-
1
-
-
3142728651
-
The role of sulphonylureas in the management of Type 2 diabetes mellitus
-
Rendell M. The role of sulphonylureas in the management of Type 2 diabetes mellitus. Drugs 64(12), 1339-1358 (2004).
-
(2004)
Drugs
, vol.64
, Issue.12
, pp. 1339-1358
-
-
Rendell, M.1
-
2
-
-
0029091094
-
Extrapancreatic effects of sulfonylureas - A comparison between glimepiride and conventional sulfonylureas
-
Müller G, Satoh Y, Geisen K. Extrapancreatic effects of sulfonylureas - a comparison between glimepiride and conventional sulfonylureas. Diabetes Res. Clin. Pract. 28(Suppl.), 115-137 (1995).
-
(1995)
Diabetes Res. Clin. Pract.
, vol.28
, Issue.SUPPL.
, pp. 115-137
-
-
Müller, G.1
Satoh, Y.2
Geisen, K.3
-
3
-
-
4544339723
-
The farnesoid X receptor: A novel drug target?
-
Claudel T, Sturm E, Kuipers F, Staels B. The farnesoid X receptor: a novel drug target? Expert Opin. Investig. Drugs 13(9), 1135-1148 (2004).
-
(2004)
Expert Opin. Investig. Drugs
, vol.13
, Issue.9
, pp. 1135-1148
-
-
Claudel, T.1
Sturm, E.2
Kuipers, F.3
Staels, B.4
-
4
-
-
26244441014
-
The farnesoid X receptor: A molecular link between bile acid and lipid and glucose metabolism
-
Claudel T, Staels B, Kuipers F. The farnesoid X receptor: a molecular link between bile acid and lipid and glucose metabolism. Arterioscler. Thromb. Vasc. Biol. 25(10), 2020-2030 (2005).
-
(2005)
Arterioscler. Thromb. Vasc. Biol.
, vol.25
, Issue.10
, pp. 2020-2030
-
-
Claudel, T.1
Staels, B.2
Kuipers, F.3
-
5
-
-
77149138381
-
Targeting farnesoid-X-receptor: From medicinal chemistry to disease treatment
-
Fiorucci S, Mencarelli A, Distrutti E, Palladino G, Cipriani S. Targeting farnesoid-X-receptor: from medicinal chemistry to disease treatment. Curr. Med. Chem. 17, 139-159 (2010).
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 139-159
-
-
Fiorucci, S.1
Mencarelli, A.2
Distrutti, E.3
Palladino, G.4
Cipriani, S.5
-
6
-
-
0037315190
-
Bile acids induce the expression of the human peroxisome proliferator-activated receptor a gene via activation of the farnesoid X receptor
-
Pineda Torra I, Claudel T, Duval C, Kosykh V, Fruchart JC, Staels B. Bile acids induce the expression of the human peroxisome proliferator-activated receptor a gene via activation of the farnesoid X receptor. Mol. Endocrinol. 17(2), 259-272 (2003).
-
(2003)
Mol. Endocrinol.
, vol.17
, Issue.2
, pp. 259-272
-
-
Pineda Torra, I.1
Claudel, T.2
Duval, C.3
Kosykh, V.4
Fruchart, J.C.5
Staels, B.6
-
7
-
-
14244264780
-
Regulation of carbohydrate metabolism by the farnesoid X receptor
-
Stayrook KR, Bramlett KS, Savkur RS et al. Regulation of carbohydrate metabolism by the farnesoid X receptor. Endocrinology 146(3), 984-991 (2005).
-
(2005)
Endocrinology
, vol.146
, Issue.3
, pp. 984-991
-
-
Stayrook, K.R.1
Bramlett, K.S.2
Savkur, R.S.3
-
8
-
-
67651123303
-
Farnesoid X receptor agonists in biliary tract disease
-
Fiorucci S, Baldelli F. Farnesoid X receptor agonists in biliary tract disease. Curr. Opin. Gastroenterol. 25(3), 252-259 (2009).
-
(2009)
Curr. Opin. Gastroenterol.
, vol.25
, Issue.3
, pp. 252-259
-
-
Fiorucci, S.1
Baldelli, F.2
-
9
-
-
76549086983
-
Bile acid-activated receptors in the treatment of dyslipidemia and related disorders
-
Fiorucci S, Cipriani S, Baldelli F, Mencarelli A. Bile acid-activated receptors in the treatment of dyslipidemia and related disorders. Prog. Lipid Res. 49(2), 171-185 (2009).
-
(2009)
Prog. Lipid Res.
, vol.49
, Issue.2
, pp. 171-185
-
-
Fiorucci, S.1
Cipriani, S.2
Baldelli, F.3
Mencarelli, A.4
-
10
-
-
0034632762
-
Identification of a chemical tool for the orphan nuclear receptor FXR
-
Maloney PR, Parks DJ, Haffner CD et al. Identification of a chemical tool for the orphan nuclear receptor FXR. J. Med. Chem. 43(16), 2971-2974 (2000).
-
(2000)
J. Med. Chem.
, vol.43
, Issue.16
, pp. 2971-2974
-
-
Maloney, P.R.1
Parks, D.J.2
Haffner, C.D.3
-
11
-
-
0037101810
-
6a-ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity
-
Pellicciari R, Fiorucci S, Camaioni E et al. 6a-ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity. J. Med. Chem. 45(17), 3569-3572 (2002).
-
(2002)
J. Med. Chem.
, vol.45
, Issue.17
, pp. 3569-3572
-
-
Pellicciari, R.1
Fiorucci, S.2
Camaioni, E.3
-
12
-
-
0037738531
-
A chemical, genetic, and structural analysis of the nuclear bile acid receptor FXR
-
Downes M, Verdecia MA, Roecker AJ et al. A chemical, genetic, and structural analysis of the nuclear bile acid receptor FXR. Mol. Cell 11(4), 1079-1092 (2003).
-
(2003)
Mol. Cell.
, vol.11
, Issue.4
, pp. 1079-1092
-
-
Downes, M.1
Verdecia, M.A.2
Roecker, A.J.3
-
13
-
-
64349115048
-
Discovery of XL335 (WAY-362450), a highly potent, selective, and orally active agonist of the farnesoid X receptor (FXR)
-
Flatt B, Martin R, Wang TL et aAY-362450), a highly potent, selective, and orally active agonist of the farnesoid X receptor (FXR). J. Med. Chem. (2009).
-
(2009)
J. Med. Chem.
-
-
Flatt, B.1
Martin, R.2
Wang, T.L.3
-
14
-
-
65349090763
-
A synthetic farnesoid X receptor (FXR) agonist promotes cholesterol lowering in models of dyslipidemia
-
Evans MJ, Mahaney PE, Borges-Marcucci L et al. A synthetic farnesoid X receptor (FXR) agonist promotes cholesterol lowering in models of dyslipidemia. Am. J. Physiol. Gastrointest. Liver Physiol. 296(3), G543-G552 (2009).
-
(2009)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.296
, Issue.3
-
-
Evans, M.J.1
Mahaney, P.E.2
Borges-Marcucci, L.3
-
15
-
-
0037470079
-
Identification of gene-selective modulators of the bile acid receptor FXR
-
Dussault I, Beard R, Lin M et al. Identification of gene-selective modulators of the bile acid receptor FXR. J. Biol. Chem. 278(9), 7027-7033 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, Issue.9
, pp. 7027-7033
-
-
Dussault, I.1
Beard, R.2
Lin, M.3
-
16
-
-
67649867896
-
Differential modulation of farnesoid X receptor signaling pathway by the thiazolidinediones
-
Kaimal R, Song X, Yan B, King R, Deng R. Differential modulation of farnesoid X receptor signaling pathway by the thiazolidinediones. J. Pharmacol. Exp. Ther. 330(1), 125-134 (2009).
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.330
, Issue.1
, pp. 125-134
-
-
Kaimal, R.1
Song, X.2
Yan, B.3
King, R.4
Deng, R.5
-
17
-
-
21244443895
-
Sulfonylurea agents exhibit peroxisome proliferator-activated receptor g agonistic activity
-
Fukuen S, Iwaki M, Yasui A, Makishima M, Matsuda M, Shimomura I. Sulfonylurea agents exhibit peroxisome proliferator-activated receptor g agonistic activity. J. Biol. Chem. 280(25), 23653-23659 (2005).
-
(2005)
J. Biol. Chem.
, vol.280
, Issue.25
, pp. 23653-23659
-
-
Fukuen, S.1
Iwaki, M.2
Yasui, A.3
Makishima, M.4
Matsuda, M.5
Shimomura, I.6
-
18
-
-
0041919542
-
Improved protein-ligand docking using gold
-
Verdonk ML, Cole JC, Hartshorn MJ, Murray CW, Taylor RD. Improved protein-ligand docking using gold. Proteins 52(4), 609-623 (2003).
-
(2003)
Proteins
, vol.52
, Issue.4
, pp. 609-623
-
-
Verdonk, M.L.1
Cole, J.C.2
Hartshorn, M.J.3
Murray, C.W.4
Taylor, R.D.5
-
19
-
-
0031226772
-
Empirical scoring functions. I. The development of a fast empirical scoring function to estimate the binding affinity of ligands in receptor complexes
-
Eldridge MD, Murray CW, Auton TR, Paolini GY, Mee RP. Empirical scoring functions. I. The development of a fast empirical scoring function to estimate the binding affinity of ligands in receptor complexes. J. Comput. Aided Mol. Des. 11(5), 425-445 (1997).
-
(1997)
J. Comput. Aided Mol. Des.
, vol.11
, Issue.5
, pp. 425-445
-
-
Eldridge, M.D.1
Murray, C.W.2
Auton, T.R.3
Paolini, G.Y.4
Mee, R.P.5
-
20
-
-
65249157397
-
Protonate 3D: Assignment of ionization states and hydrogen coordinates to macromolecular structures
-
Labute P. Protonate 3D: assignment of ionization states and hydrogen coordinates to macromolecular structures. Proteins 75(1), 187-205 (2009).
-
(2009)
Proteins
, vol.75
, Issue.1
, pp. 187-205
-
-
Labute, P.1
-
21
-
-
23444454552
-
The amber biomolecular simulation programs
-
Case DA, Cheatham TE 3rd, Darden T et al. The amber biomolecular simulation programs. J. Comput. Chem. 26(16), 1668-1688 (2005).
-
(2005)
J. Comput. Chem.
, vol.26
, Issue.16
, pp. 1668-1688
-
-
Case, D.A.1
Cheatham III, T.E.2
Darden, T.3
-
22
-
-
47749128054
-
Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW4064
-
Akwabi-Ameyaw A, Bass JY, Caldwell RD et al. Conformationally constrained farnesoid X receptor (FXR) agonists: naphthoic acid-based analogs of GW4064. Bioorg. Med. Chem. Lett. 18(15), 4339-4343 (2008).
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.15
, pp. 4339-4343
-
-
Akwabi-Ameyaw, A.1
Bass, J.Y.2
Caldwell, R.D.3
-
23
-
-
33750580948
-
Halofenate is a selective peroxisome proliferator-activated receptor g modulator with antidiabetic activity
-
Allen T, Zhang F, Moodie SA et al. Halofenate is a selective peroxisome proliferator-activated receptor g modulator with antidiabetic activity. Diabetes 55(9), 2523-2533 (2006).
-
(2006)
Diabetes
, vol.55
, Issue.9
, pp. 2523-2533
-
-
Allen, T.1
Zhang, F.2
Moodie, S.A.3
-
24
-
-
0033637121
-
A regulatory cascade of the nuclear receptors FXR SHP-1 and lRH-1 represses bile acid biosynthesis
-
Goodwin B, Jones SA, Price RR et al. A regulatory cascade of the nuclear receptors FXR, SHP-1, and lRH-1 represses bile acid biosynthesis. Mol. Cell 6(3), 517-526 (2000).
-
(2000)
Mol. Cell.
, vol.6
, Issue.3
, pp. 517-526
-
-
Goodwin, B.1
Jones, S.A.2
Price, R.R.3
-
25
-
-
0034646603
-
Farnesoid X receptor responds to bile acids and represses cholesterol 7a-hydroxylase gene (CYP7A1) transcription
-
Chiang JY, Kimmel R, Weinberger C, Stroup D. Farnesoid X receptor responds to bile acids and represses cholesterol 7a-hydroxylase gene (CYP7A1) transcription. J. Biol. Chem. 275(15), 10918-10924 (2000)
-
(2000)
J. Biol. Chem.
, vol.275
, Issue.15
, pp. 10918-10924
-
-
Chiang, J.Y.1
Kimmel, R.2
Weinberger, C.3
Stroup, D.4
-
26
-
-
0037663483
-
Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis
-
Holt JA, Luo G, Billin AN et al. Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis. Genes Dev. 17(13), 1581-1591 (2003).
-
(2003)
Genes Dev.
, vol.17
, Issue.13
, pp. 1581-1591
-
-
Holt, J.A.1
Luo, G.2
Billin, A.N.3
-
27
-
-
0035800772
-
Human bile salt export pump promoter is transactivated by the farnesoid X receptor/ bile acid receptor
-
Ananthanarayanan M, Balasubramanian N, Makishima M, Mangelsdorf DJ, Suchy FJ. Human bile salt export pump promoter is transactivated by the farnesoid X receptor/ bile acid receptor. J. Biol. Chem. 276(31), 28857-28865 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, Issue.31
, pp. 28857-28865
-
-
Ananthanarayanan, M.1
Balasubramanian, N.2
Makishima, M.3
Mangelsdorf, D.J.4
Suchy, F.J.5
-
28
-
-
0345650665
-
Activation functions 1 and 2 of nuclear receptors: Molecular strategies for transcriptional activation
-
Warnmark A, Treuter E, Wright AP, Gustafsson JA. Activation functions 1 and 2 of nuclear receptors: molecular strategies for transcriptional activation. Mol. Endocrinol. 17(10), 1901-1909 (2003).
-
(2003)
Mol. Endocrinol.
, vol.17
, Issue.10
, pp. 1901-1909
-
-
Warnmark, A.1
Treuter, E.2
Wright, A.P.3
Gustafsson, J.A.4
-
29
-
-
44449136869
-
Identification of a potent synthetic FXR agonist with an unexpected mode of binding and activation
-
Soisson SM, Parthasarathy G, Adams AD et al. Identification of a potent synthetic FXR agonist with an unexpected mode of binding and activation. Proc. Natl Acad. Sci. USA 105(14), 5337-5342 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, Issue.14
, pp. 5337-5342
-
-
Soisson, S.M.1
Parthasarathy, G.2
Adams, A.D.3
-
30
-
-
64249153603
-
Identification of an N-oxide pyridine GW4064 analog as a potent FXR agonist
-
Feng S, Yang M, Zhang Z et al. Identification of an N-oxide pyridine GW4064 analog as a potent FXR agonist. Bioorg. Med. Chem. Lett. 19, 2595-2598 (2009).
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2595-2598
-
-
Feng, S.1
Yang, M.2
Zhang, Z.3
-
31
-
-
67651108945
-
FXR agonist activity of conformationally constrained analogs of GW4064
-
Akwabi-Ameyaw A, Bass JY, Caldwell RD et al. FXR agonist activity of conformationally constrained analogs of GW4064. Bioorg. Med. Chem. Lett. 19(16), 4733-4739 (2009).
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, Issue.16
, pp. 4733-4739
-
-
Akwabi-Ameyaw, A.1
Bass, J.Y.2
Caldwell, R.D.3
-
32
-
-
65149087208
-
Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064
-
Bass JY, Caldwell RD, Caravella JA et al. Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064. Bioorg. Med. Chem. Lett. 19(11), 2969-2973 (2009).
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, Issue.11
, pp. 2969-2973
-
-
Bass, J.Y.1
Caldwell, R.D.2
Caravella, J.A.3
-
33
-
-
0038298927
-
Nuclear receptor ligands and cofactor recruitment: Is there a coactivator 'on deck'?
-
Nettles KW, Greene GL. Nuclear receptor ligands and cofactor recruitment: is there a coactivator 'on deck'? Mol. Cell 11(4), 850-851 (2003).
-
(2003)
Mol. Cell.
, vol.11
, Issue.4
, pp. 850-851
-
-
Nettles, K.W.1
Greene, G.L.2
-
34
-
-
0034521515
-
Sulphonylurea dose-response relationships: Relation to clinical practice
-
Lindblad U, Melander A. Sulphonylurea dose-response relationships: relation to clinical practice. Diabetes Obes. Metab. 2(1), 25-31 (2000).
-
(2000)
Diabetes Obes. Metab.
, vol.2
, Issue.1
, pp. 25-31
-
-
Lindblad, U.1
Melander, A.2
|