-
1
-
-
0029930899
-
Dysglycaemia and risk of cardiovascular disease
-
Gerstein, H. C.; Yusuf, S. Dysglycaemia and risk of cardiovascular disease. Lancet 1996, 347, 949-950.
-
(1996)
Lancet
, vol.347
, pp. 949-950
-
-
Gerstein, H.C.1
Yusuf, S.2
-
2
-
-
4043077286
-
11β-Hydroxysteroid dehydrogenase type 1: A tissue-specific regulator of glucocorticoid response
-
(a) Tomlinson, J. W.; Walker, E. A.; Bujalska, I. J.; Draper, N.; Lavery, G. G.; Cooper, M. S.; Hewison, M.; Stewart, P. M. 11β-Hydroxysteroid dehydrogenase type 1: a tissue-specific regulator of glucocorticoid response. Endocr. Rev. 2004, 25, 831-866.
-
(2004)
Endocr. Rev
, vol.25
, pp. 831-866
-
-
Tomlinson, J.W.1
Walker, E.A.2
Bujalska, I.J.3
Draper, N.4
Lavery, G.G.5
Cooper, M.S.6
Hewison, M.7
Stewart, P.M.8
-
3
-
-
0942290504
-
11β-Hydroxysteroid dehydrogenase type 1 in obesity and type 2 diabetes
-
(b) Stulnig, T. M.; Waldhausl, W. 11β-Hydroxysteroid dehydrogenase type 1 in obesity and type 2 diabetes. Diabetologia 2004, 47, 1-11.
-
(2004)
Diabetologia
, vol.47
, pp. 1-11
-
-
Stulnig, T.M.1
Waldhausl, W.2
-
4
-
-
0035824440
-
A transgenic model of visceral obesity and the metabolic syndrome
-
(a) Masuzaki, H.; Paterson, J.; Shinyama, H.; Morton, N. M.; Mullins, J. J.; Seckl, J. R.; Flier, J. S. A transgenic model of visceral obesity and the metabolic syndrome. Science 2001, 294, 2166-2170.
-
(2001)
Science
, vol.294
, pp. 2166-2170
-
-
Masuzaki, H.1
Paterson, J.2
Shinyama, H.3
Morton, N.M.4
Mullins, J.J.5
Seckl, J.R.6
Flier, J.S.7
-
5
-
-
2342510149
-
Metabolic syndrome without obesity: Hepatic overexpression of 11β-hydroxysteroid dehydrogenase type 1 in transgenic mice
-
(b) Paterson, J. M.; Morton, N. M.; Fievet, C.; Kenyon, C. J.; Holmes, M. C.; Staels, B.; Seckl, J. R.; Mullins, J. J. Metabolic syndrome without obesity: hepatic overexpression of 11β-hydroxysteroid dehydrogenase type 1 in transgenic mice. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 7088-7093.
-
(2004)
Proc. Natl. Acad. Sci. U.S.A
, vol.101
, pp. 7088-7093
-
-
Paterson, J.M.1
Morton, N.M.2
Fievet, C.3
Kenyon, C.J.4
Holmes, M.C.5
Staels, B.6
Seckl, J.R.7
Mullins, J.J.8
-
6
-
-
12144291638
-
Novel adipose tissue-mediated resistance to diet-induced visceral obesity in 11β-hydroxysteroid dehydrogenase type-1 deficient mice
-
(c) Morton, N. M.; Paterson, M.; Masuzaki, H.; Holmes, M.; Staels, B.; Fievet, C.; Walker, B.; Flier, J. S.; Mullins, J. J.; Seckl, J. R. Novel adipose tissue-mediated resistance to diet-induced visceral obesity in 11β-hydroxysteroid dehydrogenase type-1 deficient mice. Diabetes 2004, 53, 931-938.
-
(2004)
Diabetes
, vol.53
, pp. 931-938
-
-
Morton, N.M.1
Paterson, M.2
Masuzaki, H.3
Holmes, M.4
Staels, B.5
Fievet, C.6
Walker, B.7
Flier, J.S.8
Mullins, J.J.9
Seckl, J.R.10
-
7
-
-
0037194658
-
Arylsulfonamidothiazoles as a new class of potential antidiabetic drugs. Discovery of potent and selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1
-
Barf, T.; Vallgarda, J.; Emond, R.; Haggstrom, C.; Kurz, G.; Nygren, A.; Larwood, V.; Mosialou, E.; Axelsson, K.; Olsson, R.; Engblom, L.; Edling, N.; Ronquist-Nii, Y.; Ohman, B.; Alberts, P.; Abrahmsen, L. Arylsulfonamidothiazoles as a new class of potential antidiabetic drugs. Discovery of potent and selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1. J. Med. Chem. 2002, 45, 3813-3815.
-
(2002)
J. Med. Chem
, vol.45
, pp. 3813-3815
-
-
Barf, T.1
Vallgarda, J.2
Emond, R.3
Haggstrom, C.4
Kurz, G.5
Nygren, A.6
Larwood, V.7
Mosialou, E.8
Axelsson, K.9
Olsson, R.10
Engblom, L.11
Edling, N.12
Ronquist-Nii, Y.13
Ohman, B.14
Alberts, P.15
Abrahmsen, L.16
-
8
-
-
0242468543
-
Selection inhibition of 11β-hydroxysteroid dehydrogenase type 1 improves hepatic insulin sensitivity in hyperglycemic mice strains
-
Alberts, P.; Nilsson, C.; Selen, G.; Engblom, L. O.; Edling, N. H.; Norling, S.; Klingstrom, G.; Larsson, C.; Forsgren, M.; Ashkzari, M.; Nilsson, C. E.; Fiedler, M.; Bergqvist, E.; Ohman, B.; Jorkstrand, E.; Abrahmsen, L. B. Selection inhibition of 11β-hydroxysteroid dehydrogenase type 1 improves hepatic insulin sensitivity in hyperglycemic mice strains. Endocrinology 2003, 144, 4755-4762.
-
(2003)
Endocrinology
, vol.144
, pp. 4755-4762
-
-
Alberts, P.1
Nilsson, C.2
Selen, G.3
Engblom, L.O.4
Edling, N.H.5
Norling, S.6
Klingstrom, G.7
Larsson, C.8
Forsgren, M.9
Ashkzari, M.10
Nilsson, C.E.11
Fiedler, M.12
Bergqvist, E.13
Ohman, B.14
Jorkstrand, E.15
Abrahmsen, L.B.16
-
9
-
-
0028839840
-
Carbenoxolone increases hepatic insulin sensitivity in man: A novel role for 11-oxosteroid reductase in enhancing glucocorticoid receptor activation
-
Walker, B. R.; Connacher, A. A.; Lindsay, M.; Webb, D. J.; Edwards, C. R. W. Carbenoxolone increases hepatic insulin sensitivity in man: a novel role for 11-oxosteroid reductase in enhancing glucocorticoid receptor activation. J. Clin. Endocrinol. Metab. 1995, 80, 3155-3159.
-
(1995)
J. Clin. Endocrinol. Metab
, vol.80
, pp. 3155-3159
-
-
Walker, B.R.1
Connacher, A.A.2
Lindsay, M.3
Webb, D.J.4
Edwards, C.R.W.5
-
10
-
-
0033105754
-
Hypertension in mice lacking 11β- hydroxysteroid dehydrogenase type 2
-
Kotelevtsev, Y. V.; Brown, R. W.; Fleming, S.; Kenyon, C.; Edwards, C. R. W.; Seckl, J. R.; Mullins, J. Hypertension in mice lacking 11β- hydroxysteroid dehydrogenase type 2. J. Clin. Invest. 1999, 103, 683-689.
-
(1999)
J. Clin. Invest
, vol.103
, pp. 683-689
-
-
Kotelevtsev, Y.V.1
Brown, R.W.2
Fleming, S.3
Kenyon, C.4
Edwards, C.R.W.5
Seckl, J.R.6
Mullins, J.7
-
11
-
-
42049102780
-
The role of 11beta-hydroxysteroid dehydrogenase in metabolic disease and therapeutic potential of 11beta-HSD1 inhibitors
-
(a) Saiah, E. The role of 11beta-hydroxysteroid dehydrogenase in metabolic disease and therapeutic potential of 11beta-HSD1 inhibitors. Curr. Med. Chem. 2008, 15 (7), 642-649.
-
(2008)
Curr. Med. Chem
, vol.15
, Issue.7
, pp. 642-649
-
-
Saiah, E.1
-
12
-
-
33846927922
-
2-(S)-Phenethylaminothiazolones as potent, orally efficacious inhibitors of 11b-hydroxysteroid dehydrogenase type 1
-
(b) St. Jean, D. J.; Yuan, C.; Bercot, E. A.; Cupples, R.; Chen, M.; Fretland, J.; Hale, C.; Hungate, R. W.; Komorowski, R.; Veniant, M.; Wang, M.; Zhang, X.; Fotsch, C. 2-(S)-Phenethylaminothiazolones as potent, orally efficacious inhibitors of 11b-hydroxysteroid dehydrogenase type 1. J. Med. Chem. 2007, 50, 429-432.
-
(2007)
J. Med. Chem
, vol.50
, pp. 429-432
-
-
St. Jean, D.J.1
Yuan, C.2
Bercot, E.A.3
Cupples, R.4
Chen, M.5
Fretland, J.6
Hale, C.7
Hungate, R.W.8
Komorowski, R.9
Veniant, M.10
Wang, M.11
Zhang, X.12
Fotsch, C.13
-
13
-
-
34248655920
-
β-Keto sulfones as inhibitors of 11β- hydroxysteroid dehydrogenase type 1 and the mechanism of action
-
(c) Xiang, J.; Ipek, M.; Suri, V.; Tam, M.; Xing, Y.; Huang, N.; Zhang, Y.; Tobin, J.; Mansour, T.; McKew, J. β-Keto sulfones as inhibitors of 11β- hydroxysteroid dehydrogenase type 1 and the mechanism of action. Bioorg. Med. Chem. 2007, 15, 4396-4405.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 4396-4405
-
-
Xiang, J.1
Ipek, M.2
Suri, V.3
Tam, M.4
Xing, Y.5
Huang, N.6
Zhang, Y.7
Tobin, J.8
Mansour, T.9
McKew, J.10
-
14
-
-
33846165085
-
Adamantane sulfone and sulfonamide 11-β-HSD1 inhibitors
-
(d) Sorensen, B.; Winn, M.; Rohde, J.; Shuai, Q.; Wang, J.; Fung, S.; Monzon, K.; Chiou, W.; Stolarik, D.; Imade, H.; Pan, L.; Deng, X.; Chovan, L.; Longenecker, K.; Judge, R.; Qin, W.; Brune, M.; Camp, H.; Frevert, E. U.; Jackbson, P.; Link, J. T. Adamantane sulfone and sulfonamide 11-β-HSD1 inhibitors. Bioorg. Med. Chem. Lett. 2007, 17, 527-532.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 527-532
-
-
Sorensen, B.1
Winn, M.2
Rohde, J.3
Shuai, Q.4
Wang, J.5
Fung, S.6
Monzon, K.7
Chiou, W.8
Stolarik, D.9
Imade, H.10
Pan, L.11
Deng, X.12
Chovan, L.13
Longenecker, K.14
Judge, R.15
Qin, W.16
Brune, M.17
Camp, H.18
Frevert, E.U.19
Jackbson, P.20
Link, J.T.21
more..
-
15
-
-
33748324539
-
Synthesis and structural activity relationship of 11β-HSD1 inhibitors with novel adamantine replacements
-
(e) Yeh, V.; Kurukulasuriya, R.; Madar, D.; Patel, J.; Fung, S.; Monzon, K.; Chiou, W.; Wang, J.; Jacobson, P.; Sham, H.; Link, J. Synthesis and structural activity relationship of 11β-HSD1 inhibitors with novel adamantine replacements. Bioorg. Med. Chem. Lett. 2006, 16, 5408-5413.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 5408-5413
-
-
Yeh, V.1
Kurukulasuriya, R.2
Madar, D.3
Patel, J.4
Fung, S.5
Monzon, K.6
Chiou, W.7
Wang, J.8
Jacobson, P.9
Sham, H.10
Link, J.11
-
16
-
-
33745221417
-
The discovery of new 11β- hydroxysteroid dehydrogenase type 1 inhibitors by common feature pharmacophore modeling and virtual screening
-
(f) Schuster, D.; Maurer, E.; Laggner, C.; Nashev, L.; Wilckens, T.; Langer, T.; Odermatt, A. The discovery of new 11β- hydroxysteroid dehydrogenase type 1 inhibitors by common feature pharmacophore modeling and virtual screening. J. Med. Chem. 2006, 49, 3454-3466.
-
(2006)
J. Med. Chem
, vol.49
, pp. 3454-3466
-
-
Schuster, D.1
Maurer, E.2
Laggner, C.3
Nashev, L.4
Wilckens, T.5
Langer, T.6
Odermatt, A.7
-
17
-
-
26844460594
-
-
Gu, X.; Dragovic, J.; Koo, G. C.; Koprak, S. L.; LeGrand, C.; Mundt, S. S.; Shah, K.; Springer, M.; Tan, E.; Thieringer, R.; Hermanowski-Vosatka, A.; Zokian, H.; Balkovec, J.; Waddell, S. T. Discovery of 4-heteroarylbicyclo[2.2. 2]octyltriazoles as potent and selective inhibitors of 11β-HSD1: novel therapeutic agents for the treatment of metabolic syndrome. Bioorg. Med. Chem. Lett. 2005, 15, 5266-5269.
-
(g) Gu, X.; Dragovic, J.; Koo, G. C.; Koprak, S. L.; LeGrand, C.; Mundt, S. S.; Shah, K.; Springer, M.; Tan, E.; Thieringer, R.; Hermanowski-Vosatka, A.; Zokian, H.; Balkovec, J.; Waddell, S. T. Discovery of 4-heteroarylbicyclo[2.2. 2]octyltriazoles as potent and selective inhibitors of 11β-HSD1: novel therapeutic agents for the treatment of metabolic syndrome. Bioorg. Med. Chem. Lett. 2005, 15, 5266-5269.
-
-
-
-
18
-
-
23944454884
-
Adamantyl triazoles as selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1
-
(h) Olson, S.; Aster, S.; Brown, K.; Carbin, L.; Graham, D.; Hermanowski, A.; LeGrand, C.; Mundt, S.; Robbins, M.; Schaeffer, J.; Slossberg, L.; Szymonifka, M.; Thieringer, R.; Wright, S.; Balkovec, J. Adamantyl triazoles as selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1. Bioorg. Med. Chem. Lett. 2005, 15, 4359-4362.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 4359-4362
-
-
Olson, S.1
Aster, S.2
Brown, K.3
Carbin, L.4
Graham, D.5
Hermanowski, A.6
LeGrand, C.7
Mundt, S.8
Robbins, M.9
Schaeffer, J.10
Slossberg, L.11
Szymonifka, M.12
Thieringer, R.13
Wright, S.14
Balkovec, J.15
-
19
-
-
47749125472
-
-
Xiang, J, Saiah, E, Tam, S, McKew, J, Chen, L, Ipek, M, Lee, K, Li, H, Li, J, Li, W, Mansour, T, Suri, V, Vargas, R, Wu, Y, Wan, Z, Lee, J, Binnun, E, Wilson, D. 11-Beta HSD1 Inhibitors. WO 092435, 2007
-
Xiang, J.; Saiah, E.; Tam, S.; McKew, J.; Chen, L.; Ipek, M.; Lee, K.; Li, H. ; Li, J. ; Li, W.; Mansour, T.; Suri, V.; Vargas, R.; Wu, Y.; Wan, Z.; Lee, J.; Binnun, E.; Wilson, D. 11-Beta HSD1 Inhibitors. WO 092435, 2007.
-
-
-
|