-
1
-
-
70350680485
-
Human skin wounds: A major and snowballing threat to public health and the economy
-
Sen, C. K.; Gordillo, G. M.; Roy, S.; Kirsner, R.; Lambert, L.; Hunt, T. K.; Gottrup, F.; Gurtner, G. C.; Longaker, M. T. Human skin wounds: a major and snowballing threat to public health and the economy Wound Repair Regener. 2009, 17, 763-771
-
(2009)
Wound Repair Regener.
, vol.17
, pp. 763-771
-
-
Sen, C.K.1
Gordillo, G.M.2
Roy, S.3
Kirsner, R.4
Lambert, L.5
Hunt, T.K.6
Gottrup, F.7
Gurtner, G.C.8
Longaker, M.T.9
-
2
-
-
77749260633
-
Factors affecting wound healing
-
Guo, S.; DiPietro, L. A. Factors affecting wound healing J. Dent. Res. 2010, 89, 219-229
-
(2010)
J. Dent. Res.
, vol.89
, pp. 219-229
-
-
Guo, S.1
Dipietro, L.A.2
-
3
-
-
34248225758
-
Cellular and molecular basis of wound healing in diabetes
-
Brem, H.; Tomic-Canic, M. Cellular and molecular basis of wound healing in diabetes J. Clin. Invest. 2007, 117, 1219-1222
-
(2007)
J. Clin. Invest.
, vol.117
, pp. 1219-1222
-
-
Brem, H.1
Tomic-Canic, M.2
-
4
-
-
84907460229
-
-
Chronic wound care guidelines. (accessed Jun 12).
-
Chronic wound care guidelines. http://woundheal.org/documents/final-pocket-guide-treatment.aspx (accessed Jun 12, 2014).
-
(2014)
-
-
-
5
-
-
84901041965
-
Biology of chronic wounds and new treatment strategies
-
Montfrans, C. V.; Stok, M.; Geerkens, M. Biology of chronic wounds and new treatment strategies Phlebology 2014, 19, 165-167
-
(2014)
Phlebology
, vol.19
, pp. 165-167
-
-
Montfrans, C.V.1
Stok, M.2
Geerkens, M.3
-
7
-
-
1942509447
-
Perceived stress and cortisol levels predict speed of wound healing in healthy male adults
-
Ebrecht, M.; Hextall, J.; Kirtley, L.; Taylor, A.; Dyson, M.; Weinman, J. Perceived stress and cortisol levels predict speed of wound healing in healthy male adults Psychoneuroendocrinology 2004, 29, 798-809
-
(2004)
Psychoneuroendocrinology
, vol.29
, pp. 798-809
-
-
Ebrecht, M.1
Hextall, J.2
Kirtley, L.3
Taylor, A.4
Dyson, M.5
Weinman, J.6
-
8
-
-
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, 10265-10275
-
(2011)
J. Biol. Chem.
, vol.286
, 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
-
10
-
-
84886601180
-
Steroidogenesis in the skin: Implications for local immune functions
-
Slominski, A.; Zbytek, B.; Nikolakis, G.; Manna, P. R.; Skobowiat, C.; Zmijewski, M.; Li, W.; Janjetovic, Z.; Postlethwaite, A.; Zouboulis, C. C.; Tuckey, R. C. Steroidogenesis in the skin: implications for local immune functions J. Steroid. Biochem. Mol. Biol. 2013, 137, 107-123
-
(2013)
J. Steroid. Biochem. Mol. Biol.
, vol.137
, pp. 107-123
-
-
Slominski, A.1
Zbytek, B.2
Nikolakis, G.3
Manna, P.R.4
Skobowiat, C.5
Zmijewski, M.6
Li, W.7
Janjetovic, Z.8
Postlethwaite, A.9
Zouboulis, C.C.10
Tuckey, R.C.11
-
11
-
-
0001135767
-
Biochemical analysis of wound fluid from nonhealing and healing chronic leg ulcers
-
Trengove, N. J.; Langton, S. R.; Stacey, M. C. Biochemical analysis of wound fluid from nonhealing and healing chronic leg ulcers Wound Repair Regener. 1996, 4, 234-239
-
(1996)
Wound Repair Regener.
, vol.4
, pp. 234-239
-
-
Trengove, N.J.1
Langton, S.R.2
Stacey, M.C.3
-
12
-
-
33847420001
-
Relevance of pharmacokinetics and pharmacodynamics of inhaled corticosteroids to asthma
-
Derendorf, H.; Nave, R.; Drollmann, A.; Cerasoli, F.; Wurst, W. Relevance of pharmacokinetics and pharmacodynamics of inhaled corticosteroids to asthma Eur. Respir. J. 2006, 28, 1042-1050
-
(2006)
Eur. Respir. J.
, vol.28
, pp. 1042-1050
-
-
Derendorf, H.1
Nave, R.2
Drollmann, A.3
Cerasoli, F.4
Wurst, W.5
-
13
-
-
84864199802
-
Novel imidazol-1-ylmethyl substituted 1,2,5,6-tetrahydro-pyrrolo[3,2,1- ij ]quinolin-4-ones as potent and selective CYP11B1 inhibitors for the treatment of Cushing's syndrome
-
Yin, L.; Lucas, S.; Maurer, F.; Kazmaier, U.; Hu, Q.; Hartmann, R. W. Novel imidazol-1-ylmethyl substituted 1,2,5,6-tetrahydro-pyrrolo[3,2,1- ij ]quinolin-4-ones as potent and selective CYP11B1 inhibitors for the treatment of Cushing's syndrome J. Med. Chem. 2012, 55, 6629-6633
-
(2012)
J. Med. Chem.
, vol.55
, pp. 6629-6633
-
-
Yin, L.1
Lucas, S.2
Maurer, F.3
Kazmaier, U.4
Hu, Q.5
Hartmann, R.W.6
-
14
-
-
84880174933
-
Cushing's syndrome: Development of highly potent and selective CYP11B1 inhibitors of the (pyridylmethyl)pyridine type
-
Emmerich, J.; Hu, Q.; Hanke, N.; Hartmann, R. W. Cushing's syndrome: development of highly potent and selective CYP11B1 inhibitors of the (pyridylmethyl)pyridine type J. Med. Chem. 2013, 56, 6022-32
-
(2013)
J. Med. Chem.
, vol.56
, pp. 6022-6032
-
-
Emmerich, J.1
Hu, Q.2
Hanke, N.3
Hartmann, R.W.4
-
15
-
-
84903545504
-
Novel pyridyl- or isoquinolinyl-substituted indolines and indoles as potent and selective aldosterone synthase inhibitors
-
Yin, L.; Hu, Q.; Emmerich, J.; Lo, M. M.; Metzger, E.; Ali, A.; Hartmann, R. W. Novel pyridyl- or isoquinolinyl-substituted indolines and indoles as potent and selective aldosterone synthase inhibitors J. Med. Chem. 2014, 57, 5179-5189
-
(2014)
J. Med. Chem.
, vol.57
, pp. 5179-5189
-
-
Yin, L.1
Hu, Q.2
Emmerich, J.3
Lo, M.M.4
Metzger, E.5
Ali, A.6
Hartmann, R.W.7
-
16
-
-
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.; Muller, 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
Muller, U.4
Hartmann, R.W.5
-
17
-
-
77954326488
-
Isopropylidene substitution increases activity and selectivity of biphenyl methylene 4-pyridine type CYP17 inhibitors
-
Hu, Q.; Yin, L.; Jagusch, C.; Hille, U. E.; Hartmann, R. W. Isopropylidene substitution increases activity and selectivity of biphenyl methylene 4-pyridine type CYP17 inhibitors J. Med. Chem. 2010, 53, 5049-5053
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5049-5053
-
-
Hu, Q.1
Yin, L.2
Jagusch, C.3
Hille, U.E.4
Hartmann, R.W.5
-
18
-
-
67349083573
-
Novel CYP17 inhibitors: Synthesis, biological evaluation, structure-activity relationships and modeling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls
-
Hille, U. E.; Hu, Q.; Vock, C.; Negri, M.; Bartels, M.; Mueller-Vieira, U.; Lauterbach, T.; Hartmann, R. W. Novel CYP17 inhibitors: synthesis, biological evaluation, structure-activity relationships and modeling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls Eur. J. Med. Chem. 2009, 44, 2765-2775
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2765-2775
-
-
Hille, U.E.1
Hu, Q.2
Vock, C.3
Negri, M.4
Bartels, M.5
Mueller-Vieira, U.6
Lauterbach, T.7
Hartmann, R.W.8
-
19
-
-
53549129492
-
CYP17 inhibitors. Annulations of additional rings in methylene imidazole substituted biphenyls: Synthesis, biological evaluation and molecular modeling
-
Pinto-Bazurco Mendieta, M. A. E.; Negri, M.; Hu, Q.; Hille, U. E.; Jagusch, C.; Jahn-Hoffmann, K.; Müller-Vieira, U.; Schmidt, D.; Lauterbach, T.; Hartmann, R. W. CYP17 inhibitors. Annulations of additional rings in methylene imidazole substituted biphenyls: synthesis, biological evaluation and molecular modeling Arch. Pharm. (Weinheim, Ger.) 2008, 341, 597-609
-
(2008)
Arch. Pharm. (Weinheim, Ger.)
, vol.341
, pp. 597-609
-
-
Pinto-Bazurco Mendieta, M.A.E.1
Negri, M.2
Hu, Q.3
Hille, U.E.4
Jagusch, C.5
Jahn-Hoffmann, K.6
Müller-Vieira, U.7
Schmidt, D.8
Lauterbach, T.9
Hartmann, R.W.10
-
20
-
-
49149091871
-
Synthesis, biological evaluation, and molecular modeling studies of methylene imidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17). Part II: Core rigidification and influence of substituents at the methylene bridge
-
Hu, Q.; Negri, M.; Jahn-Hoffmann, K.; Zhuang, Y.; Olgen, S.; Bartels, M.; Müller-Vieira, U.; Lauterbach, T.; Hartmann, R. W. Synthesis, biological evaluation, and molecular modeling studies of methylene imidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17). Part II: Core rigidification and influence of substituents at the methylene bridge Bioorg. Med. Chem. 2008, 16, 7715-7727
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7715-7727
-
-
Hu, Q.1
Negri, M.2
Jahn-Hoffmann, K.3
Zhuang, Y.4
Olgen, S.5
Bartels, M.6
Müller-Vieira, U.7
Lauterbach, T.8
Hartmann, R.W.9
-
21
-
-
77955388983
-
Replacement of imidazolyl by pyridyl in biphenyl methylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer
-
Hu, Q.; Jagusch, C.; Hille, U. E.; Haupenthal, J.; Hartmann, R. W. Replacement of imidazolyl by pyridyl in biphenyl methylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer J. Med. Chem. 2010, 53, 5749-5758
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5749-5758
-
-
Hu, Q.1
Jagusch, C.2
Hille, U.E.3
Haupenthal, J.4
Hartmann, R.W.5
-
22
-
-
84893720016
-
CYP17 inhibitors-abiraterone, C17,20-lyase inhibitors and multi-targeting agents
-
Yin, L.; Hu, Q. CYP17 inhibitors-abiraterone, C17,20-lyase inhibitors and multi-targeting agents Nat. Rev. Urol. 2014, 11, 32-42
-
(2014)
Nat. Rev. Urol.
, vol.11
, pp. 32-42
-
-
Yin, L.1
Hu, Q.2
-
23
-
-
84870383585
-
Hits identified in library screening demonstrate selective CYP17A1 lyase inhibition
-
Krug, S. J.; Hu, Q.; Hartmann, R. W. Hits identified in library screening demonstrate selective CYP17A1 lyase inhibition J. Steroid Biochem. Mol. Biol. 2013, 134, 75-79
-
(2013)
J. Steroid Biochem. Mol. Biol.
, vol.134
, pp. 75-79
-
-
Krug, S.J.1
Hu, Q.2
Hartmann, R.W.3
-
24
-
-
77953104461
-
The role of fluorine substitution in biphenyl methylene imidazole type CYP17 inhibitors for the treatment of prostate carcinoma
-
Hu, Q.; Negri, M.; Olgen, S.; Hartmann, R. W. The role of fluorine substitution in biphenyl methylene imidazole type CYP17 inhibitors for the treatment of prostate carcinoma ChemMedChem 2010, 5, 899-910
-
(2010)
ChemMedChem
, vol.5
, pp. 899-910
-
-
Hu, Q.1
Negri, M.2
Olgen, S.3
Hartmann, R.W.4
-
25
-
-
71849117108
-
Steroidogenic cytochrome P450 (CYP) enzymes as drug targets: Combining substructures of known CYP inhibitors leads to compounds with different inhibitory profile
-
Hille, U. E.; Hu, Q.; Pinto-Bazurco Mendieta, M. A. E.; Bartels, M.; Vock, C. A.; Lauterbach, T.; Hartmann, R. W. Steroidogenic cytochrome P450 (CYP) enzymes as drug targets: combining substructures of known CYP inhibitors leads to compounds with different inhibitory profile C. R. Chim. 2009, 12, 1117-1126
-
(2009)
C. R. Chim.
, vol.12
, pp. 1117-1126
-
-
Hille, U.E.1
Hu, Q.2
Pinto-Bazurco Mendieta, M.A.E.3
Bartels, M.4
Vock, C.A.5
Lauterbach, T.6
Hartmann, R.W.7
-
26
-
-
38949127288
-
Synthesis, biological evaluation and molecular modeling studies of methyleneimidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17). Part I: Heterocyclic modifications of the core structure
-
Jagusch, C.; Negri, M.; Hille, U. E.; Hu, Q.; Bartels, M.; Jahn-Hoffmann, K.; Pinto-Bazurco Mendieta, M. A. E.; Rodenwaldt, B.; Müller-Vieira, U.; Schmidt, D.; Lauterbach, T.; Recanatini, M.; Cavalli, A.; Hartmann, R. W. Synthesis, biological evaluation and molecular modeling studies of methyleneimidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17). Part I: Heterocyclic modifications of the core structure Bioorg. Med. Chem. 2008, 16, 1992-2010
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1992-2010
-
-
Jagusch, C.1
Negri, M.2
Hille, U.E.3
Hu, Q.4
Bartels, M.5
Jahn-Hoffmann, K.6
Pinto-Bazurco Mendieta, M.A.E.7
Rodenwaldt, B.8
Müller-Vieira, U.9
Schmidt, D.10
Lauterbach, T.11
Recanatini, M.12
Cavalli, A.13
Hartmann, R.W.14
-
27
-
-
50249131899
-
Synthesis, biological evaluation, and molecular modeling of abiraterone analogues: Novel CYP17 inhibitors for the treatment of prostate cancer
-
Pinto-Bazurco Mendieta, M. A. E.; Negri, M.; Jagusch, C.; Müller-Vieira, U.; Lauterbach, T.; Hartmann, R. W. Synthesis, biological evaluation, and molecular modeling of abiraterone analogues: novel CYP17 inhibitors for the treatment of prostate cancer J. Med. Chem. 2008, 51, 5009-5018
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5009-5018
-
-
Pinto-Bazurco Mendieta, M.A.E.1
Negri, M.2
Jagusch, C.3
Müller-Vieira, U.4
Lauterbach, T.5
Hartmann, R.W.6
-
28
-
-
84880163967
-
Recent progress in pharmaceutical therapy for castration-resistant prostate cancer
-
Yin, L.; Hu, Q.; Hartmann, R. W. Recent progress in pharmaceutical therapy for castration-resistant prostate cancer Int. J. Mol. Sci. 2013, 14, 13958-13978
-
(2013)
Int. J. Mol. Sci.
, vol.14
, pp. 13958-13978
-
-
Yin, L.1
Hu, Q.2
Hartmann, R.W.3
-
29
-
-
31344451950
-
Synthesis and biological evaluation of 5-[(aryl)(1 H -imidazol-1-yl)methyl]-1 H -indoles: Potent and selective aromatase inhibitors
-
Lézé, M.-P.; Le Borgne, M.; Pinson, P.; Palusczak, A.; Duflos, M.; Le Bauta, G.; Hartmann, R. W. Synthesis and biological evaluation of 5-[(aryl)(1 H -imidazol-1-yl)methyl]-1 H -indoles: potent and selective aromatase inhibitors Bioorg. Med. Chem. Lett. 2006, 16, 1134-1137
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 1134-1137
-
-
Lézé, M.-P.1
Le Borgne, M.2
Pinson, P.3
Palusczak, A.4
Duflos, M.5
Le Bauta, G.6
Hartmann, R.W.7
-
30
-
-
34547607018
-
Imidazolylmethylbenzophenones as highly potent aromatase inhibitors
-
Gobbi, S.; Cavalli, A.; Negri, M.; Schewe, K. E.; Belluti, F.; Piazzi, L.; Hartmann, R. W.; Recanatini, M.; Bisi, A. Imidazolylmethylbenzophenones as highly potent aromatase inhibitors J. Med. Chem. 2007, 50, 3420-3422
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3420-3422
-
-
Gobbi, S.1
Cavalli, A.2
Negri, M.3
Schewe, K.E.4
Belluti, F.5
Piazzi, L.6
Hartmann, R.W.7
Recanatini, M.8
Bisi, A.9
-
31
-
-
0030006607
-
Synthesis and evaluation of azole-substituted tetrahydronaphthalenes as inhibitors of P450 arom, P450 17, and P450 TxA2
-
Hartmann, R. W.; Frotscher, M.; Ledergerber, D.; Wächter, G. A.; Grün, G. L.; Sergejew, T. F. Synthesis and evaluation of azole-substituted tetrahydronaphthalenes as inhibitors of P450 arom, P450 17, and P450 TxA2 Arch. Pharm. (Weinheim, Ger.) 1996, 329, 251-261
-
(1996)
Arch. Pharm. (Weinheim, Ger.)
, vol.329
, pp. 251-261
-
-
Hartmann, R.W.1
Frotscher, M.2
Ledergerber, D.3
Wächter, G.A.4
Grün, G.L.5
Sergejew, T.F.6
-
32
-
-
84874632661
-
Modulation of cytochromes P450 with xanthone-based molecules: From aromatase to aldosterone synthase and steroid 11betahydroxylase inhibition
-
Gobbi, S.; Hu, Q.; Negri, M.; Zimmer, C.; Belluti, F.; Rampa, A.; Hartmann, R. W.; Bisi, A. Modulation of cytochromes P450 with xanthone-based molecules: from aromatase to aldosterone synthase and steroid 11betahydroxylase inhibition J. Med. Chem. 2013, 56, 1723-1729
-
(2013)
J. Med. Chem.
, vol.56
, pp. 1723-1729
-
-
Gobbi, S.1
Hu, Q.2
Negri, M.3
Zimmer, C.4
Belluti, F.5
Rampa, A.6
Hartmann, R.W.7
Bisi, A.8
-
33
-
-
84864262707
-
Synthesis and biological evaluation of imidazolylmethylacridones as cytochrome P-450 enzymes inhibitors
-
Abadi, A. H.; Abou-Seri, S. M.; Hu, Q.; Negri, M.; Hartmann, R. W. Synthesis and biological evaluation of imidazolylmethylacridones as cytochrome P-450 enzymes inhibitors MedChemComm 2012, 3, 663-666
-
(2012)
MedChemComm
, vol.3
, pp. 663-666
-
-
Abadi, A.H.1
Abou-Seri, S.M.2
Hu, Q.3
Negri, M.4
Hartmann, R.W.5
-
34
-
-
84901263832
-
Aldosterone synthase inhibitors as promising treatments for mineralocorticoid dependent cardiovascular and renal diseases
-
Hu, Q.; Yin, L.; Hartmann, R. W. Aldosterone synthase inhibitors as promising treatments for mineralocorticoid dependent cardiovascular and renal diseases J. Med. Chem. 2014, 57, 5011-5022
-
(2014)
J. Med. Chem.
, vol.57
, pp. 5011-5022
-
-
Hu, Q.1
Yin, L.2
Hartmann, R.W.3
-
35
-
-
84866935329
-
Selective dual inhibitors of CYP19 and CYP11B2: Targeting cardiovascular diseases hiding in the shadow of breast cancer
-
Hu, Q.; Yin, L.; Hartmann, R. W. Selective dual inhibitors of CYP19 and CYP11B2: targeting cardiovascular diseases hiding in the shadow of breast cancer J. Med. Chem. 2012, 55, 7080-7089
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7080-7089
-
-
Hu, Q.1
Yin, L.2
Hartmann, R.W.3
-
36
-
-
84872777577
-
Tetrahydropyrroloquinolinone type dual inhibitors of aromatase/aldosterone synthase as a novel strategy for breast cancer patients with elevated cardiovascular risks
-
Yin, L.; Hu, Q.; Hartmann, R. W. Tetrahydropyrroloquinolinone type dual inhibitors of aromatase/aldosterone synthase as a novel strategy for breast cancer patients with elevated cardiovascular risks J. Med. Chem. 2013, 56, 460-470
-
(2013)
J. Med. Chem.
, vol.56
, pp. 460-470
-
-
Yin, L.1
Hu, Q.2
Hartmann, R.W.3
-
37
-
-
84875126614
-
Drug discovery for breast cancer and coinstantaneous cardiovascular disease: What is the future?
-
Yin, L.; Hu, Q. Drug discovery for breast cancer and coinstantaneous cardiovascular disease: What is the future? Future Med. Chem. 2013, 5, 359-362
-
(2013)
Future Med. Chem.
, vol.5
, pp. 359-362
-
-
Yin, L.1
Hu, Q.2
-
38
-
-
84881420660
-
Highly potent and selective non-steroidal dual inhibitors of CYP17/CYP11B2 for the treatment of prostate cancer to reduce risks of cardiovascular diseases
-
Pinto-Bazurco Mendieta, M. A. E.; Hu, Q.; Engel, M.; Hartmann, R. W. Highly potent and selective non-steroidal dual inhibitors of CYP17/CYP11B2 for the treatment of prostate cancer to reduce risks of cardiovascular diseases J. Med. Chem. 2013, 56, 6101-6107
-
(2013)
J. Med. Chem.
, vol.56
, pp. 6101-6107
-
-
Pinto-Bazurco Mendieta, M.A.E.1
Hu, Q.2
Engel, M.3
Hartmann, R.W.4
-
39
-
-
77649197692
-
Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1 H -imidazoles as selective inhibitors of aldosterone synthase (CYP11B2)
-
Roumen, L.; Peeters, J. W.; Emmen, J. M. A.; Beugels, I. P. E.; Custers, E. M. G.; de Gooyer, M.; Plate, R.; Pieterse, K.; Hilbers, P. A. J.; Smits, J. F. M.; Vekemans, J. A. J.; Leysen, D.; Ottenheijm, H. C. J.; Janssen, H. M.; Hermans, J. J. R. Synthesis, biological evaluation, and molecular modeling of 1-benzyl-1 H -imidazoles as selective inhibitors of aldosterone synthase (CYP11B2) J. Med. Chem. 2010, 53, 1712-1725
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1712-1725
-
-
Roumen, L.1
Peeters, J.W.2
Emmen, J.M.A.3
Beugels, I.P.E.4
Custers, E.M.G.5
De Gooyer, M.6
Plate, R.7
Pieterse, K.8
Hilbers, P.A.J.9
Smits, J.F.M.10
Vekemans, J.A.J.11
Leysen, D.12
Ottenheijm, H.C.J.13
Janssen, H.M.14
Hermans, J.J.R.15
-
40
-
-
84868317925
-
3-Pyridinyl substituted aliphatic cycles as CYP11B2 inhibitors: Aromaticity abolishment of the core significantly increased selectivity over CYP1A2
-
Yin, L.; Hu, Q.; Hartmann, R. W. 3-Pyridinyl substituted aliphatic cycles as CYP11B2 inhibitors: aromaticity abolishment of the core significantly increased selectivity over CYP1A2 PLoS One 2012, 7 (11) e48048
-
(2012)
PLoS One
, vol.7
, Issue.11
, pp. 48048
-
-
Yin, L.1
Hu, Q.2
Hartmann, R.W.3
-
41
-
-
58149087304
-
In vivo active aldosterone synthase inhibitors with improved selectivity: Lead optimization providing a series of pyridine substituted 3,4-dihydro-1 H -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-1 H -quinolin-2-one derivatives J. Med. Chem. 2008, 51, 8077-8087
-
(2008)
J. Med. Chem.
, vol.51
, pp. 8077-8087
-
-
Lucas, S.1
Heim, R.2
Ries, C.3
Schewe, K.E.4
Birk, B.5
Hartmann, R.W.6
-
42
-
-
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, 6138-6149
-
(2008)
J. Med. Chem.
, vol.51
, 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
-
43
-
-
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.; Müller-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, 5064-5074
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5064-5074
-
-
Heim, R.1
Lucas, S.2
Grombein, C.M.3
Ries, C.4
Schewe, K.E.5
Negri, M.6
Müller-Vieira, U.7
Birk, B.8
Hartmann, R.W.9
-
44
-
-
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.; Müller-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, 2222-2231
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2222-2231
-
-
Voets, M.1
Antes, I.2
Scherer, C.3
Müller-Vieira, U.4
Biemel, K.5
Marchais-Oberwinkler, S.6
Hartmann, R.W.7
|