biol 76 (2001) 179-186
-
(2001)
J Steroid Biochem Mol Biol
, vol.76
, pp. 179-186
-
-
Harper-Wynne, C.1
Dowsett, M.2
-
14
-
-
0035714768
-
Where do selective estrogen receptor modulators (SERMs) and aromatase inhibitors (AIs) now fit into breast cancer treatment algorithms?
-
Howell A., Howell S.J., Clarke R., and Anderson E. Where do selective estrogen receptor modulators (SERMs) and aromatase inhibitors (AIs) now fit into breast cancer treatment algorithms?. J Steroid Biochem Mol Biol 79 (2001) 227-237
-
(2001)
J Steroid Biochem Mol Biol
, vol.79
, pp. 227-237
-
-
Howell, A.1
Howell, S.J.2
Clarke, R.3
Anderson, E.4
-
15
-
-
0037130287
-
Exemestane, a new steroidal aromatase inhibitor of clinical relevance
-
Lombardi P. Exemestane, a new steroidal aromatase inhibitor of clinical relevance. Biochim Biophys Acta 1587 (2002) 326-337
-
(2002)
Biochim Biophys Acta
, vol.1587
, pp. 326-337
-
-
Lombardi, P.1
-
16
-
-
0028286267
-
6-Alkyl- and 6-arylandrost-4-ene-3,17-diones as aromatase inhibitors. Synthesis and structure-activity relationships
-
Numazawa M., and Oshibe M. 6-Alkyl- and 6-arylandrost-4-ene-3,17-diones as aromatase inhibitors. Synthesis and structure-activity relationships. J Med Chem 37 (1994) 1312-1319
-
(1994)
J Med Chem
, vol.37
, pp. 1312-1319
-
-
Numazawa, M.1
Oshibe, M.2
-
17
-
-
0029131311
-
Further studies on 6-alkylandrost-4-ene-3,17-diones as aromatase inhibitors: elongation of the 6-alkyl chain
-
Numazawa M., and Oshibe M. Further studies on 6-alkylandrost-4-ene-3,17-diones as aromatase inhibitors: elongation of the 6-alkyl chain. Steroids 60 (1995) 506-511
-
(1995)
Steroids
, vol.60
, pp. 506-511
-
-
Numazawa, M.1
Oshibe, M.2
-
18
-
-
0029971786
-
Time-dependent inactivation of aromatase by 6-alkylandrosta-1,4-diene-3,17-diones. Effects of length and configuration of the 6-alkyl group
-
Numazawa M., Oshibe M., Yamaguchi S., and Tachibana M. Time-dependent inactivation of aromatase by 6-alkylandrosta-1,4-diene-3,17-diones. Effects of length and configuration of the 6-alkyl group. J Med Chem 39 (1996) 1033-1038
-
(1996)
J Med Chem
, vol.39
, pp. 1033-1038
-
-
Numazawa, M.1
Oshibe, M.2
Yamaguchi, S.3
Tachibana, M.4
-
19
-
-
0030800838
-
6-Alkylandrosta-4,6-diene-3,17-diones and their 1,4,6-triene analogs as aromatase inhibitors
-
Numazawa M., Oshibe M., and Yamaguchi S. 6-Alkylandrosta-4,6-diene-3,17-diones and their 1,4,6-triene analogs as aromatase inhibitors. Steroids 62 (1997) 595-602
-
(1997)
Steroids
, vol.62
, pp. 595-602
-
-
Numazawa, M.1
Oshibe, M.2
Yamaguchi, S.3
-
20
-
-
0020561566
-
Synthesis and properties of the epimeric 6-hydroperoxyandrostenediones, new substrates/inhibitors of human placental aromatase
-
Tan L., Hrycay E.G., and Matsumoto K. Synthesis and properties of the epimeric 6-hydroperoxyandrostenediones, new substrates/inhibitors of human placental aromatase. J Steroid Biochem 19 (1983) 1329-1338
-
(1983)
J Steroid Biochem
, vol.19
, pp. 1329-1338
-
-
Tan, L.1
Hrycay, E.G.2
Matsumoto, K.3
-
21
-
-
0033758790
-
Probing the binding pocket of the active site of aromatase with 6-ether or 6-ester substituted androst-4-ene-3,17-diones and their diene and triene analogs
-
Numazawa M., Shelangouski M., and Nagaoka M. Probing the binding pocket of the active site of aromatase with 6-ether or 6-ester substituted androst-4-ene-3,17-diones and their diene and triene analogs. Steroids 65 (2000) 871-882
-
(2000)
Steroids
, vol.65
, pp. 871-882
-
-
Numazawa, M.1
Shelangouski, M.2
Nagaoka, M.3
-
22
-
-
0020325007
-
Synthesis and evaluation of 10β-substituted 4-estrene-3,17-diones as inhibitors of human placental microsomal aromatase
-
Marcotte P.A., and Robinson C.H. Synthesis and evaluation of 10β-substituted 4-estrene-3,17-diones as inhibitors of human placental microsomal aromatase. Steroids 39 (1982) 325-344
-
(1982)
Steroids
, vol.39
, pp. 325-344
-
-
Marcotte, P.A.1
Robinson, C.H.2
-
23
-
-
37049109882
-
Steroidal C19 sulphur and nitrogen derivatives designed as aromatase inhibitors
-
Wright N.J., Calder M.R., and Akhtar M. Steroidal C19 sulphur and nitrogen derivatives designed as aromatase inhibitors. J Chem Soc Chem Commun (1985) 1733
-
(1985)
J Chem Soc Chem Commun
, pp. 1733
-
-
Wright, N.J.1
Calder, M.R.2
Akhtar, M.3
-
24
-
-
0021848339
-
Thiol-containing androgens as suicide substrates of aromatase
-
Bednarski J.J., Porubek D.J., and Nelson S.D. Thiol-containing androgens as suicide substrates of aromatase. J Med Chem 28 (1985) 775-779
-
(1985)
J Med Chem
, vol.28
, pp. 775-779
-
-
Bednarski, J.J.1
Porubek, D.J.2
Nelson, S.D.3
-
25
-
-
0024793429
-
Recent developments in aromatase inhibition as a potential treatment for oestrogen-dependent breast cancer
-
Banting L., Nicholls P.J., Shaw M.A., and Smith H.J. Recent developments in aromatase inhibition as a potential treatment for oestrogen-dependent breast cancer. Prog Med Chem 26 (1989) 253-298
-
(1989)
Prog Med Chem
, vol.26
, pp. 253-298
-
-
Banting, L.1
Nicholls, P.J.2
Shaw, M.A.3
Smith, H.J.4
-
27
-
-
0001828104
-
Aromatase inhibitors: specific inhibitors of oestrogen biosynthesis
-
Berg D., and Plempel M. (Eds), Ellis Horwood Ltd., Chichester (England)
-
Covey D.F. Aromatase inhibitors: specific inhibitors of oestrogen biosynthesis. In: Berg D., and Plempel M. (Eds). Sterol biosynthesis inhibitors (1988), Ellis Horwood Ltd., Chichester (England) 534-571
-
(1988)
Sterol biosynthesis inhibitors
, pp. 534-571
-
-
Covey, D.F.1
-
28
-
-
0030761842
-
21-Hydroxy-6,19-oxidoprogesterone: a novel synthetic steroid with specific antiglucocorticoid properties in the rat
-
Vicent G.P., Monteserin M.C., Veleiro A.S., Burton G., Lantos C.P., and Galigniana M.D. 21-Hydroxy-6,19-oxidoprogesterone: a novel synthetic steroid with specific antiglucocorticoid properties in the rat. Mol Pharmacol 52 (1997) 749-753
-
(1997)
Mol Pharmacol
, vol.52
, pp. 749-753
-
-
Vicent, G.P.1
Monteserin, M.C.2
Veleiro, A.S.3
Burton, G.4
Lantos, C.P.5
Galigniana, M.D.6
-
29
-
-
0037325551
-
A receptor activity of a 6,19-oxido analogue of pregnanolone
-
A receptor activity of a 6,19-oxido analogue of pregnanolone. Bioorg Med Chem Lett 13 (2003) 343-346
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 343-346
-
-
Veleiro, A.S.1
Rosenstein, R.2
Grilli, M.L.3
Jaliffa, C.4
Speroni, F.5
Burton, G.6
-
30
-
-
24744441919
-
6,19-Sulfur-bridged progesterone analogues with antiimmunosuppressive activity
-
Veleiro A.S., Pecci A., Monteserin M.C., Baggio R., Garland M.T., Lantos C.P., et al. 6,19-Sulfur-bridged progesterone analogues with antiimmunosuppressive activity. J Med Chem 48 (2005) 5675-5683
-
(2005)
J Med Chem
, vol.48
, pp. 5675-5683
-
-
Veleiro, A.S.1
Pecci, A.2
Monteserin, M.C.3
Baggio, R.4
Garland, M.T.5
Lantos, C.P.6
-
31
-
-
0041318990
-
6,19-Carbon-bridged steroids. Synthesis of 6,19-methanoprogesterone
-
Joselevich M., Ghini A.A., and Burton G. 6,19-Carbon-bridged steroids. Synthesis of 6,19-methanoprogesterone. Org Biomol Chem 1 (2003) 939-943
-
(2003)
Org Biomol Chem
, vol.1
, pp. 939-943
-
-
Joselevich, M.1
Ghini, A.A.2
Burton, G.3
-
32
-
-
34547142710
-
Synthesis of 6,19-cyclopregnanes. Constrained analogues of steroid hormones
-
Chenna P.H., Veleiro A.S., Sonego J.M., Ceballos N.R., Garland M.T., Baggio R.F., et al. Synthesis of 6,19-cyclopregnanes. Constrained analogues of steroid hormones. Org Biomol Chem 5 (2007) 2453-2457
-
(2007)
Org Biomol Chem
, vol.5
, pp. 2453-2457
-
-
Chenna, P.H.1
Veleiro, A.S.2
Sonego, J.M.3
Ceballos, N.R.4
Garland, M.T.5
Baggio, R.F.6
-
33
-
-
84981840657
-
Steroids. CXCVIII. 19-Norsteroids. 4. Reductive ether cleavage of 5α-halo-6β,19-epoxysteroids
-
Kalvoda J., Heusler K., Ueberwasser H., Anner G., and Wettstein A. Steroids. CXCVIII. 19-Norsteroids. 4. Reductive ether cleavage of 5α-halo-6β,19-epoxysteroids. Helv Chim Acta 46 (1963) 1361-1369
-
(1963)
Helv Chim Acta
, vol.46
, pp. 1361-1369
-
-
Kalvoda, J.1
Heusler, K.2
Ueberwasser, H.3
Anner, G.4
Wettstein, A.5
-
35
-
-
0344902741
-
A new method for the deoxygenation of secondary alcohols
-
Barton D.H.R., and McCombie S.W. A new method for the deoxygenation of secondary alcohols. J Chem Soc, Perkin Trans I (1975) 1574-1585
-
(1975)
J Chem Soc, Perkin Trans I
, pp. 1574-1585
-
-
Barton, D.H.R.1
McCombie, S.W.2
-
36
-
-
0142216815
-
Biological aromatization of steroids
-
Ryan K.J. Biological aromatization of steroids. J Biol Chem 234 (1959) 268-272
-
(1959)
J Biol Chem
, vol.234
, pp. 268-272
-
-
Ryan, K.J.1
-
38
-
-
0041616545
-
-
Erithacus Software Limited, Surrey, UK
-
Grafit version 5.0.3 (2001), Erithacus Software Limited, Surrey, UK
-
(2001)
Grafit version 5.0.3
-
-
-
39
-
-
0001673303
-
Intramolecular olefinic aldehyde Prins reactions for the construction of five-membered rings
-
Andersen N.H., Hadley S.W., Kelly J.D., and Bacon E.R. Intramolecular olefinic aldehyde Prins reactions for the construction of five-membered rings. J Org Chem 50 (1985) 4144-4151
-
(1985)
J Org Chem
, vol.50
, pp. 4144-4151
-
-
Andersen, N.H.1
Hadley, S.W.2
Kelly, J.D.3
Bacon, E.R.4
-
40
-
-
0027291622
-
The invention of radical reactions. Part XXXI. Diphenylsilane: a reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo and iodo compounds by radical chain chemistry
-
Barton D.H.R., Jang D.O., and Jaszberenyi J.C. The invention of radical reactions. Part XXXI. Diphenylsilane: a reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo and iodo compounds by radical chain chemistry. Tetrahedron 49 (1993) 7193-7214
-
(1993)
Tetrahedron
, vol.49
, pp. 7193-7214
-
-
Barton, D.H.R.1
Jang, D.O.2
Jaszberenyi, J.C.3
|