-
1
-
-
85008135775
-
Structure of kinamycin C, and the structural relation among kinamycin A, B, C, and D
-
Omura S, Nakagawa A, Yamada H, Hata T, Furusaki A, Watanabe T. Structure of kinamycin C, and the structural relation among kinamycin A, B, C, and D. Chem Pharm Bull 1971; 19:2428-2430.
-
(1971)
Chem Pharm Bull
, vol.19
, pp. 2428-2430
-
-
Omura, S.1
Nakagawa, A.2
Yamada, H.3
Hata, T.4
Furusaki, A.5
Watanabe, T.6
-
2
-
-
0015789726
-
Structures and biological properties of kinamycin A, B, C, and D
-
Omura S, Nakagawa A, Yamada H, Hata T, Furukawa A, Watanabe T. Structures and biological properties of kinamycin A, B, C, and D. Chem Pharm Bull 1973; 21:931-940.
-
(1973)
Chem Pharm Bull
, vol.21
, pp. 931-940
-
-
Omura, S.1
Nakagawa, A.2
Yamada, H.3
Hata, T.4
Furukawa, A.5
Watanabe, T.6
-
3
-
-
0017397793
-
Bioactivation as a model for drug design bioreductive alkylation
-
Moore HW. Bioactivation as a model for drug design bioreductive alkylation. Science 1977; 197:527-532.
-
(1977)
Science
, vol.197
, pp. 527-532
-
-
Moore, H.W.1
-
5
-
-
0028050438
-
Revised structures for the kinamycin antibiotics: 5-diazobenzo[b] fluorenes rather than benzo[b]carbazole cyanamides
-
Gould SJ, Tamayo N, Melville CR, Cone MC. Revised structures for the kinamycin antibiotics: 5-diazobenzo[b]fluorenes rather than benzo[b]carbazole cyanamides. J Am Chem Soc 1994; 116:2207-2208.
-
(1994)
J Am Chem Soc
, vol.116
, pp. 2207-2208
-
-
Gould, S.J.1
Tamayo, N.2
Melville, C.R.3
Cone, M.C.4
-
6
-
-
27644487203
-
A proposal for the mechanism-of-action of diazoparaquinone natural products
-
Feldman KS, Eastman KJ. A proposal for the mechanism-of-action of diazoparaquinone natural products. J Am Chem Soc 2005; 127:15344-15345.
-
(2005)
J Am Chem Soc
, vol.127
, pp. 15344-15345
-
-
Feldman, K.S.1
Eastman, K.J.2
-
7
-
-
0034812241
-
Lomaiviticins A and B, potent antitumor antibiotics from Micromonospora lomaivitiensis
-
He H, Ding WD, Bernan VS, Richardson AD, Ireland CM, Greenstein M, et al. Lomaiviticins A and B, potent antitumor antibiotics from Micromonospora lomaivitiensis. J Am Chem Soc 2001; 123:5362-5363.
-
(2001)
J Am Chem Soc
, vol.123
, pp. 5362-5363
-
-
He, H.1
Ding, W.D.2
Bernan, V.S.3
Richardson, A.D.4
Ireland, C.M.5
Greenstein, M.6
-
8
-
-
0037028980
-
Diazo group electrophilicity in kinamycins and lomaiviticin A: Potential insights into the molecular mechanism of antibacterial and antitumor activity
-
Laufer RS, Dmitrienko GI. Diazo group electrophilicity in kinamycins and lomaiviticin A: potential insights into the molecular mechanism of antibacterial and antitumor activity. J Am Chem Soc 2002; 124:1854-1855.
-
(2002)
J Am Chem Soc
, vol.124
, pp. 1854-1855
-
-
Laufer, R.S.1
Dmitrienko, G.I.2
-
9
-
-
0024550662
-
New products related to kinamycin from Streptomyces murayamaensis. I. Taxonomy, production, isolation and biological properties
-
Cone MC, Seaton PJ, Halley KA, Gould SJ. New products related to kinamycin from Streptomyces murayamaensis. I. Taxonomy, production, isolation and biological properties. J Antibiot (Tokyo) 1989; 42:179-188.
-
(1989)
J Antibiot (Tokyo)
, vol.42
, pp. 179-188
-
-
Cone, M.C.1
Seaton, P.J.2
Halley, K.A.3
Gould, S.J.4
-
10
-
-
1642388489
-
2(levrazoxane), of the topoisomerase II inhibitors dexrazoxane (ICRF-187) and levrazoxane (ICRF-186)
-
2(levrazoxane), of the topoisomerase II inhibitors dexrazoxane (ICRF-187) and levrazoxane (ICRF-186). J Inorg Biochem 2004; 98:616-624.
-
(2004)
J Inorg Biochem
, vol.98
, pp. 616-624
-
-
Hasinoff, B.B.1
Wu, X.2
Yang, Y.3
-
11
-
-
0030739460
-
Characterization of a Chinese hamster ovary cell line with acquired resistance to the bisdioxopiperazine dexrazoxane (ICRF-187) catalytic inhibitor of topoisomerase II
-
Hasinoff BB, Kuschak TI, Creighton AM, Fattman CL, Allan WP, Thampatty P, et al. Characterization of a Chinese hamster ovary cell line with acquired resistance to the bisdioxopiperazine dexrazoxane (ICRF-187) catalytic inhibitor of topoisomerase II. Biochem Pharmacol 1997; 53:1843-1853.
-
(1997)
Biochem Pharmacol
, vol.53
, pp. 1843-1853
-
-
Hasinoff, B.B.1
Kuschak, T.I.2
Creighton, A.M.3
Fattman, C.L.4
Allan, W.P.5
Thampatty, P.6
-
12
-
-
0030733491
-
Mitindomide is a catalytic inhibitor of DNA topoisomerase II that acts at the bisdioxopiperazine binding site
-
Hasinoff BB, Kozlowska H, Creighton AM, Allan WP, Thampatty P, Yalowich JC. Mitindomide is a catalytic inhibitor of DNA topoisomerase II that acts at the bisdioxopiperazine binding site. Mol Pharmacol 1997; 52:839-845.
-
(1997)
Mol Pharmacol
, vol.52
, pp. 839-845
-
-
Hasinoff, B.B.1
Kozlowska, H.2
Creighton, A.M.3
Allan, W.P.4
Thampatty, P.5
Yalowich, J.C.6
-
13
-
-
0027487007
-
Altered gene expression in human leukemia K562 cells selected for resistance to etoposide
-
Ritke MK, Yalowich JC. Altered gene expression in human leukemia K562 cells selected for resistance to etoposide. Biochem Pharmacol 1993; 46:2007-2020.
-
(1993)
Biochem Pharmacol
, vol.46
, pp. 2007-2020
-
-
Ritke, M.K.1
Yalowich, J.C.2
-
14
-
-
0028141994
-
Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells
-
Ritke MK, Allan WP, Fattman C, Gunduz NN, Yalowich JC. Reduced phosphorylation of topoisomerase II in etoposide-resistant human leukemia K562 cells. Mol Pharmacol 1994; 46:58-66.
-
(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
-
15
-
-
0028325365
-
Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukemia K562 cells
-
Ritke MK, Roberts D, Allan WP, Raymond J, Bergoltz VV, Yalowich JC. Altered stability of etoposide-induced topoisomerase II-DNA complexes in resistant human leukemia K562 cells. Br J Cancer 1994; 69:687-697.
-
(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
-
16
-
-
0029982836
-
Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells
-
Fattman C, Allan WP, Hasinoff BB, Yalowich JC. Collateral sensitivity to the bisdioxopiperazine dexrazoxane (ICRF-187) in etoposide (VP-16) resistant human leukemia K562 cells. Biochem Pharmacol 1996; 52:635-642.
-
(1996)
Biochem Pharmacol
, vol.52
, pp. 635-642
-
-
Fattman, C.1
Allan, W.P.2
Hasinoff, B.B.3
Yalowich, J.C.4
-
17
-
-
0035119566
-
The catalytic DNA topoisomerase II inhibitor dexrazoxane (ICRF-187) induces differentiation and apoptosis in human leukemia K562 cells
-
Hasinoff BB, Abram ME, Barnabé N, Khelifa T, Allan WP, Yalowich JC. The catalytic DNA topoisomerase II inhibitor dexrazoxane (ICRF-187) induces differentiation and apoptosis in human leukemia K562 cells. Mol Pharmacol 2001; 59:453-461.
-
(2001)
Mol Pharmacol
, vol.59
, pp. 453-461
-
-
Hasinoff, B.B.1
Abram, M.E.2
Barnabé, N.3
Khelifa, T.4
Allan, W.P.5
Yalowich, J.C.6
-
18
-
-
0035812478
-
High-throughput fluorescence flow injection topoisomerase II inhibition assay
-
Barnabé N, Hasinoff BB. High-throughput fluorescence flow injection topoisomerase II inhibition assay. J Chromatogr B Biomed Sci Appl 2001; 760:263-269.
-
(2001)
J Chromatogr B Biomed Sci Appl
, vol.760
, pp. 263-269
-
-
Barnabé, N.1
Hasinoff, B.B.2
-
19
-
-
20144362708
-
Biochemical and proteomics approaches to characterize topoisomerase IIα cysteines and DNA as targets responsible for cisplatin-induced inhibition of topoisomerase IIα
-
Hasinoff BB, Wu X, Krokhin OV, Ens W, Standing KG, Nitiss JL, et al. Biochemical and proteomics approaches to characterize topoisomerase IIα cysteines and DNA as targets responsible for cisplatin-induced inhibition of topoisomerase IIα. Mol Pharmacol 2005; 67:937-947.
-
(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
-
20
-
-
0027520798
-
On the coupling between ATP usage and DNA transport by yeast DNA topoisomerase II
-
Lindsley JE, Wang JC. On the coupling between ATP usage and DNA transport by yeast DNA topoisomerase II. J Biol Chem 1993; 268:8096-9104.
-
(1993)
J Biol Chem
, vol.268
, pp. 8096-9104
-
-
Lindsley, J.E.1
Wang, J.C.2
-
22
-
-
0037075063
-
Mining the National Cancer Institute's tumor-screening database: Identification of compounds with similar cellular activities
-
Rabow AA, Shoemaker RH, Sausville EA, Covell DG. Mining the National Cancer Institute's tumor-screening database: identification of compounds with similar cellular activities. J Med Chem 2002; 45:818-840.
-
(2002)
J Med Chem
, vol.45
, pp. 818-840
-
-
Rabow, A.A.1
Shoemaker, R.H.2
Sausville, E.A.3
Covell, D.G.4
-
23
-
-
0034608083
-
Suppression by metallothionein of doxorubicin-induced cardiomyocyte apoptosis through inhibition of p38 mitogen-activated protein kinases
-
Kang YJ, Zhou ZX, Wang GW, Buridi A, Klein JB. Suppression by metallothionein of doxorubicin-induced cardiomyocyte apoptosis through inhibition of p38 mitogen-activated protein kinases. J Biol Chem 2000; 275:13690-13698.
-
(2000)
J Biol Chem
, vol.275
, pp. 13690-13698
-
-
Kang, Y.J.1
Zhou, Z.X.2
Wang, G.W.3
Buridi, A.4
Klein, J.B.5
-
24
-
-
0033628701
-
Topoisomerase II as a target for anticancer drugs: When enzymes stop being nice
-
Fortune JM, Osheroff N. Topoisomerase II as a target for anticancer drugs: when enzymes stop being nice. Prog Nucleic Acid Res Mol Biol 2000; 64:221-253.
-
(2000)
Prog Nucleic Acid Res Mol Biol
, vol.64
, pp. 221-253
-
-
Fortune, J.M.1
Osheroff, N.2
-
25
-
-
0035029153
-
Tumor cell death induced by topoisomerase-targeting drugs
-
Li TK, Liu LF. Tumor cell death induced by topoisomerase-targeting drugs. Annu Rev Pharmacol Toxicol 2001; 41:53-77.
-
(2001)
Annu Rev Pharmacol Toxicol
, vol.41
, pp. 53-77
-
-
Li, T.K.1
Liu, L.F.2
-
26
-
-
0001426296
-
Acquired resistance to ICRF-187 (dexrazoxane) in a CHO cell line is associated with a point mutation in DNA topoisomerase IIα (topo II) and decreased drug-induced DNA-enzyme complexes
-
Yalowich JC, Thampatty P, Allan WP, Chee G-L, Hasinoff BB. Acquired resistance to ICRF-187 (dexrazoxane) in a CHO cell line is associated with a point mutation in DNA topoisomerase IIα (topo II) and decreased drug-induced DNA-enzyme complexes. Proc Am Assoc Cancer Res 1998; 39:375.
-
(1998)
Proc Am Assoc Cancer Res
, vol.39
, pp. 375
-
-
Yalowich, J.C.1
Thampatty, P.2
Allan, W.P.3
Chee, G.-L.4
Hasinoff, B.B.5
-
27
-
-
0141591551
-
Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187
-
Classen S, Olland S, Berger JM. Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187. Proc Natl Acad Sci U S A 2003; 100:10629-10634.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 10629-10634
-
-
Classen, S.1
Olland, S.2
Berger, J.M.3
-
28
-
-
0141591551
-
Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187
-
Classen S, Olland S, Berger JM. Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187. Proc Natl Acad Sci U S A 2003; 100:14510.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 14510
-
-
Classen, S.1
Olland, S.2
Berger, J.M.3
-
29
-
-
0028878831
-
Topoisomerase inhibitors. A review of their therapeutic potential in cancer
-
Sinha BK. Topoisomerase inhibitors. A review of their therapeutic potential in cancer. Drugs 1995; 49:11-19.
-
(1995)
Drugs
, vol.49
, pp. 11-19
-
-
Sinha, B.K.1
-
30
-
-
85015066476
-
DNA damage and repair
-
Friedberg EC. DNA damage and repair. Nature 2003; 421:436-440.
-
(2003)
Nature
, vol.421
, pp. 436-440
-
-
Friedberg, E.C.1
-
31
-
-
0041732381
-
Characteristics of γ-H2AX foci at DNA double-strand breaks sites
-
Pilch DR, Sedelnikova OA, Redon C, Celeste A, Nussenzweig A, Bonner WM. Characteristics of γ-H2AX foci at DNA double-strand breaks sites. Biochem Cell Biol 2003; 81:123-129.
-
(2003)
Biochem Cell Biol
, vol.81
, pp. 123-129
-
-
Pilch, D.R.1
Sedelnikova, O.A.2
Redon, C.3
Celeste, A.4
Nussenzweig, A.5
Bonner, W.M.6
-
32
-
-
0032489520
-
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
-
Rogakou EP, Pilch DR, Orr AH, Ivanova VS, Bonner WM. DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem 1998; 273:5858-5868.
-
(1998)
J Biol Chem
, vol.273
, pp. 5858-5868
-
-
Rogakou, E.P.1
Pilch, D.R.2
Orr, A.H.3
Ivanova, V.S.4
Bonner, W.M.5
-
33
-
-
0027972061
-
Differential induction of etoposide-mediated apoptosis in human leukemia HL-60 and K562 cells
-
Ritke MK, Rusnak JM, Lazo JS, Allan WP, Dive C, Heer S, et al. Differential induction of etoposide-mediated apoptosis in human leukemia HL-60 and K562 cells. Mol Pharmacol 1994; 46:605-611.
-
(1994)
Mol Pharmacol
, vol.46
, pp. 605-611
-
-
Ritke, M.K.1
Rusnak, J.M.2
Lazo, J.S.3
Allan, W.P.4
Dive, C.5
Heer, S.6
-
34
-
-
0027979832
-
BCR-ABL maintains resistance of chronic myelogenous leukemia cells to apoptotic cell death
-
McGahon A, Bissonnette R, Schmitt M, Cotter KM, Green DR, Cotter TG. BCR-ABL maintains resistance of chronic myelogenous leukemia cells to apoptotic cell death. Blood 1994; 83:1179-1187.
-
(1994)
Blood
, vol.83
, pp. 1179-1187
-
-
McGahon, A.1
Bissonnette, R.2
Schmitt, M.3
Cotter, K.M.4
Green, D.R.5
Cotter, T.G.6
-
35
-
-
0029796045
-
The effect of dexrazoxane (ICRF-187) on doxorubicin- and daunorubicin-mediated growth inhibition of Chinese hamster ovary cells
-
Hasinoff BB, Yalowich JC, Ling Y, Buss JL. The effect of dexrazoxane (ICRF-187) on doxorubicin- and daunorubicin-mediated growth inhibition of Chinese hamster ovary cells. Anticancer Drugs 1996; 7:558-567.
-
(1996)
Anticancer Drugs
, vol.7
, pp. 558-567
-
-
Hasinoff, B.B.1
Yalowich, J.C.2
Ling, Y.3
Buss, J.L.4
-
36
-
-
28844482331
-
Structure-activity study of the interaction of bioreductive benzoquinone alkylating agents with DNA topoisomerase II
-
Hasinoff BB, Wu X, Begleiter A, Guziec L, Guziec F, Giorgianni A, et al. Structure-activity study of the interaction of bioreductive benzoquinone alkylating agents with DNA topoisomerase II. Cancer Chemother Pharmacol 2006; 57:221-233.
-
(2006)
Cancer Chemother Pharmacol
, vol.57
, pp. 221-233
-
-
Hasinoff, B.B.1
Wu, X.2
Begleiter, A.3
Guziec, L.4
Guziec, F.5
Giorgianni, A.6
-
37
-
-
0036239375
-
Maleimide is a potent inhibitor of topoisomerase II in vitro and in vivo: A new mode of catalytic inhibition
-
Jensen LH, Renodon-Corniere A, Wessel I, Langer SW, Sokilde B, Carstensen EV, et al. Maleimide is a potent inhibitor of topoisomerase II in vitro and in vivo: a new mode of catalytic inhibition. Mol Pharmacol 2002; 61:1235-1243.
-
(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
-
38
-
-
0031978752
-
The ortho-quinone metabolite of the anticancer drug etoposide (VP-16) is a potent inhibitor of the topoisomerase II/DNA cleavable complex
-
Gantchev TG, Hunting DJ. The ortho-quinone metabolite of the anticancer drug etoposide (VP-16) is a potent inhibitor of the topoisomerase II/DNA cleavable complex. Mol Pharmacol 1998; 53:422-428.
-
(1998)
Mol Pharmacol
, vol.53
, pp. 422-428
-
-
Gantchev, T.G.1
Hunting, D.J.2
-
39
-
-
0035916938
-
Stimulation of topoisomerase II-mediated DNA damage via a mechanism involving protein thiolation
-
Wang H, Mao Y, Chen AY, Zhou N, LaVoie EJ, Liu LF. Stimulation of topoisomerase II-mediated DNA damage via a mechanism involving protein thiolation. Biochemistry 2001; 40:3316-3323.
-
(2001)
Biochemistry
, vol.40
, pp. 3316-3323
-
-
Wang, H.1
Mao, Y.2
Chen, A.Y.3
Zhou, N.4
Lavoie, E.J.5
Liu, L.F.6
-
40
-
-
2942555034
-
1,4-Benzoquinone is a topoisomerase II poison
-
Lindsey RH Jr, Bromberg KD, Felix CA, Osheroff N. 1,4-Benzoquinone is a topoisomerase II poison. Biochemistry 2004; 43:7563-7574.
-
(2004)
Biochemistry
, vol.43
, pp. 7563-7574
-
-
Lindsey Jr., R.H.1
Bromberg, K.D.2
Felix, C.A.3
Osheroff, N.4
-
41
-
-
0035818011
-
Reductive activation of mitomycin a by thiols
-
Paz MM, Tomasz M. Reductive activation of mitomycin A by thiols. Org Lett 2001; 3:2789-2792.
-
(2001)
Org Lett
, vol.3
, pp. 2789-2792
-
-
Paz, M.M.1
Tomasz, M.2
|