-
1
-
-
0343629854
-
The inhibition of ribonucleotide reductase by α-(N)-heterocyclic carboxaldehyde thiosemicarbazones
-
A. Sartorelli, International encyclopedia of pharmacology and therapeutics Pergamon New York
-
E.C. Moore, and A.C. Sartorelli The inhibition of ribonucleotide reductase by α-(N)-heterocyclic carboxaldehyde thiosemicarbazones A. Sartorelli, Inhibitors of ribonucleoside diphosphate reductase activity International encyclopedia of pharmacology and therapeutics vol. 128 1989 Pergamon New York 203 215
-
(1989)
Inhibitors of Ribonucleoside Diphosphate Reductase Activity
, vol.128
, pp. 203-215
-
-
Moore, E.C.1
Sartorelli, A.C.2
-
2
-
-
0033975268
-
Triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity
-
R.A. Finch, M. Liu, S.P. Grill, W.C. Rose, R. Loomis, and K.M. Vasquez Triapine (3-aminopyridine-2-carboxaldehyde-thiosemicarbazone): a potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity Biochem Pharmacol 59 2000 983 991
-
(2000)
Biochem Pharmacol
, vol.59
, pp. 983-991
-
-
Finch, R.A.1
Liu, M.2
Grill, S.P.3
Rose, W.C.4
Loomis, R.5
Vasquez, K.M.6
-
3
-
-
33750471953
-
Dipyridyl thiosemicarbazone chelators with potent and selective antitumor activity form iron complexes with redox activity
-
D.R. Richardson, P.C. Sharpe, D.B. Lovejoy, D. Senaratne, D.S. Kalinowski, and M. Islam Dipyridyl thiosemicarbazone chelators with potent and selective antitumor activity form iron complexes with redox activity J Med Chem 49 2006 6510 6521
-
(2006)
J Med Chem
, vol.49
, pp. 6510-6521
-
-
Richardson, D.R.1
Sharpe, P.C.2
Lovejoy, D.B.3
Senaratne, D.4
Kalinowski, D.S.5
Islam, M.6
-
4
-
-
79952752677
-
The medicinal chemistry of novel iron chelators for the treatment of cancer
-
Z. Kovacevic, D.S. Kalinowski, D.B. Lovejoy, Y. Yu, Y.S. Rahmanto, and P.C. Sharpe The medicinal chemistry of novel iron chelators for the treatment of cancer Curr Top Med Chem 11 2011 483 499
-
(2011)
Curr Top Med Chem
, vol.11
, pp. 483-499
-
-
Kovacevic, Z.1
Kalinowski, D.S.2
Lovejoy, D.B.3
Yu, Y.4
Rahmanto, Y.S.5
Sharpe, P.C.6
-
5
-
-
67650394382
-
Phase II study of 3-AP triapine in patients with recurrent or metastatic head and neck squamous cell carcinoma
-
C.M. Nutting, C.M. van Herpen, A.B. Miah, S.A. Bhide, J.P. Machiels, and J. Buter Phase II study of 3-AP triapine in patients with recurrent or metastatic head and neck squamous cell carcinoma Ann Oncol 20 2009 1275 1279
-
(2009)
Ann Oncol
, vol.20
, pp. 1275-1279
-
-
Nutting, C.M.1
Van Herpen, C.M.2
Miah, A.B.3
Bhide, S.A.4
MacHiels, J.P.5
Buter, J.6
-
6
-
-
4444248453
-
Novel di-2-pyridyl-derived iron chelators with marked and selective antitumor activity: In vitro and in vivo assessment
-
J. Yuan, D.B. Lovejoy, and D.R. Richardson Novel di-2-pyridyl-derived iron chelators with marked and selective antitumor activity: in vitro and in vivo assessment Blood 104 2004 1450 1458
-
(2004)
Blood
, vol.104
, pp. 1450-1458
-
-
Yuan, J.1
Lovejoy, D.B.2
Richardson, D.R.3
-
7
-
-
33749515083
-
A class of iron chelators with a wide spectrum of potent antitumor activity that overcomes resistance to chemotherapeutics
-
M. Whitnall, J. Howard, P. Ponka, and D.R. Richardson A class of iron chelators with a wide spectrum of potent antitumor activity that overcomes resistance to chemotherapeutics Proc Natl Acad Sci USA 103 2006 14901 14906
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 14901-14906
-
-
Whitnall, M.1
Howard, J.2
Ponka, P.3
Richardson, D.R.4
-
8
-
-
80052221642
-
Antitumor activity of metal-chelating compound Dp44mT is mediated by formation of a redox-active copper complex that accumulates in lysosomes
-
D.B. Lovejoy, P.J. Jansson, U.T. Brunk, J. Wong, P. Ponka, and D.R. Richardson Antitumor activity of metal-chelating compound Dp44mT is mediated by formation of a redox-active copper complex that accumulates in lysosomes Cancer Res 71 2011 5871 5880
-
(2011)
Cancer Res
, vol.71
, pp. 5871-5880
-
-
Lovejoy, D.B.1
Jansson, P.J.2
Brunk, U.T.3
Wong, J.4
Ponka, P.5
Richardson, D.R.6
-
9
-
-
67449126645
-
The iron chelator Dp44mT does not protect myocytes against doxorubicin
-
B.B. Hasinoff, and D. Patel The iron chelator Dp44mT does not protect myocytes against doxorubicin J Inorg Biochem 103 2009 1093 1101
-
(2009)
J Inorg Biochem
, vol.103
, pp. 1093-1101
-
-
Hasinoff, B.B.1
Patel, D.2
-
10
-
-
82455175282
-
The iron chelator Dp44mT inhibits the proliferation of cancer cells but fails to protect from doxorubicin-induced cardiotoxicity in spontaneously hypertensive rats
-
V.A. Rao, J. Zhang, S.R. Klein, P. Espandiari, A. Knapton, and J.S. Dickey The iron chelator Dp44mT inhibits the proliferation of cancer cells but fails to protect from doxorubicin-induced cardiotoxicity in spontaneously hypertensive rats Cancer Chemother Pharmacol 68 2011 1125 1134
-
(2011)
Cancer Chemother Pharmacol
, vol.68
, pp. 1125-1134
-
-
Rao, V.A.1
Zhang, J.2
Klein, S.R.3
Espandiari, P.4
Knapton, A.5
Dickey, J.S.6
-
11
-
-
79956293094
-
The potent and novel thiosemicarbazone chelators di-2-pyridylketone-4,4- dimethyl-3-thiosemicarbazone and 2-benzoylpyridine-4,4-dimethyl-3- thiosemicarbazone affect crucial thiol systems required for ribonucleotide reductase activity
-
Y. Yu, Y.S. Rahmanto, C.L. Hawkins, and D.R. Richardson The potent and novel thiosemicarbazone chelators di-2-pyridylketone-4,4-dimethyl-3- thiosemicarbazone and 2-benzoylpyridine-4,4-dimethyl-3-thiosemicarbazone affect crucial thiol systems required for ribonucleotide reductase activity Mol Pharmacol 79 2011 921 931
-
(2011)
Mol Pharmacol
, vol.79
, pp. 921-931
-
-
Yu, Y.1
Rahmanto, Y.S.2
Hawkins, C.L.3
Richardson, D.R.4
-
12
-
-
79955462543
-
Cellular iron depletion stimulates the JNK and p38 MAPK signaling transduction pathways, dissociation of ASK1-thioredoxin, and activation of ASK1
-
Y. Yu, and D.R. Richardson Cellular iron depletion stimulates the JNK and p38 MAPK signaling transduction pathways, dissociation of ASK1-thioredoxin, and activation of ASK1 J Biol Chem 286 2011 15413 15427
-
(2011)
J Biol Chem
, vol.286
, pp. 15413-15427
-
-
Yu, Y.1
Richardson, D.R.2
-
13
-
-
59149089078
-
The iron chelator Dp44mT causes DNA damage and selective inhibition of topoisomerase IIα in breast cancer cells
-
V.A. Rao, S.R. Klein, K.K. Agama, E. Toyoda, N. Adachi, and Y. Pommier The iron chelator Dp44mT causes DNA damage and selective inhibition of topoisomerase IIα in breast cancer cells Cancer Res 69 2009 948 957
-
(2009)
Cancer Res
, vol.69
, pp. 948-957
-
-
Rao, V.A.1
Klein, S.R.2
Agama, K.K.3
Toyoda, E.4
Adachi, N.5
Pommier, Y.6
-
14
-
-
64649090292
-
Targeting DNA topoisomerase II in cancer chemotherapy
-
J.L. Nitiss Targeting DNA topoisomerase II in cancer chemotherapy Nat Rev Cancer 9 2009 338 350
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 338-350
-
-
Nitiss, J.L.1
-
15
-
-
63349086953
-
The DNA cleavage reaction of topoisomerase II: Wolf in sheep's clothing
-
J.E. Deweese, and N. Osheroff The DNA cleavage reaction of topoisomerase II: wolf in sheep's clothing Nucleic Acids Res 37 2009 738 748
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 738-748
-
-
Deweese, J.E.1
Osheroff, N.2
-
16
-
-
77954187741
-
DNA topoisomerases and their poisoning by anticancer and antibacterial drugs
-
Y. Pommier, E. Leo, H. Zhang, and C. Marchand DNA topoisomerases and their poisoning by anticancer and antibacterial drugs Chem Biol 17 2010 421 433
-
(2010)
Chem Biol
, vol.17
, pp. 421-433
-
-
Pommier, Y.1
Leo, E.2
Zhang, H.3
Marchand, C.4
-
17
-
-
0032482306
-
Synthesis of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP)
-
C. Niu, J. Li, T.W. Doyle, and S-H. Chen Synthesis of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) Tetrahedron 54 1998 6311 6318
-
(1998)
Tetrahedron
, vol.54
, pp. 6311-6318
-
-
Niu, C.1
Li, J.2
Doyle, T.W.3
Chen, S.-H.4
-
18
-
-
33748157438
-
Kinamycins A and C, bacterial metabolites that contain an unusual diazo group, as potential new anticancer agents: Antiproliferative and cell cycle effects
-
B.B. Hasinoff, X. Wu, J.C. Yalowich, V. Goodfellow, R.S. Laufer, and O. Adedayo Kinamycins A and C, bacterial metabolites that contain an unusual diazo group, as potential new anticancer agents: antiproliferative and cell cycle effects Anticancer Drugs 17 2006 825 837
-
(2006)
Anticancer Drugs
, vol.17
, pp. 825-837
-
-
Hasinoff, B.B.1
Wu, X.2
Yalowich, J.C.3
Goodfellow, V.4
Laufer, R.S.5
Adedayo, O.6
-
19
-
-
0029982836
-
Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells
-
C. Fattman, W.P. Allan, B.B. Hasinoff, and J.C. Yalowich Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells Biochem Pharmacol 52 1996 635 642
-
(1996)
Biochem Pharmacol
, vol.52
, pp. 635-642
-
-
Fattman, C.1
Allan, W.P.2
Hasinoff, B.B.3
Yalowich, J.C.4
-
20
-
-
0027487007
-
Altered gene expression in human leukemia K562 cells selected for resistance to etoposide
-
M.K. Ritke, and J.C. Yalowich Altered gene expression in human leukemia K562 cells selected for resistance to etoposide Biochem Pharmacol 46 1993 2007 2020
-
(1993)
Biochem Pharmacol
, vol.46
, pp. 2007-2020
-
-
Ritke, M.K.1
Yalowich, J.C.2
-
21
-
-
80655123142
-
Design, synthesis, and biological evaluation of a novel series of bisintercalating DNA-binding piperazine-linked bisanthrapyrazole compounds as anticancer agents
-
R. Zhang, X. Wu, J.C. Yalowich, and B.B. Hasinoff Design, synthesis, and biological evaluation of a novel series of bisintercalating DNA-binding piperazine-linked bisanthrapyrazole compounds as anticancer agents Bioorg Med Chem 19 2011 7023 7032
-
(2011)
Bioorg Med Chem
, vol.19
, pp. 7023-7032
-
-
Zhang, R.1
Wu, X.2
Yalowich, J.C.3
Hasinoff, B.B.4
-
22
-
-
20144362708
-
Biochemical and proteomics approaches to characterize topoisomerase IIα cysteines and DNA as targets responsible for cisplatin-induced inhibition of topoisomerase IIα
-
B.B. Hasinoff, X. Wu, O.V. Krokhin, W. Ens, K.G. Standing, and J.L. Nitiss Biochemical and proteomics approaches to characterize topoisomerase IIα cysteines and DNA as targets responsible for cisplatin-induced inhibition of topoisomerase IIα Mol Pharmacol 67 2005 937 947
-
(2005)
Mol Pharmacol
, vol.67
, pp. 937-947
-
-
Hasinoff, B.B.1
Wu, X.2
Krokhin, O.V.3
Ens, W.4
Standing, K.G.5
Nitiss, J.L.6
-
23
-
-
33746893422
-
A structure-based 3D-QSAR study of anthrapyrazole analogs of the anticancer agents losoxantrone and piroxantrone
-
H. Liang, X. Wu, L.J. Guziec, F.S. Guziec Jr., K.K. Larson, and J. Lang A structure-based 3D-QSAR study of anthrapyrazole analogs of the anticancer agents losoxantrone and piroxantrone J Chem Inf Model 46 2006 1827 1835
-
(2006)
J Chem Inf Model
, vol.46
, pp. 1827-1835
-
-
Liang, H.1
Wu, X.2
Guziec, L.J.3
Guziec, Jr.F.S.4
Larson, K.K.5
Lang, J.6
-
26
-
-
84860679077
-
A novel validated quantitiative pharmacodynamic topoisomerase i covalent-complex immunoassay
-
Abstract Number: C224
-
Pfister TD, Khin S, Agama K, Hollingshead M, Sooryakumar D, Pommier Y, et al. A novel validated quantitiative pharmacodynamic topoisomerase I covalent-complex immunoassay. AACR-NCI-EORTC International Conference 2009. Abstract Number: C224.
-
(2009)
AACR-NCI-EORTC International Conference
-
-
Pfister, T.D.1
Khin, S.2
Agama, K.3
Hollingshead, M.4
Sooryakumar, D.5
Pommier, Y.6
-
27
-
-
0028141994
-
Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells
-
M.K. Ritke, W.P. Allan, C. Fattman, N.N. Gunduz, and J.C. Yalowich Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells Mol Pharmacol 46 1994 58 66
-
(1994)
Mol Pharmacol
, vol.46
, pp. 58-66
-
-
Ritke, M.K.1
Allan, W.P.2
Fattman, C.3
Gunduz, N.N.4
Yalowich, J.C.5
-
28
-
-
0036239375
-
Maleimide is a potent inhibitor of topoisomerase II in vitro and in vivo: A new mode of catalytic inhibition
-
L.H. Jensen, A. Renodon-Corniere, I. Wessel, S.W. Langer, B. Sokilde, and E.V. Carstensen Maleimide is a potent inhibitor of topoisomerase II in vitro and in vivo: a new mode of catalytic inhibition Mol Pharmacol 61 2002 1235 1243
-
(2002)
Mol Pharmacol
, vol.61
, pp. 1235-1243
-
-
Jensen, L.H.1
Renodon-Corniere, A.2
Wessel, I.3
Langer, S.W.4
Sokilde, B.5
Carstensen, E.V.6
-
29
-
-
0028325365
-
Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukaemia K562 cells
-
M.K. Ritke, D. Roberts, W.P. Allan, J. Raymond, V.V. Bergoltz, and J.C. Yalowich Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukaemia K562 cells Br J Cancer 69 1994 687 697
-
(1994)
Br J Cancer
, vol.69
, pp. 687-697
-
-
Ritke, M.K.1
Roberts, D.2
Allan, W.P.3
Raymond, J.4
Bergoltz, V.V.5
Yalowich, J.C.6
-
30
-
-
0024456572
-
Characterization of an amsacrine-resistant line of human leukemia cells: Evidence for a drug-resistant form of topoisomerase II
-
L.A. Zwelling, M. Hinds, D. Chan, J. Mayes, K.L. Sie, and E. Parker Characterization of an amsacrine-resistant line of human leukemia cells: evidence for a drug-resistant form of topoisomerase II J Biol Chem 264 1989 16411 16420
-
(1989)
J Biol Chem
, vol.264
, pp. 16411-16420
-
-
Zwelling, L.A.1
Hinds, M.2
Chan, D.3
Mayes, J.4
Sie, K.L.5
Parker, E.6
-
31
-
-
64649105115
-
DNA topoisomerase II and its growing repertoire of biological functions
-
J.L. Nitiss DNA topoisomerase II and its growing repertoire of biological functions Nat Rev Cancer 9 2009 327 337
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 327-337
-
-
Nitiss, J.L.1
-
32
-
-
34548299563
-
Dexrazoxane: How it works in cardiac and tumor cells. Is it a prodrug or is it a drug?
-
B.B. Hasinoff, and E.H. Herman Dexrazoxane: how it works in cardiac and tumor cells. Is it a prodrug or is it a drug? Cardiovasc Toxicol 7 2007 140 144
-
(2007)
Cardiovasc Toxicol
, vol.7
, pp. 140-144
-
-
Hasinoff, B.B.1
Herman, E.H.2
-
33
-
-
77953126769
-
Design, synthesis and biological evaluation of a novel series of anthrapyrazoles linked with netropsin-like oligopyrrole carboxamides as anticancer agents
-
R. Zhang, X. Wu, L.J. Guziec, F. Guziec Jr., G-L. Chee, and J.C. Yalowich Design, synthesis and biological evaluation of a novel series of anthrapyrazoles linked with netropsin-like oligopyrrole carboxamides as anticancer agents Bioorg Med Chem 18 2010 3974 3984
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 3974-3984
-
-
Zhang, R.1
Wu, X.2
Guziec, L.J.3
Guziec, Jr.F.4
Chee, G.-L.5
Yalowich, J.C.6
-
34
-
-
0034050902
-
Systematic variation in gene expression patterns in human cancer cell lines
-
D.T. Ross, U. Scherf, M.B. Eisen, C.M. Perou, C. Rees, and P. Spellman Systematic variation in gene expression patterns in human cancer cell lines Nat Genet 24 2000 227 235
-
(2000)
Nat Genet
, vol.24
, pp. 227-235
-
-
Ross, D.T.1
Scherf, U.2
Eisen, M.B.3
Perou, C.M.4
Rees, C.5
Spellman, P.6
-
35
-
-
14844345208
-
Exocyclic DNA lesions stimulate DNA cleavage mediated by human topoisomerase IIα in vitro and in cultured cells
-
R. Velez-Cruz, J.N. Riggins, J.S. Daniels, H. Cai, F.P. Guengerich, and L.J. Marnett Exocyclic DNA lesions stimulate DNA cleavage mediated by human topoisomerase IIα in vitro and in cultured cells Biochemistry 44 2005 3972 3981
-
(2005)
Biochemistry
, vol.44
, pp. 3972-3981
-
-
Velez-Cruz, R.1
Riggins, J.N.2
Daniels, J.S.3
Cai, H.4
Guengerich, F.P.5
Marnett, L.J.6
-
36
-
-
0034193242
-
Sensitivity of human type II topoisomerases to DNA damage: Stimulation of enzyme-mediated DNA cleavage by abasic, oxidized and alkylated lesions
-
M. Sabourin, and N. Osheroff Sensitivity of human type II topoisomerases to DNA damage: stimulation of enzyme-mediated DNA cleavage by abasic, oxidized and alkylated lesions Nucleic Acids Res 28 2000 1947 1954
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 1947-1954
-
-
Sabourin, M.1
Osheroff, N.2
|