-
1
-
-
37849027240
-
Novel PPAR gamma agonists identified from a natural product library: A virtual screening, induced-fit docking and biological assay study
-
Salam, N. K.; Huang, T. H. W.; Kota, B. P.; Kim, M. S.; Li, Y.; Hibbs, D. E. Novel PPAR gamma agonists identified from a natural product library: A virtual screening, induced-fit docking and biological assay study. Chem. Biol. Drug Des. 2008, 71, 57-70.
-
(2008)
Chem. Biol. Drug Des.
, vol.71
, pp. 57-70
-
-
Salam, N.K.1
Huang, T.H.W.2
Kota, B.P.3
Kim, M.S.4
Li, Y.5
Hibbs, D.E.6
-
2
-
-
44049108337
-
Peroxisome proliferator-activated receptor gamma agonists and diabetes: Current evidence and future perspectives
-
Chiarelli, F.; Marzio, D. D. Peroxisome proliferator-activated receptor gamma agonists and diabetes: current evidence and future perspectives. Vasc. Health Risk Manage. 2008, 4, 297-304.
-
(2008)
Vasc. Health Risk Manage.
, vol.4
, pp. 297-304
-
-
Chiarelli, F.1
Marzio, D.D.2
-
3
-
-
59149084957
-
Peroxisome proliferator-activated receptor gamma agonists as insulin sensitizers: From the discovery to recent progress
-
Nobuo, C.; Yu, M. Peroxisome proliferator-activated receptor gamma agonists as insulin sensitizers: From the discovery to recent progress. Curr. Top. Med. Chem. 2008, 8, 1483-1507.
-
(2008)
Curr. Top. Med. Chem.
, vol.8
, pp. 1483-1507
-
-
Nobuo, C.1
Yu, M.2
-
4
-
-
26844431513
-
Dual and pan-peroxisome proliferator-activated receptors (PPAR) co-agonism: The bezafibrate lessons
-
Tenenbaum, A.; Motro, M.; Fisman, E. Z. Dual and pan-peroxisome proliferator-activated receptors (PPAR) co-agonism: The bezafibrate lessons. Cardiovasc. Diabetol. 2005, 4, 14.
-
(2005)
Cardiovasc. Diabetol.
, vol.4
, pp. 14
-
-
Tenenbaum, A.1
Motro, M.2
Fisman, E.Z.3
-
5
-
-
33744503414
-
Selective PPAR agonists for the treatment of type 2 diabetes
-
Nehlin, J. O.; Mogensen, J. P.; Petterson, I.; Jeppesen, L.; Fleckner, J.; Wulff, E. M.; Sauerberg, P. Selective PPAR agonists for the treatment of type 2 diabetes. Ann. N.Y. Acad. Sci. 2006, 1067, 448-453.
-
(2006)
Ann. N.Y. Acad. Sci.
, vol.1067
, pp. 448-453
-
-
Nehlin, J.O.1
Mogensen, J.P.2
Petterson, I.3
Jeppesen, L.4
Fleckner, J.5
Wulff, E.M.6
Sauerberg, P.7
-
6
-
-
43049168651
-
The PPAR gamma coding region and its role in visceral obesity
-
Khoo, B. Y.; Najimudin Nazalan Muhammad; Tengku, T. S. The PPAR gamma coding region and its role in visceral obesity. Biochem. Biophys. Res. Commun. 2008, 371, 177-179.
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.371
, pp. 177-179
-
-
Khoo, B.Y.1
Muhammad, N.N.2
Tengku, T.S.3
-
8
-
-
60549092887
-
PPAR gamma and its ligands: Therapeutic implications in cardiovascular disease
-
Villacorta, L.; Schopfer, F. J.; Zhang, J.; Freeman, B. A.; Chen, E. Y. PPAR gamma and its ligands: therapeutic implications in cardiovascular disease. Clin. Sci. 2009, 116, 205-218.
-
(2009)
Clin. Sci.
, vol.116
, pp. 205-218
-
-
Villacorta, L.1
Schopfer, F.J.2
Zhang, J.3
Freeman, B.A.4
Chen, E.Y.5
-
9
-
-
53149098608
-
Potential of peroxisome proliferator-activated receptor gamma antagonist compounds as therapeutic agents for a wide range of cancer types
-
Burton, J. D.; Goldenberg, D. M.; Blumenthal, R. D. Potential of peroxisome proliferator-activated receptor gamma antagonist compounds as therapeutic agents for a wide range of cancer types. PPAR Res. 2008, 2008, 494161.
-
(2008)
PPAR Res.
, vol.2008
, pp. 494161
-
-
Burton, J.D.1
Goldenberg, D.M.2
Blumenthal, R.D.3
-
10
-
-
27944505915
-
PPARs in diseases: Control mechanisms of inflammation
-
Kostadinova, R.; Wahli, W.; Michalik, L. PPARs in diseases: control mechanisms of inflammation. Curr. Med. Chem. 2005, 12, 2995-3009.
-
(2005)
Curr. Med. Chem.
, vol.12
, pp. 2995-3009
-
-
Kostadinova, R.1
Wahli, W.2
Michalik, L.3
-
11
-
-
46749115113
-
PPARgamma agonists as therapeutics for the treatment of Alzheimer0s disease
-
Landreth, G.; Jiang, Q.; Mandrekar, S.; Heneka, M.PPARgamma agonists as therapeutics for the treatment of Alzheimer0s disease. Neurotherapeutics 2008, 5, 481-489.
-
(2008)
Neurotherapeutics
, vol.5
, pp. 481-489
-
-
Landreth, G.1
Jiang, Q.2
Mandrekar, S.3
Heneka, M.4
-
12
-
-
54349086581
-
Thiazolidinediones anti-inflammatory and anti-atherosclerotic effects in type 2 diabetes mellitus
-
Pastromas, S.; Sakellariou, D.; Koulouris, S. Thiazolidinediones anti-inflammatory and anti-atherosclerotic effects in type 2 diabetes mellitus. Anti-Inflammatory Anti-Allergy Agents Med. Chem. 2008, 7, 217-223.
-
(2008)
Anti-Inflammatory Anti-Allergy Agents Med. Chem.
, vol.7
, pp. 217-223
-
-
Pastromas, S.1
Sakellariou, D.2
Koulouris, S.3
-
13
-
-
69249083643
-
Peroxisome proliferator-activated receptors: Targets for the treatment of metabolic illnesses
-
review
-
Rodrigo, M.-C.; Poblete, B. M.; Gonzalez, G. O.; Leiva, M. E.; Mujica, E. V.; Aranguez, A. C.; Ivan, P. Peroxisome proliferator-activated receptors: targets for the treatment of metabolic illnesses (review). Mol. Med. Rep. 2008, 1, 317-324.
-
(2008)
Mol. Med. Rep.
, vol.1
, pp. 317-324
-
-
Rodrigo, M.-C.1
Poblete, B.M.2
Gonzalez, G.O.3
Leiva, M.E.4
Mujica, E.V.5
Aranguez, A.C.6
Ivan, P.7
-
14
-
-
33847122993
-
Dual PPAR alpha and gamma agonists: Promises and pitfalls in type 2 diabetes
-
Ahmed, I.; Furlong, K.; Flood, J.; Treat, V. P.; Goldstein, B. J. Dual PPAR alpha and gamma agonists: promises and pitfalls in type 2 diabetes. Am. J. Ther. 2007, 14, 49-62.
-
(2007)
Am. J. Ther.
, vol.14
, pp. 49-62
-
-
Ahmed, I.1
Furlong, K.2
Flood, J.3
Treat, V.P.4
Goldstein, B.J.5
-
15
-
-
48449090661
-
Design and synthesis of novel oxazole containing 1,3-dioxane-2-carboxylic acid derivatives as PPAR alpha and gamma dual agonists
-
Pingali, H.; Jain, M.; Shah, S.; Makadia, P.; Zaware, P.; Goel, A.; Patel, M.; Giri, S.; Patel, H.; Patel, P. Design and synthesis of novel oxazole containing 1,3-dioxane-2-carboxylic acid derivatives as PPAR alpha and gamma dual agonists. Bioorg. Med. Chem. 2008, 16, 7117-7127.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7117-7127
-
-
Pingali, H.1
Jain, M.2
Shah, S.3
Makadia, P.4
Zaware, P.5
Goel, A.6
Patel, M.7
Giri, S.8
Patel, H.9
Patel, P.10
-
16
-
-
0016394077
-
A Potent Antihypercholesterolemic Agent: [4-Chloro-6-(2,3-xylidino)-2- pyrimidinylthio] acetic Acid (WY-14643)
-
Santilli, A. A.; Scotese, A. C.; Tomarelli, R. M. A Potent Antihypercholesterolemic Agent: [4-Chloro-6-(2,3-xylidino)-2-pyrimidinylthio] acetic Acid (WY-14643). Experientia 1974, 30, 1110-1111.
-
(1974)
Experientia
, vol.30
, pp. 1110-1111
-
-
Santilli, A.A.1
Scotese, A.C.2
Tomarelli, R.M.3
-
17
-
-
53149149804
-
Renal and vascular mechanisms of thiazolidinedione- Induced fluid retention
-
Yang, T.; Soodvilai, S. Renal and vascular mechanisms of thiazolidinedione- induced fluid retention. PPAR Res. 2008, 2008, 943614.
-
(2008)
PPAR Res.
, vol.2008
, pp. 943614
-
-
Yang, T.1
Soodvilai, S.2
-
18
-
-
0031898610
-
PPAR-gamma: Adipogenic regulator and thiazolidinedione receptor
-
Spiegelman, B. M. PPAR-gamma: adipogenic regulator and thiazolidinedione receptor. Diabetes 1998, 47, 507-514
-
(1998)
Diabetes
, vol.47
, pp. 507-514
-
-
Spiegelman, B.M.1
-
19
-
-
37049029469
-
Synthesis and evaluation of the antiproliferative activities of derivatives of carboxyalkyl isoflavones linked to N-t-Boc-hexylenediamine
-
Kohen, F.; Gayer, B.; Kulik, T.; Frydman, V.; Nevo, N.; Katzburg, S.; Limor, R.; Sharon, O.; Stern, N.; Somjen, D. Synthesis and evaluation of the antiproliferative activities of derivatives of carboxyalkyl isoflavones linked to N-t-Boc-hexylenediamine. J. Med. Chem. 2007, 50, 6405-6410.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 6405-6410
-
-
Kohen, F.1
Gayer, B.2
Kulik, T.3
Frydman, V.4
Nevo, N.5
Katzburg, S.6
Limor, R.7
Sharon, O.8
Stern, N.9
Somjen, D.10
-
20
-
-
0346887168
-
Antiproliferative activity of various flavonoids and related compounds: Additive effect of interferon-α2b
-
Blank, V. C.; Poli, C.; Marder, M.; Roguin, L. P. Antiproliferative activity of various flavonoids and related compounds: additive effect of interferon-α2b. Bioorg. Med. Chem. Lett. 2004, 14, 133-136.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 133-136
-
-
Blank, V.C.1
Poli, C.2
Marder, M.3
Roguin, L.P.4
-
21
-
-
47349110359
-
Synthesis and biological activity of some new flavonyl-2,4- thiazolidinediones
-
Bozdaǧ-Dundar, O. B.; Verspohl, E. J.; Daş-Evcimen, N.; Kaup, R. M.; Bauer, K.; Saríkaya, M.; Evranos, B.; Ertan, R. Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones. Bioorg. Med. Chem. 2008, 16, 6747-6751.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 6747-6751
-
-
Bozdaǧ-Dundar, O.B.1
Verspohl, E.J.2
Daş-Evcimen, N.3
Kaup, R.M.4
Bauer, K.5
Saríkaya, M.6
Evranos, B.7
Ertan, R.8
-
22
-
-
12244291214
-
Fatty acid synthase inhibitors from plants: Isolation, structure elucidation, and SAR studies
-
Li, X.-C.; Joshi, A. S.; ElSohly, H. N.; Khan, S. I.; Jacob, M. R.; Zhang, Z.; Khan, I. A.; Ferreira, D.; Walker, L. A.; Broedel, S. E.; Raulli, R. E.; Cihlar, R. L. Fatty acid synthase inhibitors from plants: isolation, structure elucidation, and SAR studies. J. Nat. Prod. 2002, 65, 1909-1914.
-
(2002)
J. Nat. Prod.
, vol.65
, pp. 1909-1914
-
-
Li, X.-C.1
Joshi, A.S.2
Elsohly, H.N.3
Khan, S.I.4
Jacob, M.R.5
Zhang, Z.6
Khan, I.A.7
Ferreira, D.8
Walker, L.A.9
Broedel, S.E.10
Raulli, R.E.11
Cihlar, R.L.12
-
23
-
-
0037176744
-
Antiviral isoflavonoid sulfate and steroidal glycosides from the fruits of Solanum torvum
-
DOI 10.1016/S0031-9422(01)00417-4, PII S0031942201004174
-
Arthan, D.; Svasti, J.; Kittakoop, P.; Pittayakhachonwut, D.; Tanticharoen, M.; Thebtaranonth, Y. Antiviral isoflavonoid sulfate and steroidal glycosides from the fruits of Solanum torvum. Phytochemistry 2002, 59, 459-463. (Pubitemid 34202567)
-
(2002)
Phytochemistry
, vol.59
, Issue.4
, pp. 459-463
-
-
Arthan, D.1
Svasti, J.2
Kittakoop, P.3
Pittayakhachonwut, D.4
Tanticharoen, M.5
Thebtaranonth, Y.6
-
24
-
-
3042716672
-
Antiinflammatory isoflavonoids from the stems of Derris scandens
-
Laupattarakasem, P.; Houghton, P. J.; Robin, J.; Hoult, S. Antiinflammatory isoflavonoids from the stems of Derris scandens. Planta Med. 2004, 70, 496-501.
-
(2004)
Planta Med.
, vol.70
, pp. 496-501
-
-
Laupattarakasem, P.1
Houghton, P.J.2
Robin, J.3
Hoult, S.4
-
25
-
-
38849204284
-
Protective effect of irisolidone, a metabolite of kakkalide, against hydrogen peroxide induced cell damage via antioxidant effect
-
Kang, K. A.; Zhang, R.; Piao, M. J.; Ko, D. O.; Wang, Z. H.; Kim, B. J.; Park, J. W.; Kim, H. S.; Kim, D. H.; Hyun, J. W. Protective effect of irisolidone, a metabolite of kakkalide, against hydrogen peroxide induced cell damage via antioxidant effect. Bioorg. Med. Chem. 2008, 16, 1133-1141.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1133-1141
-
-
Kang, K.A.1
Zhang, R.2
Piao, M.J.3
Ko, D.O.4
Wang, Z.H.5
Kim, B.J.6
Park, J.W.7
Kim, H.S.8
Kim, D.H.9
Hyun, J.W.10
-
26
-
-
41149144696
-
Understanding the cardioprotective effects of flavonols: Discovery of relaxant flavonols without antioxidant activity
-
Qin, C. H.; Chen, X.; Hughes, R. A.; Williams, S. J.; Woodman, O. L. Understanding the cardioprotective effects of flavonols: discovery of relaxant flavonols without antioxidant activity. J. Med. Chem. 2007, 51, 1874-1884.
-
(2007)
J. Med. Chem.
, vol.51
, pp. 1874-1884
-
-
Qin, C.H.1
Chen, X.2
Hughes, R.A.3
Williams, S.J.4
Woodman, O.L.5
-
27
-
-
0037451845
-
Synthesis and estrogen receptor binding affnities of 7-hydroxy- 3-(4-hydroxyphenyl)- 4H-1-benzopyran-4-ones containing a basic side chain
-
Kim, Y.-W.; Mobley, J. A.; Brueggemeier, R. W. Synthesis and estrogen receptor binding affnities of 7-hydroxy- 3-(4-hydroxyphenyl)- 4H-1-benzopyran-4-ones containing a basic side chain. Bioorg. Med. Chem. Lett. 2003, 13, 1475-1478.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1475-1478
-
-
Kim, Y.-W.1
Mobley, J.A.2
Brueggemeier, R.W.3
-
28
-
-
3242794236
-
Synthesis and aromatase inhibitory activity of novel pyridine-containing isoflavones
-
Kim, Y.-W.; Hackett, J. C.; Brueggemeier, R. W. Synthesis and aromatase inhibitory activity of novel pyridine-containing isoflavones. J. Med. Chem. 2004, 47, 4032-4040.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 4032-4040
-
-
Kim, Y.-W.1
Hackett, J.C.2
Brueggemeier, R.W.3
-
29
-
-
3042598800
-
A convenient and biogenetic type synthesis of few naturally occurring chromeno dihydrochalcones and their in vitro antileishmanial activity
-
Tadigoppula, N.; Shweta, G. S. A convenient and biogenetic type synthesis of few naturally occurring chromeno dihydrochalcones and their in vitro antileishmanial activity. Bioorg. Med. Chem. Lett. 2004, 14, 3913-3916.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 3913-3916
-
-
Tadigoppula, N.1
Shweta, G.S.2
-
30
-
-
33847260626
-
Practical and efficient entry to isoflavones by Pd(0)/C-mediated Suzuki-Miyaura reaction. Total synthesis of geranylated isoflavones
-
Felpin, F. X.; Lory, C.; Sow, H.; Acherar, S. Practical and efficient entry to isoflavones by Pd(0)/C-mediated Suzuki-Miyaura reaction. Total synthesis of geranylated isoflavones. Tetrahedron 2007, 63, 3010-3016.
-
(2007)
Tetrahedron
, vol.63
, pp. 3010-3016
-
-
Felpin, F.X.1
Lory, C.2
Sow, H.3
Acherar, S.4
-
31
-
-
10644284737
-
Catecholic flavonoids acting as telomerase inhibitors
-
Menichincheri, M.; Ballinari, D.; Bargiotti, A.; Bonomini, L.; Ceccarelli,W.; D'Alessio, R.; Fretta, A.;Moll, J.; Polucci, P.; Soncini, C.; Tibolla,M.; Trosset, J. Y.; Vanotti, E. Catecholic flavonoids acting as telomerase inhibitors. J. Med. Chem. 2004, 47, 6466-6475.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6466-6475
-
-
Menichincheri, M.1
Ballinari, D.2
Bargiotti, A.3
Bonomini, L.4
Ceccarelli, W.5
D'Alessio, R.6
Fretta, A.7
Moll, J.8
Polucci, P.9
Soncini, C.10
Tibolla, M.11
Trosset, J.Y.12
Vanotti, E.13
-
32
-
-
35148862752
-
Structure-activity relationship studies of flavonoids as potent inhibitors of human platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2
-
Vasquez-Martinez, Y.; Ohri, R. V.; Kenyon, V.; Holmanb, T. R.; Sepúlveda-Bozaa, S. Structure-activity relationship studies of flavonoids as potent inhibitors of human platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2. Bioorg. Med. Chem. 2007, 15, 7408-7425.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 7408-7425
-
-
Vasquez-Martinez, Y.1
Ohri, R.V.2
Kenyon, V.3
Holmanb, T.R.4
Sepúlveda- Bozaa, S.5
-
33
-
-
0037179186
-
A convenient one-pot synthesis of 2-alkylthio isoflavones from deoxybenzoins using a phase transfer catalyst
-
Kim, Y. W.; Brueggemeier, R. W. A convenient one-pot synthesis of 2-alkylthio isoflavones from deoxybenzoins using a phase transfer catalyst. Tetrahedron Lett. 2002, 43, 6113-6115.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6113-6115
-
-
Kim, Y.W.1
Brueggemeier, R.W.2
-
34
-
-
21244505104
-
Novel, potent small-molecule inhibitors of the molecular chaperone Hsp90 discovered through structure-based design
-
Dymock, B. W.; Barril, X.; Brough, P. A.; Cansfield, J. E.; Massey, A.; McDonald, E.; Hubbard, R. E.; Surgenor, S.; Roughley, S. D.; Webb, P.; Workman, P.; Wright, L.; Drysdale, M. J. Novel, potent small-molecule inhibitors of the molecular chaperone Hsp90 discovered through structure-based design. J. Med. Chem. 2005, 48, 4212-4215.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4212-4215
-
-
Dymock, B.W.1
Barril, X.2
Brough, P.A.3
Cansfield, J.E.4
Massey, A.5
McDonald, E.6
Hubbard, R.E.7
Surgenor, S.8
Roughley, S.D.9
Webb, P.10
Workman, P.11
Wright, L.12
Drysdale, M.J.13
-
35
-
-
0141854072
-
A natural product ligand of the oxysterol receptor, liver X receptor
-
Bramlett, K. S.; Houck, K. A.; Borchert, K. M.; Dowless, M. S.; Kulanthaivel, P.; Zhang, Y.; Beyer, T. P.; Schmidt, R.; Thomas, J. S.; Michael, L. F.; Barr, R.; Montrose, C.; Eacho, P. I.; Cao, G.; Burris, T. P. A natural product ligand of the oxysterol receptor, liver X receptor. J. Pharmacol. Exp. Ther. 2003, 307, 291-296.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.307
, pp. 291-296
-
-
Bramlett, K.S.1
Houck, K.A.2
Borchert, K.M.3
Dowless, M.S.4
Kulanthaivel, P.5
Zhang, Y.6
Beyer, T.P.7
Schmidt, R.8
Thomas, J.S.9
Michael, L.F.10
Barr, R.11
Montrose, C.12
Eacho, P.I.13
Cao, G.14
Burris, T.P.15
-
36
-
-
33645217958
-
Synthesis and PPAR-gamma ligand-binding activity of the new series of 2́-hydroxychalcone and thiazolidinedione derivatives
-
Jung, S. H.; Park, S. Y.; Kim-Pak, Y.; Lee, H. K.; Park, K. S.; Shin, K. H.; Ohuchi, K.; Shin, H.-K.; Keum, S. R.; Lim, S. S. Synthesis and PPAR-gamma ligand-binding activity of the new series of 2́-hydroxychalcone and thiazolidinedione derivatives. Chem. Pharm. Bull. 2006, 54, 368-371.
-
(2006)
Chem. Pharm. Bull.
, vol.54
, pp. 368-371
-
-
Jung, S.H.1
Park, S.Y.2
Kim-Pak, Y.3
Lee, H.K.4
Park, K.S.5
Shin, K.H.6
Ohuchi, K.7
Shin, H.-K.8
Keum, S.R.9
Lim, S.S.10
-
37
-
-
0035805144
-
Suppression of inducible cyclooxygenase and nitric oxide synthase through activation of peroxisome proliferator-activated receptorgamma by flavonoids in mouse macrophages
-
Liang, Y.-C.; Tsai, S.-H.; Tsai, D.-C.; Lin-Shiau, S.-Y.; Lin, J.-K. Suppression of inducible cyclooxygenase and nitric oxide synthase through activation of peroxisome proliferator-activated receptorgamma by flavonoids in mouse macrophages. FEBS Lett. 2001, 496, 12-18.
-
(2001)
FEBS Lett.
, vol.496
, pp. 12-18
-
-
Liang, Y.-C.1
Tsai, S.-H.2
Tsai, D.-C.3
Lin-Shiau, S.-Y.4
Lin, J.-K.5
-
38
-
-
33846816486
-
Antiinflammatory effects of isoflavones are dependent on flow and human endothelial cell PPAR gamma
-
Chacko, B. K.; Chandler, R. T.; D'Alessandro, T. L.; Mundhekar, A.; Khoo, N. K. H.; Botting, N.; Barnes, S.; Patel, R. P. Antiinflammatory effects of isoflavones are dependent on flow and human endothelial cell PPAR gamma. J. Nutr. 2007, 137, 351-356.
-
(2007)
J. Nutr.
, vol.137
, pp. 351-356
-
-
Chacko, B.K.1
Chandler, R.T.2
D'Alessandro, T.L.3
Mundhekar, A.4
Khoo, N.K.H.5
Botting, N.6
Barnes, S.7
Patel, R.P.8
-
39
-
-
7844224790
-
N-(2-Benzoylphenyl)-L-tyrosine PPARγ Agonists. 1. Discovery of a Novel Series of Potent Antihyperglycemic and Antihyperlipidemic Agents
-
Henke, B. R.; Blanchard, S. G.; Brackeen, M. F.; Brown, K. K.; Cobb, J. E.; Collins, J. L.; Harrington, W. W.; Hashim, M. A.; Hull-Ryde, E. A.; Kaldor, I.; Kliewer, S. A.; Lake, D. H.; Leesnitzer, L. M.; Lehmann, J. M.; Lenhard, J. M.; Orband-Miller, L. A.; Miller, J.F.; Mook, R. A.; Noble, S. A.; Oliver, W.; Parks, D. J.; Plunket, K. D.; Szewczyk, J. R.; Willson, T. M. N-(2-Benzoylphenyl)-L-tyrosine PPARγ Agonists. 1. Discovery of a Novel Series of Potent Antihyperglycemic and Antihyperlipidemic Agents. J. Med. Chem. 1998, 41, 5020-5036.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5020-5036
-
-
Henke, B.R.1
Blanchard, S.G.2
Brackeen, M.F.3
Brown, K.K.4
Cobb, J.E.5
Collins, J.L.6
Harrington, W.W.7
Hashim, M.A.8
Hull-Ryde, E.A.9
Kaldor, I.10
Kliewer, S.A.11
Lake, D.H.12
Leesnitzer, L.M.13
Lehmann, J.M.14
Lenhard, J.M.15
Orband-Miller, L.A.16
Miller, J.F.17
Mook, R.A.18
Noble, S.A.19
Oliver, W.20
Parks, D.J.21
Plunket, K.D.22
Szewczyk, J.R.23
Willson, T.M.24
more..
-
40
-
-
0033998334
-
The PPARs: From Orphan Receptors to Drug Discovery
-
Willson, T. M.; Brown, P. J.; Sternbach, D. D.; Henke, B. R. The PPARs: From Orphan Receptors to Drug Discovery. J. Med. Chem. 2000, 43, 527-550.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 527-550
-
-
Willson, T.M.1
Brown, P.J.2
Sternbach, D.D.3
Henke, B.R.4
-
41
-
-
33750481268
-
Anti-hyperlipidemic properties of CM108 (a flavone derivative) in vitro and in vivo
-
Guo, L.; Hu, W.-R.; Lian, J.-H.; Ji, W.; Deng, T.; Qian, M.; Gong, B.-Q. Anti-hyperlipidemic properties of CM108 (a flavone derivative) in vitro and in vivo. Eur. J. Pharmacol. 2006, 551, 80-86.
-
(2006)
Eur. J. Pharmacol.
, vol.551
, pp. 80-86
-
-
Guo, L.1
Hu, W.-R.2
Lian, J.-H.3
Ji, W.4
Deng, T.5
Qian, M.6
Gong, B.-Q.7
|