-
1
-
-
37249031349
-
Antitumor metal compounds: More than theme and variations
-
Jakupec, M. A.; Galanski, M.; Arion, V. B.; Hartinger, C. G.; Keppler, B. K. Antitumor metal compounds: more than theme and variations Dalton Trans. 2008, 183-194
-
(2008)
Dalton Trans.
, pp. 183-194
-
-
Jakupec, M.A.1
Galanski, M.2
Arion, V.B.3
Hartinger, C.G.4
Keppler, B.K.5
-
2
-
-
55149098114
-
Medicinal applications of metal complexes binding to biological macromolecules
-
Reedijk, J. Medicinal applications of metal complexes binding to biological macromolecules Macromol. Symp. 2008, 270, 193-201
-
(2008)
Macromol. Symp.
, vol.270
, pp. 193-201
-
-
Reedijk, J.1
-
3
-
-
35548986156
-
Metal based drugs: From serendipity to design
-
Fricker, S. P. Metal based drugs: from serendipity to design Dalton Trans. 2007, 4903-4917
-
(2007)
Dalton Trans.
, pp. 4903-4917
-
-
Fricker, S.P.1
-
4
-
-
0042948708
-
Ruthenium metallopharmaceuticals
-
Clarke, M. J. Ruthenium metallopharmaceuticals Coord. Chem. Rev. 2003, 236, 209-233
-
(2003)
Coord. Chem. Rev.
, vol.236
, pp. 209-233
-
-
Clarke, M.J.1
-
5
-
-
37149008995
-
Ruthenium Anticancer Compounds: Challenges and Expectations
-
Bratsos, I.; Jedner, S.; Gianferrara, T.; Alessio, E. Ruthenium Anticancer Compounds: Challenges and Expectations Chimia 2007, 61, 692-697
-
(2007)
Chimia
, vol.61
, pp. 692-697
-
-
Bratsos, I.1
Jedner, S.2
Gianferrara, T.3
Alessio, E.4
-
6
-
-
2542625358
-
A Phase i and Pharmacological Study with Imidazolium- trans -DMSO-imidazole-tetrachlororuthenate, a Novel Ruthenium Anticancer Agent
-
Rademaker-Lakhai, J. M.; Van Den Bongard, D.; Pluim, D.; Beijnen, J. H.; Schellens, J. H. M. A Phase I and Pharmacological Study with Imidazolium- trans -DMSO-imidazole-tetrachlororuthenate, a Novel Ruthenium Anticancer Agent Clin. Cancer Res. 2004, 10, 3717-3727
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 3717-3727
-
-
Rademaker-Lakhai, J.M.1
Van Den Bongard, D.2
Pluim, D.3
Beijnen, J.H.4
Schellens, J.H.M.5
-
7
-
-
59449101302
-
Pharmacokinetics of a novel anticancer ruthenium complex (KP1019, FFC14A) in a phase i dose-escalation study
-
Lentz, F.; Drescher, A.; Lindauer, A.; Henke, M.; Hilger, R. A.; Hartinger, C. G.; Scheulen, M. E.; Dittrich, C.; Keppler, B. K.; Jaehde, U. Pharmacokinetics of a novel anticancer ruthenium complex (KP1019, FFC14A) in a phase I dose-escalation study Anti-Cancer Drugs 2009, 20, 97-103
-
(2009)
Anti-Cancer Drugs
, vol.20
, pp. 97-103
-
-
Lentz, F.1
Drescher, A.2
Lindauer, A.3
Henke, M.4
Hilger, R.A.5
Hartinger, C.G.6
Scheulen, M.E.7
Dittrich, C.8
Keppler, B.K.9
Jaehde, U.10
-
8
-
-
70349281567
-
A categorization of metal anticancer compounds based on their mode of action
-
Gianferrara, T.; Bratsos, I.; Alessio, E. A categorization of metal anticancer compounds based on their mode of action Dalton Trans. 2009, 7588-7598
-
(2009)
Dalton Trans.
, pp. 7588-7598
-
-
Gianferrara, T.1
Bratsos, I.2
Alessio, E.3
-
9
-
-
55449107748
-
Medicinal organometallic chemistry: Designing metal arene complexes as anticancer agents
-
Peacock, A. F. A.; Sadler, P. J. Medicinal organometallic chemistry: designing metal arene complexes as anticancer agents Chem. Asian J. 2008, 3, 1890-1899
-
(2008)
Chem. Asian J.
, vol.3
, pp. 1890-1899
-
-
Peacock, A.F.A.1
Sadler, P.J.2
-
10
-
-
75749151659
-
Arene ruthenium complexes as anticancer agents
-
Suess-Fink, G. Arene ruthenium complexes as anticancer agents Dalton Trans. 2010, 39, 1673-1688
-
(2010)
Dalton Trans.
, vol.39
, pp. 1673-1688
-
-
Suess-Fink, G.1
-
11
-
-
33845772944
-
Diversity in guanine-selective DNA binding modes for an organometallic ruthenium arene complex
-
Liu, H. K.; Berners-Price, S. J.; Wang, F.; Parkinson, J. A.; Xu, J.; Bella, J.; Sadler, P. J. Diversity in guanine-selective DNA binding modes for an organometallic ruthenium arene complex Angew. Chem., Int. Ed. 2006, 45, 8153-8156
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 8153-8156
-
-
Liu, H.K.1
Berners-Price, S.J.2
Wang, F.3
Parkinson, J.A.4
Xu, J.5
Bella, J.6
Sadler, P.J.7
-
12
-
-
29444455073
-
Controlling ligand substitution reactions of organometallic complexes: Tuning cancer cell cytotoxicity
-
Wang, F.; Habtemariam, A.; van der Geer, E. P. L; Fernandez, R.; Melchart, M.; Deeth, R. J.; Aird, R.; Guichard, S.; Fabbiani, F. P. A; Lozano-Casal, P.; Oswald, I. D. H.; Jodrell, D. I.; Parsons, S.; Sadler, P. J. Controlling ligand substitution reactions of organometallic complexes: tuning cancer cell cytotoxicity Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 18269-18274
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 18269-18274
-
-
Wang, F.1
Habtemariam, A.2
Van Der Geer, E.P.L.3
Fernandez, R.4
Melchart, M.5
Deeth, R.J.6
Aird, R.7
Guichard, S.8
Fabbiani, F.P.A.9
Lozano-Casal, P.10
Oswald, I.D.H.11
Jodrell, D.I.12
Parsons, S.13
Sadler, P.J.14
-
13
-
-
33750969384
-
Structure-Activity Relationships for Cytotoxic Ruthenium(II) Arene Complexes Containing N, N -, N, O -, and O, O -Chelating Ligands
-
Habtemariam, A.; Melchart, M.; Fernandez, R.; Parsons, S.; Oswald, I. D. H.; Parkin, A.; Fabbiani, F. P. A; Davidson, J. E.; Dawson, A.; Aird, R. E.; Jodrell, D. I.; Sadler, P. J. Structure-Activity Relationships for Cytotoxic Ruthenium(II) Arene Complexes Containing N, N -, N, O -, and O, O -Chelating Ligands J. Med. Chem. 2006, 49, 6858-6868
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6858-6868
-
-
Habtemariam, A.1
Melchart, M.2
Fernandez, R.3
Parsons, S.4
Oswald, I.D.H.5
Parkin, A.6
Fabbiani, F.P.A.7
Davidson, J.E.8
Dawson, A.9
Aird, R.E.10
Jodrell, D.I.11
Sadler, P.J.12
-
14
-
-
37149042962
-
Systematic design of a targeted organometallic antitumor drug in preclinical development
-
Dyson, P. J. Systematic design of a targeted organometallic antitumor drug in preclinical development Chimia 2007, 61, 698-703
-
(2007)
Chimia
, vol.61
, pp. 698-703
-
-
Dyson, P.J.1
-
15
-
-
35548947955
-
Tuning the hydrophobicity of ruthenium(II)-arene (RAPTA) drugs to modify uptake, biomolecular interactions and efficacy
-
Scolaro, C.; Chaplin, A. B.; Hartinger, C. G.; Bergamo, A.; Cocchietto, M.; Keppler, B. K.; Sava, G.; Dyson, P. J. Tuning the hydrophobicity of ruthenium(II)-arene (RAPTA) drugs to modify uptake, biomolecular interactions and efficacy Dalton Trans. 2007, 5065-5072
-
(2007)
Dalton Trans.
, pp. 5065-5072
-
-
Scolaro, C.1
Chaplin, A.B.2
Hartinger, C.G.3
Bergamo, A.4
Cocchietto, M.5
Keppler, B.K.6
Sava, G.7
Dyson, P.J.8
-
16
-
-
33751403575
-
Development of Organometallic Ruthenium-Arene Anticancer Drugs That Resist Hydrolysis
-
Ang, W. H.; Daldini, E.; Scolaro, C.; Scopelliti, R.; Juillerat-Jeannerat, L.; Dyson, P. J. Development of Organometallic Ruthenium-Arene Anticancer Drugs That Resist Hydrolysis Inorg. Chem. 2006, 45, 9006-9013
-
(2006)
Inorg. Chem.
, vol.45
, pp. 9006-9013
-
-
Ang, W.H.1
Daldini, E.2
Scolaro, C.3
Scopelliti, R.4
Juillerat-Jeannerat, L.5
Dyson, P.J.6
-
17
-
-
63749127483
-
Kinome signaling through regulated protein-protein interactions in normal and cancer cells
-
Pawson, T.; Kofler, M. Kinome signaling through regulated protein-protein interactions in normal and cancer cells Curr. Opin. Cell Biol. 2009, 21, 147-153
-
(2009)
Curr. Opin. Cell Biol.
, vol.21
, pp. 147-153
-
-
Pawson, T.1
Kofler, M.2
-
18
-
-
63449112585
-
Therapeutic Protein Kinase Inhibitors
-
Grant, S. K. Therapeutic Protein Kinase Inhibitors Cell. Mol. Life Sci. 2009, 66, 1163-1177
-
(2009)
Cell. Mol. Life Sci.
, vol.66
, pp. 1163-1177
-
-
Grant, S.K.1
-
19
-
-
1642323740
-
Protein kinase inhibitors: Insights into drug design from structure
-
Noble, M. E.; Endicott, J. A.; Johnson, L. N. Protein kinase inhibitors: insights into drug design from structure Science 2004, 303, 1800-1805
-
(2004)
Science
, vol.303
, pp. 1800-1805
-
-
Noble, M.E.1
Endicott, J.A.2
Johnson, L.N.3
-
20
-
-
6444236961
-
An Organometallic Inhibitor for Glycogen Synthase Kinase 3
-
Bregman, H.; Williams, D. S.; Atilla, G. E.; Carroll, P. J.; Meggers, E. An Organometallic Inhibitor for Glycogen Synthase Kinase 3 J. Am. Chem. Soc. 2004, 126, 13594-13595
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13594-13595
-
-
Bregman, H.1
Williams, D.S.2
Atilla, G.E.3
Carroll, P.J.4
Meggers, E.5
-
21
-
-
56749178863
-
Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes
-
Maksimoska, J.; Feng, L.; Harms, K.; Yi, C.; Kissil, J.; Marmorstein, R.; Meggers, E. Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes J. Am. Chem. Soc. 2008, 130, 15764-15765
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 15764-15765
-
-
Maksimoska, J.1
Feng, L.2
Harms, K.3
Yi, C.4
Kissil, J.5
Marmorstein, R.6
Meggers, E.7
-
22
-
-
59649119743
-
Extremely Tight Binding of a Ruthenium Complex to Glycogen Synthase Kinase 3
-
Atilla-Gokcumen, G. E.; Pagano, N.; Streu, C.; Maksimoska, J.; Filippakopoulos, P.; Knapp, S.; Meggers, E. Extremely Tight Binding of a Ruthenium Complex to Glycogen Synthase Kinase 3 ChemBioChem 2008, 9, 2933-2936
-
(2008)
ChemBioChem
, vol.9
, pp. 2933-2936
-
-
Atilla-Gokcumen, G.E.1
Pagano, N.2
Streu, C.3
Maksimoska, J.4
Filippakopoulos, P.5
Knapp, S.6
Meggers, E.7
-
23
-
-
61849162674
-
Targeting proteins with metal complexes
-
Meggers, E. Targeting proteins with metal complexes Chem. Commun. 2009, 1001-1010
-
(2009)
Chem. Commun.
, pp. 1001-1010
-
-
Meggers, E.1
-
24
-
-
64349099558
-
Kinase Domain Mutations in Cancer: Implications for Small Molecule Drug Design Strategies
-
Bikker, J. A.; Brooijmans, N.; Wissner, A.; Mansour, T. S. Kinase Domain Mutations in Cancer: Implications for Small Molecule Drug Design Strategies J. Med. Chem. 2009, 52, 1493-1509
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1493-1509
-
-
Bikker, J.A.1
Brooijmans, N.2
Wissner, A.3
Mansour, T.S.4
-
25
-
-
0033128165
-
Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases
-
Hoessel, R.; Leclerc, S.; Endicott, J. A.; Noble, M. E. M.; Lawrie, A.; Tunnah, P.; Leost, M.; Damiens, E.; Marie, D.; Marko, D.; Niederberger, E.; Tang, W.; Eisenbrand, G.; Meijer, L. Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases Nature Cell Biol. 1999, 1, 60-67
-
(1999)
Nature Cell Biol.
, vol.1
, pp. 60-67
-
-
Hoessel, R.1
Leclerc, S.2
Endicott, J.A.3
Noble, M.E.M.4
Lawrie, A.5
Tunnah, P.6
Leost, M.7
Damiens, E.8
Marie, D.9
Marko, D.10
Niederberger, E.11
Tang, W.12
Eisenbrand, G.13
Meijer, L.14
-
26
-
-
8644224855
-
Molecular mechanisms of indirubin and its derivatives: Novel anticancer molecules with their origin in traditional Chinese phytomedicine
-
Eisenbrand, G.; Hippe, F.; Jakobs, S.; Muehlbeyer, S. Molecular mechanisms of indirubin and its derivatives: novel anticancer molecules with their origin in traditional Chinese phytomedicine J. Cancer Res. Clin. Oncol. 2004, 130, 627-635
-
(2004)
J. Cancer Res. Clin. Oncol.
, vol.130
, pp. 627-635
-
-
Eisenbrand, G.1
Hippe, F.2
Jakobs, S.3
Muehlbeyer, S.4
-
27
-
-
20944435625
-
Indirubin derivatives inhibit Stat3 signaling and induce apoptosis in human cancer cells
-
Nam, S.; Buettner, R.; Turkson, J.; Kim, D.; Cheng, J. Q.; Muehlbeyer, S.; Hippe, F.; Vatter, S.; Merz, K.; Eisenbrand, G.; Jove, R. Indirubin derivatives inhibit Stat3 signaling and induce apoptosis in human cancer cells Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 5998-6003
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 5998-6003
-
-
Nam, S.1
Buettner, R.2
Turkson, J.3
Kim, D.4
Cheng, J.Q.5
Muehlbeyer, S.6
Hippe, F.7
Vatter, S.8
Merz, K.9
Eisenbrand, G.10
Jove, R.11
-
28
-
-
43949085683
-
Indirubin-3′-monoxime, a derivative of a Chinese anti-leukemia medicine, inhibits Notch1 signaling
-
Lee, M. J.; Kim, M. Y.; Mo, J. S.; Ann, E. J.; Seo, M.-S.; Hong, J.-A.; Kim, Y.-C.; Park, H. S. Indirubin-3′-monoxime, a derivative of a Chinese anti-leukemia medicine, inhibits Notch1 signaling Cancer Lett. 2008, 265, 215-225
-
(2008)
Cancer Lett.
, vol.265
, pp. 215-225
-
-
Lee, M.J.1
Kim, M.Y.2
Mo, J.S.3
Ann, E.J.4
Seo, M.-S.5
Hong, J.-A.6
Kim, Y.-C.7
Park, H.S.8
-
29
-
-
33747364467
-
Synthesis of novel 5-substituted indirubins as protein kinases inhibitors
-
Beauchard, A.; Ferandin, Y.; Frere, S.; Lozach, O.; Blairvacq, M.; Meijer, L.; Thiery, V.; Besson, T. Synthesis of novel 5-substituted indirubins as protein kinases inhibitors Bioorg. Med. Chem. 2006, 14, 6434-6443
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 6434-6443
-
-
Beauchard, A.1
Ferandin, Y.2
Frere, S.3
Lozach, O.4
Blairvacq, M.5
Meijer, L.6
Thiery, V.7
Besson, T.8
-
30
-
-
20444445904
-
From the insoluble dye indirubin towards highly active, soluble CDK2-inhibitors
-
Jautelat, R.; Brumby, T.; Schaefer, M.; Briem, H.; Eisenbrand, G.; Schwahn, S.; Krueger, M.; Luecking, U.; Prien, O.; Siemeister, G. From the insoluble dye indirubin towards highly active, soluble CDK2-inhibitors ChemBioChem 2005, 6, 531-540
-
(2005)
ChemBioChem
, vol.6
, pp. 531-540
-
-
Jautelat, R.1
Brumby, T.2
Schaefer, M.3
Briem, H.4
Eisenbrand, G.5
Schwahn, S.6
Krueger, M.7
Luecking, U.8
Prien, O.9
Siemeister, G.10
-
31
-
-
3042629590
-
Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediate the antiproliferative effects of indirubins
-
Knockaert, M.; Blondel, M.; Bach, S.; Leost, M.; Elbi, C.; Hager, G. L.; Nagy, S. R.; Han, D.; Denison, M.; Ffrench, M.; Ryan, X. P.; Magiatis, P.; Polychronopoulos, P.; Greengard, P.; Skaltsounis, L.; Meijer, L. Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediate the antiproliferative effects of indirubins Oncogene 2004, 23, 4400-4412
-
(2004)
Oncogene
, vol.23
, pp. 4400-4412
-
-
Knockaert, M.1
Blondel, M.2
Bach, S.3
Leost, M.4
Elbi, C.5
Hager, G.L.6
Nagy, S.R.7
Han, D.8
Denison, M.9
Ffrench, M.10
Ryan, X.P.11
Magiatis, P.12
Polychronopoulos, P.13
Greengard, P.14
Skaltsounis, L.15
Meijer, L.16
-
32
-
-
84859801379
-
-
Int. PatentWO 02/092079 A1, November 21.
-
Siemeister, G.; Thierauch, K. H.; Prien, O.; Jautelat, R.; Eisenbrand, G. Therapeutic use of selective indirubin derivatives as VEGF receptor inhibitors. Int. PatentWO 02/092079 A1, November 21, 2002.
-
(2002)
Therapeutic Use of Selective Indirubin Derivatives As VEGF Receptor Inhibitors
-
-
Siemeister, G.1
Thierauch, K.H.2
Prien, O.3
Jautelat, R.4
Eisenbrand, G.5
-
33
-
-
0034988970
-
Inhibitor Binding to Active and Inactive CDK2 the Crystal Structure of CDK2-Cyclin A/ Indirubin-5-Sulphonate
-
Davies, T. G.; Tunnah, P.; Meijer, L.; Marko, D.; Eisenbrand, G.; Endicott, J. A.; Noble, M. E. M. Inhibitor Binding to Active and Inactive CDK2 The Crystal Structure of CDK2-Cyclin A/ Indirubin-5-Sulphonate Structure 2001, 9, 389-397
-
(2001)
Structure
, vol.9
, pp. 389-397
-
-
Davies, T.G.1
Tunnah, P.2
Meijer, L.3
Marko, D.4
Eisenbrand, G.5
Endicott, J.A.6
Noble, M.E.M.7
-
34
-
-
84859806134
-
-
Int. Patent WO 02/22598 A1, March 21.
-
Renhowe, P.; Pecchi, S.; Machajewski, T.; Shafer, C.; Taylor, C.; McCrea, B.; McBride, C.; Jazan, E.; Wernette-Hammond, M. E.; Harris, A. Quinolinone Derivatives as Tyrosine Kinase Inhibitors. Int. Patent WO 02/22598 A1, March 21, 2002.
-
(2002)
Quinolinone Derivatives As Tyrosine Kinase Inhibitors
-
-
Renhowe, P.1
Pecchi, S.2
MacHajewski, T.3
Shafer, C.4
Taylor, C.5
McCrea, B.6
McBride, C.7
Jazan, E.8
Wernette-Hammond, M.E.9
Harris, A.10
-
35
-
-
33644803645
-
Design and structure-activity relationship of heterocyclic analogs of 4-amino-3-benzimidazol-2-ylhydroquinolin-2-ones as inhibitors of receptor tyrosine kinases
-
Frazier, K.; Jazan, E.; McBride, C. M.; Pecchi, S.; Renhowe, P. A.; Shafer, C. M.; Taylor, C.; Bussiere, D.; Min, He M.; Jansen, J. M.; Lapointe, G.; Ma, S.; Vora, J.; Wiesmann, M. Design and structure-activity relationship of heterocyclic analogs of 4-amino-3-benzimidazol-2-ylhydroquinolin-2-ones as inhibitors of receptor tyrosine kinases Bioorg. Med. Chem. Lett. 2006, 16, 2247-2251
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2247-2251
-
-
Frazier, K.1
Jazan, E.2
McBride, C.M.3
Pecchi, S.4
Renhowe, P.A.5
Shafer, C.M.6
Taylor, C.7
Bussiere, D.8
Min, H.M.9
Jansen, J.M.10
Lapointe, G.11
Ma, S.12
Vora, J.13
Wiesmann, M.14
-
36
-
-
60549084927
-
Design, Structure-Activity Relationships and in Vivo Characterization of 4-Amino-3-benzimidazol-2-ylhydroquinolin-2-ones: A Novel Class of Receptor Tyrosine Kinase Inhibitors
-
Renhowe, P. A.; Pecchi, S.; Shafer, C. M.; Machajewski, T. D.; Jazan, E. M.; Taylor, C.; Antonios-McCrea, W.; McBride, C. M.; Frazier, K.; Wiesmann, M.; Lapointe, G. R.; Feucht, P. H.; Warne, R. L.; Heise, C. C.; Menezes, D.; Aardalen, K.; Ye, H.; He, M.; Le, V.; Vora, J.; Jansen, J. M.; Wernette-Hammond, M. E.; Harris, A. L. Design, Structure-Activity Relationships and in Vivo Characterization of 4-Amino-3-benzimidazol-2-ylhydroquinolin-2-ones: A Novel Class of Receptor Tyrosine Kinase Inhibitors J. Med. Chem. 2009, 52, 278-292
-
(2009)
J. Med. Chem.
, vol.52
, pp. 278-292
-
-
Renhowe, P.A.1
Pecchi, S.2
Shafer, C.M.3
MacHajewski, T.D.4
Jazan, E.M.5
Taylor, C.6
Antonios-Mccrea, W.7
McBride, C.M.8
Frazier, K.9
Wiesmann, M.10
Lapointe, G.R.11
Feucht, P.H.12
Warne, R.L.13
Heise, C.C.14
Menezes, D.15
Aardalen, K.16
Ye, H.17
He, M.18
Le, V.19
Vora, J.20
Jansen, J.M.21
Wernette-Hammond, M.E.22
Harris, A.L.23
more..
-
37
-
-
84859795035
-
-
Int. Patent WO 2004/043950 A1, May 27.
-
Ladouceur, G. H.; Bear, B.; Bi, C.; Brittelli, D. R.; Burke, M. J.; Chen, G.; Cook, J.; Dumas, J.; Sibley, R.; Turner, M. R. Indolyl pyrazinone derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis. Int. Patent WO 2004/043950 A1, May 27, 2004.
-
(2004)
Indolyl Pyrazinone Derivatives Useful for Treating Hyper-proliferative Disorders and Diseases Associated with Angiogenesis
-
-
Ladouceur, G.H.1
Bear, B.2
Bi, C.3
Brittelli, D.R.4
Burke, M.J.5
Chen, G.6
Cook, J.7
Dumas, J.8
Sibley, R.9
Turner, M.R.10
-
38
-
-
34250023992
-
Convenient synthetic method for 3-(3-substituted indol-2-yl)quinoxalin-2- ones as VEGF inhibitor
-
Aoki, K.; Koseki, J.; Takeda, S.; Aburada, M.; Miyamoto, K. Convenient synthetic method for 3-(3-substituted indol-2-yl)quinoxalin-2-ones as VEGF inhibitor Chem. Pharm. Bull. 2007, 55, 922-925
-
(2007)
Chem. Pharm. Bull.
, vol.55
, pp. 922-925
-
-
Aoki, K.1
Koseki, J.2
Takeda, S.3
Aburada, M.4
Miyamoto, K.5
-
39
-
-
0017018732
-
Reactions with pyridinium pyruvates
-
Westphal, G.; Scheybal, A.; Lipke, B.; Weber, F. G. Reactions with pyridinium pyruvates Pharmazie 1976, 31, 770-773
-
(1976)
Pharmazie
, vol.31
, pp. 770-773
-
-
Westphal, G.1
Scheybal, A.2
Lipke, B.3
Weber, F.G.4
-
40
-
-
0017658103
-
Preparation of several 3-hetaryl-2-quinoxalinones
-
Westphal, G.; Scheybal, A.; Lipke, B.; Weber, F. G. Preparation of several 3-hetaryl-2-quinoxalinones Pharmazie 1977, 32, 563-565
-
(1977)
Pharmazie
, vol.32
, pp. 563-565
-
-
Westphal, G.1
Scheybal, A.2
Lipke, B.3
Weber, F.G.4
-
41
-
-
84859805573
-
Quinoxaline series. III. Synthesis, reactions, and infrared spectra of some 3-hydroxy-2-carboxymethylquinoxaline derivatives
-
Klicnar, J.; Hajek, M.; Dobas, I. Quinoxaline series. III. Synthesis, reactions, and infrared spectra of some 3-hydroxy-2-carboxymethylquinoxaline derivatives Collect. Czech. Chem. Commun. 1965, 30, 3092-3101
-
(1965)
Collect. Czech. Chem. Commun.
, vol.30
, pp. 3092-3101
-
-
Klicnar, J.1
Hajek, M.2
Dobas, I.3
-
42
-
-
60749086476
-
Tuning the anticancer activity of maltol-derived ruthenium complexes by derivatization of the 3-hydroxy-4-pyrone moiety
-
Kandioller, W.; Hartinger, C. G.; Nazarov, A. A.; Kasser, J.; John, R.; Jakupec, M. A.; Arion, V. B.; Dyson, P. J.; Keppler, B. K. Tuning the anticancer activity of maltol-derived ruthenium complexes by derivatization of the 3-hydroxy-4-pyrone moiety J. Organomet. Chem. 2009, 694, 922-929
-
(2009)
J. Organomet. Chem.
, vol.694
, pp. 922-929
-
-
Kandioller, W.1
Hartinger, C.G.2
Nazarov, A.A.3
Kasser, J.4
John, R.5
Jakupec, M.A.6
Arion, V.B.7
Dyson, P.J.8
Keppler, B.K.9
-
43
-
-
68149164662
-
From Pyrone to Thiopyrone Ligands-Rendering Maltol-Derived Ruthenium(II)-Arene Complexes That Are Anticancer Active in Vitro
-
Kandioller, W.; Hartinger, C. G.; Nazarov, A. A.; Kuznetsov, M. L.; John, R. O.; Bartel, C.; Jakupec, M. A.; Arion, V. B.; Keppler, B. K. From Pyrone to Thiopyrone Ligands-Rendering Maltol-Derived Ruthenium(II)-Arene Complexes That Are Anticancer Active in Vitro Organometallics 2009, 28, 4249-4251
-
(2009)
Organometallics
, vol.28
, pp. 4249-4251
-
-
Kandioller, W.1
Hartinger, C.G.2
Nazarov, A.A.3
Kuznetsov, M.L.4
John, R.O.5
Bartel, C.6
Jakupec, M.A.7
Arion, V.B.8
Keppler, B.K.9
-
44
-
-
20344380450
-
Cationic arene ruthenium complexes containing chelating 1,10-phenanthroline ligands
-
Canivet, J.; Karmazin-Brelot, L.; Suess-Fink, G. Cationic arene ruthenium complexes containing chelating 1,10-phenanthroline ligands J. Organomet. Chem. 2005, 690, 3202-3211
-
(2005)
J. Organomet. Chem.
, vol.690
, pp. 3202-3211
-
-
Canivet, J.1
Karmazin-Brelot, L.2
Suess-Fink, G.3
-
45
-
-
0347624091
-
Kinetics of aquation and anation of ruthenium(II) arene anticancer complexes, acidity and X-ray structures of aqua adducts
-
Wang, F.; Chen, H.; Parsons, S.; Oswald, I. D. H.; Davidson, J. E.; Sadler, P. J. Kinetics of aquation and anation of ruthenium(II) arene anticancer complexes, acidity and X-ray structures of aqua adducts Chem.-Eur. J. 2003, 9, 5810-5820
-
(2003)
Chem.-Eur. J.
, vol.9
, pp. 5810-5820
-
-
Wang, F.1
Chen, H.2
Parsons, S.3
Oswald, I.D.H.4
Davidson, J.E.5
Sadler, P.J.6
-
46
-
-
32244442894
-
Tuning the Reactivity of Osmium(II) and Ruthenium(II) Arene Complexes under Physiological Conditions
-
Peacock, A. F. A.; Habtemariam, A.; Fernandez, R.; Walland, V.; Fabbiani, F. P. A; Parsons, S.; Aird, R. E.; Jodrell, D. I.; Sadler, P. J. Tuning the Reactivity of Osmium(II) and Ruthenium(II) Arene Complexes under Physiological Conditions J. Am. Chem. Soc. 2006, 128, 1739-1748
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 1739-1748
-
-
Peacock, A.F.A.1
Habtemariam, A.2
Fernandez, R.3
Walland, V.4
Fabbiani, F.P.A.5
Parsons, S.6
Aird, R.E.7
Jodrell, D.I.8
Sadler, P.J.9
-
47
-
-
0030558056
-
Solvatochromism and prototropic reactions of 2-quinoxalinone
-
Santra, S.; Dogra, S. K. Solvatochromism and prototropic reactions of 2-quinoxalinone Chem. Phys. 1996, 207, 103-113
-
(1996)
Chem. Phys.
, vol.207
, pp. 103-113
-
-
Santra, S.1
Dogra, S.K.2
-
48
-
-
0002526520
-
Ï€-Arene Aqua Complexes of Cobalt, Rhodium, Iridium, and Ruthenium: Preparation, Structure, and Kinetics of Water Exchange and Water Substitution
-
Dadci, L.; Elias, H.; Frey, U.; Hoernig, A.; Koelle, U.; Merbach, A. E.; Paulus, H.; Schneider, J. S. π-Arene Aqua Complexes of Cobalt, Rhodium, Iridium, and Ruthenium: Preparation, Structure, and Kinetics of Water Exchange and Water Substitution Inorg. Chem. 1995, 34, 306-315
-
(1995)
Inorg. Chem.
, vol.34
, pp. 306-315
-
-
Dadci, L.1
Elias, H.2
Frey, U.3
Hoernig, A.4
Koelle, U.5
Merbach, A.E.6
Paulus, H.7
Schneider, J.S.8
-
49
-
-
34249689999
-
Chloro half-sandwich osmium(II) complexes: Influence of chelated N, N -ligands on hydrolysis, guanine binding, and cytotoxicity
-
Peacock, A. F. A.; Habtemariam, A.; Moggach, S. A.; Prescimone, A.; Parsons, S.; Sadler, P. J. Chloro half-sandwich osmium(II) complexes: influence of chelated N, N -ligands on hydrolysis, guanine binding, and cytotoxicity Inorg. Chem. 2007, 46, 4049-4059
-
(2007)
Inorg. Chem.
, vol.46
, pp. 4049-4059
-
-
Peacock, A.F.A.1
Habtemariam, A.2
Moggach, S.A.3
Prescimone, A.4
Parsons, S.5
Sadler, P.J.6
-
50
-
-
0035963318
-
Anti-mitotic properties of indirubin-3′-monoxime, a CDK/GSK-3 inhibitor: Induction of endoreplication following prophase arrest
-
Damiens, E.; Baratte, B.; Marie, D.; Eisenbrand, G.; Meijer, L. Anti-mitotic properties of indirubin-3′-monoxime, a CDK/GSK-3 inhibitor: induction of endoreplication following prophase arrest Oncogene 2001, 20, 3786-3797
-
(2001)
Oncogene
, vol.20
, pp. 3786-3797
-
-
Damiens, E.1
Baratte, B.2
Marie, D.3
Eisenbrand, G.4
Meijer, L.5
-
51
-
-
84859795033
-
-
Manuscript in preparation.
-
Ginzinger, W.; Egger, A.; Mühlgassner, G.; Arion, V. B.; Jakupec, M. A.; Galanski, M.; Berger, W.; Keppler, B. K. Water soluble indirubin derivatives with a quaternary ammonium moiety. Manuscript in preparation.
-
Water Soluble Indirubin Derivatives with A Quaternary Ammonium Moiety
-
-
Ginzinger, W.1
Egger, A.2
Mühlgassner, G.3
Arion, V.B.4
Jakupec, M.A.5
Galanski, M.6
Berger, W.7
Keppler, B.K.8
-
52
-
-
37049118608
-
Arene ruthenium(II) complexes formed by dehydrogenation by cyclohexadienes with ruthenium(III) trichloride
-
Bennett, M. A.; Smith, A. K. Arene ruthenium(II) complexes formed by dehydrogenation by cyclohexadienes with ruthenium(III) trichloride J. Chem. Soc., Dalton Trans. 1974, 233-241
-
(1974)
J. Chem. Soc., Dalton Trans.
, pp. 233-241
-
-
Bennett, M.A.1
Smith, A.K.2
-
55
-
-
84859801381
-
-
3rd ed. Brauer, G. Ferdinand Enke Verlag: Stuttgart
-
Brauer, G.; Fehlhammer, W. P.; Glemser, O.; Grube, H. J.; Gustav, K.; Herrmann, W. A.; Herzog, S.; Lux, H.; Müller, H.; Ofele, K.; Schill, E.; Scholdert, R.; Schwärzt, H.; Schwarzmann, E.; Schwochau, K.; Simon, A.; Strähle, J. In Handbuch der Präparativen Anorganischen Chemie, 3rd ed.; Brauer, G., Ed.; Ferdinand Enke Verlag: Stuttgart, 1981; Vol. 3, p 1743.
-
(1981)
Handbuch der Präparativen Anorganischen Chemie
, vol.3
, pp. 1743
-
-
Brauer, G.1
Fehlhammer, W.P.2
Glemser, O.3
Grube, H.J.4
Gustav, K.5
Herrmann, W.A.6
Herzog, S.7
Lux, H.8
Müller, H.9
Ofele, K.10
Schill, E.11
Scholdert, R.12
Schwärzt, H.13
Schwarzmann, E.14
Schwochau, K.15
Simon, A.16
Strähle, J.17
-
58
-
-
0141452964
-
WinGX suite for small-molecule single-crystal crystallography
-
Farrugia, L. J. WinGX suite for small-molecule single-crystal crystallography J. Appl. Crystallogr. 1999, 32, 837-838
-
(1999)
J. Appl. Crystallogr.
, vol.32
, pp. 837-838
-
-
Farrugia, L.J.1
-
60
-
-
0001792356
-
Single-crystal structure validation with the program PLATON
-
Spek, A. L. Single-crystal structure validation with the program PLATON J. Appl. Crystallogr. 2003, 36, 7-13
-
(2003)
J. Appl. Crystallogr.
, vol.36
, pp. 7-13
-
-
Spek, A.L.1
-
62
-
-
0003872738
-
-
Kluwer Academic Press: Dodrecht, The Netherlands, Tables 4.2.6.8 and 6.1.1.4
-
International Tables for X-ray Crystallography; Kluwer Academic Press: Dodrecht, The Netherlands, 1992; Vol. C, Tables 4.2.6.8 and 6.1.1.4.
-
(1992)
International Tables for X-ray Crystallography
, vol.100
-
-
-
63
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann, T. J. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 1983, 65, 55-63
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.J.1
-
64
-
-
0032743259
-
-
Aubry, J.-P.; Blaecke, A.; Lecoanet-Henchoz, S.; Jeannin, P.; Herbault, N.; Caron, G.; Moine, V.; Bonnefoy, J.-Y. Cytometry 1999, 37, 197-204
-
(1999)
Cytometry
, vol.37
, pp. 197-204
-
-
Aubry, J.-P.1
Blaecke, A.2
Lecoanet-Henchoz, S.3
Jeannin, P.4
Herbault, N.5
Caron, G.6
Moine, V.7
Bonnefoy, J.-Y.8
-
65
-
-
36649023786
-
Pyrazolo[4′,3′:5,6]pyrano[2,3- b ]quinoxalin-4(1 H)-one: Synthesis and characterization of a novel tetracyclic ring system
-
Eller, G. A.; Datterl, B.; Holzer, W. Pyrazolo[4′,3′:5,6] pyrano[2,3- b ]quinoxalin-4(1 H)-one: synthesis and characterization of a novel tetracyclic ring system J. Heterocycl. Chem. 2007, 44, 1139-1143
-
(2007)
J. Heterocycl. Chem.
, vol.44
, pp. 1139-1143
-
-
Eller, G.A.1
Datterl, B.2
Holzer, W.3
|