-
1
-
-
79960657926
-
Orphans in the human cytochrome P450 superfamily: Approaches to discovering functions and relevance in pharmacology
-
Guengerich, F. P.; Cheng, Q. Orphans in the human cytochrome P450 superfamily: approaches to discovering functions and relevance in pharmacology. Pharmacol Rev. 2011, 63 (3), 684-99.
-
(2011)
Pharmacol Rev.
, vol.63
, Issue.3
, pp. 684-699
-
-
Guengerich, F.P.1
Cheng, Q.2
-
2
-
-
34548394436
-
Inhibition of cytochromes P450: Existing and new promising therapeutic targets
-
Schuster, I.; Bernhardt, R. Inhibition of cytochromes P450: existing and new promising therapeutic targets. Drug Metab Rev. 2007, 39 (2-3), 481-99.
-
(2007)
Drug Metab Rev.
, vol.39
, Issue.2-3
, pp. 481-499
-
-
Schuster, I.1
Bernhardt, R.2
-
3
-
-
34248330459
-
Inhibitors of steroidal cytochrome P450 enzymes as targets for drug development
-
Baston, E.; Leroux, F. R. Inhibitors of steroidal cytochrome P450 enzymes as targets for drug development. Recent Pat Anticancer Drug Discov. 2007, 2 (1), 31-58.
-
(2007)
Recent Pat Anticancer Drug Discov.
, vol.2
, Issue.1
, pp. 31-58
-
-
Baston, E.1
Leroux, F.R.2
-
4
-
-
34249930470
-
Targeting cytochrome P450 enzymes: A new approach in anti-cancer drug development
-
Bruno, R. D.; Njar, V. C. Targeting cytochrome P450 enzymes: a new approach in anti-cancer drug development. Bioorg Med Chem. 2007, 15 (15), 5047-60.
-
(2007)
Bioorg Med Chem.
, vol.15
, Issue.15
, pp. 5047-5060
-
-
Bruno, R.D.1
Njar, V.C.2
-
5
-
-
33847676287
-
Cytochrome P450-catalyzed pathways in human brain: Metabolism meets pharmacology or old drugs with new mechanism of action?
-
Haining, R. L.; Nichols-Haining, M. Cytochrome P450-catalyzed pathways in human brain: metabolism meets pharmacology or old drugs with new mechanism of action? Pharmacol Ther. 2007, 113 (3), 537-45.
-
(2007)
Pharmacol Ther.
, vol.113
, Issue.3
, pp. 537-545
-
-
Haining, R.L.1
Nichols-Haining, M.2
-
6
-
-
77952784905
-
Adrenocortical zonation in humans under normal and pathological conditions
-
Nishimoto, K.; Nakagawa, K.; Li, D.; Kosaka, T.; Oya, M.; Mikami, S.; Shibata, H.; Itoh, H.; Mitani, F.; Yamazaki, T.; Ogishima, T.; Suematsu, M.; Mukai, K. Adrenocortical zonation in humans under normal and pathological conditions. J Clin Endocrinol Metab. 2010, 95 (5), 2296-305.
-
(2010)
J Clin Endocrinol Metab.
, vol.95
, Issue.5
, pp. 2296-2305
-
-
Nishimoto, K.1
Nakagawa, K.2
Li, D.3
Kosaka, T.4
Oya, M.5
Mikami, S.6
Shibata, H.7
Itoh, H.8
Mitani, F.9
Yamazaki, T.10
Ogishima, T.11
Suematsu, M.12
Mukai, K.13
-
7
-
-
0034641677
-
Crystal structures of adrenodoxin reductase in complex with NADP+ and NADPH suggesting a mechanism for the electron transfer of an enzyme family
-
Ziegler, G. A.; Schulz, G. E. Crystal structures of adrenodoxin reductase in complex with NADP+ and NADPH suggesting a mechanism for the electron transfer of an enzyme family. Biochemistry. 2000, 39 (36), 10986-95.
-
(2000)
Biochemistry.
, vol.39
, Issue.36
, pp. 10986-10995
-
-
Ziegler, G.A.1
Schulz, G.E.2
-
8
-
-
78649442579
-
Adrenodoxin: The archetype of vertebrate-type [2Fe-2S] cluster ferredoxins
-
Ewen, K. M.; Kleser, M.; Bernhardt, R. Adrenodoxin: the archetype of vertebrate-type [2Fe-2S] cluster ferredoxins. Biochim Biophys Acta 2011, 1814 (1), 111-25.
-
(2011)
Biochim Biophys Acta
, vol.1814
, Issue.1
, pp. 111-125
-
-
Ewen, K.M.1
Kleser, M.2
Bernhardt, R.3
-
9
-
-
10644266103
-
Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones
-
Payne, A. H.; Hales, D. B. Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones. Endocr Rev. 2004, 25 (6), 947-70.
-
(2004)
Endocr Rev.
, vol.25
, Issue.6
, pp. 947-970
-
-
Payne, A.H.1
Hales, D.B.2
-
10
-
-
76149083519
-
Aldosterone and arterial hypertension
-
Tomaschitz, A.; Pilz, S.; Ritz, E.; Obermayer-Pietsch, B.; Pieber, T. R. Aldosterone and arterial hypertension. Nat Rev Endocrinol 2009, 6 (2), 83-93.
-
(2009)
Nat Rev Endocrinol
, vol.6
, Issue.2
, pp. 83-93
-
-
Tomaschitz, A.1
Pilz, S.2
Ritz, E.3
Obermayer-Pietsch, B.4
Pieber, T.R.5
-
11
-
-
79956364204
-
Cell membrane-associated mineralocorticoid receptors? New evidence
-
Krug, A. W.; Pojoga, L. H.; Williams, G. H.; Adler, G. K. Cell membrane-associated mineralocorticoid receptors? New evidence. Hypertension 2011, 57 (6), 1019-25.
-
(2011)
Hypertension
, vol.57
, Issue.6
, pp. 1019-1025
-
-
Krug, A.W.1
Pojoga, L.H.2
Williams, G.H.3
Adler, G.K.4
-
12
-
-
77953298335
-
Aldosterone: Role in edematous disorders, hypertension, chronic renal failure, and metabolic syndrome
-
Schrier, R. W.; Masoumi, A.; Elhassan, E. Aldosterone: role in edematous disorders, hypertension, chronic renal failure, and metabolic syndrome. Clin J Am Soc Nephrol 2010, 5 (6), 1132-40.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, Issue.6
, pp. 1132-1140
-
-
Schrier, R.W.1
Masoumi, A.2
Elhassan, E.3
-
13
-
-
77949881587
-
Expanding view of aldosterone action, with an emphasis on rapid action
-
Vinson, G. P.; Coghlan, J. P. Expanding view of aldosterone action, with an emphasis on rapid action. Clin Exp Pharmacol Physiol. 2010, 37 (4), 410-6.
-
(2010)
Clin Exp Pharmacol Physiol.
, vol.37
, Issue.4
, pp. 410-416
-
-
Vinson, G.P.1
Coghlan, J.P.2
-
14
-
-
84856339877
-
Aldosterone, mineralocorticoid receptor, and heart failure
-
Messaoudi, S.; Azibani, F.; Delcayre, C.; Jaisser, F. Aldosterone, mineralocorticoid receptor, and heart failure. Mol Cell Endocrinol. 2012, 350 (2), 266-72.
-
(2012)
Mol Cell Endocrinol.
, vol.350
, Issue.2
, pp. 266-272
-
-
Messaoudi, S.1
Azibani, F.2
Delcayre, C.3
Jaisser, F.4
-
15
-
-
77951879058
-
Aldosterone: Effects on the kidney and cardiovascular system
-
Briet, M.; Schiffrin, E. L. Aldosterone: effects on the kidney and cardiovascular system. Nat Rev Nephrol 2010, 6 (5), 261-73.
-
(2010)
Nat Rev Nephrol
, vol.6
, Issue.5
, pp. 261-273
-
-
Briet, M.1
Schiffrin, E.L.2
-
16
-
-
79955974994
-
The role of aldosterone in the metabolic syndrome
-
Briet, M.; Schiffrin, E. L. The role of aldosterone in the metabolic syndrome. Curr Hypertens Rep. 2011, 13 (2), 163-72.
-
(2011)
Curr Hypertens Rep.
, vol.13
, Issue.2
, pp. 163-172
-
-
Briet, M.1
Schiffrin, E.L.2
-
17
-
-
0030587794
-
Effectiveness of spironolactone added to an angiotensin-converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure (the Randomized Aldactone Evaluation Study [RALES])
-
Effectiveness of spironolactone added to an angiotensin-converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure (the Randomized Aldactone Evaluation Study [RALES]). Am J Cardiol. 1996, 78 (8), 902-7.
-
(1996)
Am J Cardiol.
, vol.78
, Issue.8
, pp. 902-907
-
-
-
18
-
-
0034916015
-
The EPHESUS trial: Eplerenone in patients with heart failure due to systolic dysfunction complicating acute myocardial infarction. Eplerenone Post-AMI Heart Failure Efficacy and Survival Study
-
Pitt, B.; Williams, G.; Remme, W.; Martinez, F.; Lopez-Sendon, J.; Zannad, F.; Neaton, J.; Roniker, B.; Hurley, S.; Burns, D.; Bittman, R.; Kleiman, J. The EPHESUS trial: eplerenone in patients with heart failure due to systolic dysfunction complicating acute myocardial infarction. Eplerenone Post-AMI Heart Failure Efficacy and Survival Study. Cardiovasc Drugs Ther. 2001, 15 (1), 79-87.
-
(2001)
Cardiovasc Drugs Ther.
, vol.15
, Issue.1
, pp. 79-87
-
-
Pitt, B.1
Williams, G.2
Remme, W.3
Martinez, F.4
Lopez-Sendon, J.5
Zannad, F.6
Neaton, J.7
Roniker, B.8
Hurley, S.9
Burns, D.10
Bittman, R.11
Kleiman, J.12
-
19
-
-
0037417252
-
Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction
-
Pitt, B.; Remme, W.; Zannad, F.; Neaton, J.; Martinez, F.; Roniker, B.; Bittman, R.; Hurley, S.; Kleiman, J.; Gatlin, M. Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction. N Engl J Med. 2003, 348 (14), 1309-21.
-
(2003)
N Engl J Med.
, vol.348
, Issue.14
, pp. 1309-1321
-
-
Pitt, B.1
Remme, W.2
Zannad, F.3
Neaton, J.4
Martinez, F.5
Roniker, B.6
Bittman, R.7
Hurley, S.8
Kleiman, J.9
Gatlin, M.10
-
20
-
-
76349121327
-
Aldosterone 'escape' vs 'breakthrough'
-
Schrier, R. W. Aldosterone 'escape' vs 'breakthrough'. Nat Rev Nephrol. 2011, 6 (2), 61.
-
(2011)
Nat Rev Nephrol.
, vol.6
, Issue.2
, pp. 61
-
-
Schrier, R.W.1
-
21
-
-
34548163060
-
The incidence and implications of aldosterone breakthrough
-
Bomback, A. S.; Klemmer, P. J. The incidence and implications of aldosterone breakthrough. Nat Clin Pract Nephrol. 2007, 3 (9), 486-92.
-
(2007)
Nat Clin Pract Nephrol.
, vol.3
, Issue.9
, pp. 486-492
-
-
Bomback, A.S.1
Klemmer, P.J.2
-
22
-
-
79955622277
-
Mineralocorticoid receptor activation and blockade: An emerging paradigm in chronic kidney disease
-
Bertocchio, J. P.; Warnock, D. G.; Jaisser, F. Mineralocorticoid receptor activation and blockade: an emerging paradigm in chronic kidney disease. Kidney Int 2011, 79 (10), 1051-60.
-
(2011)
Kidney Int
, vol.79
, Issue.10
, pp. 1051-1060
-
-
Bertocchio, J.P.1
Warnock, D.G.2
Jaisser, F.3
-
23
-
-
79959516061
-
Aldosterone blockade: Current research and future trends
-
Bramlage, P.; Turgonyi, E.; Montalescot, G. Aldosterone blockade: current research and future trends. Eur Heart J Supp. 2011, 13 (Suppl. B), B46-B50.
-
(2011)
Eur Heart J Supp.
, vol.13
, Issue.SUPPL. B
-
-
Bramlage, P.1
Turgonyi, E.2
Montalescot, G.3
-
24
-
-
79959950762
-
Novel therapeutic targets for the treatment of heart failure
-
Tamargo, J.; Lopez-Sendon, J. Novel therapeutic targets for the treatment of heart failure. Nat Rev Drug Discov 1038, 10 (7), 536-55.
-
(1038)
Nat Rev Drug Discov
, vol.10
, Issue.7
, pp. 536-555
-
-
Tamargo, J.1
Lopez-Sendon, J.2
-
25
-
-
0030989625
-
Heme-coordinating analogs of lauric acid as inhibitors of fatty acid omega-hydroxylation
-
Lu, P.; Alterman, M. A.; Chaurasia, C. S.; Bambal, R. B.; Hanzlik, R. P. Heme-coordinating analogs of lauric acid as inhibitors of fatty acid omega-hydroxylation. Arch Biochem Biophys. 1997, 337 (1), 1-7.
-
(1997)
Arch Biochem Biophys.
, vol.337
, Issue.1
, pp. 1-7
-
-
Lu, P.1
Alterman, M.A.2
Chaurasia, C.S.3
Bambal, R.B.4
Hanzlik, R.P.5
-
26
-
-
0024842845
-
Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta)
-
Mornet, E.; Dupont, J.; Vitek, A.; White, P. C. Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta). J Biol Chem. 1989, 264 (35), 20961-7.
-
(1989)
J Biol Chem.
, vol.264
, Issue.35
, pp. 20961-20967
-
-
Mornet, E.1
Dupont, J.2
Vitek, A.3
White, P.C.4
-
27
-
-
79953184635
-
Cortisol synthesis in epidermis is induced by IL-1 and tissue injury
-
Vukelic, S.; Stojadinovic, O.; Pastar, I.; Rabach, M.; Krzyzanowska, A.; Lebrun, E.; Davis, S. C.; Resnik, S.; Brem, H.; Tomic-Canic, M. Cortisol synthesis in epidermis is induced by IL-1 and tissue injury. J Biol Chem 2011, 286 (12), 10265-75.
-
(2011)
J Biol Chem
, vol.286
, Issue.12
, pp. 10265-10275
-
-
Vukelic, S.1
Stojadinovic, O.2
Pastar, I.3
Rabach, M.4
Krzyzanowska, A.5
Lebrun, E.6
Davis, S.C.7
Resnik, S.8
Brem, H.9
Tomic-Canic, M.10
-
28
-
-
0030591713
-
Adrenal insufficiency
-
Oelkers, W. Adrenal insufficiency. N Engl J Med. 1996, 335 (16), 1206-12.
-
(1996)
N Engl J Med.
, vol.335
, Issue.16
, pp. 1206-1212
-
-
Oelkers, W.1
-
29
-
-
0021738890
-
Etomidate inhibits adrenocortical function in surgical patients
-
Wagner, R. L.; White, P. F. Etomidate inhibits adrenocortical function in surgical patients. Anesthesiology. 1984, 61 (6), 647-51.
-
(1984)
Anesthesiology.
, vol.61
, Issue.6
, pp. 647-651
-
-
Wagner, R.L.1
White, P.F.2
-
30
-
-
0021253073
-
Inhibition of adrenal steroidogenesis by the anesthetic etomidate
-
Wagner, R. L.; White, P. F.; Kan, P. B.; Rosenthal, M. H.; Feldman, D. Inhibition of adrenal steroidogenesis by the anesthetic etomidate. N Engl J Med. 1984, 310 (22), 1415-21.
-
(1984)
N Engl J Med.
, vol.310
, Issue.22
, pp. 1415-1421
-
-
Wagner, R.L.1
White, P.F.2
Kan, P.B.3
Rosenthal, M.H.4
Feldman, D.5
-
31
-
-
2342632561
-
Development of test systems for the discovery of selective human aldosterone synthase (CYP11B2) and 11betahydroxylase (CYP11B1) inhibitors. Discovery of a new lead compound for the therapy of congestive heart failure, myocardial fibrosis and hypertension
-
Bureik, M.; Hubel, K.; Dragan, C. A.; Scher, J.; Becker, H.; Lenz, N.; Bernhardt, R. Development of test systems for the discovery of selective human aldosterone synthase (CYP11B2) and 11betahydroxylase (CYP11B1) inhibitors. Discovery of a new lead compound for the therapy of congestive heart failure, myocardial fibrosis and hypertension. Mol Cell Endocrinol. 2004, 217 (1-2), 249-54.
-
(2004)
Mol Cell Endocrinol.
, vol.217
, Issue.1-2
, pp. 249-254
-
-
Bureik, M.1
Hubel, K.2
Dragan, C.A.3
Scher, J.4
Becker, H.5
Lenz, N.6
Bernhardt, R.7
-
32
-
-
27544515571
-
Molecular identity and gene expression of aldosterone synthase cytochrome P450
-
Okamoto, M.; Nonaka, Y.; Takemori, H.; Doi, J. Molecular identity and gene expression of aldosterone synthase cytochrome P450. Biochem Biophys Res Commun. 2005, 338 (1), 325-30.
-
(2005)
Biochem Biophys Res Commun.
, vol.338
, Issue.1
, pp. 325-330
-
-
Okamoto, M.1
Nonaka, Y.2
Takemori, H.3
Doi, J.4
-
33
-
-
0027401686
-
Isolation and characterization of rat CYP11B genes involved in late steps of mineralo-and glucocorticoid syntheses
-
Mukai, K.; Imai, M.; Shimada, H.; Ishimura, Y. Isolation and characterization of rat CYP11B genes involved in late steps of mineralo-and glucocorticoid syntheses. J Biol Chem. 1993, 268 (12), 9130-7.
-
(1993)
J Biol Chem.
, vol.268
, Issue.12
, pp. 9130-9137
-
-
Mukai, K.1
Imai, M.2
Shimada, H.3
Ishimura, Y.4
-
34
-
-
0031759098
-
18-Vinyldeoxycorticosterone: A potent inhibitor of the bovine cytochrome P-450(11) beta
-
Davioud, E.; Piffeteau, A.; Delorme, C.; Coustal, S.; Marquet, A. 18-Vinyldeoxycorticosterone: a potent inhibitor of the bovine cytochrome P-450(11) beta. Bioorg Med Chem. 1998, 6 (10), 1781-8.
-
(1998)
Bioorg Med Chem.
, vol.6
, Issue.10
, pp. 1781-1788
-
-
Davioud, E.1
Piffeteau, A.2
Delorme, C.3
Coustal, S.4
Marquet, A.5
-
35
-
-
0038054903
-
Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosis
-
Hartmann, R. W.; Muller, U.; Ehmer, P. B. Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosis. Eur J Med Chem. 2003, 38 (4), 363-6.
-
(2003)
Eur J Med Chem.
, vol.38
, Issue.4
, pp. 363-366
-
-
Hartmann, R.W.1
Muller, U.2
Ehmer, P.B.3
-
36
-
-
0027292450
-
Cloning and expression of a rat cytochrome P-450 11 beta-hydroxylase/aldosterone synthase (CYP11B2) cDNA variant
-
Zhou, M.; Gomez-Sanchez, C. E. Cloning and expression of a rat cytochrome P-450 11 beta-hydroxylase/aldosterone synthase (CYP11B2) cDNA variant. Biochem Biophys Res Commun. 1993, 194 (1), 112-7.
-
(1993)
Biochem Biophys Res Commun.
, vol.194
, Issue.1
, pp. 112-117
-
-
Zhou, M.1
Gomez-Sanchez, C.E.2
-
37
-
-
0028856369
-
Cloning and expression of the rat adrenal cytochrome P-450 11B3 (CYP11B3) enzyme cDNA: Preferential 18-hydroxylation over 11 beta-hydroxylation of DOC
-
Zhou, M. Y.; Gomez-Sanchez, E. P.; Foecking, M. F.; Gomez-Sanchez, C. E. Cloning and expression of the rat adrenal cytochrome P-450 11B3 (CYP11B3) enzyme cDNA: preferential 18-hydroxylation over 11 beta-hydroxylation of DOC. Mol Cell Endocrinol. 1995, 114 (1-2), 137-45.
-
(1995)
Mol Cell Endocrinol.
, vol.114
, Issue.1-2
, pp. 137-145
-
-
Zhou, M.Y.1
Gomez-Sanchez, E.P.2
Foecking, M.F.3
Gomez-Sanchez, C.E.4
-
38
-
-
0025144462
-
Cloning of cDNA and genomic DNA for human cytochrome P-45011 beta
-
Kawamoto, T.; Mitsuuchi, Y.; Toda, K.; Miyahara, K.; Yokoyama, Y.; Nakao, K.; Hosoda, K.; Yamamoto, Y.; Imura, H.; Shizuta, Y. Cloning of cDNA and genomic DNA for human cytochrome P-45011 beta. FEBS Lett. 1990, 269 (2), 345-9.
-
(1990)
FEBS Lett.
, vol.269
, Issue.2
, pp. 345-349
-
-
Kawamoto, T.1
Mitsuuchi, Y.2
Toda, K.3
Miyahara, K.4
Yokoyama, Y.5
Nakao, K.6
Hosoda, K.7
Yamamoto, Y.8
Imura, H.9
Shizuta, Y.10
-
39
-
-
0035149863
-
Immunoelectron microscopic localization of three key steroidogenic enzymes (cytochrome P450(scc), 3 betahydroxysteroid dehydrogenase and cytochrome P450(c17) in rat adrenal cortex and gonads
-
Pelletier, G.; Li, S.; Luu-The, V.; Tremblay, Y.; Belanger, A.; Labrie, F. Immunoelectron microscopic localization of three key steroidogenic enzymes (cytochrome P450(scc), 3 betahydroxysteroid dehydrogenase and cytochrome P450(c17) in rat adrenal cortex and gonads. J Endocrinol. 2001, 171 (2), 373-83.
-
(2001)
J Endocrinol.
, vol.171
, Issue.2
, pp. 373-383
-
-
Pelletier, G.1
Li, S.2
Luu-The, V.3
Tremblay, Y.4
Belanger, A.5
Labrie, F.6
-
40
-
-
0033514376
-
Biochemical differences between rat and human cytochrome P450c17 support the different steroidogenic needs of these two species
-
Brock, B. J.; Waterman, M. R. Biochemical differences between rat and human cytochrome P450c17 support the different steroidogenic needs of these two species. Biochemistry. 1999, 38 (5), 1598-606.
-
(1999)
Biochemistry.
, vol.38
, Issue.5
, pp. 1598-1606
-
-
Brock, B.J.1
Waterman, M.R.2
-
41
-
-
67650690564
-
Selective aldosterone synthase inhibitors reduce aldosterone formation in vitro and in vivo
-
Ries, C.; Lucas, S.; Heim, R.; Birk, B.; Hartmann, R. W. Selective aldosterone synthase inhibitors reduce aldosterone formation in vitro and in vivo. J Steroid Biochem Mol Biol. 2009, 116 (3-5), 121-6.
-
(2009)
J Steroid Biochem Mol Biol.
, vol.116
, Issue.3-5
, pp. 121-126
-
-
Ries, C.1
Lucas, S.2
Heim, R.3
Birk, B.4
Hartmann, R.W.5
-
42
-
-
77953749176
-
Pharmacodynamic and pharmacokinetic characterization of the aldosterone synthase inhibitor FAD286 in two rodent models of hyperaldosteronism: Comparison with the 11beta-hydroxylase inhibitor metyrapone
-
Rigel, D. F.; Fu, F.; Beil, M.; Hu, C. W.; Liang, G.; Jeng, A. Y. Pharmacodynamic and pharmacokinetic characterization of the aldosterone synthase inhibitor FAD286 in two rodent models of hyperaldosteronism: comparison with the 11beta-hydroxylase inhibitor metyrapone. J Pharmacol Exp Ther. 2010, 334 (1), 232-43.
-
(2010)
J Pharmacol Exp Ther.
, vol.334
, Issue.1
, pp. 232-243
-
-
Rigel, D.F.1
Fu, F.2
Beil, M.3
Hu, C.W.4
Liang, G.5
Jeng, A.Y.6
-
43
-
-
0032401583
-
Structure/function relationship of CYP11B1 associated with Dahl's salt-resistant rats--expression of rat CYP11B1 and CYP11B2 in Escherichia coli
-
Nonaka, Y.; Fujii, T.; Kagawa, N.; Waterman, M. R.; Takemori, H.; Okamoto, M. Structure/function relationship of CYP11B1 associated with Dahl's salt-resistant rats--expression of rat CYP11B1 and CYP11B2 in Escherichia coli. Eur J Biochem. 1998, 258 (2), 869-78.
-
(1998)
Eur J Biochem.
, vol.258
, Issue.2
, pp. 869-878
-
-
Nonaka, Y.1
Fujii, T.2
Kagawa, N.3
Waterman, M.R.4
Takemori, H.5
Okamoto, M.6
-
44
-
-
38549165088
-
Purification and functional characterization of human 11beta hydroxylase expressed in Escherichia coli
-
Zollner, A.; Kagawa, N.; Waterman, M. R.; Nonaka, Y.; Takio, K.; Shiro, Y.; Hannemann, F.; Bernhardt, R. Purification and functional characterization of human 11beta hydroxylase expressed in Escherichia coli. FEBS J. 2008, 275 (4), 799-810.
-
(2008)
FEBS J.
, vol.275
, Issue.4
, pp. 799-810
-
-
Zollner, A.1
Kagawa, N.2
Waterman, M.R.3
Nonaka, Y.4
Takio, K.5
Shiro, Y.6
Hannemann, F.7
Bernhardt, R.8
-
45
-
-
84864458519
-
Human aldosterone synthase: Recombinant expression in E. coli and purification enables a detailed biochemical analysis of the protein on the molecular level
-
Hobler, A.; Kagawa, N.; Hutter, M. C.; Hartmann, M. F.; Wudy, S. A.; Hannemann, F.; Bernhardt, R. Human aldosterone synthase: Recombinant expression in E. coli and purification enables a detailed biochemical analysis of the protein on the molecular level. J Steroid Biochem Mol Biol 2012, 132(1-2), 57-65.
-
(2012)
J Steroid Biochem Mol Biol
, vol.132
, Issue.1-2
, pp. 57-65
-
-
Hobler, A.1
Kagawa, N.2
Hutter, M.C.3
Hartmann, M.F.4
Wudy, S.A.5
Hannemann, F.6
Bernhardt, R.7
-
46
-
-
0017794351
-
Measurement of substrate and inhibitor binding to microsomal cytochrome P-450 by optical-difference spectroscopy
-
Jefcoate, C. R. Measurement of substrate and inhibitor binding to microsomal cytochrome P-450 by optical-difference spectroscopy. Methods Enzymol. 1978, 52, 258-79.
-
(1978)
Methods Enzymol.
, vol.52
, pp. 258-279
-
-
Jefcoate, C.R.1
-
47
-
-
33845358503
-
Synthetic inhibitors of cytochrome P450 2A6: Inhibitory activity, difference spectra, mechanism of inhibition, and protein cocrystallization
-
Yano, J. K.; Denton, T. T.; Cerny, M. A.; Zhang, X.; Johnson, E. F.; Cashman, J. R. Synthetic inhibitors of cytochrome P450 2A6: inhibitory activity, difference spectra, mechanism of inhibition, and protein cocrystallization. J Med Chem. 2006, 49 (24), 6987-7001.
-
(2006)
J Med Chem.
, vol.49
, Issue.24
, pp. 6987-7001
-
-
Yano, J.K.1
Denton, T.T.2
Cerny, M.A.3
Zhang, X.4
Johnson, E.F.5
Cashman, J.R.6
-
48
-
-
0001006147
-
Observations on the chromosomes of Chinese hamster cells in tissue culture
-
Ford, D. K.; Yerganian, G. Observations on the chromosomes of Chinese hamster cells in tissue culture. J Natl Cancer Inst. 1958, 21 (2), 393-425.
-
(1958)
J Natl Cancer Inst.
, vol.21
, Issue.2
, pp. 393-425
-
-
Ford, D.K.1
Yerganian, G.2
-
49
-
-
0014387212
-
Mammalian cell genetics. II. Chemical induction of specific locus mutations in Chinese hamster cells in vitro
-
Chu, E. H.; Malling, H. V. Mammalian cell genetics. II. Chemical induction of specific locus mutations in Chinese hamster cells in vitro. Proc Natl Acad Sci U S A. 1968, 61 (4), 1306-12.
-
(1968)
Proc Natl Acad Sci U S A.
, vol.61
, Issue.4
, pp. 1306-1312
-
-
Chu, E.H.1
Malling, H.V.2
-
50
-
-
0019812701
-
Mutagenesis by chemical agents in V79 chinese hamster cells: A review and analysis of the literature. A report of the Gene-Tox Program
-
Bradley, M. O.; Bhuyan, B.; Francis, M. C.; Langenbach, R.; Peterson, A.; Huberman, E. Mutagenesis by chemical agents in V79 chinese hamster cells: a review and analysis of the literature. A report of the Gene-Tox Program. Mutat Res. 1981, 87 (2), 81-142.
-
(1981)
Mutat Res.
, vol.87
, Issue.2
, pp. 81-142
-
-
Bradley, M.O.1
Bhuyan, B.2
Francis, M.C.3
Langenbach, R.4
Peterson, A.5
Huberman, E.6
-
51
-
-
0023001132
-
Metabolizing systems in short-term in vitro tests for carcinogenicity
-
Platt, K. L.; Utesch, D.; Gemperlein-Mertes, I.; Glatt, H. R.; Oesch, F. Metabolizing systems in short-term in vitro tests for carcinogenicity. Food Chem Toxicol. 1986, 24 (6-7), 721-9.
-
(1986)
Food Chem Toxicol.
, vol.24
, Issue.6-7
, pp. 721-729
-
-
Platt, K.L.1
Utesch, D.2
Gemperlein-Mertes, I.3
Glatt, H.R.4
Oesch, F.5
-
52
-
-
0343543122
-
Stable expression of rat cytochrome P-450IIB1 cDNA in Chinese hamster cells (V79) and metabolic activation of aflatoxin B1
-
Doehmer, J.; Dogra, S.; Friedberg, T.; Monier, S.; Adesnik, M.; Glatt, H.; Oesch, F. Stable expression of rat cytochrome P-450IIB1 cDNA in Chinese hamster cells (V79) and metabolic activation of aflatoxin B1. Proc Natl Acad Sci U S A. 1988, 85 (16), 5769-73.
-
(1988)
Proc Natl Acad Sci U S A.
, vol.85
, Issue.16
, pp. 5769-5773
-
-
Doehmer, J.1
Dogra, S.2
Friedberg, T.3
Monier, S.4
Adesnik, M.5
Glatt, H.6
Oesch, F.7
-
53
-
-
0029848607
-
Identification of intermediates in the conversion of cholesterol to pregnenolone with a reconstituted cytochrome p-450scc system: Accumulation of the intermediate modulated by the adrenodoxin level
-
Sugano, S.; Miura, R.; Morishima, N. Identification of intermediates in the conversion of cholesterol to pregnenolone with a reconstituted cytochrome p-450scc system: accumulation of the intermediate modulated by the adrenodoxin level. J Biochem. 1996, 120 (4), 780-7.
-
(1996)
J Biochem.
, vol.120
, Issue.4
, pp. 780-787
-
-
Sugano, S.1
Miura, R.2
Morishima, N.3
-
54
-
-
79251470430
-
Inactivation of cytochrome P450 (P450) 3A4 but not P450 3A5 by OSI-930, a thiophene-containing anticancer drug
-
Lin, H. L.; Zhang, H.; Medower, C.; Hollenberg, P. F.; Johnson, W. W. Inactivation of cytochrome P450 (P450) 3A4 but not P450 3A5 by OSI-930, a thiophene-containing anticancer drug. Drug Metab Dispos. 2011, 39 (2), 345-50.
-
(2011)
Drug Metab Dispos.
, vol.39
, Issue.2
, pp. 345-350
-
-
Lin, H.L.1
Zhang, H.2
Medower, C.3
Hollenberg, P.F.4
Johnson, W.W.5
-
55
-
-
79953148368
-
Structural basis for three-step sequential catalysis by the cholesterol side chain cleavage enzyme CYP11A1
-
Mast, N.; Annalora, A. J.; Lodowski, D. T.; Palczewski, K.; Stout, C. D.; Pikuleva, I. A. Structural basis for three-step sequential catalysis by the cholesterol side chain cleavage enzyme CYP11A1. J Biol Chem. 2011, 286 (7), 5607-13.
-
(2011)
J Biol Chem.
, vol.286
, Issue.7
, pp. 5607-5613
-
-
Mast, N.1
Annalora, A.J.2
Lodowski, D.T.3
Palczewski, K.4
Stout, C.D.5
Pikuleva, I.A.6
-
56
-
-
79951561142
-
The interaction of microsomal cytochrome P450 2B4 with its redox partners, cytochrome P450 reductase and cytochrome b(5)
-
Im, S. C.; Waskell, L. The interaction of microsomal cytochrome P450 2B4 with its redox partners, cytochrome P450 reductase and cytochrome b(5). Arch Biochem Biophys. 2011, 507 (1), 144-53.
-
(2011)
Arch Biochem Biophys.
, vol.507
, Issue.1
, pp. 144-153
-
-
Im, S.C.1
Waskell, L.2
-
57
-
-
0025873636
-
Human placental estrogen synthetase (aromatase). Effect of environment on the kinetics of protein-protein and substrate-protein interactions and the production of 19-oxygenated androgen intermediates in the purified reconstituted cytochrome P450 enzyme system
-
Sethumadhavan, K.; Bellino, F. L. Human placental estrogen synthetase (aromatase). Effect of environment on the kinetics of protein-protein and substrate-protein interactions and the production of 19-oxygenated androgen intermediates in the purified reconstituted cytochrome P450 enzyme system. J Steroid Biochem Mol Biol. 1991, 39 (3), 381-94.
-
(1991)
J Steroid Biochem Mol Biol.
, vol.39
, Issue.3
, pp. 381-394
-
-
Sethumadhavan, K.1
Bellino, F.L.2
-
58
-
-
69249206536
-
Coexpression of CYP11B2 or CYP11B1 with adrenodoxin and adrenodoxin reductase for assessing the potency and selectivity of aldosterone synthase inhibitors
-
LaSala, D.; Shibanaka, Y.; Jeng, A. Y. Coexpression of CYP11B2 or CYP11B1 with adrenodoxin and adrenodoxin reductase for assessing the potency and selectivity of aldosterone synthase inhibitors. Anal Biochem. 2009, 394 (1), 56-61.
-
(2009)
Anal Biochem.
, vol.394
, Issue.1
, pp. 56-61
-
-
LaSala, D.1
Shibanaka, Y.2
Jeng, A.Y.3
-
59
-
-
33750010974
-
Mitochondrial P450s
-
Omura, T. Mitochondrial P450s. Chem Biol Interact. 2006, 163 (1-2), 86-93.
-
(2006)
Chem Biol Interact.
, vol.163
, Issue.1-2
, pp. 86-93
-
-
Omura, T.1
-
60
-
-
84857120661
-
Human adrenocortical carcinoma cell lines
-
Wang, T.; Rainey, W. E. Human adrenocortical carcinoma cell lines. Mol and Cell Endocrinol 2012, 351 (1), 58-65.
-
(2012)
Mol and Cell Endocrinol
, vol.351
, Issue.1
, pp. 58-65
-
-
Wang, T.1
Rainey, W.E.2
-
61
-
-
33845416182
-
Regulation of steroid hormone biosynthesis enzymes and organic anion transporters by forskolin and DHEA-S treatment in adrenocortical cells
-
Asif, A. R.; Ljubojevic, M.; Sabolic, I.; Shnitsar, V.; Metten, M.; Anzai, N.; Muller, G. A.; Burckhardt, G.; Hagos, Y. Regulation of steroid hormone biosynthesis enzymes and organic anion transporters by forskolin and DHEA-S treatment in adrenocortical cells. Am J Physiol Endocrinol Metab. 2006, 291 (6), E1351-9.
-
(2006)
Am J Physiol Endocrinol Metab.
, vol.291
, Issue.6
-
-
Asif, A.R.1
Ljubojevic, M.2
Sabolic, I.3
Shnitsar, V.4
Metten, M.5
Anzai, N.6
Muller, G.A.7
Burckhardt, G.8
Hagos, Y.9
-
62
-
-
18744370748
-
Presence of organic anion transporters 3 (OAT3) and 4 (OAT4) in human adrenocortical cells
-
Asif, A. R.; Steffgen, J.; Metten, M.; Grunewald, R. W.; Muller, G. A.; Bahn, A.; Burckhardt, G.; Hagos, Y. Presence of organic anion transporters 3 (OAT3) and 4 (OAT4) in human adrenocortical cells. Pflugers Arch. 2005, 450 (2), 88-95.
-
(2005)
Pflugers Arch.
, vol.450
, Issue.2
, pp. 88-95
-
-
Asif, A.R.1
Steffgen, J.2
Metten, M.3
Grunewald, R.W.4
Muller, G.A.5
Bahn, A.6
Burckhardt, G.7
Hagos, Y.8
-
63
-
-
0033946019
-
Role of multidrug resistance P-glycoprotein in the secretion of aldosterone by human adrenal NCI-H295 cells
-
Bello-Reuss, E.; Ernest, S.; Holland, O. B.; Hellmich, M. R. Role of multidrug resistance P-glycoprotein in the secretion of aldosterone by human adrenal NCI-H295 cells. Am J Physiol Cell Physiol. 2000, 278 (6), C1256-65.
-
(2000)
Am J Physiol Cell Physiol.
, vol.278
, Issue.6
-
-
Bello-Reuss, E.1
Ernest, S.2
Holland, O.B.3
Hellmich, M.R.4
-
64
-
-
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 (1), 2-6.
-
(2011)
ACS Med Chem Lett
, vol.2
, Issue.1
, pp. 2-6
-
-
Hille, U.E.1
Zimmer, C.2
Vock, C.A.3
Hartmann, R.W.4
-
65
-
-
34548752270
-
Construction of 3D models of the CYP11B family as a tool to predict ligand binding characteristics
-
Roumen, L.; Sanders, M. P. A.; Pieterse, K.; Hilbers, P. A. J.; Plate, R.; Custers, E.; Gooyer, M.; Smits, J. F. M.; Beugels, I.; Emmen, J.; Ottenheijm, H. C. J.; Leysen, D.; Hermans, J. J. R. Construction of 3D models of the CYP11B family as a tool to predict ligand binding characteristics. J Comput Aided Mol Des. 2007, 21 (8), 455-471.
-
(2007)
J Comput Aided Mol Des.
, vol.21
, Issue.8
, pp. 455-471
-
-
Roumen, L.1
Sanders, M.P.A.2
Pieterse, K.3
Hilbers, P.A.J.4
Plate, R.5
Custers, E.6
Gooyer, M.7
Smits, J.F.M.8
Beugels, I.9
Emmen, J.10
Ottenheijm, H.C.J.11
Leysen, D.12
Hermans, J.J.R.13
-
66
-
-
0034484013
-
New mechanisms of adrenostatic compounds in a human adrenocortical cancer cell line
-
Fassnacht, M.; Hahner, S.; Beuschlein, F.; Klink, A.; Reincke, M.; Allolio, B. New mechanisms of adrenostatic compounds in a human adrenocortical cancer cell line. Eur J Clin Invest. 2000, 30 (Suppl 3), 76-82.
-
(2000)
Eur J Clin Invest.
, vol.30
, Issue.SUPPL. 3
, pp. 76-82
-
-
Fassnacht, M.1
Hahner, S.2
Beuschlein, F.3
Klink, A.4
Reincke, M.5
Allolio, B.6
-
67
-
-
0036550024
-
Effects of 3-MeSO2-DDE and some CYP inhibitors on glucocorticoid steroidogenesis in the H295R human adrenocortical carcinoma cell line
-
Johansson, M. K.; Sanderson, J. T.; Lund, B. O. Effects of 3-MeSO2-DDE and some CYP inhibitors on glucocorticoid steroidogenesis in the H295R human adrenocortical carcinoma cell line. Toxicol In vitro. 2002, 16 (2), 113-21.
-
(2002)
Toxicol In vitro.
, vol.16
, Issue.2
, pp. 113-121
-
-
Johansson, M.K.1
Sanderson, J.T.2
Lund, B.O.3
-
68
-
-
33645662194
-
Synthesis and evaluation of heteroaryl-substituted dihydronaphthalenes and indenes: Potent and selective inhibitors of aldosterone synthase (CYP11B2) for the treatment of congestive heart failure and myocardial fibrosis
-
Voets, M.; Antes, I.; Scherer, C.; Muller-Vieira, U.; Biemel, K.; Marchais-Oberwinkler, S.; Hartmann, R. W. Synthesis and evaluation of heteroaryl-substituted dihydronaphthalenes and indenes: potent and selective inhibitors of aldosterone synthase (CYP11B2) for the treatment of congestive heart failure and myocardial fibrosis. J Med Chem. 2006, 49 (7), 2222-31.
-
(2006)
J Med Chem.
, vol.49
, Issue.7
, pp. 2222-2231
-
-
Voets, M.1
Antes, I.2
Scherer, C.3
Muller-Vieira, U.4
Biemel, K.5
Marchais-Oberwinkler, S.6
Hartmann, R.W.7
-
69
-
-
77953481424
-
Etomidate unmasks intraadrenal regulation of steroidogenesis and proliferation in adrenal cortical cell lines
-
Hahner, S.; Sturmer, A.; Fassnacht, M.; Hartmann, R. W.; Schewe, K.; Cochran, S.; Zink, M.; Schirbel, A.; Allolio, B. Etomidate unmasks intraadrenal regulation of steroidogenesis and proliferation in adrenal cortical cell lines. Horm Metab Res. 2010, 42 (7), 528-34.
-
(2010)
Horm Metab Res.
, vol.42
, Issue.7
, pp. 528-534
-
-
Hahner, S.1
Sturmer, A.2
Fassnacht, M.3
Hartmann, R.W.4
Schewe, K.5
Cochran, S.6
Zink, M.7
Schirbel, A.8
Allolio, B.9
-
70
-
-
41849083040
-
New selective inhibitors of steroid 11betahydroxylation in the adrenal cortex. Synthesis and structure-activity relationship of potent etomidate analogues
-
Zolle, I. M.; Berger, M. L.; Hammerschmidt, F.; Hahner, S.; Schirbel, A.; Peric-Simov, B. New selective inhibitors of steroid 11betahydroxylation in the adrenal cortex. Synthesis and structure-activity relationship of potent etomidate analogues. J Med Chem. 2008, 51 (7), 2244-53.
-
(2008)
J Med Chem.
, vol.51
, Issue.7
, pp. 2244-2253
-
-
Zolle, I.M.1
Berger, M.L.2
Hammerschmidt, F.3
Hahner, S.4
Schirbel, A.5
Peric-Simov, B.6
-
71
-
-
77649146802
-
Carboetomidate: A pyrrole analog of etomidate designed not to suppress adrenocortical function
-
Cotten, J. F.; Forman, S. A.; Laha, J. K.; Cuny, G. D.; Husain, S. S.; Miller, K. W.; Nguyen, H. H.; Kelly, E. W.; Stewart, D.; Liu, A.; Raines, D. E. Carboetomidate: a pyrrole analog of etomidate designed not to suppress adrenocortical function. Anesthesiology. 2010, 112 (3), 637-44.
-
(2010)
Anesthesiology.
, vol.112
, Issue.3
, pp. 637-644
-
-
Cotten, J.F.1
Forman, S.A.2
Laha, J.K.3
Cuny, G.D.4
Husain, S.S.5
Miller, K.W.6
Nguyen, H.H.7
Kelly, E.W.8
Stewart, D.9
Liu, A.10
Raines, D.E.11
-
72
-
-
14944355617
-
Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/-indanes and structurally modified derivatives: Potent and selective inhibitors of aldosterone synthase
-
Ulmschneider, S.; Muller-Vieira, U.; Klein, C. D.; Antes, I.; Lengauer, T.; Hartmann, R. W. Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/-indanes and structurally modified derivatives: potent and selective inhibitors of aldosterone synthase. J Med Chem. 2005, 48 (5), 1563-75.
-
(2005)
J Med Chem.
, vol.48
, Issue.5
, pp. 1563-1575
-
-
Ulmschneider, S.1
Muller-Vieira, U.2
Klein, C.D.3
Antes, I.4
Lengauer, T.5
Hartmann, R.W.6
-
73
-
-
77649197692
-
Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1H-imidazoles as selective inhibitors of aldosterone synthase (CYP11B2)
-
Roumen, L.; Peeters, J. W.; Emmen, J. M.; Beugels, I. P.; Custers, E. M.; de Gooyer, M.; Plate, R.; Pieterse, K.; Hilbers, P. A.; Smits, J. F.; Vekemans, J. A.; Leysen, D.; Ottenheijm, H. C.; Janssen, H. M.; Hermans, J. J. Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1H-imidazoles as selective inhibitors of aldosterone synthase (CYP11B2). J Med Chem 2010, 53 (4), 1712-25.
-
(2010)
J Med Chem
, vol.53
, Issue.4
, pp. 1712-1725
-
-
Roumen, L.1
Peeters, J.W.2
Emmen, J.M.3
Beugels, I.P.4
Custers, E.M.5
de Gooyer, M.6
Plate, R.7
Pieterse, K.8
Hilbers, P.A.9
Smits, J.F.10
Vekemans, J.A.11
Leysen, D.12
Ottenheijm, H.C.13
Janssen, H.M.14
Hermans, J.J.15
-
74
-
-
20544453256
-
Aldosterone synthase inhibitor ameliorates angiotensin II-induced organ damage
-
Fiebeler, A.; Nussberger, J.; Shagdarsuren, E.; Rong, S.; Hilfenhaus, G.; Al-Saadi, N.; Dechend, R.; Wellner, M.; Meiners, S.; Maser-Gluth, C.; Jeng, A. Y.; Webb, R. L.; Luft, F. C.; Muller, D. N. Aldosterone synthase inhibitor ameliorates angiotensin II-induced organ damage. Circulation. 2005, 111 (23), 3087-94.
-
(2005)
Circulation.
, vol.111
, Issue.23
, pp. 3087-3094
-
-
Fiebeler, A.1
Nussberger, J.2
Shagdarsuren, E.3
Rong, S.4
Hilfenhaus, G.5
Al-Saadi, N.6
Dechend, R.7
Wellner, M.8
Meiners, S.9
Maser-Gluth, C.10
Jeng, A.Y.11
Webb, R.L.12
Luft, F.C.13
Muller, D.N.14
-
75
-
-
84881325307
-
-
2011-US211002011088188, 20110113
-
Hu, Q.-Y.; Ksander, G.; Meredith, E.; Monovich, L. G.; Papillon, J.; Schumacher, C. Use of an adrenal hormone-modifying agent. 2011-US211002011088188, 20110113., 2011.
-
(2011)
Use of an adrenal hormone-modifying agent
-
-
Hu, Q.-Y.1
Ksander, G.2
Meredith, E.3
Monovich, L.G.4
Papillon, J.5
Schumacher, C.6
-
76
-
-
79953774542
-
-
2006-US329122007024945, 20060823
-
Ksander, G. M.; Meredith, E.; Monovich, L. G.; Papillon, J.; Firooznia, F.; Hu, Q.-Y. Preparation of condensed imidazole derivatives for the inhibition of aldosterone synthase and aromatase. 2006-US329122007024945, 20060823., 2007.
-
(2007)
Preparation of condensed imidazole derivatives for the inhibition of aldosterone synthase and aromatase
-
-
Ksander, G.M.1
Meredith, E.2
Monovich, L.G.3
Papillon, J.4
Firooznia, F.5
Hu, Q.-Y.6
-
77
-
-
0028850596
-
Extra-adrenal effects of metyrapone include inhibition of the 11-oxoreductase activity of 11 beta-hydroxysteroid dehydrogenase: A model for 11-HSD I deficiency
-
Raven, P. W.; Checkley, S. A.; Taylor, N. F. Extra-adrenal effects of metyrapone include inhibition of the 11-oxoreductase activity of 11 beta-hydroxysteroid dehydrogenase: a model for 11-HSD I deficiency. Clin Endocrinol (Oxf). 1995, 43 (5), 637-44.
-
(1995)
Clin Endocrinol (Oxf).
, vol.43
, Issue.5
, pp. 637-644
-
-
Raven, P.W.1
Checkley, S.A.2
Taylor, N.F.3
-
78
-
-
0021350019
-
Structure-activity relationship study of the inhibition of adrenal cortical 11 beta-hydroxylase by new metyrapone analogues
-
Hays, S. J.; Tobes, M. C.; Gildersleeve, D. L.; Wieland, D. M.; Beierwaltes, W. H. Structure-activity relationship study of the inhibition of adrenal cortical 11 beta-hydroxylase by new metyrapone analogues. J Med Chem. 1984, 27 (1), 15-9.
-
(1984)
J Med Chem.
, vol.27
, Issue.1
, pp. 15-19
-
-
Hays, S.J.1
Tobes, M.C.2
Gildersleeve, D.L.3
Wieland, D.M.4
Beierwaltes, W.H.5
-
79
-
-
0021918248
-
Adrenal cortical 11 beta-hydroxylase and sidechain cleavage enzymes. Requirement for the A-or B-pyridyl ring in metyrapone for inhibition
-
Tobes, M. C.; Hays, S. J.; Gildersleeve, D. L.; Wieland, D. M.; Beierwaltes, W. H. Adrenal cortical 11 beta-hydroxylase and sidechain cleavage enzymes. Requirement for the A-or B-pyridyl ring in metyrapone for inhibition. J Steroid Biochem. 1985, 22 (1), 103-10.
-
(1985)
J Steroid Biochem.
, vol.22
, Issue.1
, pp. 103-110
-
-
Tobes, M.C.1
Hays, S.J.2
Gildersleeve, D.L.3
Wieland, D.M.4
Beierwaltes, W.H.5
-
80
-
-
79956132010
-
CYP17 inhibitors for prostate cancer therapy
-
Vasaitis, T. S.; Bruno, R. D.; Njar, V. C. CYP17 inhibitors for prostate cancer therapy. J Steroid Biochem Mol Biol. 2011, 125 (1-2), 23-31.
-
(2011)
J Steroid Biochem Mol Biol.
, vol.125
, Issue.1-2
, pp. 23-31
-
-
Vasaitis, T.S.1
Bruno, R.D.2
Njar, V.C.3
-
81
-
-
0029012814
-
Cloning and stable expression of the human mitochondrial cytochrome P45011B1 cDNA in V79 Chinese hamster cells and their application for testing of potential inhibitors
-
Denner, K.; Vogel, R.; Schmalix, W.; Doehmer, J.; Bernhardt, R. Cloning and stable expression of the human mitochondrial cytochrome P45011B1 cDNA in V79 Chinese hamster cells and their application for testing of potential inhibitors. Pharmacogenetics. 1995, 5 (2), 89-96.
-
(1995)
Pharmacogenetics.
, vol.5
, Issue.2
, pp. 89-96
-
-
Denner, K.1
Vogel, R.2
Schmalix, W.3
Doehmer, J.4
Bernhardt, R.5
-
82
-
-
80051710067
-
Optimization of the First Selective Steroid-11b-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-11b-hydroxylase (CYP11B1) Inhibitors for the Treatment of Cortisol Dependent Diseases. ACS Med Chem Lett 2011, 2 (8), 559-564.
-
(2011)
ACS Med Chem Lett
, vol.2
, Issue.8
, pp. 559-564
-
-
Hille, U.E.1
Zimmer, C.2
Haupenthal, J.3
Hartmann, R.W.4
-
83
-
-
79952043405
-
Clinical and molecular pharmacology of etomidate
-
Forman, S. A. Clinical and molecular pharmacology of etomidate. Anesthesiology. 2011, 114 (3), 695-707.
-
(2011)
Anesthesiology.
, vol.114
, Issue.3
, pp. 695-707
-
-
Forman, S.A.1
-
84
-
-
0037456430
-
Corticosteroid insufficiency in acutely ill patients
-
Cooper, M. S.; Stewart, P. M. Corticosteroid insufficiency in acutely ill patients. N Engl J Med. 2003, 348 (8), 727-34.
-
(2003)
N Engl J Med.
, vol.348
, Issue.8
, pp. 727-734
-
-
Cooper, M.S.1
Stewart, P.M.2
-
85
-
-
68249158184
-
Methoxycarbonyl-etomidate: A novel rapidly metabolized and ultra-short-acting etomidate analogue that does not produce prolonged adrenocortical suppression
-
Cotten, J. F.; Husain, S. S.; Forman, S. A.; Miller, K. W.; Kelly, E. W.; Nguyen, H. H.; Raines, D. E. Methoxycarbonyl-etomidate: a novel rapidly metabolized and ultra-short-acting etomidate analogue that does not produce prolonged adrenocortical suppression. Anesthesiology. 2009, 111 (2), 240-9.
-
(2009)
Anesthesiology.
, vol.111
, Issue.2
, pp. 240-249
-
-
Cotten, J.F.1
Husain, S.S.2
Forman, S.A.3
Miller, K.W.4
Kelly, E.W.5
Nguyen, H.H.6
Raines, D.E.7
-
86
-
-
84864405859
-
In vivo and In vitro Pharmacological Studies of Methoxycarbonyl-Carboetomidate
-
Pejo, E.; Cotten, J. F.; Kelly, E. W.; Le Ge, R.; Cuny, G. D.; Laha, J. K.; Liu, J.; Lin, X. J.; Raines, D. E. In vivo and In vitro Pharmacological Studies of Methoxycarbonyl-Carboetomidate. Anesth Analg 2011, 2011, 14.
-
(2011)
Anesth Analg
, vol.2011
, pp. 14
-
-
Pejo, E.1
Cotten, J.F.2
Kelly, E.W.3
Le Ge, R.4
Cuny, G.D.5
Laha, J.K.6
Liu, J.7
Lin, X.J.8
Raines, D.E.9
-
87
-
-
84055195125
-
Differential effects of etomidate and its pyrrole analogue carboetomidate on the adrenocortical and cytokine responses to endotoxemia
-
Pejo, E.; Feng, Y.; Chao, W.; Cotten, J. F.; Le Ge, R.; Raines, D. E. Differential effects of etomidate and its pyrrole analogue carboetomidate on the adrenocortical and cytokine responses to endotoxemia. Crit Care Med. 2012, 40 (1), 187-92.
-
(2012)
Crit Care Med.
, vol.40
, Issue.1
, pp. 187-192
-
-
Pejo, E.1
Feng, Y.2
Chao, W.3
Cotten, J.F.4
Le Ge, R.5
Raines, D.E.6
-
88
-
-
0031838388
-
In vitro and in vivo primate evaluation of carbon-11-etomidate and carbon-11-metomidate as potential tracers for PET imaging of the adrenal cortex and its tumors
-
Bergstrom, M.; Bonasera, T. A.; Lu, L.; Bergstrom, E.; Backlin, C.; Juhlin, C.; Langstrom, B. In vitro and in vivo primate evaluation of carbon-11-etomidate and carbon-11-metomidate as potential tracers for PET imaging of the adrenal cortex and its tumors. J Nucl Med. 1998, 39 (6), 982-9.
-
(1998)
J Nucl Med.
, vol.39
, Issue.6
, pp. 982-989
-
-
Bergstrom, M.1
Bonasera, T.A.2
Lu, L.3
Bergstrom, E.4
Backlin, C.5
Juhlin, C.6
Langstrom, B.7
-
89
-
-
0037246562
-
Double-blind randomised trial comparing the non-steroidal aromatase inhibitors letrozole and fadrozole in postmenopausal women with advanced breast cancer
-
Tominaga, T.; Adachi, I.; Sasaki, Y.; Tabei, T.; Ikeda, T.; Takatsuka, Y.; Toi, M.; Suwa, T.; Ohashi, Y. Double-blind randomised trial comparing the non-steroidal aromatase inhibitors letrozole and fadrozole in postmenopausal women with advanced breast cancer. Ann Oncol. 2003, 14 (1), 62-70.
-
(2003)
Ann Oncol.
, vol.14
, Issue.1
, pp. 62-70
-
-
Tominaga, T.1
Adachi, I.2
Sasaki, Y.3
Tabei, T.4
Ikeda, T.5
Takatsuka, Y.6
Toi, M.7
Suwa, T.8
Ohashi, Y.9
-
90
-
-
0025361466
-
The effects of CGS 16949A, an aromatase inhibitor on adrenal mineralocorticoid biosynthesis
-
Demers, L. M.; Melby, J. C.; Wilson, T. E.; Lipton, A.; Harvey, H. A.; Santen, R. J. The effects of CGS 16949A, an aromatase inhibitor on adrenal mineralocorticoid biosynthesis. J Clin Endocrinol Metab 1990, 70 (4), 1162-6.
-
(1990)
J Clin Endocrinol Metab
, vol.70
, Issue.4
, pp. 1162-1166
-
-
Demers, L.M.1
Melby, J.C.2
Wilson, T.E.3
Lipton, A.4
Harvey, H.A.5
Santen, R.J.6
-
91
-
-
0025327094
-
Potency and selectivity of the non-steroidal aromatase inhibitor CGS 16949A in postmenopausal breast cancer patients
-
Dowsett, M.; Stein, R. C.; Mehta, A.; Coombes, R. C. Potency and selectivity of the non-steroidal aromatase inhibitor CGS 16949A in postmenopausal breast cancer patients. Clin Endocrinol (Oxf) 1990, 32 (5), 623-34.
-
(1990)
Clin Endocrinol (Oxf)
, vol.32
, Issue.5
, pp. 623-634
-
-
Dowsett, M.1
Stein, R.C.2
Mehta, A.3
Coombes, R.C.4
-
92
-
-
0027157717
-
The effects of long term fadrozole hydrochloride treatment in patients with advanced stage breast cancer
-
Demers, L. M.; Lipton, A.; Harvey, H. A.; Hanagan, J.; Mulagha, M.; Santen, R. J. The effects of long term fadrozole hydrochloride treatment in patients with advanced stage breast cancer. J Steroid Biochem Mol Biol. 1993, 44 (4-6), 683-5.
-
(1993)
J Steroid Biochem Mol Biol.
, vol.44
, Issue.4-6
, pp. 683-685
-
-
Demers, L.M.1
Lipton, A.2
Harvey, H.A.3
Hanagan, J.4
Mulagha, M.5
Santen, R.J.6
-
93
-
-
0025740676
-
Specificity of low dose fadrozole hydrochloride (CGS 16949A) as an aromatase inhibitor
-
Santen, R. J.; Demers, L. M.; Lynch, J.; Harvey, H.; Lipton, A.; Mulagha, M.; Hanagan, J.; Garber, J. E.; Henderson, I. C.; Navari, R. M.; et al., Specificity of low dose fadrozole hydrochloride (CGS 16949A) as an aromatase inhibitor. J Clin Endocrinol Metab. 1991, 73 (1), 99-106.
-
(1991)
J Clin Endocrinol Metab.
, vol.73
, Issue.1
, pp. 99-106
-
-
Santen, R.J.1
Demers, L.M.2
Lynch, J.3
Harvey, H.4
Lipton, A.5
Mulagha, M.6
Hanagan, J.7
Garber, J.E.8
Henderson, I.C.9
Navari, R.M.10
-
94
-
-
84865760148
-
The effects of aldosterone synthase inhibition on aldosterone and cortisol in patients with hypertension: A phase II, randomized, double-blind, placebo-controlled, multicenter study
-
Andersen, K.; Hartman, D.; Peppard, T.; Hermann, D.; Van Ess, P.; Lefkowitz, M.; Trapani, A. The effects of aldosterone synthase inhibition on aldosterone and cortisol in patients with hypertension: a phase II, randomized, double-blind, placebo-controlled, multicenter study. J Clin Hypertens 2012, 14 (9), 580-7.
-
(2012)
J Clin Hypertens
, vol.14
, Issue.9
, pp. 580-587
-
-
Andersen, K.1
Hartman, D.2
Peppard, T.3
Hermann, D.4
van Ess, P.5
Lefkowitz, M.6
Trapani, A.7
-
95
-
-
0035893679
-
Modelling of three-dimensional structures of cytochromes P450 11B1 and 11B2
-
Belkina, N. V.; Lisurek, M.; Ivanov, A. S.; Bernhardt, R. Modelling of three-dimensional structures of cytochromes P450 11B1 and 11B2. J Inorg Biochem. 2001, 87 (4), 197-207.
-
(2001)
J Inorg Biochem.
, vol.87
, Issue.4
, pp. 197-207
-
-
Belkina, N.V.1
Lisurek, M.2
Ivanov, A.S.3
Bernhardt, R.4
-
96
-
-
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 (7), 2307-19.
-
(2011)
J Med Chem.
, vol.54
, Issue.7
, pp. 2307-2319
-
-
Lucas, S.1
Negri, M.2
Heim, R.3
Zimmer, C.4
Hartmann, R.W.5
-
97
-
-
0030737703
-
Mechanismbased inactivation of bovine cytochrome P-450(11beta) by 18-unsaturated progesterone derivatives
-
Delorme, C.; Piffeteau, A.; Sobrio, F.; Marquet, A. Mechanismbased inactivation of bovine cytochrome P-450(11beta) by 18-unsaturated progesterone derivatives. Eur J Biochem. 1997, 248 (1), 252-60.
-
(1997)
Eur J Biochem.
, vol.248
, Issue.1
, pp. 252-260
-
-
Delorme, C.1
Piffeteau, A.2
Sobrio, F.3
Marquet, A.4
-
98
-
-
0029135315
-
Inhibition of bovine cytochrome P-450(11 beta) by 18-unsaturated progesterone derivatives
-
Delorme, C.; Piffeteau, A.; Viger, A.; Marquet, A. Inhibition of bovine cytochrome P-450(11 beta) by 18-unsaturated progesterone derivatives. Eur J Biochem. 1995, 232 (1), 247-56.
-
(1995)
Eur J Biochem.
, vol.232
, Issue.1
, pp. 247-256
-
-
Delorme, C.1
Piffeteau, A.2
Viger, A.3
Marquet, A.4
-
99
-
-
0024464221
-
18-Substituted progesterone derivatives as inhibitors of aldosterone biosynthesis
-
Viger, A.; Coustal, S.; Perard, S.; Piffeteau, A.; Marquet, A. 18-Substituted progesterone derivatives as inhibitors of aldosterone biosynthesis. J Steroid Biochem. 1989, 33 (1), 119-24.
-
(1989)
J Steroid Biochem.
, vol.33
, Issue.1
, pp. 119-124
-
-
Viger, A.1
Coustal, S.2
Perard, S.3
Piffeteau, A.4
Marquet, A.5
-
100
-
-
0030661602
-
Inhibition of steroidogenesis in rat adrenal cells by 18-ethynyldeoxycorticosterone: Evidence for an alternative pathway of aldosterone biosynthesis
-
Gomez-Sanchez, C. E.; Gomez-Sanchez, E. P.; Foecking, M. F.; Zhou, M. Y. Inhibition of steroidogenesis in rat adrenal cells by 18-ethynyldeoxycorticosterone: evidence for an alternative pathway of aldosterone biosynthesis. J Steroid Biochem Mol Biol. 1997, 62 (2/3), 207-212.
-
(1997)
J Steroid Biochem Mol Biol.
, vol.62
, Issue.2-3
, pp. 207-212
-
-
Gomez-Sanchez, C.E.1
Gomez-Sanchez, E.P.2
Foecking, M.F.3
Zhou, M.Y.4
-
103
-
-
0028831852
-
Enzyme-activated inhibitors of steroidal hydroxylases
-
Johnston, J. O.; Wright, C. L.; Holbert, G. W. Enzyme-activated inhibitors of steroidal hydroxylases. J Steroid Biochem Mol Biol. 1995, 52 (1), 17-34.
-
(1995)
J Steroid Biochem Mol Biol.
, vol.52
, Issue.1
, pp. 17-34
-
-
Johnston, J.O.1
Wright, C.L.2
Holbert, G.W.3
-
104
-
-
0025788412
-
Inhibition of aldosterone biosynthesis by 18-ethynyl-deoxycorticosterone
-
Yamakita, N.; Chiou, S.; Gomez-Sanchez, C. E. Inhibition of aldosterone biosynthesis by 18-ethynyl-deoxycorticosterone. Endocrinology. 1991, 129 (5), 2361-6.
-
(1991)
Endocrinology.
, vol.129
, Issue.5
, pp. 2361-2366
-
-
Yamakita, N.1
Chiou, S.2
Gomez-Sanchez, C.E.3
-
105
-
-
0025837758
-
Renal action of progesterone and 18-substituted derivatives
-
Rafestin-Oblin, M. E.; Couette, B.; Barlet-Bas, C.; Cheval, L.; Viger, A.; Doucet, A. Renal action of progesterone and 18-substituted derivatives. Am J Physiol. 1991, 260 (6 Pt 2), F828-32.
-
(1991)
Am J Physiol.
, vol.260
, Issue.6 Pt 2
-
-
Rafestin-Oblin, M.E.1
Couette, B.2
Barlet-Bas, C.3
Cheval, L.4
Viger, A.5
Doucet, A.6
-
106
-
-
0028026819
-
Selective inhibition of steroidogenic P450 enzymes: Current status and future perspectives
-
Hartmann, R. W. Selective inhibition of steroidogenic P450 enzymes: current status and future perspectives. Eur J Pharm Sci 1994, 2 (1-2), 15-16.
-
(1994)
Eur J Pharm Sci
, vol.2
, Issue.1-2
, pp. 15-16
-
-
Hartmann, R.W.1
-
107
-
-
20144370140
-
Synthesis and evaluation of imidazolylmethylenetetrahydronaphthalenes and imidazolylmethyleneindanes: Potent inhibitors of aldosterone synthase
-
Ulmschneider, S.; Muller-Vieira, U.; Mitrenga, M.; Hartmann, R. W.; Oberwinkler-Marchais, S.; Klein, C. D.; Bureik, M.; Bernhardt, R.; Antes, I.; Lengauer, T. Synthesis and evaluation of imidazolylmethylenetetrahydronaphthalenes and imidazolylmethyleneindanes: potent inhibitors of aldosterone synthase. J Med Chem. 2005, 48 (6), 1796-805.
-
(2005)
J Med Chem.
, vol.48
, Issue.6
, pp. 1796-1805
-
-
Ulmschneider, S.1
Muller-Vieira, U.2
Mitrenga, M.3
Hartmann, R.W.4
Oberwinkler-Marchais, S.5
Klein, C.D.6
Bureik, M.7
Bernhardt, R.8
Antes, I.9
Lengauer, T.10
-
108
-
-
27144472491
-
Heteroaryl-substituted naphthalenes and structurally modified derivatives: Selective inhibitors of CYP11B2 for the treatment of congestive heart failure and myocardial fibrosis
-
Voets, M.; Antes, I.; Scherer, C.; Muller-Vieira, U.; Biemel, K.; Barassin, C.; Marchais-Oberwinkler, S.; Hartmann, R. W. Heteroaryl-substituted naphthalenes and structurally modified derivatives: selective inhibitors of CYP11B2 for the treatment of congestive heart failure and myocardial fibrosis. J Med Chem. 2005, 48 (21), 6632-42.
-
(2005)
J Med Chem.
, vol.48
, Issue.21
, pp. 6632-6642
-
-
Voets, M.1
Antes, I.2
Scherer, C.3
Muller-Vieira, U.4
Biemel, K.5
Barassin, C.6
Marchais-Oberwinkler, S.7
Hartmann, R.W.8
-
109
-
-
27744485786
-
Development and evaluation of a pharmacophore model for inhibitors of aldosterone synthase (CYP11B2)
-
Ulmschneider, S.; Negri, M.; Voets, M.; Hartmann, R. W. Development and evaluation of a pharmacophore model for inhibitors of aldosterone synthase (CYP11B2). Bioorg Med Chem Lett. 2006, 16 (1), 25-30.
-
(2006)
Bioorg Med Chem Lett.
, vol.16
, Issue.1
, pp. 25-30
-
-
Ulmschneider, S.1
Negri, M.2
Voets, M.3
Hartmann, R.W.4
-
110
-
-
0023189253
-
Activation mechanisms to chemical toxicity
-
Parke, D. V. Activation mechanisms to chemical toxicity. Arch Toxicol. 1987, 60 (1-3), 5-15.
-
(1987)
Arch Toxicol.
, vol.60
, Issue.1-3
, pp. 5-15
-
-
Parke, D.V.1
-
111
-
-
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.; Muller-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 (16), 5064-74.
-
(2008)
J Med Chem.
, vol.51
, Issue.16
, pp. 5064-5074
-
-
Heim, R.1
Lucas, S.2
Grombein, C.M.3
Ries, C.4
Schewe, K.E.5
Negri, M.6
Muller-Vieira, U.7
Birk, B.8
Hartmann, R.W.9
-
112
-
-
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 (19), 6138-49.
-
(2008)
J Med Chem.
, vol.51
, Issue.19
, 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
-
113
-
-
58149087304
-
In vivo active aldosterone synthase inhibitors with improved selectivity: Lead optimization providing a series of pyridine substituted 3,4-dihydro-1H-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-1H-quinolin-2-one derivatives. J Med Chem. 2008, 51 (24), 8077-87.
-
(2008)
J Med Chem.
, vol.51
, Issue.24
, pp. 8077-8087
-
-
Lucas, S.1
Heim, R.2
Ries, C.3
Schewe, K.E.4
Birk, B.5
Hartmann, R.W.6
-
114
-
-
78650514131
-
N-(Pyridin-3-yl)benzamides as selective inhibitors of human aldosterone synthase (CYP11B2)
-
Zimmer, C.; Hafner, M.; Zender, M.; Ammann, D.; Hartmann, R. W.; Vock, C. A. N-(Pyridin-3-yl)benzamides as selective inhibitors of human aldosterone synthase (CYP11B2). Bioorg Med Chem Lett. 2010, 21 (1), 186-90.
-
(2010)
Bioorg Med Chem Lett.
, vol.21
, Issue.1
, pp. 186-190
-
-
Zimmer, C.1
Hafner, M.2
Zender, M.3
Ammann, D.4
Hartmann, R.W.5
Vock, C.A.6
-
115
-
-
77955426300
-
The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-beta-hydroxylase
-
Adams, C. M.; Hu, C. W.; Jeng, A. Y.; Karki, R.; Ksander, G.; Lasala, D.; Leung-Chu, J.; Liang, G.; Liu, Q.; Meredith, E.; Rao, C.; Rigel, D. F.; Shi, J.; Smith, S.; Springer, C.; Zhang, C. The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-beta-hydroxylase. Bioorg Med Chem Lett. 2010, 20 (15), 4324-7.
-
(2010)
Bioorg Med Chem Lett.
, vol.20
, Issue.15
, pp. 4324-4327
-
-
Adams, C.M.1
Hu, C.W.2
Jeng, A.Y.3
Karki, R.4
Ksander, G.5
Lasala, D.6
Leung-Chu, J.7
Liang, G.8
Liu, Q.9
Meredith, E.10
Rao, C.11
Rigel, D.F.12
Shi, J.13
Smith, S.14
Springer, C.15
Zhang, C.16
-
116
-
-
0001072162
-
DL-1-(1-Arylalkyl)imidazole-5-carboxylate esters. A novel type of hypnotic agents
-
Godefroi, E. F.; Janssen, P. A.; Vandereycken, C. A.; Vanheertum, A. H.; Niemegeers, C. J. DL-1-(1-Arylalkyl)imidazole-5-carboxylate esters. A novel type of hypnotic agents. J Med Chem. 1965, 8, 220-3.
-
(1965)
J Med Chem.
, vol.8
, pp. 220-223
-
-
Godefroi, E.F.1
Janssen, P.A.2
Vandereycken, C.A.3
Vanheertum, A.H.4
Niemegeers, C.J.5
-
117
-
-
78149282496
-
Hormonal and electrolyte responses to the aldosterone synthase inhibitor LCI699 in sodium depleted healthy subjects
-
Menard, J.; Watson, C.; Rebello, S.; Zhang, Y. M.; Dole, W. P. Hormonal and electrolyte responses to the aldosterone synthase inhibitor LCI699 in sodium depleted healthy subjects. J Am Coll Cardiol 2010, 55 (10), A61. E583.
-
(2010)
J Am Coll Cardiol
, vol.55
, Issue.10
-
-
Menard, J.1
Watson, C.2
Rebello, S.3
Zhang, Y.M.4
Dole, W.P.5
-
118
-
-
78149238346
-
Aldosterone synthase inhibition with LCI699: A proof-ofconcept study in patients with primary aldosteronism
-
Amar, L.; Azizi, M.; Menard, J.; Peyrard, S.; Watson, C.; Plouin, P. F. Aldosterone synthase inhibition with LCI699: a proof-ofconcept study in patients with primary aldosteronism. Hypertension. 2010, 56 (5), 831-8.
-
(2010)
Hypertension.
, vol.56
, Issue.5
, pp. 831-838
-
-
Amar, L.1
Azizi, M.2
Menard, J.3
Peyrard, S.4
Watson, C.5
Plouin, P.F.6
|