-
1
-
-
0026543213
-
Role of steroid 11β-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans
-
Kawamoto, T.; Mitsuuchi, Y.; Toda, K.; Yokoyama, Y.; Miyakara, K.; Miura, S.; Onishi, T.; Ichihawa, Y.; Nakao, K.; Imura, H.; Ulick, S.; Shizuta, Y. Role of steroid 11β-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans. Proc. Natl. Acad. Sci. U.S.A. 1992, 89, 1458-1462.
-
(1992)
Proc. Natl. Acad. Sci. U.S.A.
, vol.89
, pp. 1458-1462
-
-
Kawamoto, T.1
Mitsuuchi, Y.2
Toda, K.3
Yokoyama, Y.4
Miyakara, K.5
Miura, S.6
Onishi, T.7
Ichihawa, Y.8
Nakao, K.9
Imura, H.10
Ulick, S.11
Shizuta, Y.12
-
2
-
-
0033935122
-
Aldosterone and myocardial fibrosis in heart failure
-
Brilla, C. G. Aldosterone and myocardial fibrosis in heart failure. Herz 2000, 25, 299-306.
-
(2000)
Herz
, vol.25
, pp. 299-306
-
-
Brilla, C.G.1
-
3
-
-
0033840926
-
Induction of cardiac fibrosis by aldosterone
-
Lijnen, P.; Petrov, V. Induction of cardiac fibrosis by aldosterone. J. Mol. Cell. Cardiol. 2000, 32, 865-879.
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 865-879
-
-
Lijnen, P.1
Petrov, V.2
-
4
-
-
0033517302
-
The effect of spironolactone on morbidity and mortality in patients with severe heart failure
-
Pitt, B.; Zannad, F.; Remme, W. J.; Cody, R.; Castaigne, A.; Perez, A.; Palensky, J.; Wittes, J. The effect of spironolactone on morbidity and mortality in patients with severe heart failure. N. Eng. J. Med. 1999, 341, 709-717.
-
(1999)
N. Eng. J. Med.
, vol.341
, pp. 709-717
-
-
Pitt, B.1
Zannad, F.2
Remme, W.J.3
Cody, R.4
Castaigne, A.5
Perez, A.6
Palensky, J.7
Wittes, J.8
-
5
-
-
0037417252
-
Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction
-
Pitt, B.; Remme, W. J.; 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. Eng. J. Med. 2003, 348, 1309-21.
-
(2003)
N. Eng. J. Med.
, vol.348
, pp. 1309-1321
-
-
Pitt, B.1
Remme, W.J.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
-
6
-
-
3042616446
-
The role of aldosterone and aldosterone-receptor antagonists in heart failure
-
Khan, N. U. A.; Movahed, A. The role of aldosterone and aldosterone-receptor antagonists in heart failure. Rev. Cardiovasc. Med. 2004, 5, 71-81.
-
(2004)
Rev. Cardiovasc. Med.
, vol.5
, pp. 71-81
-
-
Khan, N.U.A.1
Movahed, A.2
-
7
-
-
3442886513
-
Rates of hyperkalemia after publication of the randomized aldactone evaluation study
-
Juurlink, D. N.; Mamdani, M. M.; Lee, D. S.; Kopp, A.; Austin, P. C.; Laupacis, A.; Redelmeier, D. A. Rates of hyperkalemia after publication of the randomized aldactone evaluation study. N. Engl. J. Med. 2004, 351, 543-551.
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 543-551
-
-
Juurlink, D.N.1
Mamdani, M.M.2
Lee, D.S.3
Kopp, A.4
Austin, P.C.5
Laupacis, A.6
Redelmeier, D.A.7
-
8
-
-
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, 15-16.
-
(1994)
Eur. J. Pharm. Sci.
, vol.2
, pp. 15-16
-
-
Hartmann, R.W.1
-
9
-
-
0036345081
-
Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): Screening in fission yeast and evaluation of selectivity in V79 cells
-
Ehmer, P. B.; Bureik, M.; Bernhardt, R.; Müller, U.; Hartmann, R. W. Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): Screening in fission yeast and evaluation of selectivity in V79 cells. J. Steroid Biochem. Mol. Biol. 2002, 81, 173-179.
-
(2002)
J. Steroid Biochem. Mol. Biol.
, vol.81
, pp. 173-179
-
-
Ehmer, P.B.1
Bureik, M.2
Bernhardt, R.3
Müller, U.4
Hartmann, R.W.5
-
10
-
-
0038054903
-
Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosis
-
Hartmann, R. W.; Müller, 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, 363-366.
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 363-366
-
-
Hartmann, R.W.1
Müller, U.2
Ehmer, P.B.3
-
11
-
-
0029044427
-
Pyridyl-substituted tetrahydrocyclopropa[α]naphthalenes: Highly active and selective inhibitors of P450 arom
-
(a) Hartmann, R. W.; Bayer, H.; Grün, G.; Sergejew, T.; Bartz, U.; Mitrenga, M. Pyridyl-substituted tetrahydrocyclopropa[α]naphthalenes: Highly active and selective inhibitors of P450 arom. J. Med. Chem. 1995, 38, 2103-2111.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2103-2111
-
-
Hartmann, R.W.1
Bayer, H.2
Grün, G.3
Sergejew, T.4
Bartz, U.5
Mitrenga, M.6
-
13
-
-
84872647271
-
A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-hydroxylase/C17,20-lyase
-
(c) Recanatini, M.; Bisi, A.; Cavalli, A.; Belluti, F.; Gobbi, S.; Rampa, A.; Valenti, P.; Palzer, M.; Palusczak, A.; Hartmann, R. W. A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17α-hydroxylase/C17,20-lyase. J. Med. Chem. 2001, 44, 672-680.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 672-680
-
-
Recanatini, M.1
Bisi, A.2
Cavalli, A.3
Belluti, F.4
Gobbi, S.5
Rampa, A.6
Valenti, P.7
Palzer, M.8
Palusczak, A.9
Hartmann, R.W.10
-
14
-
-
11144224747
-
Design, synthesis and 3D QSAR of novel potent and selective aromatase inhibitors
-
(d) Leonetti, F.; Favia, A.; Rao, A.; Aliano, R.; Palusczak, A.; Hartmann, R. W.; Carotti, A. Design, synthesis and 3D QSAR of novel potent and selective aromatase inhibitors. J. Med. Chem. 2004, 47, 6792-6803.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6792-6803
-
-
Leonetti, F.1
Favia, A.2
Rao, A.3
Aliano, R.4
Palusczak, A.5
Hartmann, R.W.6
Carotti, A.7
-
15
-
-
0032835607
-
Imidazole substituted biphenyls: A new class of highly potent and in vivo active inhibitors of P450 17 as potential therapeutics for treatment of prostate cancer
-
(a) Wachall, B. G.; Hector, M.; Zhuang, Y.; Hartmann, R. W. Imidazole substituted biphenyls: A new class of highly potent and in vivo active inhibitors of P450 17 as potential therapeutics for treatment of prostate cancer. Bioorg. Med. Chem. 1999, 7, 1913-1924.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 1913-1924
-
-
Wachall, B.G.1
Hector, M.2
Zhuang, Y.3
Hartmann, R.W.4
-
16
-
-
0034676307
-
Synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17α-hydroxylase/C17-20-lyase (P450 17)
-
(b) Hartmann, R. W.; Hector, M.; Wachall, B. G.; Palusczak, A.; Palzer, M.; Huch, V.; Veith, M. Synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17α-hydroxylase/C17-20- lyase (P450 17). J. Med. Chem. 2000, 43, 4437-4445.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4437-4445
-
-
Hartmann, R.W.1
Hector, M.2
Wachall, B.G.3
Palusczak, A.4
Palzer, M.5
Huch, V.6
Veith, M.7
-
17
-
-
0034088239
-
Novel imidazolyl and triazolyl substituted biphenyl compounds: Synthesis and evaluation as nonsteroidal inhibitors of human 17α-hydroxylase-C17,20- lyase (P450 17)
-
(c) Zhuang, Y.; Wachall, B. G.; Hartmann, R. W. Novel imidazolyl and triazolyl substituted biphenyl compounds: Synthesis and evaluation as nonsteroidal inhibitors of human 17α-hydroxylase-C17,20-lyase (P450 17). Bioorg. Med. Chem. 2000, 8, 1245-1252.
-
(2000)
Bioorg. Med. Chem.
, vol.8
, pp. 1245-1252
-
-
Zhuang, Y.1
Wachall, B.G.2
Hartmann, R.W.3
-
18
-
-
0038062686
-
Effects of novel 17α-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo
-
(d) Haidar, S.; Ehmer, P. B.; Barassin, S.; Batzl-Hartmann, C.; Hartmann, R. W. Effects of novel 17α-hydroxylase/C17,20-lyase (P450 17, CYP 17) inhibitors on androgen biosynthesis in vitro and in vivo. J. Steroid Biochem. Mol. Biol. 2003, 84, 555-562.
-
(2003)
J. Steroid Biochem. Mol. Biol.
, vol.84
, pp. 555-562
-
-
Haidar, S.1
Ehmer, P.B.2
Barassin, S.3
Batzl-Hartmann, C.4
Hartmann, R.W.5
-
19
-
-
0031733012
-
Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3
-
Taymans, S. E.; Pack, S.; Pak, E.; Torpy, D. J.; Zhuang, Z.; Stratakis, C. A. Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3. J. Clin. Endocrinol. Metab. 1998, 83, 1033-1036.
-
(1998)
J. Clin. Endocrinol. Metab.
, vol.83
, pp. 1033-1036
-
-
Taymans, S.E.1
Pack, S.2
Pak, E.3
Torpy, D.J.4
Zhuang, Z.5
Stratakis, C.A.6
-
20
-
-
0024850612
-
Evidence that corticosterone is not an obligatory intermediate in aldosterone biosynthesis in the rat adrenal
-
Häusler, A.; Monnet, G.; Borer, C.; Bhatnagar, A. S. Evidence that corticosterone is not an obligatory intermediate in aldosterone biosynthesis in the rat adrenal. J. Steroid Biochem. 1989, 34, 567-570.
-
(1989)
J. Steroid Biochem.
, vol.34
, pp. 567-570
-
-
Häusler, A.1
Monnet, G.2
Borer, C.3
Bhatnagar, A.S.4
-
21
-
-
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, 1162-1166.
-
(1990)
J. Clin. Endocrinol. Metab.
, vol.70
, 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
-
22
-
-
2342632561
-
Development of test systems for the discovery of selective human aldosterone synthase (CYP11B2) and 11beta-hydroxylase (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 11beta-hydroxylase (CYP11B1) inhibitors. Discovery of a new lead compound for the therapy of congestive heart failure, myocardial fibrosis and hypertension. Mol. Cell. Endocrinol. 2004, 217, 249-254.
-
(2004)
Mol. Cell. Endocrinol.
, vol.217
, 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
-
23
-
-
20144370140
-
Synthesis and evaluation of imidazolylmethylene-tetrahydronaphthalenes and imidazolylmethylene-indanes: Potent inhibitors of aldosterone synthase
-
Ulmschneider, S.; Müller-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 imidazolylmethylene- tetrahydronaphthalenes and imidazolylmethylene-indanes: Potent inhibitors of aldosterone synthase. J. Med. Chem. 2005, 48, 1796-1805.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1796-1805
-
-
Ulmschneider, S.1
Müller-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
-
24
-
-
14944355617
-
Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/- indanes and structurally modified derivatives: Potent and selective inhibitors of aldosterone synthase
-
Ulmschneider, S.; Müller-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, 1563-1575.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1563-1575
-
-
Ulmschneider, S.1
Müller-Vieira, U.2
Klein, C.D.3
Antes, I.4
Lengauer, T.5
Hartmann, R.W.6
-
25
-
-
2042507954
-
Palladium-catalyzed cross-coupling reactions of organoboron compounds
-
Miyaura, N.; Suzuki, N. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95, 2457-2483.
-
(1995)
Chem. Rev.
, vol.95
, pp. 2457-2483
-
-
Miyaura, N.1
Suzuki, N.2
-
26
-
-
84918727092
-
Orientating phenomena in the substitution on aromatic bicyclic compounds. III. Radical substitutions in the naphthalene group
-
Huisgen, R.; Sorge, G. Orientating phenomena in the substitution on aromatic bicyclic compounds. III. Radical substitutions in the naphthalene group. Liebigs Ann. Chem. 1950, 566, 162-184.
-
(1950)
Liebigs Ann. Chem.
, vol.566
, pp. 162-184
-
-
Huisgen, R.1
Sorge, G.2
-
27
-
-
0033390320
-
Preparation and pharmacological evaluation of novel glycoprotein (Gp) IIb/IIIa antagonists. 1. The selection of naphthalene derivatives
-
Ono, S.; Inoue, Y.; Yoshida, T.; Ashimori, A.; Kosaka, K.; Imada, T.; Fukaya, C.; Nakamura, N. Preparation and pharmacological evaluation of novel glycoprotein (Gp) IIb/IIIa antagonists. 1. The selection of naphthalene derivatives. Chem. Pharm. Bull. 1999, 49, 1685-1693.
-
(1999)
Chem. Pharm. Bull.
, vol.49
, pp. 1685-1693
-
-
Ono, S.1
Inoue, Y.2
Yoshida, T.3
Ashimori, A.4
Kosaka, K.5
Imada, T.6
Fukaya, C.7
Nakamura, N.8
-
28
-
-
27144556191
-
-
(Wyeth). Substituted phenyl naphthalenes as estrogenic agents. Patent WO03051805, 2003
-
Mewshaw, R. E.; Edsall, R. J.; Yang, C.; Harris, H. A.; Keith, J. C.; Albert, L. M. (Wyeth). Substituted phenyl naphthalenes as estrogenic agents. Patent WO03051805, 2003.
-
-
-
Mewshaw, R.E.1
Edsall, R.J.2
Yang, C.3
Harris, H.A.4
Keith, J.C.5
Albert, L.M.6
-
29
-
-
27144459656
-
Halogen reactivities. Certain heterocyclic iminohalide systems
-
Young, T. E.; Amstutz, E. D. Halogen reactivities. Certain heterocyclic iminohalide systems. J. Am. Chem. Soc. 1951, 4773-4775.
-
(1951)
J. Am. Chem. Soc.
, pp. 4773-4775
-
-
Young, T.E.1
Amstutz, E.D.2
-
30
-
-
0001444643
-
A mild efficient procedure for the conversion of carboxylic acid esters to primary amides using formamide/methanolic sodium methoxide
-
Jagdmann, G. E.; Munson, H. R.; Gero, T. W. A mild efficient procedure for the conversion of carboxylic acid esters to primary amides using formamide/methanolic sodium methoxide. Synth. Commun. 1990, 20, 1203-1208.
-
(1990)
Synth. Commun.
, vol.20
, pp. 1203-1208
-
-
Jagdmann, G.E.1
Munson, H.R.2
Gero, T.W.3
-
31
-
-
0032493017
-
New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
-
Lam, P. Y. S.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M. T.; Combs, A. New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation. Tetrahedron Lett. 1998, 39, 2941-2944.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2941-2944
-
-
Lam, P.Y.S.1
Clark, C.G.2
Saubern, S.3
Adams, J.4
Winters, M.P.5
Chan, D.M.T.6
Combs, A.7
-
32
-
-
1642480209
-
A simple copper salt catalysed the coupling of imidazole with arylboronic acids in protic solvent
-
Lan, J.; Chen, L.; Yu, X.; You, J.; Xie, R. A simple copper salt catalysed the coupling of imidazole with arylboronic acids in protic solvent. Chem. Commun. 2004, 2, 188-189.
-
(2004)
Chem. Commun.
, vol.2
, pp. 188-189
-
-
Lan, J.1
Chen, L.2
Yu, X.3
You, J.4
Xie, R.5
-
33
-
-
84979394958
-
Imidazolsynthesen mit formamid
-
Bredereck, H.; Theilig, G. Imidazolsynthesen mit Formamid. Chem. Ber. 1953, 86, 88-96.
-
(1953)
Chem. Ber.
, vol.86
, pp. 88-96
-
-
Bredereck, H.1
Theilig, G.2
-
34
-
-
0029016986
-
Cloning of CYP11B1 and CYP11B2 from normal human adrenal and their functional expression in COS-7 and V79 chinese hamster cells
-
Denner, K.; Doehmer, J.; Bernhardt, R. Cloning of CYP11B1 and CYP11B2 from normal human adrenal and their functional expression in COS-7 and V79 chinese hamster cells. Endocr. Res. 1995, 21, 443-448.
-
(1995)
Endocr. Res.
, vol.21
, pp. 443-448
-
-
Denner, K.1
Doehmer, J.2
Bernhardt, R.3
-
35
-
-
0016293443
-
Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione
-
Thompson, E. A.; Siiteri, P. K. Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione. J. Biol. Chem. 1974, 249, 5364-5372.
-
(1974)
J. Biol. Chem.
, vol.249
, pp. 5364-5372
-
-
Thompson, E.A.1
Siiteri, P.K.2
-
36
-
-
0022470925
-
Aromatase inhibitors. Synthesis and evaluation of mammary tumor inhibiting activity of 3-alkylated 3-(4-aminophenyl)piperidine-2,6-diones
-
Hartmann, R. W.; Batzl, C. Aromatase inhibitors. Synthesis and evaluation of mammary tumor inhibiting activity of 3-alkylated 3-(4-aminophenyl) piperidine-2,6-diones. J. Med. Chem. 1986, 29, 1362-1369.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1362-1369
-
-
Hartmann, R.W.1
Batzl, C.2
-
37
-
-
0034484809
-
17,20-lyase (P450c17) by coexpression of P450c17 with NADPH-cytochrome-P450-reductase in Escherichia coli
-
17,20-lyase (P450c17) by coexpression of P450c17 with NADPH-cytochrome-P450-reductase in Escherichia coli. J. Steroid Biochem. Mol. Biol. 2000, 75, 57-63.
-
(2000)
J. Steroid Biochem. Mol. Biol.
, vol.75
, pp. 57-63
-
-
Ehmer, P.B.1
Jose, J.2
Hartmann, R.W.3
-
38
-
-
1242352932
-
Synthesis of hydroxy derivatives of highly potent nonsteroidal CYP17 inhibitors as potential metabolites and evaluation of their activity by a non cellular assay using recombinant enzyme
-
Hutschenreuter, T. U.; Ehmer, P. B.; Hartmann, R. W. Synthesis of hydroxy derivatives of highly potent nonsteroidal CYP17 inhibitors as potential metabolites and evaluation of their activity by a non cellular assay using recombinant enzyme. J. Enzyme Inhib. Med. Chem. 2004, 19, 17-32.
-
(2004)
J. Enzyme Inhib. Med. Chem.
, vol.19
, pp. 17-32
-
-
Hutschenreuter, T.U.1
Ehmer, P.B.2
Hartmann, R.W.3
-
39
-
-
0035524138
-
Assessing the absorption of new pharmaceuticals
-
Hidalgo, I. J. Assessing the absorption of new pharmaceuticals. Curr. Top. Med. Chem. 2001, 1, 385-401.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 385-401
-
-
Hidalgo, I.J.1
-
40
-
-
0030990079
-
In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in men - Fact or myth
-
Yee, S. In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in men - fact or myth. Pharm. Res. 1997, 14, 763-766.
-
(1997)
Pharm. Res.
, vol.14
, pp. 763-766
-
-
Yee, S.1
-
41
-
-
0035048583
-
Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity
-
Tannergren, C.; Langguth, P.; Hoffmann, K. J. Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity. Pharmazie 2001, 56, 337-342.
-
(2001)
Pharmazie
, vol.56
, pp. 337-342
-
-
Tannergren, C.1
Langguth, P.2
Hoffmann, K.J.3
-
42
-
-
0037331839
-
N-in-one permeability studies of heterogeneous sets of compounds across Caco-2 cell monolayers
-
Laitinen, L.; Kangas, H.; Kaukonen, A. M.; Hakala, K.; Kotiaho, R.; Kostiainen, R.; Hirvonen, J. N-in-one permeability studies of heterogeneous sets of compounds across Caco-2 cell monolayers. Pharm. Res. 2003, 20, 187-197.
-
(2003)
Pharm. Res.
, vol.20
, pp. 187-197
-
-
Laitinen, L.1
Kangas, H.2
Kaukonen, A.M.3
Hakala, K.4
Kotiaho, R.5
Kostiainen, R.6
Hirvonen, J.7
-
43
-
-
0033844748
-
Carrier-mediated transport of macrolide antimicrobial agents across Caco-2 cell monolayers
-
Saito, H.; Fukasawa, Y.; Otsubo, Y.; Yamada, K.; Sezaki, H.; Yamashita, S. Carrier-mediated transport of macrolide antimicrobial agents across Caco-2 cell monolayers. Pharm. Res. 2000, 17, 761-765.
-
(2000)
Pharm. Res.
, vol.17
, pp. 761-765
-
-
Saito, H.1
Fukasawa, Y.2
Otsubo, Y.3
Yamada, K.4
Sezaki, H.5
Yamashita, S.6
-
44
-
-
0035893679
-
Modelling of three-dimensional structures of cytochromes P450 11B2 and 11B1
-
Belkina, N. V.; Lisurek, M.; Ivanov, A. S.; Bernhardt, R. Modelling of three-dimensional structures of cytochromes P450 11B2 and 11B1. J. Inorg. Biochem. 2001, 87, 197-207.
-
(2001)
J. Inorg. Biochem.
, vol.87
, pp. 197-207
-
-
Belkina, N.V.1
Lisurek, M.2
Ivanov, A.S.3
Bernhardt, R.4
-
45
-
-
0033595869
-
Palladium catalyzed cross-coupling between phenyl- Or naphthylboronic acids and benzylic bromides
-
Chowdhury, S.; Georghiou, P. E. Palladium catalyzed cross-coupling between phenyl- or naphthylboronic acids and benzylic bromides. Tetrahedron Lett. 1999, 40, 7599-7603.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7599-7603
-
-
Chowdhury, S.1
Georghiou, P.E.2
-
46
-
-
0037178508
-
An improved protocol for the preparation of 3-pyridyl- and some arylboronic acids
-
Li, W.; Nelson, D. P.; Jensen, M. S.; Hoerrner, R. S.; Cai, D.; Larsen, R. D.; Reider, P. J. An improved protocol for the preparation of 3-pyridyl- and some arylboronic acids. J. Org. Chem. 2002, 67, 5394-5397.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 5394-5397
-
-
Li, W.1
Nelson, D.P.2
Jensen, M.S.3
Hoerrner, R.S.4
Cai, D.5
Larsen, R.D.6
Reider, P.J.7
-
47
-
-
84984207285
-
Kondensation von 3-(1-Imidazolyl)- und -(1-benzimidazolyl)-chinolin zu heterocyclotetraaromaten
-
Kauffmann, T.; Tigler, D.; Woltermann, A. Kondensation von 3-(1-Imidazolyl)- und -(1-Benzimidazolyl)-chinolin zu Heterocyclotetraaromaten. Chem. Ber. 1982, 115, 452-458.
-
(1982)
Chem. Ber.
, vol.115
, pp. 452-458
-
-
Kauffmann, T.1
Tigler, D.2
Woltermann, A.3
-
48
-
-
0000213449
-
Synthesis of bromoacetyl derivatives by use of tetrabutylammonium tribromide
-
Kajigaeshi, S.; Kakinami, T.; Okamoto, T.; Fujisaki, S. Synthesis of bromoacetyl derivatives by use of tetrabutylammonium tribromide. Bull. Chem. Soc. Jpn. 1987, 60, 1159-1160.
-
(1987)
Bull. Chem. Soc. Jpn.
, vol.60
, pp. 1159-1160
-
-
Kajigaeshi, S.1
Kakinami, T.2
Okamoto, T.3
Fujisaki, S.4
-
49
-
-
84981838580
-
Über die katalytische hydrogenolyse von derivaten des p-phenylbenzylamins
-
Dahn, H.; Zoller, P. Über die katalytische Hydrogenolyse von Derivaten des p-Phenylbenzylamins. Helv. Chim. Acta 1952, 35, 1348-1351.
-
(1952)
Helv. Chim. Acta
, vol.35
, pp. 1348-1351
-
-
Dahn, H.1
Zoller, P.2
-
50
-
-
0042265520
-
Crystal structure of human cytochrome P4502C9 with bound warfarin
-
Williams, P. A.; Cosme, J.; Ward, A.; Angove, H. C.; Matak Vinkovic, D.; Jhoti, H. Crystal structure of human cytochrome P4502C9 with bound warfarin. Nature 2003, 424, 464-468.
-
(2003)
Nature
, vol.424
, pp. 464-468
-
-
Williams, P.A.1
Cosme, J.2
Ward, A.3
Angove, H.C.4
Matak Vinkovic, D.5
Jhoti, H.6
-
51
-
-
0036022958
-
Flexible docking under pharmacophore type constraints
-
Hindle, S. A.; Rarey, M.; Buning, C.; Lengauer, T. Flexible docking under pharmacophore type constraints. J. Comput. Aided Mol. Des. 2002, 16, 129-149.
-
(2002)
J. Comput. Aided Mol. Des.
, vol.16
, pp. 129-149
-
-
Hindle, S.A.1
Rarey, M.2
Buning, C.3
Lengauer, T.4
-
52
-
-
0008819754
-
The GROMOS biomolecular simulation program package
-
Scott, W. R. P.; Hünenberger, P. H.; Tironi, I. G.; Mark, A. E.; Billeter, S. R.; Fennen, J.; Torda, A. E.; Huber, T.; Krüger, P.; van Gunsteren, W. F. The GROMOS Biomolecular Simulation Program Package. J. Phys. Chem. A 1999, 103, 3596-3607.
-
(1999)
J. Phys. Chem. A
, vol.103
, pp. 3596-3607
-
-
Scott, W.R.P.1
Hünenberger, P.H.2
Tironi, I.G.3
Mark, A.E.4
Billeter, S.R.5
Fennen, J.6
Torda, A.E.7
Huber, T.8
Krüger, P.9
Van Gunsteren, W.F.10
-
53
-
-
0035789518
-
GROMACS 3.0: A package for molecular simulation and trajectory analysis
-
Lindahl, E.; Hess, B.; van der Spoel, D. GROMACS 3.0: a package for molecular simulation and trajectory analysis. J. Mol. Mod. 2001, 7, 306-317.
-
(2001)
J. Mol. Mod.
, vol.7
, pp. 306-317
-
-
Lindahl, E.1
Hess, B.2
Van Der Spoel, D.3
-
54
-
-
0002775934
-
Interaction models for water in relation to protein hydration
-
Pullman, B., Ed.; Reidel Publishing Co.: Dordrecht
-
Berendsen, H. J. C.; Postma, J. P. M.; van Gunsteren, W. F.; Hermans, J. Interaction models for water in relation to protein hydration. In Intermolecular Forces; Pullman, B., Ed.; Reidel Publishing Co.: Dordrecht, 1981; pp 331-342.
-
(1981)
Intermolecular Forces
, pp. 331-342
-
-
Berendsen, H.J.C.1
Postma, J.P.M.2
Van Gunsteren, W.F.3
Hermans, J.4
|