-
1
-
-
0003964363
-
-
American Cancer Society
-
Cancer Facts & Figures 2013 American Cancer Society http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-036845.pdf
-
(2013)
Cancer Facts & Figures
-
-
-
2
-
-
84896789649
-
-
IARC
-
Globocan 2012 IARC
-
(2012)
Globocan
-
-
-
4
-
-
0036463649
-
Apoptosis-based therapies
-
J.C. Reed Apoptosis-based therapies Nat. Rev. Drug Discov. 1 2002 111 121
-
(2002)
Nat. Rev. Drug Discov.
, vol.1
, pp. 111-121
-
-
Reed, J.C.1
-
5
-
-
22144460556
-
Apoptosis-based therapies for hematologic malignancies
-
J.C. Reed M. Pellecchia Apoptosis-based therapies for hematologic malignancies Blood 106 2005 408 418
-
(2005)
Blood
, vol.106
, pp. 408-418
-
-
Reed, J.C.1
Pellecchia, M.2
-
6
-
-
70349433777
-
Procaspase-3 activation as an anti-cancer strategy: Structure-activity relationship of procaspase-activating compound 1 (PAC-1) and its cellular colocalization with caspase-3
-
Q.P. Peterson D.C. Hsu D.R. Goode C.J. Novotny R.K. Totten P.J. Hergenrother Procaspase-3 activation as an anti-cancer strategy: structure-activity relationship of procaspase-activating compound 1 (PAC-1) and its cellular colocalization with caspase-3 J. Med. Chem. 52 2009 5721 5731
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5721-5731
-
-
Peterson, Q.P.1
Hsu, D.C.2
Goode, D.R.3
Novotny, C.J.4
Totten, R.K.5
Hergenrother, P.J.6
-
7
-
-
0038778278
-
Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell-and caspase-based high throughput screening assay
-
S.X. Cai B. Nguyen S. Jia J. Herich J. Guastella S. Reddy B. Tseng J. Drewe S. Kasibhatla Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell-and caspase-based high throughput screening assay J. Med. Chem. 46 2003 2474 2481
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2474-2481
-
-
Cai, S.X.1
Nguyen, B.2
Jia, S.3
Herich, J.4
Guastella, J.5
Reddy, S.6
Tseng, B.7
Drewe, J.8
Kasibhatla, S.9
-
9
-
-
0037187361
-
Novel 5-substituted 2,4-thiazolidinedione and 2,4-oxazolidinedione derivatives as insulin sensitizers and anti-diabetic activities
-
M. Yu M. Tsuyoshi Y. Tohru K. Mitsuru O. Hiroyuki I. Hitoshi S. Takashi Novel 5-substituted 2,4-thiazolidinedione and 2,4-oxazolidinedione derivatives as insulin sensitizers and anti-diabetic activities J. Med. Chem. 45 2002 1518 1534
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1518-1534
-
-
Yu, M.1
Tsuyoshi, M.2
Tohru, Y.3
Mitsuru, K.4
Hiroyuki, O.5
Hitoshi, I.6
Takashi, S.7
-
10
-
-
77953326342
-
Synthesis and anti-inflammatory activity of new arylidene-thiazolidine-2,4-dione as PPAR ligands
-
C.D. Barros A.A. Amato T.B. Oliveira K.B.R. Iannini A.L. Silva T.G. Silva E.S. Leite M.Z. Hernandes M.C.A. Lima S.L. Galdino F.A.R. Neves I.R. Pitta Synthesis and anti-inflammatory activity of new arylidene-thiazolidine-2,4-dione as PPAR ligands Bioorg. Med. Chem. 18 2010 3805 3811
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3805-3811
-
-
Barros, C.D.1
Amato, A.A.2
Oliveira, T.B.3
Iannini, K.B.R.4
Silva, A.L.5
Silva, T.G.6
Leite, E.S.7
Hernandes, M.Z.8
Lima, M.C.A.9
Galdino, S.L.10
Neves, F.A.R.11
Pitta, I.R.12
-
11
-
-
84858983819
-
Synthesis, quantum mechanical calculation and biological evaluation of 5-(4-substituted aryl/hetero aryl methylidene)-1,3-thiazolidine-2,4-diones
-
N. Swathi Y. Ramu C.V.S. Subrahmanyam K. Satyanarayana Synthesis, quantum mechanical calculation and biological evaluation of 5-(4-substituted aryl/hetero aryl methylidene)-1,3-thiazolidine-2,4-diones Int. J. Pharm. Sci. 4 2012 561 566
-
(2012)
Int. J. Pharm. Sci.
, vol.4
, pp. 561-566
-
-
Swathi, N.1
Ramu, Y.2
Subrahmanyam, C.V.S.3
Satyanarayana, K.4
-
12
-
-
77954902048
-
Synthesis and evaluation of some 5-[1-{4-4-substituted phenyl amino}-meth-(Z)-ylidene]-thiazolidine-2,4-dione for antitubercular activity
-
S.R. Pattan K.R. Alagwadi A.R. Bhat V.V.K. Reddy J.S. Pattan A.B. Khade K.G. Bhatt Synthesis and evaluation of some 5-[1-{4-4-substituted phenyl amino}-meth-(Z)-ylidene]-thiazolidine-2,4-dione for antitubercular activity Indian Drugs 45 2008 532 535
-
(2008)
Indian Drugs
, vol.45
, pp. 532-535
-
-
Pattan, S.R.1
Alagwadi, K.R.2
Bhat, A.R.3
Reddy, V.V.K.4
Pattan, J.S.5
Khade, A.B.6
Bhatt, K.G.7
-
13
-
-
34447628509
-
Synthesis and antimicrobial activity of some new thiazolyl thiazolidine-2,4-dione derivatives
-
B. Oya O. Ozen M. Arzu K. Engin E. Rahmiye Synthesis and antimicrobial activity of some new thiazolyl thiazolidine-2,4-dione derivatives Bioorg. Med. Chem. 15 2007 6012 6017
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 6012-6017
-
-
Oya, B.1
Ozen, O.2
Arzu, M.3
Engin, K.4
Rahmiye, E.5
-
14
-
-
0027742233
-
Synthesis and anticonvulsant properties of some novel quinazolinone thiazolidine and 4-thiazolidone derivatives
-
S.A.H. El-Feky Synthesis and anticonvulsant properties of some novel quinazolinone thiazolidine and 4-thiazolidone derivatives Pharmazie 48 1993 894 896
-
(1993)
Pharmazie
, vol.48
, pp. 894-896
-
-
El-Feky, S.A.H.1
-
15
-
-
84861919344
-
New thiazolidinedione-5-acetic acid amide derivatives: Synthesis, characterization and investigation of antimicrobial and cytotoxic properties
-
G.A. Shankar R.A. Kallanagouda New thiazolidinedione-5-acetic acid amide derivatives: synthesis, characterization and investigation of antimicrobial and cytotoxic properties Med. Chem. Res. 21 2012 816 824
-
(2012)
Med. Chem. Res.
, vol.21
, pp. 816-824
-
-
Shankar, G.A.1
Kallanagouda, R.A.2
-
16
-
-
38949125112
-
Hybrid molecules with a dual mode of action: Dream or reality?
-
B. Meunier Hybrid molecules with a dual mode of action: dream or reality? Acc. Chem. Res. 41 2008 69 77
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 69-77
-
-
Meunier, B.1
-
17
-
-
68849122747
-
Enhanced targeting with heterobivalent ligands
-
L. Xu J. Vagner J. Josan R.M. Lynch D.L. Morse B. Baggett H. Han E.A. Mash V.J. Hruby J. Robert Enhanced targeting with heterobivalent ligands Mol. Cancer Ther. 8 8 2009 2356 2365
-
(2009)
Mol. Cancer Ther.
, vol.8
, Issue.8
, pp. 2356-2365
-
-
Xu, L.1
Vagner, J.2
Josan, J.3
Lynch, R.M.4
Morse, D.L.5
Baggett, B.6
Han, H.7
Mash, E.A.8
Hruby, V.J.9
Robert, J.10
-
18
-
-
84855758265
-
3,5-Disubstituted-thiazolidine-2,4-dione analogs as anticancer agents: Design, synthesis and biological characterization
-
K. Liu W. Rao H. Parikh Q. Li T.L. Guo S. Grant G.E. Kellogg S. Zhang 3,5-Disubstituted-thiazolidine-2,4-dione analogs as anticancer agents: design, synthesis and biological characterization Eur. J. Med. Chem. 47 2012 125 137
-
(2012)
Eur. J. Med. Chem.
, vol.47
, pp. 125-137
-
-
Liu, K.1
Rao, W.2
Parikh, H.3
Li, Q.4
Guo, T.L.5
Grant, S.6
Kellogg, G.E.7
Zhang, S.8
-
20
-
-
16644393169
-
Thiazolidinedione, a peroxisome proliferator-activated receptor-γ ligand, inhibits growth and metastasis of HT-29 human colon cancer cells through differentiation-promoting effects
-
T. Yoshizumi T. Ohta I. Ninomiya I. Terada S. Fushida T. Fujimura G.I. Nishimura K. Shimizu S. Yi K. Miwa Thiazolidinedione, a peroxisome proliferator-activated receptor-γ ligand, inhibits growth and metastasis of HT-29 human colon cancer cells through differentiation-promoting effects Int. J. Oncol. 25 3 2004 631
-
(2004)
Int. J. Oncol.
, vol.25
, Issue.3
, pp. 631
-
-
Yoshizumi, T.1
Ohta, T.2
Ninomiya, I.3
Terada, I.4
Fushida, S.5
Fujimura, T.6
Nishimura, G.I.7
Shimizu, K.8
Yi, S.9
Miwa, K.10
-
21
-
-
33751533892
-
Peroxisome proliferator-activated receptors
-
L. Michalik J. Auwerx J.P. Berger V.K. Chatterjee C.K. Glass F.J. Gonzalez P.A. Grimaldi T. Kadowaki M.A. Lazar S. O'Rahilly C.N. Palmer J. Plutzky J.K. Reddy B.M. Spiegelman B. Staels W. Wahli Peroxisome proliferator-activated receptors Pharmacol. Rev. 58 4 2006 726 741
-
(2006)
Pharmacol. Rev.
, vol.58
, Issue.4
, pp. 726-741
-
-
Michalik, L.1
Auwerx, J.2
Berger, J.P.3
Chatterjee, V.K.4
Glass, C.K.5
Gonzalez, F.J.6
Grimaldi, P.A.7
Kadowaki, T.8
Lazar, M.A.9
O'Rahilly, S.10
Palmer, C.N.11
Plutzky, J.12
Reddy, J.K.13
Spiegelman, B.M.14
Staels, B.15
Wahli, W.16
-
22
-
-
0002890043
-
Molecular mechanisms of hepatocarcinogenic peroxisome proliferators
-
A. Puga K.B. Wallace Taylor & Francis Philadelphia
-
P.J. Lapinskas J.C. Corton Molecular mechanisms of hepatocarcinogenic peroxisome proliferators A. Puga K.B. Wallace Molecular Biology of the Toxic Response 1998 Taylor & Francis Philadelphia 219 253
-
(1998)
Molecular Biology of the Toxic Response
, pp. 219-253
-
-
Lapinskas, P.J.1
Corton, J.C.2
-
23
-
-
0028802627
-
Differential activation of peroxisome proliferator-activated receptors by eicosanoids
-
K. Yu W. Bayona C.B. Kallen H.P. Harding C.P. Ravera G. McMahon M. Brown M.A. Lazar Differential activation of peroxisome proliferator-activated receptors by eicosanoids J. Biol. Chem. 270 1995 23975 23983
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 23975-23983
-
-
Yu, K.1
Bayona, W.2
Kallen, C.B.3
Harding, H.P.4
Ravera, C.P.5
McMahon, G.6
Brown, M.7
Lazar, M.A.8
-
24
-
-
68949128792
-
PPAR-gamma agonists and their effects on IGF-I receptor signaling: Implications for cancer
-
A. Belfiore M. Genua R. Malaguarnera PPAR-gamma agonists and their effects on IGF-I receptor signaling: implications for cancer PPAR Res. 2009 2009 830501
-
(2009)
PPAR Res.
, vol.2009
, pp. 830501
-
-
Belfiore, A.1
Genua, M.2
Malaguarnera, R.3
-
25
-
-
0036183630
-
The mechanisms of action of PPARs
-
J. Berger D.E. Moller The mechanisms of action of PPARs Annu. Rev. Med. 53 2002 409 435
-
(2002)
Annu. Rev. Med.
, vol.53
, pp. 409-435
-
-
Berger, J.1
Moller, D.E.2
-
26
-
-
32644460092
-
From molecular action to physiological outputs: Peroxisome proliferator-activated receptors are nuclear receptors at the crossroads of key cellular functions
-
J.N. Feige L. Gelman L. Michalik B. Desvergne W. Wahli From molecular action to physiological outputs: peroxisome proliferator-activated receptors are nuclear receptors at the crossroads of key cellular functions Prog. Lipid Res. 45 2 2006 120 159
-
(2006)
Prog. Lipid Res.
, vol.45
, Issue.2
, pp. 120-159
-
-
Feige, J.N.1
Gelman, L.2
Michalik, L.3
Desvergne, B.4
Wahli, W.5
-
27
-
-
84871393949
-
Targeting PPARγ signaling cascade for the prevention and treatment of prostate cancer
-
S. Sikka L. Chen G. Sethi A.P. Kumar Targeting PPARγ signaling cascade for the prevention and treatment of prostate cancer PPAR Res. 2012 2012 968040
-
(2012)
PPAR Res.
, vol.2012
, pp. 968040
-
-
Sikka, S.1
Chen, L.2
Sethi, G.3
Kumar, A.P.4
-
28
-
-
0035204352
-
Limited cooperation between peroxisome proliferator-activated receptors and retinoid X receptor agonists in sebocyte growth and development
-
M.J. Kim D. Deplewski N. Ciletti S. Michel U. Reichert R.L. Rosenfield Limited cooperation between peroxisome proliferator-activated receptors and retinoid X receptor agonists in sebocyte growth and development Mol. Genet. Metab. 74 2001 362 369
-
(2001)
Mol. Genet. Metab.
, vol.74
, pp. 362-369
-
-
Kim, M.J.1
Deplewski, D.2
Ciletti, N.3
Michel, S.4
Reichert, U.5
Rosenfield, R.L.6
-
29
-
-
0030818756
-
Polarity and specific sequence requirements of peroxisome proliferator-activated receptor (PPAR)/retinoid X receptor heterodimer binding to DNA: A functional analysis of the malic enzyme gene PPAR response element
-
A. Ijpenberg E. Jeannin W. Wahli B. Desvergne Polarity and specific sequence requirements of peroxisome proliferator-activated receptor (PPAR)/retinoid X receptor heterodimer binding to DNA: a functional analysis of the malic enzyme gene PPAR response element J. Biol. Chem. 272 1997 20108 20117
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 20108-20117
-
-
Ijpenberg, A.1
Jeannin, E.2
Wahli, W.3
Desvergne, B.4
-
30
-
-
0029294531
-
Peroxisome proliferator activated receptors: Transcriptional regulators of adipogenesis, lipid metabolism and more
-
W. Wahli O. Braissant B. Desvergne Peroxisome proliferator activated receptors: transcriptional regulators of adipogenesis, lipid metabolism and more Chem. Biol. 2 1995 261 266
-
(1995)
Chem. Biol.
, vol.2
, pp. 261-266
-
-
Wahli, W.1
Braissant, O.2
Desvergne, B.3
-
32
-
-
0029016829
-
An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor gamma (PPAR gamma)
-
J.M. Lehmann L.B. Moore T.A. Smith-Oliver W.O. Wilkison T.M. Willson S.A. Kliewer An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor gamma (PPAR gamma) J. Biol. Chem. 270 1995 12953 12956
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 12953-12956
-
-
Lehmann, J.M.1
Moore, L.B.2
Smith-Oliver, T.A.3
Wilkison, W.O.4
Willson, T.M.5
Kliewer, S.A.6
-
33
-
-
0025726848
-
Two cis-acting regulatory sequences in the peroxisome proliferator-responsive enhancer region of rat acyl-CoA oxidase gene
-
T. Osumi J.K. Wen T. Hashimoto Two cis-acting regulatory sequences in the peroxisome proliferator-responsive enhancer region of rat acyl-CoA oxidase gene Biochem. Biophys. Res. Commun. 175 1991 866 871
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.175
, pp. 866-871
-
-
Osumi, T.1
Wen, J.K.2
Hashimoto, T.3
-
35
-
-
0035977861
-
Peroxisome proliferator-activated receptor gamma (PPARgamma) activation and its consequences in humans
-
J. Bar-Tana Peroxisome proliferator-activated receptor gamma (PPARgamma) activation and its consequences in humans Toxicol. Lett. 120 2001 9 19
-
(2001)
Toxicol. Lett.
, vol.120
, pp. 9-19
-
-
Bar-Tana, J.1
-
36
-
-
0028355391
-
Peroxisome proliferator-activated receptors: Finding the orphan a home
-
S. Green W. Wahli Peroxisome proliferator-activated receptors: finding the orphan a home Mol. Cell. Endocrinol. 100 1994 149 153
-
(1994)
Mol. Cell. Endocrinol.
, vol.100
, pp. 149-153
-
-
Green, S.1
Wahli, W.2
-
37
-
-
0037405057
-
Modulation of PPARγ activity with pharmaceutical agents: Treatment of insulin resistance and atherosclerosis
-
M. Wang S. Tafuri Modulation of PPARγ activity with pharmaceutical agents: treatment of insulin resistance and atherosclerosis J. Cell. Biochem. 89 2003 38 47
-
(2003)
J. Cell. Biochem.
, vol.89
, pp. 38-47
-
-
Wang, M.1
Tafuri, S.2
-
39
-
-
0035325163
-
Histone acetylation and chromatin remodeling
-
P.D. Gregory K. Wagner W. Hörz Histone acetylation and chromatin remodeling Exp. Cell Res. 265 2 2001 195 202
-
(2001)
Exp. Cell Res.
, vol.265
, Issue.2
, pp. 195-202
-
-
Gregory, P.D.1
Wagner, K.2
Hörz, W.3
-
42
-
-
0032565868
-
Activation of human aortic smooth-muscle cells is inhibited by PPARα but not PPARγ activators
-
B. Staels K. Wolfgang A. Habib R. Merval M. Lebret I.P. Torra P. Delerive A. Fadel G. Chinetti J.C. Fruchart J. Najib J. Maclouf A. Tedgui Activation of human aortic smooth-muscle cells is inhibited by PPARα but not PPARγ activators Nature 393 1998 790 793
-
(1998)
Nature
, vol.393
, pp. 790-793
-
-
Staels, B.1
Wolfgang, K.2
Habib, A.3
Merval, R.4
Lebret, M.5
Torra, I.P.6
Delerive, P.7
Fadel, A.8
Chinetti, G.9
Fruchart, J.C.10
Najib, J.11
Maclouf, J.12
Tedgui, A.13
-
43
-
-
0033564698
-
Cyclo-oxygenase-2-derived prostacyclin mediates embryo implantation in the mouse via PPARd
-
H. Lim R.A. Gupta W. Ma B.C. Paria D.E. Moller J.D. Morrow R.N. DuBois J.M. Trzaskos S.K. Dey Cyclo-oxygenase-2-derived prostacyclin mediates embryo implantation in the mouse via PPARd Genes Dev. 13 1999 561 574
-
(1999)
Genes Dev.
, vol.13
, pp. 561-574
-
-
Lim, H.1
Gupta, R.A.2
Ma, W.3
Paria, B.C.4
Moller, D.E.5
Morrow, J.D.6
Dubois, R.N.7
Trzaskos, J.M.8
Dey, S.K.9
-
44
-
-
0029102676
-
Structural organization of mouse peroxisome proliferatoractivated receptor gamma (mPPAR) gamma gene: Alternative promoter use and different splicing yield two mPPAR gamma isoforms
-
Y. Zhu C. Qi J.R. Korenberg X.N. Chen D. Noya M.S. Rao J.K. Reddy Structural organization of mouse peroxisome proliferatoractivated receptor gamma (mPPAR) gamma gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms Proc. Natl. Acad. Sci. 92 1995 7921 7925
-
(1995)
Proc. Natl. Acad. Sci.
, vol.92
, pp. 7921-7925
-
-
Zhu, Y.1
Qi, C.2
Korenberg, J.R.3
Chen, X.N.4
Noya, D.5
Rao, M.S.6
Reddy, J.K.7
-
45
-
-
0033067952
-
Regulation of differentiation of sheep subcutaneous and abdominal preadipocytes in culture
-
B. Soret H.J. Lee E. Finley S.C. Lee R.G. Vernon Regulation of differentiation of sheep subcutaneous and abdominal preadipocytes in culture J. Endocrinol. 161 1999 517 524
-
(1999)
J. Endocrinol.
, vol.161
, pp. 517-524
-
-
Soret, B.1
Lee, H.J.2
Finley, E.3
Lee, S.C.4
Vernon, R.G.5
-
46
-
-
0141621135
-
The orphan nuclear receptor Rev-Erbb is a peroxisome proliferator-activated receptor (PPAR)-g target gene and promotes PPAR-γ-induced adipocyte differentiation
-
C. Fontaine G. Dubois Y. Duguay T. Helledie N. Vu-Dac P. Gervois F. Soncin S. Mandrup J.C. Fruchart J. Fruchart-Najib B. Staels The orphan nuclear receptor Rev-Erbb is a peroxisome proliferator-activated receptor (PPAR)-g target gene and promotes PPAR-γ-induced adipocyte differentiation J. Biol. Chem. 278 2003 37672 37680
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 37672-37680
-
-
Fontaine, C.1
Dubois, G.2
Duguay, Y.3
Helledie, T.4
Vu-Dac, N.5
Gervois, P.6
Soncin, F.7
Mandrup, S.8
Fruchart, J.C.9
Fruchart-Najib, J.10
Staels, B.11
-
47
-
-
0031993322
-
Terminal differentiation of human breast cancer through PPAR-γ
-
E. Mueller P. Sarraf P. Tontonoz R.M. Evans K.J. Martin M. Zhang C. Fletcher S. Singer B.M. Spiegelman Terminal differentiation of human breast cancer through PPAR-γ Mol. Cell 1 1998 465 470
-
(1998)
Mol. Cell
, vol.1
, pp. 465-470
-
-
Mueller, E.1
Sarraf, P.2
Tontonoz, P.3
Evans, R.M.4
Martin, K.J.5
Zhang, M.6
Fletcher, C.7
Singer, S.8
Spiegelman, B.M.9
-
48
-
-
18144388677
-
Selective activation of PPARgamma in breast, colon, and lung cancer cell lines
-
C.D. Allred M.W. Kilogore Selective activation of PPARgamma in breast, colon, and lung cancer cell lines Mol. Cell. Endocrinol. 235 2005 21 29
-
(2005)
Mol. Cell. Endocrinol.
, vol.235
, pp. 21-29
-
-
Allred, C.D.1
Kilogore, M.W.2
-
50
-
-
33746218695
-
Differentiation and growth inhibition mediated via the RXR: PPARgamma heterodimer in colon cancer
-
R.M. Cesario J. Stone W.C. Yen R.P. Bissonnette W.W. Lamph Differentiation and growth inhibition mediated via the RXR: PPARgamma heterodimer in colon cancer Cancer Lett. 240 2006 225 233
-
(2006)
Cancer Lett.
, vol.240
, pp. 225-233
-
-
Cesario, R.M.1
Stone, J.2
Yen, W.C.3
Bissonnette, R.P.4
Lamph, W.W.5
-
51
-
-
33751303104
-
Peroxisome proliferator-activated receptor gamma is highly expressed in pancreatic cancer and is associated with shorter overall survival times
-
G. Kristiansen J. Jacob A.C. Buckendahl R. Grutzmann M. Dietel C. Pilarsky Peroxisome proliferator-activated receptor gamma is highly expressed in pancreatic cancer and is associated with shorter overall survival times Clin. Cancer Res. 12 2006 6444 6451
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 6444-6451
-
-
Kristiansen, G.1
Jacob, J.2
Buckendahl, A.C.3
Grutzmann, R.4
Dietel, M.5
Pilarsky, C.6
-
52
-
-
0345687980
-
Growth arrest by troglitazone is mediated by p27Kip1 accumulation, which results from dual inhibition of proteasome activity and Skp2 expression in human hepatocellular carcinoma cells
-
W. Motomura N. Takahashi M. Nagamine M. Sawamukai S. Tanno Y. Kohgo T. Okimura Growth arrest by troglitazone is mediated by p27Kip1 accumulation, which results from dual inhibition of proteasome activity and Skp2 expression in human hepatocellular carcinoma cells Int. J. Cancer 108 2004 41 46
-
(2004)
Int. J. Cancer
, vol.108
, pp. 41-46
-
-
Motomura, W.1
Takahashi, N.2
Nagamine, M.3
Sawamukai, M.4
Tanno, S.5
Kohgo, Y.6
Okimura, T.7
-
53
-
-
1642381346
-
Up-regulation of p21 gene expression by peroxisome proliferator-activated receptor gamma in human lung carcinoma cells
-
S. Han N. Sidell P.B. Fisher J. Roman Up-regulation of p21 gene expression by peroxisome proliferator-activated receptor gamma in human lung carcinoma cells Clin. Cancer Res. 10 2004 1911 1919
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 1911-1919
-
-
Han, S.1
Sidell, N.2
Fisher, P.B.3
Roman, J.4
-
54
-
-
25444511570
-
The PPAR-gamma agonist pioglitazone post-transcriptionally induces p21 in PC3 prostate cancer but not in other cell lines
-
S.K. Radhakrishnan A. Gartel The PPAR-gamma agonist pioglitazone post-transcriptionally induces p21 in PC3 prostate cancer but not in other cell lines Cell Cycle 4 2005 582 584
-
(2005)
Cell Cycle
, vol.4
, pp. 582-584
-
-
Radhakrishnan, S.K.1
Gartel, A.2
-
55
-
-
3242679874
-
The ligands of peroxisome proliferator-activated receptor (PPAR) gamma inhibit growth of human esophageal carcinoma cells through induction of apoptosis and cell cycle arrest
-
D. Fujii K. Yoshida K. Tanabe J. Hihara T. Toge The ligands of peroxisome proliferator-activated receptor (PPAR) gamma inhibit growth of human esophageal carcinoma cells through induction of apoptosis and cell cycle arrest Anticancer Res. 24 2004 1409 1416
-
(2004)
Anticancer Res.
, vol.24
, pp. 1409-1416
-
-
Fujii, D.1
Yoshida, K.2
Tanabe, K.3
Hihara, J.4
Toge, T.5
-
57
-
-
0033741281
-
Expression of peroxisome proliferator-activated receptor (PPAR)gamma in gastric cancer and inhibitory effects of PPARgamma agonists
-
H. Sato S. Ishihara K. Kawashima N. Moriyama H. Suetsugu H. Kazumori T. Okuyama M.A. Rumi R. Fukuda N. Nagasue Y. Kinoshita Expression of peroxisome proliferator-activated receptor (PPAR)gamma in gastric cancer and inhibitory effects of PPARgamma agonists Br. J. Cancer 83 2000 1394 1400
-
(2000)
Br. J. Cancer
, vol.83
, pp. 1394-1400
-
-
Sato, H.1
Ishihara, S.2
Kawashima, K.3
Moriyama, N.4
Suetsugu, H.5
Kazumori, H.6
Okuyama, T.7
Rumi, M.A.8
Fukuda, R.9
Nagasue, N.10
Kinoshita, Y.11
-
58
-
-
0035458324
-
PPAR-gamma ligands inhibit growth of human esophageal adenocarcinoma cells through induction of apoptosis, cell cycle arrest and reduction of ornithine decarboxylase activity
-
T. Takashima Y. Fujiwara K. Higuchi T. Arakawa Y. Yano T. Hasuma S. Otani PPAR-gamma ligands inhibit growth of human esophageal adenocarcinoma cells through induction of apoptosis, cell cycle arrest and reduction of ornithine decarboxylase activity Int. J. Oncol. 19 2001 465 471
-
(2001)
Int. J. Oncol.
, vol.19
, pp. 465-471
-
-
Takashima, T.1
Fujiwara, Y.2
Higuchi, K.3
Arakawa, T.4
Yano, Y.5
Hasuma, T.6
Otani, S.7
-
59
-
-
21144439861
-
Chemopreventive effect of peroxisome proliferator-activated receptor gamma on gastric carcinogenesis in mice
-
J. Lu K. Imamura S. Nomura K. Mafune A. Nakajima T. Kadowaki N. Kubota Y. Terauchi G. Ishii A. Ochiai H. Esumi M. Kaminishi Chemopreventive effect of peroxisome proliferator-activated receptor gamma on gastric carcinogenesis in mice Cancer Res. 65 2005 4769 4774
-
(2005)
Cancer Res.
, vol.65
, pp. 4769-4774
-
-
Lu, J.1
Imamura, K.2
Nomura, S.3
Mafune, K.4
Nakajima, A.5
Kadowaki, T.6
Kubota, N.7
Terauchi, Y.8
Ishii, G.9
Ochiai, A.10
Esumi, H.11
Kaminishi, M.12
-
60
-
-
34250901928
-
Effects of thiazolidinediones on differentiation, proliferation, and apoptosis
-
F.S. Chou P.S. Wang S. Kulp Joseph J. Pinzone Effects of thiazolidinediones on differentiation, proliferation, and apoptosis Mol. Cancer Res. 5 6 2007 523 530
-
(2007)
Mol. Cancer Res.
, vol.5
, Issue.6
, pp. 523-530
-
-
Chou, F.S.1
Wang, P.S.2
Kulp, S.3
Pinzone, J.J.4
-
61
-
-
84896105072
-
A new dawn for the use of thiazolidinediones in cancer therapy
-
H. Joshi T. Pal C. Ramaa A new dawn for the use of thiazolidinediones in cancer therapy Expert Opin. Investig. Drugs 23 4 2014 501 510
-
(2014)
Expert Opin. Investig. Drugs
, vol.23
, Issue.4
, pp. 501-510
-
-
Joshi, H.1
Pal, T.2
Ramaa, C.3
-
62
-
-
84893794489
-
Peroxisome proliferator-activated receptors and their ligands: Nutritional and clinical implications
-
B. Grygiel-Górniak Peroxisome proliferator-activated receptors and their ligands: nutritional and clinical implications Nutr. J. 13 1 2014 17
-
(2014)
Nutr. J.
, vol.13
, Issue.1
, pp. 17
-
-
Grygiel-Górniak, B.1
-
63
-
-
84884991460
-
Synthesis, characterization, and evaluation of a novel inhibitor of WNT/β-catenin signaling pathway
-
Z. Yan Z. Zhu J. Wang J. Sun Y. Chen G. Yang W. Chen Y. Deng Synthesis, characterization, and evaluation of a novel inhibitor of WNT/β-catenin signaling pathway Mol. Cancer 12 2013 116
-
(2013)
Mol. Cancer
, vol.12
, pp. 116
-
-
Yan, Z.1
Zhu, Z.2
Wang, J.3
Sun, J.4
Chen, Y.5
Yang, G.6
Chen, W.7
Deng, Y.8
-
64
-
-
84957591389
-
Roles of Wnt/β-catenin signaling in the gastric cancer stem cells proliferation and salinomycin treatment
-
J. Mao S. Fan W. Ma P. Fan B. Wang J. Zhang H. Wang B. Tang Q. Zhang X. Yu L. Wang B. Song L. Li Roles of Wnt/β-catenin signaling in the gastric cancer stem cells proliferation and salinomycin treatment Cell Death Dis. 5 2014 e1039
-
(2014)
Cell Death Dis.
, vol.5
, pp. 1039
-
-
Mao, J.1
Fan, S.2
Ma, W.3
Fan, P.4
Wang, B.5
Zhang, J.6
Wang, H.7
Tang, B.8
Zhang, Q.9
Yu, X.10
Wang, L.11
Song, B.12
Li, L.13
-
65
-
-
19944403876
-
Wnt/beta-catenin signaling pathway as a novel cancer drug target
-
H.H. Luu R. Zhang R.C. Haydon E. Rayburn Q. Kang W. Si J.K. Park H. Wang Y. Peng W. Jiang T.C. He Wnt/beta-catenin signaling pathway as a novel cancer drug target Curr. Cancer Drug Targets 4 8 2004 653 671
-
(2004)
Curr. Cancer Drug Targets
, vol.4
, Issue.8
, pp. 653-671
-
-
Luu, H.H.1
Zhang, R.2
Haydon, R.C.3
Rayburn, E.4
Kang, Q.5
Si, W.6
Park, J.K.7
Wang, H.8
Peng, Y.9
Jiang, W.10
He, T.C.11
-
66
-
-
84855579880
-
Inhibition of lymphoma cell proliferation by peroxisomal proliferator-activated receptor-γ ligands via Wnt signaling pathway
-
J. Liu X. Dai Y. Xu P. Liu Y. Zhang X. Liu Z. Fang D. Lin R. Xiao R. Huang Inhibition of lymphoma cell proliferation by peroxisomal proliferator-activated receptor-γ ligands via Wnt signaling pathway Cell Biochem. Biophys. 62 1 2012 19 27
-
(2012)
Cell Biochem. Biophys.
, vol.62
, Issue.1
, pp. 19-27
-
-
Liu, J.1
Dai, X.2
Xu, Y.3
Liu, P.4
Zhang, Y.5
Liu, X.6
Fang, Z.7
Lin, D.8
Xiao, R.9
Huang, R.10
-
67
-
-
84862656024
-
Troglitazone attenuates TGF-β1-induced EMT in alveolar epithelial cells via a PPARγ-independent mechanism
-
B. Zhou S.T. Buckley V. Patel Y. Liu J. Luo M.S. Krishnaveni M. Ivan L. DeMaio K.J. Kim C. Ehrhardt E.D. Crandall Z. Borok Troglitazone attenuates TGF-β1-induced EMT in alveolar epithelial cells via a PPARγ-independent mechanism PLoS One 7 6 2012 e38827
-
(2012)
PLoS One
, vol.7
, Issue.6
, pp. 38827
-
-
Zhou, B.1
Buckley, S.T.2
Patel, V.3
Liu, Y.4
Luo, J.5
Krishnaveni, M.S.6
Ivan, M.7
Demaio, L.8
Kim, K.J.9
Ehrhardt, C.10
Crandall, E.D.11
Borok, Z.12
-
68
-
-
64849091190
-
Thiazolidinediones downregulate Wnt/beta-catenin signaling via multiple mechanisms in breast cancer cells
-
P.S. Wang F.S. Chou M. Bloomston M.S. Vonau M. Saji A. Espinosa J.J. Pinzone Thiazolidinediones downregulate Wnt/beta-catenin signaling via multiple mechanisms in breast cancer cells J. Surg. Res. 153 2 2009 210 216
-
(2009)
J. Surg. Res.
, vol.153
, Issue.2
, pp. 210-216
-
-
Wang, P.S.1
Chou, F.S.2
Bloomston, M.3
Vonau, M.S.4
Saji, M.5
Espinosa, A.6
Pinzone, J.J.7
-
69
-
-
0036983115
-
The Ras-Raf-MEK-ERK pathway in the treatment of cancer
-
R.A. Hilger M.E. Scheulen D. Strumberg The Ras-Raf-MEK-ERK pathway in the treatment of cancer Onkologie 25 2002 511 518
-
(2002)
Onkologie
, vol.25
, pp. 511-518
-
-
Hilger, R.A.1
Scheulen, M.E.2
Strumberg, D.3
-
71
-
-
0037400975
-
A pivotal role for ERK in the oncogenic behaviour of malignant melanoma?
-
K.S. Smalley A pivotal role for ERK in the oncogenic behaviour of malignant melanoma? Int. J. Cancer 104 2003 527 532
-
(2003)
Int. J. Cancer
, vol.104
, pp. 527-532
-
-
Smalley, K.S.1
-
72
-
-
0033607784
-
Differentiation stage-specific inhibition of the Raf-MEK-ERK pathway by Akt
-
C. Rommel B.A. Clarke S. Zimmermann L. Nunez R. Rossman K. Reid K. Moelling G.D. Yancopoulos D.J. Glass Differentiation stage-specific inhibition of the Raf-MEK-ERK pathway by Akt Science 286 1999 1738
-
(1999)
Science
, vol.286
, pp. 1738
-
-
Rommel, C.1
Clarke, B.A.2
Zimmermann, S.3
Nunez, L.4
Rossman, R.5
Reid, K.6
Moelling, K.7
Yancopoulos, G.D.8
Glass, D.J.9
-
73
-
-
0037810249
-
Signal transduction mediated by the Ras/Raf/MEK/ERK pathway from cytokine receptors to transcription factors: Potential targeting for therapeutic intervention
-
F. Chang L.S. Steelman J.T. Lee J.G. Shelton P.M. Navolanic W.L. Blalock R.A. Franklin J.A. McCubrey Signal transduction mediated by the Ras/Raf/MEK/ERK pathway from cytokine receptors to transcription factors: potential targeting for therapeutic intervention Leukemia 17 2003 1263 1293
-
(2003)
Leukemia
, vol.17
, pp. 1263-1293
-
-
Chang, F.1
Steelman, L.S.2
Lee, J.T.3
Shelton, J.G.4
Navolanic, P.M.5
Blalock, W.L.6
Franklin, R.A.7
McCubrey, J.A.8
-
75
-
-
0034898803
-
Thiazolidinediones, peroxisome proliferator-activated receptor gamma agonists, regulate endothelial cell growth and secretion of vasoactive peptides
-
Y. Fukunaga H. Itoh K. Doi T. Tanaka J. Yamashita T.H. Chun M. Inoue K. Masatsugu N. Sawada T. Saito K. Hosoda H. Kook M. Ueda K. Nakao Thiazolidinediones, peroxisome proliferator-activated receptor gamma agonists, regulate endothelial cell growth and secretion of vasoactive peptides Atherosclerosis 158 1 2001 113 119
-
(2001)
Atherosclerosis
, vol.158
, Issue.1
, pp. 113-119
-
-
Fukunaga, Y.1
Itoh, H.2
Doi, K.3
Tanaka, T.4
Yamashita, J.5
Chun, T.H.6
Inoue, M.7
Masatsugu, K.8
Sawada, N.9
Saito, T.10
Hosoda, K.11
Kook, H.12
Ueda, M.13
Nakao, K.14
-
76
-
-
77951242981
-
Energy restriction as an antitumor target of thiazolidinediones
-
S. Wei S.K. Kulp C.S. Chen Energy restriction as an antitumor target of thiazolidinediones J. Biol. Chem. 285 13 2010 9780 9791
-
(2010)
J. Biol. Chem.
, vol.285
, Issue.13
, pp. 9780-9791
-
-
Wei, S.1
Kulp, S.K.2
Chen, C.S.3
-
77
-
-
84875332058
-
Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione
-
R. Romagnoli P.G. Baraldi M.K. Salvador M.E. Camacho J. Balzarini J. Bermejo F. Estévez Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione Eur. J. Med. Chem. 63 2013 544 557
-
(2013)
Eur. J. Med. Chem.
, vol.63
, pp. 544-557
-
-
Romagnoli, R.1
Baraldi, P.G.2
Salvador, M.K.3
Camacho, M.E.4
Balzarini, J.5
Bermejo, J.6
Estévez, F.7
-
78
-
-
84879689641
-
The inhibitory effect of a synthetic compound, (Z)-5-(2,4-dihydroxybenzylidene) thiazolidine-2,4-dione (MHY498), on nitric oxide-induced melanogenesis
-
S.H. Kim Y.J. Choi K.M. Moon H.J. Lee Y. Wooc K.W. Chung Y. Jung S. Kim P. Chun Y. Byun Y.M. Ha H.R. Moon H.Y. Chung The inhibitory effect of a synthetic compound, (Z)-5-(2,4-dihydroxybenzylidene) thiazolidine-2,4-dione (MHY498), on nitric oxide-induced melanogenesis Bioorg. Med. Chem. Lett. 23 2013 4332 4335
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 4332-4335
-
-
Kim, S.H.1
Choi, Y.J.2
Moon, K.M.3
Lee, H.J.4
Wooc, Y.5
Chung, K.W.6
Jung, Y.7
Kim, S.8
Chun, P.9
Byun, Y.10
Ha, Y.M.11
Moon, H.R.12
Chung, H.Y.13
-
79
-
-
84870155584
-
2H-Chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents
-
M. Azizmohammadi M. Khoobi A. Ramazani S. Emami A. Zarrin O. Firuzi R. Miri A. Shafiee 2H-Chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents Eur. J. Med. Chem. 59 2013 15 22
-
(2013)
Eur. J. Med. Chem.
, vol.59
, pp. 15-22
-
-
Azizmohammadi, M.1
Khoobi, M.2
Ramazani, A.3
Emami, S.4
Zarrin, A.5
Firuzi, O.6
Miri, R.7
Shafiee, A.8
-
80
-
-
84878701268
-
Inhibition of endotrophin, a cleavage product of collagen VI, confers cisplatin sensitivity to tumours
-
J. Park T.S. Morley P.E. Scherer Inhibition of endotrophin, a cleavage product of collagen VI, confers cisplatin sensitivity to tumours EMBO Mol. Med. 5 6 2013 935 948
-
(2013)
EMBO Mol. Med.
, vol.5
, Issue.6
, pp. 935-948
-
-
Park, J.1
Morley, T.S.2
Scherer, P.E.3
-
81
-
-
84883877783
-
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents
-
T.C. Chen D.S. Yu K.F. Huang Y.C. Fu C.C. Lee C.L. Chen F.C. Huang H.H. Hsieh J.J. Lin H.S. Huang Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents Eur. J. Med. Chem. 69 2013 278 293
-
(2013)
Eur. J. Med. Chem.
, vol.69
, pp. 278-293
-
-
Chen, T.C.1
Yu, D.S.2
Huang, K.F.3
Fu, Y.C.4
Lee, C.C.5
Chen, C.L.6
Huang, F.C.7
Hsieh, H.H.8
Lin, J.J.9
Huang, H.S.10
-
82
-
-
84862782325
-
Design, synthesis and evaluation of telomerase inhibitory, hTERT repressing, and anti-proliferation activities of symmetrical 1,8-disubstituted amidoanthraquinones
-
C.C. Lee K.F. Huang D.M. Chang J.J. Hsu F.C. Huang K.N. Shih C.L. Chen T.C. Chen R.H. Chen J.J. Lin H.S. Huang Design, synthesis and evaluation of telomerase inhibitory, hTERT repressing, and anti-proliferation activities of symmetrical 1,8-disubstituted amidoanthraquinones Eur. J. Med. Chem. 50 2012 102 112
-
(2012)
Eur. J. Med. Chem.
, vol.50
, pp. 102-112
-
-
Lee, C.C.1
Huang, K.F.2
Chang, D.M.3
Hsu, J.J.4
Huang, F.C.5
Shih, K.N.6
Chen, C.L.7
Chen, T.C.8
Chen, R.H.9
Lin, J.J.10
Huang, H.S.11
-
84
-
-
84875384373
-
Novel quinolone substituted thiazolidin-4-ones as anti-inflammatory, anticancer agents: Design, synthesis and biological screening
-
S.K. Suthar V. Jaiswal S. Lohan S. Bansal A. Chaudhary A. Tiwari A.T. Alex A. Joesph Novel quinolone substituted thiazolidin-4-ones as anti-inflammatory, anticancer agents: design, synthesis and biological screening Eur. J. Med. Chem. 63 2013 589 602
-
(2013)
Eur. J. Med. Chem.
, vol.63
, pp. 589-602
-
-
Suthar, S.K.1
Jaiswal, V.2
Lohan, S.3
Bansal, S.4
Chaudhary, A.5
Tiwari, A.6
Alex, A.T.7
Joesph, A.8
-
85
-
-
84861851126
-
Design, synthesis, and biological evaluation of novel 2,4-thiazolidinedione derivatives as histone deacetylase inhibitors targeting liver cancer cell line
-
R. Mohan A.K. Sharma S. Gupta C.S. Ramaa Design, synthesis, and biological evaluation of novel 2,4-thiazolidinedione derivatives as histone deacetylase inhibitors targeting liver cancer cell line Med. Chem. Res. 21 2012 1156 1165
-
(2012)
Med. Chem. Res.
, vol.21
, pp. 1156-1165
-
-
Mohan, R.1
Sharma, A.K.2
Gupta, S.3
Ramaa, C.S.4
-
86
-
-
71749119790
-
Structure-activity relationship (SAR) studies of 3-(2-amino-ethyl)-5-(4-ethoxybenzylidene)-thiazolidine-2,4-dione: Development of potential substratespecific ERK1/2 inhibitors
-
Q. Li A. Al-Ayoubi T. Guo H. Zheng A. Sarkar T. Nguyen S.T. Eblen S. Grant G.E. Kellogg S. Zhang Structure-activity relationship (SAR) studies of 3-(2-amino-ethyl)-5-(4-ethoxybenzylidene)-thiazolidine-2,4-dione: development of potential substratespecific ERK1/2 inhibitors Bioorg. Med. Chem. Lett. 19 2009 6042 6046
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6042-6046
-
-
Li, Q.1
Al-Ayoubi, A.2
Guo, T.3
Zheng, H.4
Sarkar, A.5
Nguyen, T.6
Eblen, S.T.7
Grant, S.8
Kellogg, G.E.9
Zhang, S.10
-
87
-
-
19344376702
-
Involvement of MEK-ERK signaling pathway in the inhibition of cell growth by troglitazone in human pancreatic cancer cells
-
W. Motomura S. Tanno N. Takahashi M. Nagamine M. Fukuda Y. Kohgo T. Okumura Involvement of MEK-ERK signaling pathway in the inhibition of cell growth by troglitazone in human pancreatic cancer cells Biochem. Biophys. Res. Commun. 332 1 2005 89 94
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.332
, Issue.1
, pp. 89-94
-
-
Motomura, W.1
Tanno, S.2
Takahashi, N.3
Nagamine, M.4
Fukuda, M.5
Kohgo, Y.6
Okumura, T.7
-
88
-
-
0033546710
-
Troglitazone suppresses cell growth of myeloid leukemia cell lines by induction of p21WAF1/CIP1 cyclin-dependent kinase inhibitor
-
A. Sugimura Y. Kiriyama H. Nochi H. Tsuchiya K. Tamoto Y. Sakurada M. Ui Y. Tokumitsu Troglitazone suppresses cell growth of myeloid leukemia cell lines by induction of p21WAF1/CIP1 cyclin-dependent kinase inhibitor Biochem. Biophys. Res. Commun. 261 3 1999 833 837
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.261
, Issue.3
, pp. 833-837
-
-
Sugimura, A.1
Kiriyama, Y.2
Nochi, H.3
Tsuchiya, H.4
Tamoto, K.5
Sakurada, Y.6
Ui, M.7
Tokumitsu, Y.8
-
89
-
-
77955413802
-
Discovery of 3-(2-aminoethyl)-5-(3-phenyl-propylidene)-thiazolidine-2,4-dione as a dual inhibitor of the Raf/MEK/ERK and the PI3K/Akt signaling pathways
-
Q. Li J. Wua H. Zheng K. Liu T.L. Guo Y. Liu S.T. Eblen S. Grant S. Zhang Discovery of 3-(2-aminoethyl)-5-(3-phenyl-propylidene)-thiazolidine-2,4-dione as a dual inhibitor of the Raf/MEK/ERK and the PI3K/Akt signaling pathways Bioorg. Med. Chem. Lett. 20 2010 4526 4530
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 4526-4530
-
-
Li, Q.1
Wua, J.2
Zheng, H.3
Liu, K.4
Guo, T.L.5
Liu, Y.6
Eblen, S.T.7
Grant, S.8
Zhang, S.9
-
90
-
-
5344277530
-
Synthesis and biological evaluation of thiazolidine-2,4-dione and 2,4-thione derivatives as inhibitors of translation initiation
-
H. Chen Y.H. Fan A. Natarajan Y. Guo J. Iyasere F. Harbinski L. Luus W. Christ H. Aktasa J.A. Halperin Synthesis and biological evaluation of thiazolidine-2,4-dione and 2,4-thione derivatives as inhibitors of translation initiation Bioorg. Med. Chem. Lett. 14 2004 5401 5405
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 5401-5405
-
-
Chen, H.1
Fan, Y.H.2
Natarajan, A.3
Guo, Y.4
Iyasere, J.5
Harbinski, F.6
Luus, L.7
Christ, W.8
Aktasa, H.9
Halperin, J.A.10
-
92
-
-
84866738128
-
Synthesis, characterization and biological evaluation of some novel 2,4 thiazolidinediones as potential cytotoxic, antimicrobial and antihyperglycemic agents
-
V.R. Avupati R.P. Yejella A. Akula G.S. Guntuku B.R. Doddi V.R. Vutla S.R. Anagani L.S. Adimulam A.K. Vyricharla Synthesis, characterization and biological evaluation of some novel 2,4 thiazolidinediones as potential cytotoxic, antimicrobial and antihyperglycemic agents Bioorg. Med. Chem. Lett. 22 2012 6442 6450
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 6442-6450
-
-
Avupati, V.R.1
Yejella, R.P.2
Akula, A.3
Guntuku, G.S.4
Doddi, B.R.5
Vutla, V.R.6
Anagani, S.R.7
Adimulam, L.S.8
Vyricharla, A.K.9
-
93
-
-
84888139352
-
Studies on the synthetic and structural aspects of benzosuberones bearing 2, 4-thiazolidenone moiety as potential anti-cancer agents
-
L. Nagarapu B. Yadagiri R. Bantu C.G. Kumar S. Pombala J. Nanubolu Studies on the synthetic and structural aspects of benzosuberones bearing 2, 4-thiazolidenone moiety as potential anti-cancer agents Eur. J. Med. Chem. 71 2014 91 97
-
(2014)
Eur. J. Med. Chem.
, vol.71
, pp. 91-97
-
-
Nagarapu, L.1
Yadagiri, B.2
Bantu, R.3
Kumar, C.G.4
Pombala, S.5
Nanubolu, J.6
-
94
-
-
84886562346
-
Synthesis of 1,3-thiazine-2,4-diones with potential anticancer activity
-
M. Ferreira L.S. Assunção F.B. Filippin-Monteiro T.B. Creczynski-Pasa M.M. Sa Synthesis of 1,3-thiazine-2,4-diones with potential anticancer activity Eur. J. Med. Chem. 70 2013 411 418
-
(2013)
Eur. J. Med. Chem.
, vol.70
, pp. 411-418
-
-
Ferreira, M.1
Assunção, L.S.2
Filippin-Monteiro, F.B.3
Creczynski-Pasa, T.B.4
Sa, M.M.5
-
95
-
-
84861189060
-
Synthesis and cytotoxic activity of new acridine-thiazolidine derivatives
-
F.W.A. Barros T.G. Silva M.G.R. Pitta D.P. Bezerra L.V. Costa-Lotufo M.O. de Moraes C. Pessoa M.A.F.B. de Moura F.C. de Abreu M.C.A. de Lima S.L. Galdino I.R. Pitta M.O.F. Goulart Synthesis and cytotoxic activity of new acridine-thiazolidine derivatives Bioorg. Med. Chem. 20 2013 3533 3539
-
(2013)
Bioorg. Med. Chem.
, vol.20
, pp. 3533-3539
-
-
Barros, F.W.A.1
Silva, T.G.2
Pitta, M.G.R.3
Bezerra, D.P.4
Costa-Lotufo, L.V.5
De Moraes, M.O.6
Pessoa, C.7
De Moura, M.A.F.B.8
De Abreu, F.C.9
De Lima, M.C.A.10
Galdino, S.L.11
Pitta, I.R.12
Goulart, M.O.F.13
-
97
-
-
84863447425
-
Discovery of novel benzylidene-1,3-thiazolidine-2,4-diones as potent and selective inhibitors of the PIM-1, PIM-2, and PIM-3 protein kinases
-
L.A. Dakin M.H. Block H. Chen E. Code J.E. Dowling X. Feng A.D. Ferguson I. Green A.W. Hird T. Howard E.K. Keeton M.L. Lamb P.D. Lyne H. Pollard J. Read A.J. Wu T. Zhang X. Zheng Discovery of novel benzylidene-1,3-thiazolidine-2,4-diones as potent and selective inhibitors of the PIM-1, PIM-2, and PIM-3 protein kinases Bioorg. Med. Chem. Lett. 22 2012 4599 4604
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 4599-4604
-
-
Dakin, L.A.1
Block, M.H.2
Chen, H.3
Code, E.4
Dowling, J.E.5
Feng, X.6
Ferguson, A.D.7
Green, I.8
Hird, A.W.9
Howard, T.10
Keeton, E.K.11
Lamb, M.L.12
Lyne, P.D.13
Pollard, H.14
Read, J.15
Wu, A.J.16
Zhang, T.17
Zheng, X.18
-
98
-
-
84862794769
-
Design and synthesis of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors
-
Y.M. Ha Y.J. Park J.A. Kim D. Park J.Y. Park H.J. Lee J.Y. Lee H.R. Moon H.Y. Chung Design and synthesis of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors Eur. J. Med. Chem. 49 2012 245 252
-
(2012)
Eur. J. Med. Chem.
, vol.49
, pp. 245-252
-
-
Ha, Y.M.1
Park, Y.J.2
Kim, J.A.3
Park, D.4
Park, J.Y.5
Lee, H.J.6
Lee, J.Y.7
Moon, H.R.8
Chung, H.Y.9
-
99
-
-
84908027654
-
-
F. Sandrine D. Catherine V. Karina R. Caroline L. Stéphanie L. Nathalie B. Carlo D. Samuel B. Nicoletta M. Giorgio A. Jean-Pierre S. Paul R. Eric Safety, pharmacokinetic, and antitumor activity of SU11248, a novel oral multitarget tyrosine kinase inhibitor, in patients with cancer 24 2006 25 35
-
(2006)
Safety, pharmacokinetic, and antitumor activity of SU11248, a novel oral multitarget tyrosine kinase inhibitor, in patients with cancer
, vol.24
, pp. 25-35
-
-
Sandrine, F.1
Catherine, D.2
Karina, V.3
Caroline, R.4
Stéphanie, L.5
Nathalie, L.6
Carlo, B.7
Samuel, D.8
Nicoletta, B.9
Giorgio, M.10
Jean-Pierre, A.11
Paul, S.12
Eric, R.13
|