-
1
-
-
33750986811
-
Antitumor activity of substituted E-3-(3,4,5-trimethoxybenzylidene)-1,3- dihydroindol-2-ones
-
A. Andreani, S. Burnelli, M. Granaiola, A. Leoni, A. Locatelli, R. Morigi, M. Rambaldi, L. Varoli, and M.W. Kunkel Antitumor activity of substituted E-3-(3,4,5-trimethoxybenzylidene)-1,3-dihydroindol-2-ones J. Med. Chem. 49 2006 6922 6924
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6922-6924
-
-
Andreani, A.1
Burnelli, S.2
Granaiola, M.3
Leoni, A.4
Locatelli, A.5
Morigi, R.6
Rambaldi, M.7
Varoli, L.8
Kunkel, M.W.9
-
2
-
-
1342300731
-
Substituted E-3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones with antitumor activity
-
A. Andreani, M. Granaiola, A. Leoni, A. Locatelli, R. Morigi, M. Rambaldi, V. Garaliene, G. Farruggia, and L. Masotti Substituted E-3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones with antitumor activity Bioorg. Med. Chem. 12 2004 1121 1128
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 1121-1128
-
-
Andreani, A.1
Granaiola, M.2
Leoni, A.3
Locatelli, A.4
Morigi, R.5
Rambaldi, M.6
Garaliene, V.7
Farruggia, G.8
Masotti, L.9
-
3
-
-
34447542806
-
Substituted E-3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones with antitumor activity. Effect on the cell cycle and apoptosis
-
A. Andreani, S. Burnelli, M. Granaiola, A. Leoni, A. Locatelli, R. Morigi, M. Rambaldi, L. Varoli, N. Calonghi, C. Cappadone, G. Farruggia, M. Zini, C. Stefanelli, and L. Masotti Substituted E-3-(2-chloro-3- indolylmethylene)1,3-dihydroindol-2-ones with antitumor activity. Effect on the cell cycle and apoptosis J. Med. Chem. 50 2007 3167 3172
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3167-3172
-
-
Andreani, A.1
Burnelli, S.2
Granaiola, M.3
Leoni, A.4
Locatelli, A.5
Morigi, R.6
Rambaldi, M.7
Varoli, L.8
Calonghi, N.9
Cappadone, C.10
Farruggia, G.11
Zini, M.12
Stefanelli, C.13
Masotti, L.14
-
4
-
-
72249084715
-
New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis, tubulin polymerization, cell growth inhibition, and molecular modeling studies
-
G. La Regina, T. Sarkar, R. Bai, M.C. Edler, R. Saletti, A. Coluccia, F. Piscitelli, L. Minelli, V. Gatti, C. Mazzoccoli, V. Palermo, C. Mazzoni, C. Falcone, A.I. Scovassi, V. Giansanti, P. Campiglia, A. Porta, B. Maresca, E. Hamel, A. Brancale, E. Novellino, and R. Silvestri New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis, tubulin polymerization, cell growth inhibition, and molecular modeling studies J. Med. Chem. 52 2009 7512 7527
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7512-7527
-
-
La Regina, G.1
Sarkar, T.2
Bai, R.3
Edler, M.C.4
Saletti, R.5
Coluccia, A.6
Piscitelli, F.7
Minelli, L.8
Gatti, V.9
Mazzoccoli, C.10
Palermo, V.11
Mazzoni, C.12
Falcone, C.13
Scovassi, A.I.14
Giansanti, V.15
Campiglia, P.16
Porta, A.17
Maresca, B.18
Hamel, E.19
Brancale, A.20
Novellino, E.21
Silvestri, R.22
more..
-
5
-
-
77956764327
-
Small-molecule inhibitors of NADPH oxidase 4
-
G. Borbély, I. Szabadkai, Z. Horvath, P. Marko, Z. Varga, N. Breza, F. Baska, T. Vantus, M. Huszar, M. Geiszt, L. Hunyady, L. Buday, L. Orfi, and G. Keri Small-molecule inhibitors of NADPH oxidase 4 J. Med. Chem. 53 2010 6758 6762
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6758-6762
-
-
Borbély, G.1
Szabadkai, I.2
Horvath, Z.3
Marko, P.4
Varga, Z.5
Breza, N.6
Baska, F.7
Vantus, T.8
Huszar, M.9
Geiszt, M.10
Hunyady, L.11
Buday, L.12
Orfi, L.13
Keri, G.14
-
7
-
-
33846794822
-
The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology
-
K. Bedard, and K.H. Krause The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology Physiol. Rev. 87 2007 245 313
-
(2007)
Physiol. Rev.
, vol.87
, pp. 245-313
-
-
Bedard, K.1
Krause, K.H.2
-
8
-
-
2942593991
-
ROS stress in cancer cells and therapeutic implications
-
H. Pelicano, D. Carney, and P. Huang ROS stress in cancer cells and therapeutic implications Drug Resist. Updates 7 2004 97 110
-
(2004)
Drug Resist. Updates
, vol.7
, pp. 97-110
-
-
Pelicano, H.1
Carney, D.2
Huang, P.3
-
9
-
-
33745518361
-
Inhibition of NADPH oxidase 4 activates apoptosis via the AKT/apoptosis signal-regulating kinase 1 pathway in pancreatic cancer PANC-1 cells
-
T. Mochizuki, S. Furuta, J. Mitsushita, W.H. Shang, M. Ito, Y. Yokoo, M. Yamaura, S. Ishizone, J. Nakayama, A. Konagai, K. Hirose, K. Kiyosawa, and T. Kamata Inhibition of NADPH oxidase 4 activates apoptosis via the AKT/apoptosis signal-regulating kinase 1 pathway in pancreatic cancer PANC-1 cells Oncogene 25 2006 3699 3707
-
(2006)
Oncogene
, vol.25
, pp. 3699-3707
-
-
Mochizuki, T.1
Furuta, S.2
Mitsushita, J.3
Shang, W.H.4
Ito, M.5
Yokoo, Y.6
Yamaura, M.7
Ishizone, S.8
Nakayama, J.9
Konagai, A.10
Hirose, K.11
Kiyosawa, K.12
Kamata, T.13
-
10
-
-
77955493991
-
NADPH oxidase 4 is an oncoprotein localized to mitochondria
-
K.A. Graham, M. Kulawiec, K.M. Owens, X. Li, M.M. Desouki, D. Chandra, and K.K. Singh NADPH oxidase 4 is an oncoprotein localized to mitochondria Cancer Biol. Ther. 10 2010 223 231
-
(2010)
Cancer Biol. Ther.
, vol.10
, pp. 223-231
-
-
Graham, K.A.1
Kulawiec, M.2
Owens, K.M.3
Li, X.4
Desouki, M.M.5
Chandra, D.6
Singh, K.K.7
-
11
-
-
80052831432
-
NADPH oxidase subunit 4-mediated reactive oxygen species contribute to cycling hypoxia-promoted tumor progression in glioblastoma multiforme
-
C.H. Hsieh, W.C. Shyu, C.Y. Chiang, J.W. Kuo, W.C. Shen, and R.S. Liu NADPH oxidase subunit 4-mediated reactive oxygen species contribute to cycling hypoxia-promoted tumor progression in glioblastoma multiforme PLoS One 6 2011 e23945
-
(2011)
PLoS One
, vol.6
, pp. 23945
-
-
Hsieh, C.H.1
Shyu, W.C.2
Chiang, C.Y.3
Kuo, J.W.4
Shen, W.C.5
Liu, R.S.6
-
12
-
-
77951518839
-
VEGF-induced ROS generation from NAD(P)H oxidases protects human leukemic cells from apoptosis
-
T. Maraldi, C. Prata, C. Caliceti, F. Vieceli Dalla Sega, L. Zambonin, D. Fiorentini, and G. Hakim VEGF-induced ROS generation from NAD(P)H oxidases protects human leukemic cells from apoptosis Int. J. Oncol. 36 2010 1581 1589
-
(2010)
Int. J. Oncol.
, vol.36
, pp. 1581-1589
-
-
Maraldi, T.1
Prata, C.2
Caliceti, C.3
Vieceli Dalla Sega, F.4
Zambonin, L.5
Fiorentini, D.6
Hakim, G.7
-
13
-
-
60649107567
-
Nox4 overexpression activates reactive oxygen species and p38 MAPK in human endothelial cells
-
C. Goettsch, W. Goettsch, G. Muller, J. Seebach, H.J. Schnittler, and H. Morawietz Nox4 overexpression activates reactive oxygen species and p38 MAPK in human endothelial cells Biochem. Biophys. Res. Commun. 380 2009 355 360
-
(2009)
Biochem. Biophys. Res. Commun.
, vol.380
, pp. 355-360
-
-
Goettsch, C.1
Goettsch, W.2
Muller, G.3
Seebach, J.4
Schnittler, H.J.5
Morawietz, H.6
-
14
-
-
80051790391
-
NADPH oxidase 4 promotes endothelial angiogenesis through endothelial nitric oxide synthase activation
-
S.M. Craige, K. Chen, Y. Pei, C. Li, X. Huang, C. Chen, R. Shibata, K. Sato, K. Walsh, and J.F. Keaney Jr. NADPH oxidase 4 promotes endothelial angiogenesis through endothelial nitric oxide synthase activation Circulation 124 2011 731 740
-
(2011)
Circulation
, vol.124
, pp. 731-740
-
-
Craige, S.M.1
Chen, K.2
Pei, Y.3
Li, C.4
Huang, X.5
Chen, C.6
Shibata, R.7
Sato, K.8
Walsh, K.9
Keaney, Jr.J.F.10
-
15
-
-
44449125132
-
Reactive oxygen species and angiogenesis: NADPH oxidase as target for cancer therapy
-
M. Ushio-Fukai, and Y. Nakamura Reactive oxygen species and angiogenesis: NADPH oxidase as target for cancer therapy Cancer Lett. 266 2008 37 52
-
(2008)
Cancer Lett.
, vol.266
, pp. 37-52
-
-
Ushio-Fukai, M.1
Nakamura, Y.2
-
16
-
-
58149474871
-
Synthesis and structure-activity relationship studies of 3-substituted indolin-2-ones as effective neuroprotective agents
-
M. Balderamos, H. Ankati, S. Kumar Akubathini, A.V. Patel, S. Kamila, C. Mukherjee, L. Wang, E.R. Biehl, and S.R. D'Mello Synthesis and structure-activity relationship studies of 3-substituted indolin-2-ones as effective neuroprotective agents Exp. Biol. Med. 233 2008 1395 1402
-
(2008)
Exp. Biol. Med.
, vol.233
, pp. 1395-1402
-
-
Balderamos, M.1
Ankati, H.2
Kumar Akubathini, S.3
Patel, A.V.4
Kamila, S.5
Mukherjee, C.6
Wang, L.7
Biehl, E.R.8
D'Mello, S.R.9
-
17
-
-
77949522116
-
Constitutive NADPH-dependent electron transferase activity of the Nox4 dehydrogenase domain
-
Y. Nisimoto, H.M. Jackson, H. Ogawa, T. Kawahara, and J.D. Lambeth Constitutive NADPH-dependent electron transferase activity of the Nox4 dehydrogenase domain Biochemistry 49 2010 2433 2442
-
(2010)
Biochemistry
, vol.49
, pp. 2433-2442
-
-
Nisimoto, Y.1
Jackson, H.M.2
Ogawa, H.3
Kawahara, T.4
Lambeth, J.D.5
-
18
-
-
46649100691
-
Nox-generated ROS modulate glucose uptake in a leukaemic cell line
-
C. Prata, T. Maraldi, D. Fiorentini, L. Zambonin, G. Hakim, and L. Landi Nox-generated ROS modulate glucose uptake in a leukaemic cell line Free Radic. Res. 42 2008 405 414
-
(2008)
Free Radic. Res.
, vol.42
, pp. 405-414
-
-
Prata, C.1
Maraldi, T.2
Fiorentini, D.3
Zambonin, L.4
Hakim, G.5
Landi, L.6
-
19
-
-
46449129179
-
Nox4 oxidase overexpression specifically decreases endogenous Nox4 mRNA and inhibits angiotensin II-induced adventitial myofibroblast migration
-
M.J. Haurani, M.E. Cifuentes, A.D. Shepard, and P.J. Pagano Nox4 oxidase overexpression specifically decreases endogenous Nox4 mRNA and inhibits angiotensin II-induced adventitial myofibroblast migration Hypertension 52 2008 143 149
-
(2008)
Hypertension
, vol.52
, pp. 143-149
-
-
Haurani, M.J.1
Cifuentes, M.E.2
Shepard, A.D.3
Pagano, P.J.4
-
20
-
-
85047049058
-
Piper sarmentosum inhibits ICAM-1 and Nox4 gene expression in oxidative stress-induced human umbilical vein endothelial cells
-
A. Ugusman, Z. Zakaria, C.K. Hui, and N.A. Nordin Piper sarmentosum inhibits ICAM-1 and Nox4 gene expression in oxidative stress-induced human umbilical vein endothelial cells BMC Complement. Altern. Med. 16 2011 11 31
-
(2011)
BMC Complement. Altern. Med.
, vol.16
, pp. 11-31
-
-
Ugusman, A.1
Zakaria, Z.2
Hui, C.K.3
Nordin, N.A.4
-
23
-
-
51849143181
-
Synthesis of ferrocenyl oxindole compounds with potential anticancer activity
-
B.V. Silva, N.M. Ribeiro, A.C. Pinto, M.D. Vargas, and L.C. Dias Synthesis of ferrocenyl oxindole compounds with potential anticancer activity J. Braz. Chem. Soc. 19 2008 1244 1247
-
(2008)
J. Braz. Chem. Soc.
, vol.19
, pp. 1244-1247
-
-
Silva, B.V.1
Ribeiro, N.M.2
Pinto, A.C.3
Vargas, M.D.4
Dias, L.C.5
-
24
-
-
0037030611
-
Synthesis and antitumor activity of 1,5,6-substituted 3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones
-
A. Andreani, M. Granaiola, A. Leoni, A. Locatelli, R. Morigi, M. Rambaldi, and V. Garaliene Synthesis and antitumor activity of 1,5,6-substituted 3-(2-chloro-3-indolylmethylene)1,3-dihydroindol-2-ones J. Med. Chem. 45 2002 2666 2669
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2666-2669
-
-
Andreani, A.1
Granaiola, M.2
Leoni, A.3
Locatelli, A.4
Morigi, R.5
Rambaldi, M.6
Garaliene, V.7
-
25
-
-
37049162897
-
Monothiophthalimide and some derivatives of oxindole
-
J.C. Porter, R. Robinson, and M. Wyler Monothiophthalimide and some derivatives of oxindole J. Chem. Soc. 1941 620 624
-
(1941)
J. Chem. Soc.
, pp. 620-624
-
-
Porter, J.C.1
Robinson, R.2
Wyler, M.3
-
26
-
-
49449106062
-
Amminazione Radicalica di Composti Aromatici Attivati: Acetammidi. Nuovo Processo per la Sintesi di para-Ammino-N, N-dialchilaniline
-
F. Minisci, R. Galli, and M. Cecere Amminazione Radicalica di Composti Aromatici Attivati: Acetammidi. Nuovo Processo per la Sintesi di para-Ammino-N, N-dialchilaniline La Chim. e l'Industria 48 1966 1324 1326
-
(1966)
La Chim. e l'Industria
, vol.48
, pp. 1324-1326
-
-
Minisci, F.1
Galli, R.2
Cecere, M.3
-
27
-
-
65949085145
-
Ruthenium-catalyzed alkylation of oxindole with alcohols
-
T. Jensen, and R. Madsen Ruthenium-catalyzed alkylation of oxindole with alcohols J. Org. Chem. 74 2009 3990 3992
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3990-3992
-
-
Jensen, T.1
Madsen, R.2
-
28
-
-
15044344246
-
Microwave-assisted Sequential amide bond formation and intramolecular amidation: A rapid entry to functionalized oxindoles
-
R.R. Poondra, and N.J. Turner Microwave-assisted Sequential amide bond formation and intramolecular amidation: a rapid entry to functionalized oxindoles Org. Lett. 7 2005 863 866
-
(2005)
Org. Lett.
, vol.7
, pp. 863-866
-
-
Poondra, R.R.1
Turner, N.J.2
-
29
-
-
0000549233
-
Nucleophilic aromatic substitutions. XVIII. New ring closures through arynes
-
R. Huisgen, H. Konig, and A.R. Lepley Nucleophilic aromatic substitutions. XVIII. New ring closures through arynes Chem. Ber. 93 1960 1496 1506
-
(1960)
Chem. Ber.
, vol.93
, pp. 1496-1506
-
-
Huisgen, R.1
Konig, H.2
Lepley, A.R.3
-
30
-
-
77951203766
-
Antitumor activity and COMPARE analysis of bis-indole derivatives
-
A. Andreani, S. Burnelli, M. Granaiola, A. Leoni, A. Locatelli, R. Morigi, M. Rambaldi, L. Varoli, L. Landi, C. Prata, F. Vieceli Dalla Sega, C. Caliceti, and R.H. Shoemaker Antitumor activity and COMPARE analysis of bis-indole derivatives Biorg. Med. Chem. 18 2010 3004 3011
-
(2010)
Biorg. Med. Chem.
, vol.18
, pp. 3004-3011
-
-
Andreani, A.1
Burnelli, S.2
Granaiola, M.3
Leoni, A.4
Locatelli, A.5
Morigi, R.6
Rambaldi, M.7
Varoli, L.8
Landi, L.9
Prata, C.10
Vieceli Dalla Sega, F.11
Caliceti, C.12
Shoemaker, R.H.13
-
31
-
-
0032474915
-
Synthesis and biological evaluations of 3-substituted indolin-2-ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases
-
L. Sun, N. Tran, F. Tang, H. App, P. Hirth, G. McMahon, and C. Tang Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases J. Med. Chem. 41 1998 2588 2603
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2588-2603
-
-
Sun, L.1
Tran, N.2
Tang, F.3
App, H.4
Hirth, P.5
McMahon, G.6
Tang, C.7
-
32
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
-
A. Monks, D. Scudiero, P. Skehan, R. Shoemaker, K. Paull, D. Vistica, C. Hose, J. Langley, P. Cronise, A. Vaigro-Wolff, M. Gray-Goodrich, H. Campbell, J. Mayo, and M. Boyd Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines J. Natl. Cancer Inst. 83 1991 757 766
-
(1991)
J. Natl. Cancer Inst.
, vol.83
, pp. 757-766
-
-
Monks, A.1
Scudiero, D.2
Skehan, P.3
Shoemaker, R.4
Paull, K.5
Vistica, D.6
Hose, C.7
Langley, J.8
Cronise, P.9
Vaigro-Wolff, A.10
Gray-Goodrich, M.11
Campbell, H.12
Mayo, J.13
Boyd, M.14
-
33
-
-
0021163546
-
Separation of active tubulin and microtubule-associated proteins by ultracentrifugation, and isolation of a component causing the formation of microtubule bundles
-
E. Hamel, and C.M. Lin Separation of active tubulin and microtubule-associated proteins by ultracentrifugation, and isolation of a component causing the formation of microtubule bundles Biochemistry 23 1984 4173 4184
-
(1984)
Biochemistry
, vol.23
, pp. 4173-4184
-
-
Hamel, E.1
Lin, C.M.2
-
34
-
-
0142036683
-
Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin
-
E. Hamel Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin Cell Biochem. Biophys. 38 2003 1 21
-
(2003)
Cell Biochem. Biophys.
, vol.38
, pp. 1-21
-
-
Hamel, E.1
-
35
-
-
0031913357
-
Structure-activity analysis of the interaction of curacin a, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells
-
P. Verdier-Pinard, J.-Y. Lai, H.-D. Yoo, J. Yu, B. Marquez, D.G. Nagle, M. Nambu, J.D. White, J.R. Falck, W.H. Gerwick, B.W. Day, and E. Hamel Structure-activity analysis of the interaction of curacin a, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells Mol. Pharmacol. 53 1998 62 67
-
(1998)
Mol. Pharmacol.
, vol.53
, pp. 62-67
-
-
Verdier-Pinard, P.1
Lai, J.-Y.2
Yoo, H.-D.3
Yu, J.4
Marquez, B.5
Nagle, D.G.6
Nambu, M.7
White, J.D.8
Falck, J.R.9
Gerwick, W.H.10
Day, B.W.11
Hamel, E.12
|