-
1
-
-
0037900979
-
Minireview: lipid metabolism, metabolic diseases, and peroxisome proliferator-activated receptors
-
Lee C.H., Olson P., Evans R.M. (2003) Minireview: lipid metabolism, metabolic diseases, and peroxisome proliferator-activated receptors. Endocrinology;144:2201-2207.
-
(2003)
Endocrinology
, vol.144
, pp. 2201-2207
-
-
Lee, C.H.1
Olson, P.2
Evans, R.M.3
-
3
-
-
77954082797
-
Synthesis of isosteric selenium analog of the PPARbeta/delta agonist GW501516 and comparison of biological activity
-
Sharma A.K., Sk U.H., He P., Peters J.M., Amin S. (2010) Synthesis of isosteric selenium analog of the PPARbeta/delta agonist GW501516 and comparison of biological activity. Bioorg Med Chem Lett;20:4050-4052.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 4050-4052
-
-
Sharma, A.K.1
Sk, U.H.2
He, P.3
Peters, J.M.4
Amin, S.5
-
4
-
-
2342466734
-
Global prevalence of diabetes: estimates for the year 2000 and projections for 2030
-
Wild S., Roglic G., Green A., Sicree R., King H. (2004) Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care;27:1047-1053.
-
(2004)
Diabetes Care
, vol.27
, pp. 1047-1053
-
-
Wild, S.1
Roglic, G.2
Green, A.3
Sicree, R.4
King, H.5
-
5
-
-
84861594164
-
Synthesis, in vitro and in silico screening of ethyl 2-(6-substituted benzo[d]thiazol-2-ylamino)-2-oxoacetates as protein-tyrosine phosphatase 1B inhibitors
-
Navarrete-Vazquez G., Ramírez-Martínez M., Estrada-Soto S., Nava-Zuazo C., Paoli P., Camici G., Escalante-García J., Medina-Franco J.L., López-Vallejo F., Ortiz-Andrade R. (2012) Synthesis, in vitro and in silico screening of ethyl 2-(6-substituted benzo[d]thiazol-2-ylamino)-2-oxoacetates as protein-tyrosine phosphatase 1B inhibitors. Eur J Med Chem;53:346-355.
-
(2012)
Eur J Med Chem
, vol.53
, pp. 346-355
-
-
Navarrete-Vazquez, G.1
Ramírez-Martínez, M.2
Estrada-Soto, S.3
Nava-Zuazo, C.4
Paoli, P.5
Camici, G.6
Escalante-García, J.7
Medina-Franco, J.L.8
López-Vallejo, F.9
Ortiz-Andrade, R.10
-
6
-
-
34548182594
-
PPAR dual agonists: are they opening Pandora's Box?
-
Balakumar P., Rose M., Ganti S.S., Krishan P., Singh M. (2007) PPAR dual agonists: are they opening Pandora's Box? Pharmacol Res;56:91-98.
-
(2007)
Pharmacol Res
, vol.56
, pp. 91-98
-
-
Balakumar, P.1
Rose, M.2
Ganti, S.S.3
Krishan, P.4
Singh, M.5
-
7
-
-
80455125821
-
Medicinal chemistry and actions of dual and pan PPAR modulators
-
Adeghate E., Adem A., Hasan M.Y., Tekes K., Kalasz H. (2011) Medicinal chemistry and actions of dual and pan PPAR modulators. Open Med Chem J;5(Suppl. 2):93-98.
-
(2011)
Open Med Chem J
, vol.5
, Issue.SUPPL. 2
, pp. 93-98
-
-
Adeghate, E.1
Adem, A.2
Hasan, M.Y.3
Tekes, K.4
Kalasz, H.5
-
8
-
-
33646269938
-
Tesaglitazar: a promising approach in type 2 diabetes
-
Cox S.L. (2006) Tesaglitazar: a promising approach in type 2 diabetes. Drugs Today (Barc);42:139-146.
-
(2006)
Drugs Today (Barc)
, vol.42
, pp. 139-146
-
-
Cox, S.L.1
-
9
-
-
51349147434
-
New PPARgamma ligands based on barbituric acid: virtual screening, synthesis and receptor binding studies
-
Sundriyal S., Viswanad B., Ramarao P., Chakraborti A.K., Bharatam P.V. (2008) New PPARgamma ligands based on barbituric acid: virtual screening, synthesis and receptor binding studies. Bioorg Med Chem Lett;18:4959-4962.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 4959-4962
-
-
Sundriyal, S.1
Viswanad, B.2
Ramarao, P.3
Chakraborti, A.K.4
Bharatam, P.V.5
-
10
-
-
0037187361
-
Novel 5-substituted 2,4-thiazolidinedione and 2,4-oxazolidinedione derivatives as insulin sensitizers with antidiabetic activities
-
Momose Y., Maekawa T., Yamano T., Kawada M., Odaka H., Ikeda H., Sohda T. (2002) Novel 5-substituted 2, 4-thiazolidinedione and 2, 4-oxazolidinedione derivatives as insulin sensitizers with antidiabetic activities. J Med Chem;45:1518-1534.
-
(2002)
J Med Chem
, vol.45
, pp. 1518-1534
-
-
Momose, Y.1
Maekawa, T.2
Yamano, T.3
Kawada, M.4
Odaka, H.5
Ikeda, H.6
Sohda, T.7
-
11
-
-
0036357952
-
Novel 5-substituted-1H-tetrazole derivatives as potent glucose and lipid lowering agents
-
Momose Y., Maekawa T., Odaka H., Ikeda H., Sohda T. (2002) Novel 5-substituted-1H-tetrazole derivatives as potent glucose and lipid lowering agents. Chem Pharm Bull;50:100-111.
-
(2002)
Chem Pharm Bull
, vol.50
, pp. 100-111
-
-
Momose, Y.1
Maekawa, T.2
Odaka, H.3
Ikeda, H.4
Sohda, T.5
-
12
-
-
44249094595
-
Glycine increases mRNA adiponectin and diminishes pro-inflammatory adipokines expression in 3T3-L1 cells
-
Garcia-Macedo R., Sanchez-Muñoz F., Almanza-Perez J.C., Duran-Reyes G., Alarcon-Aguilar F., Cruz M. (2008) Glycine increases mRNA adiponectin and diminishes pro-inflammatory adipokines expression in 3T3-L1 cells. Eur J Pharmacol;587:317-321.
-
(2008)
Eur J Pharmacol
, vol.587
, pp. 317-321
-
-
Garcia-Macedo, R.1
Sanchez-Muñoz, F.2
Almanza-Perez, J.C.3
Duran-Reyes, G.4
Alarcon-Aguilar, F.5
Cruz, M.6
-
13
-
-
77956877625
-
Glycine regulates inflammatory markers modifying the energetic balance through PPAR and UCP-2
-
Almanza-Perez J.C., Alarcon-Aguilar F.J., Blancas-Flores G., Campos-Sepulveda A.E., Roman-Ramos R., Garcia-Macedo R., Cruz M. (2010) Glycine regulates inflammatory markers modifying the energetic balance through PPAR and UCP-2. Biomed Pharmacother;64:534-540.
-
(2010)
Biomed Pharmacother
, vol.64
, pp. 534-540
-
-
Almanza-Perez, J.C.1
Alarcon-Aguilar, F.J.2
Blancas-Flores, G.3
Campos-Sepulveda, A.E.4
Roman-Ramos, R.5
Garcia-Macedo, R.6
Cruz, M.7
-
14
-
-
70349932423
-
Autodock4 and AutoDockTools4: automated docking with selective receptor flexibility
-
Morris G.M., Huey R., Lindstrom W., Sanner M.F., Belew R.K., Goodsell D.S., Olson A.J. (2009) Autodock4 and AutoDockTools4: automated docking with selective receptor flexibility. J Comput Chem;16:2785-2791.
-
(2009)
J Comput Chem
, vol.16
, pp. 2785-2791
-
-
Morris, G.M.1
Huey, R.2
Lindstrom, W.3
Sanner, M.F.4
Belew, R.K.5
Goodsell, D.S.6
Olson, A.J.7
-
15
-
-
77950917531
-
A comparative study of flavonoid analogues on streptozotocin-nicotinamide induced diabetic rats: quercetin as a potential antidiabetic agent acting via 11β-hydroxysteroid dehydrogenase type 1 inhibition
-
Torres-Piedra M., Ortiz-Andrade R., Villalobos-Molina R., Singh N., Medina-Franco J.L., Webster S.P., Binnie M., Navarrete-Vázquez G., Estrada-Soto S. (2010) A comparative study of flavonoid analogues on streptozotocin-nicotinamide induced diabetic rats: quercetin as a potential antidiabetic agent acting via 11β-hydroxysteroid dehydrogenase type 1 inhibition. Eur J Med Chem;45:2606-2612.
-
(2010)
Eur J Med Chem
, vol.45
, pp. 2606-2612
-
-
Torres-Piedra, M.1
Ortiz-Andrade, R.2
Villalobos-Molina, R.3
Singh, N.4
Medina-Franco, J.L.5
Webster, S.P.6
Binnie, M.7
Navarrete-Vázquez, G.8
Estrada-Soto, S.9
-
16
-
-
84055183812
-
Rational targeting of peroxisome proliferating activated receptor subtypes
-
Nevin D.K., Lloyd D.G., Fayne D. (2011) Rational targeting of peroxisome proliferating activated receptor subtypes. Curr Med Chem;18:5598-5623.
-
(2011)
Curr Med Chem
, vol.18
, pp. 5598-5623
-
-
Nevin, D.K.1
Lloyd, D.G.2
Fayne, D.3
-
17
-
-
0035074525
-
Metabolic adaptations in skeletal muscle overexpressing GLUT4: effects on muscle and physical activity
-
Tsao T.S., Li J., Chang K.S., Stenbit A.E., Galuska D., Anderson J.E., Zierath J.R., McCarter R.J., Charron M.J. (2001) Metabolic adaptations in skeletal muscle overexpressing GLUT4: effects on muscle and physical activity. FASEB J;15:958-969.
-
(2001)
FASEB J
, vol.15
, pp. 958-969
-
-
Tsao, T.S.1
Li, J.2
Chang, K.S.3
Stenbit, A.E.4
Galuska, D.5
Anderson, J.E.6
Zierath, J.R.7
McCarter, R.J.8
Charron, M.J.9
-
18
-
-
0033834248
-
Targeted disruption of the glucose transporter 4 selectively in muscle causes insulin resistance and glucose intolerance
-
Zisman A., Peroni O.D., Abel E.D., Michael M.D., Mauvais-Jarvis F., Lowell B.B., Wojtaszewski J.F., Hirshman M.F., Virkamaki A., Goodyear L.J., Kahn C.R., Kahn B.B. (2000) Targeted disruption of the glucose transporter 4 selectively in muscle causes insulin resistance and glucose intolerance. Nat Med;6:924-928.
-
(2000)
Nat Med
, vol.6
, pp. 924-928
-
-
Zisman, A.1
Peroni, O.D.2
Abel, E.D.3
Michael, M.D.4
Mauvais-Jarvis, F.5
Lowell, B.B.6
Wojtaszewski, J.F.7
Hirshman, M.F.8
Virkamaki, A.9
Goodyear, L.J.10
Kahn, C.R.11
Kahn, B.B.12
-
20
-
-
71049127036
-
Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator
-
Xu L., Chen Y., Pan Y., Skiles G.L., Shou M. (2009) Prediction of human drug-drug interactions from time-dependent inactivation of CYP3A4 in primary hepatocytes using a population-based simulator. Drug Metab Dispos;37:2330-2339.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 2330-2339
-
-
Xu, L.1
Chen, Y.2
Pan, Y.3
Skiles, G.L.4
Shou, M.5
-
21
-
-
79955713610
-
In silico predictions of hERG channel blockers in drug discovery: from ligand-based and target-based approaches to systems chemical biology
-
Taboureau O., Jørgensen F.S. (2011) In silico predictions of hERG channel blockers in drug discovery: from ligand-based and target-based approaches to systems chemical biology. Comb Chem High Throughput Screen;14:375-387.
-
(2011)
Comb Chem High Throughput Screen
, vol.14
, pp. 375-387
-
-
Taboureau, O.1
Jørgensen, F.S.2
-
22
-
-
43049119332
-
Antidiabetic activity of N-(6-substituted-1,3-benzothiazol-2-yl)benzenesulfonamides
-
Moreno-Díaz H., Villalobos-Molina R., Ortiz-Andrade R., Díaz-Coutiño D., Medina-Franco J.L., Webster S.P., Binnie M., Estrada-Soto S., Ibarra-Barajas M., León-Rivera I., Navarrete-Vázquez G. (2008) Antidiabetic activity of N-(6-substituted-1, 3-benzothiazol-2-yl)benzenesulfonamides. Bioorg Med Chem Lett;18:2871-2877.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 2871-2877
-
-
Moreno-Díaz, H.1
Villalobos-Molina, R.2
Ortiz-Andrade, R.3
Díaz-Coutiño, D.4
Medina-Franco, J.L.5
Webster, S.P.6
Binnie, M.7
Estrada-Soto, S.8
Ibarra-Barajas, M.9
León-Rivera, I.10
Navarrete-Vázquez, G.11
|