-
1
-
-
0025132245
-
Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators
-
I. Issemann, and S. Green Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators Nature 347 1990 645 650
-
(1990)
Nature
, vol.347
, pp. 645-650
-
-
Issemann, I.1
Green, S.2
-
2
-
-
67349155584
-
Significance of peroxisome proliferator-activated receptors in the cardiovascular system in health and disease
-
E. Robinson, and D.J. Grieve Significance of peroxisome proliferator-activated receptors in the cardiovascular system in health and disease Pharmacol. Ther. 122 2009 246 263
-
(2009)
Pharmacol. Ther.
, vol.122
, pp. 246-263
-
-
Robinson, E.1
Grieve, D.J.2
-
3
-
-
11144310564
-
An overview on biological mechanisms of PPARs
-
DOI 10.1016/j.phrs.2004.07.012, PII S104366180400194X
-
B.P. Kota, T.H.-W.Huang, and B.D. Roufogalis An overview on biological mechanisms of PPARs Pharm. Res. 51 2005 85 94 (Pubitemid 40040538)
-
(2005)
Pharmacological Research
, vol.51
, Issue.2
, pp. 85-94
-
-
Kota, B.P.1
Huang, T.H.-W.2
Roufogalis, B.D.3
-
4
-
-
67449108376
-
Peroxisome proliferator-activated receptor-alpha (PPARα): At the crossroads of obesity, diabetes and cardiovascular disease
-
J.-C. Fruchart Peroxisome proliferator-activated receptor-alpha (PPARα): at the crossroads of obesity, diabetes and cardiovascular disease Atherosclerosis 205 2009 1 8
-
(2009)
Atherosclerosis
, vol.205
, pp. 1-8
-
-
Fruchart, J.-C.1
-
5
-
-
78049257829
-
PPARγ: A circadian transcription factor in adipogenesis and osteogenesis
-
M. Kawai, and C.J. Rosen PPARγ: a circadian transcription factor in adipogenesis and osteogenesis Natl. Rev. 6 2010 629 636
-
(2010)
Natl. Rev.
, vol.6
, pp. 629-636
-
-
Kawai, M.1
Rosen, C.J.2
-
6
-
-
68449095060
-
PPARδ in humans: Genetic and pharmacological evidence for a significant metabolic function
-
F. Karpe, and E.E. Ehrenborg PPARδ in humans: genetic and pharmacological evidence for a significant metabolic function Curr. Opin. Lipidol. 20 2009 333 336
-
(2009)
Curr. Opin. Lipidol.
, vol.20
, pp. 333-336
-
-
Karpe, F.1
Ehrenborg, E.E.2
-
8
-
-
33645076793
-
Mode of action of fibrates in the regulation of triglyceride and HDL-cholesterol metabolism
-
J.-C. Fruchart, and P. Duriez Mode of action of fibrates in the regulation of triglyceride and HDL-cholesterol metabolism Drugs Today 42 2006 39 64
-
(2006)
Drugs Today
, vol.42
, pp. 39-64
-
-
Fruchart, J.-C.1
Duriez, P.2
-
10
-
-
0037870337
-
α-asarone inhibits HMG-CoA reductase, lowers serum LDL-cholesterol levels and reduces biliary CSI in hypercholesterolemic rats
-
DOI 10.1078/0944-7113-00274
-
L. Rodríguez-Páez, M. Juárez-Sanchez, J. Antúnez-Solís, I. Baeza, and C. Wong α-Asarone inhibits HMG-CoA reductase, lowers serum LDL-cholesterol levels and reduces biliary CSI in hypercholesterolemic rats Phytomedicine 10 2003 397 404 (Pubitemid 36745163)
-
(2003)
Phytomedicine
, vol.10
, Issue.5
, pp. 397-404
-
-
Rodriguez-Paez, L.1
Juarez-Sanchez, M.2
Antunez-Solis, J.3
Baeza, I.4
Wong, C.5
-
11
-
-
0346727388
-
Potent Hypolipidemic Activity of Mimetic Amides of Fibrates Based on the 2-Methoxy-4-(2-propenyl)phenoxyacetic Scaffold
-
DOI 10.1002/ddr.10333
-
D. Hernández, P. Bernal, A. Cruz, Y. Garciafigueroa, L. Garduño, M. Salazar, F. Díaz, G. Chamorro, and J. Tamariz Potent hypolipidemic activity of mimetic amides of fibrates based on the 2-methoxy-4-(2-propenyl)phenoxyacetic scaffold Drug Dev. Res. 61 2004 19 36 (Pubitemid 38056080)
-
(2004)
Drug Development Research
, vol.61
, Issue.1
, pp. 19-36
-
-
Hernandez, D.1
Bernal, P.2
Cruz, A.3
Garciafigueroa, Y.4
Garduno, L.5
Salazar, M.6
Diaz, F.7
Chamorro, G.8
Tamariz, J.9
-
13
-
-
49649150734
-
Flavonoid frond exudates from two Jamaican ferns, Pityrogramma tartarea and P. calomelanos
-
A.E. Star, and T.J. Mabry Flavonoid frond exudates from two Jamaican ferns, Pityrogramma tartarea and P. calomelanos Phytochemistry 10 1971 2817 2818
-
(1971)
Phytochemistry
, vol.10
, pp. 2817-2818
-
-
Star, A.E.1
Mabry, T.J.2
-
14
-
-
41649120931
-
Design, synthesis, biological evaluation and docking studies of pterostilbene analogs inside PPARα
-
DOI 10.1016/j.bmc.2008.01.051, PII S0968089608000710
-
C.S. Mizuno, G. Ma, S. Khan, A. Patny, M.A. Avery, and A.M. Rimando Design, synthesis, biological evaluation and docking studies of pterostilbene analogs inside PPARα Bioorg. Med. Chem. 16 2008 3800 3808 (Pubitemid 351484033)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.7
, pp. 3800-3808
-
-
Mizuno, C.S.1
Ma, G.2
Khan, S.3
Patny, A.4
Avery, M.A.5
Rimando, A.M.6
-
15
-
-
36649022448
-
Structure-based drug design of a novel family of chalcones as PPARα agonists: Virtual screening, synthesis, and biological activities in vitro
-
DOI 10.1111/j.1745-7254.2007.00670.x
-
X.-H. Li, H.-J. Zou, A.-H. Wu, Y.-L. Ye, and J.-H. Shen Structure-based drug design of a novel family of chalcones as PPARα agonists: virtual screening, synthesis, and biological activities in vitro Acta Pharm. Sin. 28 2007 2040 2052 (Pubitemid 350198339)
-
(2007)
Acta Pharmacologica Sinica
, vol.28
, Issue.12
, pp. 2040-2052
-
-
Li, X.-H.1
Zou, H.-J.2
Wu, A.-H.3
Ye, Y.-L.4
Shen, J.-H.5
-
16
-
-
78651501250
-
Pan-PPAR agonists based on the resveratrol scaffold: Biological evaluation and docking studies
-
W. Li, X. He, W. Shi, H. Jia, and B. Zhong Pan-PPAR agonists based on the resveratrol scaffold: biological evaluation and docking studies ChemMedChem 5 2010 1977 1982
-
(2010)
ChemMedChem
, vol.5
, pp. 1977-1982
-
-
Li, W.1
He, X.2
Shi, W.3
Jia, H.4
Zhong, B.5
-
17
-
-
70350061743
-
Synthesis and biological evaluation of 2-heteroarylthioalkanoic acid analogues of clofibric acid as peroxisome proliferator-activated receptor α agonists
-
L. Giampietro, A. Ammazzalorso, A. Giancristofaro, F. Lannutti, G. Bettoni, B. De Filippis, M. Fantacuzzi, C. Maccallini, M. Petruzzelli, A. Morgano, A. Moschetta, and R. Amoroso Synthesis and biological evaluation of 2-heteroarylthioalkanoic acid analogues of clofibric acid as peroxisome proliferator-activated receptor α agonists J. Med. Chem. 52 2009 6224 6232
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6224-6232
-
-
Giampietro, L.1
Ammazzalorso, A.2
Giancristofaro, A.3
Lannutti, F.4
Bettoni, G.5
De Filippis, B.6
Fantacuzzi, M.7
MacCallini, C.8
Petruzzelli, M.9
Morgano, A.10
Moschetta, A.11
Amoroso, R.12
-
18
-
-
79952332433
-
Synthesis and biological evaluation of gemfibrozil chiral analogues as potential PPARα agonists
-
B. De Filippis, L. Giampietro, A. Giancristofaro, A. Ammazzalorso, M. Fantacuzzi, C. Maccallini, M. Petruzzelli, and R. Amoroso Synthesis and biological evaluation of gemfibrozil chiral analogues as potential PPARα agonists Lett. Drug Des. Disc. 8 2011 154 158
-
(2011)
Lett. Drug Des. Disc.
, vol.8
, pp. 154-158
-
-
De Filippis, B.1
Giampietro, L.2
Giancristofaro, A.3
Ammazzalorso, A.4
Fantacuzzi, M.5
MacCallini, C.6
Petruzzelli, M.7
Amoroso, R.8
-
19
-
-
29644433541
-
Synthesis and phase transition in new chalcone derivatives: Crystal structure of 1-phenyl-3-(4'-undecylcarbonyloxyphenyl)-2-propen-1-one
-
DOI 10.1080/154214090964753, PII G5244165136318
-
G.Y. Yeap, I. Susanti, B.S. Teoh, W.A.K. Mahmood, and W.T.A. Harrison Synthesis and phase transition in new chalcone derivatives: crystal structure of 1-phenyl-3-(4'-undecylcarbonyloxyphenyl)-2-propen-1-one Mol. Cryst. Liq. Cryst. 442 2005 133 146 (Pubitemid 43019132)
-
(2005)
Molecular Crystals and Liquid Crystals
, vol.442
, pp. 133-146
-
-
Yeap, G.-Y.1
Susanti, I.2
Teoh, B.-S.3
Mahmood, W.A.K.4
Harrison, W.T.A.5
-
20
-
-
0021921508
-
Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 3. Modifications to the linkage region (region 3)
-
DOI 10.1021/jm00381a006
-
D.M. Stout, W.L. Matier, C. Barcelon-Yang, R.D. Reynolds, and B.S. Brown Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 3. Modifications to the linkage region (region 3) J. Med. Chem. 28 1985 295 298 (Pubitemid 15137932)
-
(1985)
Journal of Medicinal Chemistry
, vol.28
, Issue.3
, pp. 295-298
-
-
Stout, D.M.1
Matier, W.L.2
Barcelon-Yang, C.3
-
21
-
-
0023621454
-
Thromboxane synthase inhibitors. Synthesis and pharmacological activity of (R)-, (S)-, and (±)-2,2-dimethyl-6-[2-(1H-imidazol-1-yl)-1-[[(4 methoxyphenyl)-methoxy]methyl]ethoxy]hexanoic acids
-
P.W. Manley, D.P. Tuffin, N.M. Allanson, P.E. Buckle, N. Lad, S.M.F. Lai, D.O. Lunt, R.A. Porter, and P.J. Wade Thromboxane synthase inhibitors. Synthesis and pharmacological activity of (R)-, (S)-, and (+-)-2,2-dimethyl-6- [2-(1H-imidazol-1-yl)-1-[[(4-methoxyphenyl)methoxy]methyl]ethoxy] hexanoic acids J. Med. Chem. 30 1987 1812 1818 (Pubitemid 18020910)
-
(1987)
Journal of Medicinal Chemistry
, vol.30
, Issue.10
, pp. 1812-1818
-
-
Manley, P.W.1
Tuffin, D.P.2
Allanson, N.M.3
Buckle, P.E.4
Lad, N.5
Lai, S.M.F.6
Lunt, D.O.7
Porter, R.A.8
Wade, P.J.9
-
22
-
-
2642551635
-
The flip side: Identifying small molecule regulators of nuclear receptors
-
DOI 10.1016/j.chembiol.2003.12.021, PII S1074552104001206
-
I.G. Schulman, and R.A. Heyman The flip side: identifying small molecule regulators of nuclear receptors Chem. Biol. 11 2009 639 646 (Pubitemid 38708832)
-
(2004)
Chemistry and Biology
, vol.11
, Issue.5
, pp. 639-646
-
-
Schulman, I.G.1
Heyman, R.A.2
-
23
-
-
0032810113
-
Reporter gene technology: The future looks bright
-
DOI 10.1016/S0006-2952(99)00096-9, PII S0006295299000969
-
L.H. Naylor Reporter gene technology: the future looks bright Biochem. Pharmacol. 58 1999 749 757 (Pubitemid 29329523)
-
(1999)
Biochemical Pharmacology
, vol.58
, Issue.5
, pp. 749-757
-
-
Naylor, L.H.1
-
24
-
-
0031043030
-
The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis
-
J.D. McGarry, and N.F. Brown The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis Eur. J. Biochem. 244 1997 1 14 (Pubitemid 27079689)
-
(1997)
European Journal of Biochemistry
, vol.244
, Issue.1
, pp. 1-14
-
-
McGarry, J.D.1
Brown, N.F.2
-
25
-
-
0035943681
-
Differential gene regulation in human versus rodent hepatocytes by peroxisome proliferator-activated receptor (PPAR) alpha. PPAR alpha fails to induce peroxisome proliferation-associated genes in human cells independently of the level of receptor expression
-
J.W. Lawrence, Y. Li, S. Chen, J.G. De Luca, J.P. Berger, D.R. Umbenhauer, D.E. Moller, and G. Zhou Differential gene regulation in human versus rodent hepatocytes by peroxisome proliferator-activated receptor (PPAR) alpha. PPAR alpha fails to induce peroxisome proliferation-associated genes in human cells independently of the level of receptor expression J. Biol. Chem. 276 2001 31521 31527
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 31521-31527
-
-
Lawrence, J.W.1
Li, Y.2
Chen, S.3
De Luca, J.G.4
Berger, J.P.5
Umbenhauer, D.R.6
Moller, D.E.7
Zhou, G.8
|