메뉴 건너뛰기




Volumn 46, Issue 10, 2011, Pages 5218-5224

Discovery of gemfibrozil analogues that activate PPARα and enhance the expression of gene CPT1A involved in fatty acids catabolism

Author keywords

Analogues of gemfibrozil; Fibrates; Nuclear receptors modulators; PPAR ; Stilbene

Indexed keywords

2 [4 [2 [3 CYCLOHEXYL 1 (4 CYCLOHEXYLBUTYL)UREIDO]ETHYL]PHENYLTHIO] 2 METHYLPROPIONIC ACID; 2,2 DIMETHYL 5 (4 PHENOXYPHENOXY)PENTANOIC ACID; 2,2 DIMETHYL 5 [4 (2 PHENYLVINYL)PHENOXY]PENTANOIC ACID; 2,2 DIMETHYL 5 [4 (PHENYLDIAZENYL)PHENOXY]PENTANOIC ACID; 5 (2 METHOXY 4 ALLYLPHENOXY) 2,2 DIMETHYLPENTANOIC ACID; 5 (4 ALLYL 2 METHOXYPHENOXY)PENTANOIC ACID; 5 (4 BENZOYLPHENOXY) 2,2 DIMETHYLPENTANOIC ACID; 5 (4 BENZOYLPHENOXY)PENTANOIC ACID; 5 [4 ((ANILINOCARBONYL)AMINO)PHENOXY]PENTANOIC ACID; 5 [4 (2 PHENYLVINYL)PHENOXY]PENTANOIC ACID; ALPHA ASARONE; CARNITINE PALMITOYL ACYL COENZYME A TRANSFERASE 1; CHALCONE; COENZYME A TRANSFERASE; FATTY ACID; GEMFIBROZIL; METHYL GROUP; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA AGONIST; PHENYL GROUP; STILBENE; UNCLASSIFIED DRUG;

EID: 80053213260     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2011.08.022     Document Type: Article
Times cited : (31)

References (25)
  • 1
    • 0025132245 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 12
    • 70349239032 scopus 로고    scopus 로고
    • Natural stilbenes: An overview
    • T. Shen, X.N. Wang, and H.X. Lou Natural stilbenes: an overview Nat. Prod. Rep. 26 2009 916 935
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 916-935
    • Shen, T.1    Wang, X.N.2    Lou, H.X.3
  • 13
    • 49649150734 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 19
    • 29644433541 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.