메뉴 건너뛰기




Volumn 16, Issue 10, 2009, Pages 1192-1213

Naphthalimides and azonafides as promising anti-cancer agents

Author keywords

[No Author keywords available]

Indexed keywords

6 ETHOXYAZONAFIDE; AMONAFIDE; AMP 53; ANTINEOPLASTIC AGENT; ARISTOLOCHIC ACID; AZAPHENANTHRENE DERIVATIVE; AZONAFIDE DERIVATIVE; BIBENOLINE; BISNAFIDE MESYLATE; CYCLOHEXIMIDE; DNA; DNA TOPOISOMERASE (ATP HYDROLYSING); DOXORUBICIN; ELINAFIDE; ETHONAFIDE; ETOPOSIDE; GLUTARIMIDE; IMIDAZONAPHTHALIMIDE DERIVATIVE; IMIDE; LU 79553; MITONAFIDE; NAPHTHALIMIDE DERIVATIVE; NAPHTHALMUSTINE; PHENANTHRENE DERIVATIVE; PLATINUM COMPLEX; TETRAHYDROAZONAFIDE DERIVATIVE; THIAZONAPHTHALIMIDE DERIVATIVE; TILORONE; UNBS 5162; UNCLASSIFIED DRUG; UNINDEXED DRUG; UREA DERIVATIVE;

EID: 65649135129     PISSN: 09298673     EISSN: None     Source Type: Journal    
DOI: 10.2174/092986709787846659     Document Type: Review
Times cited : (140)

References (92)
  • 1
    • 65649133789 scopus 로고
    • Butyramiden und verfahren zu dessen herstelling.
    • Patent DE2318136
    • Roldan, C. M.; Braña, M. F.; Berlanga, J. M. C. Butyramiden und verfahren zu dessen herstelling. Patent DE2318136, 1973.
    • (1973)
    • Roldan, C.M.1    Braña, M.F.2    Berlanga, J.M.C.3
  • 2
    • 65649145953 scopus 로고
    • Naphthalimides substitutes
    • Patent FR2279396
    • Roldan, C. M.; Braña, M. F.; Berlanga, J. M. C. Naphthalimides substitutes. Patent FR2279396, 1976.
    • (1976)
    • Roldan, C.M.1    Braña, M.F.2    Berlanga, J.M.C.3
  • 3
    • 0001116731 scopus 로고    scopus 로고
    • Naphthalimides as anticancer agents: Synthesis and biological activity
    • Braña, M. F.; Ramos, A. Naphthalimides as anticancer agents: synthesis and biological activity. Curr. Med. Chem. - Anti-Cancer Agents, 2001, 1, 237-255.
    • (2001) Curr. Med. Chem. - Anti-Cancer Agents , vol.1 , pp. 237-255
    • Braña, M.F.1    Ramos, A.2
  • 4
    • 65649115315 scopus 로고    scopus 로고
    • NCI database
    • NCI database: http://dtp.nci.nih.gov/.
  • 5
    • 0022179935 scopus 로고
    • N-(Aminoalkyl)imide antineo-plastic agents. Synthesis and biological activity
    • Zee-Cheng, R. K. Y.; Cheng, C. C. N-(Aminoalkyl)imide antineo-plastic agents. Synthesis and biological activity. J. Med. Chem., 1985, 28, 1216-1222.
    • (1985) J. Med. Chem , vol.28 , pp. 1216-1222
    • Zee-Cheng, R.K.Y.1    Cheng, C.C.2
  • 7
    • 0029080878 scopus 로고
    • Synthesis and cytostatic activity of enynes, enediynes and dienediynes linked to intercalators
    • Braña, M. F.; Morán, M.; Pérez de Vega, M. J.; Pita-Romero, I.; Walker, N. Synthesis and cytostatic activity of enynes, enediynes and dienediynes linked to intercalators. Tetrahedron, 1995, 51, 9127-9138.
    • (1995) Tetrahedron , vol.51 , pp. 9127-9138
    • Braña, M.F.1    Morán, M.2    Pérez de Vega, M.J.3    Pita-Romero, I.4    Walker, N.5
  • 9
    • 21744451160 scopus 로고    scopus 로고
    • Novel thiazonaphthalimides as efficient antitumor and DNA photocleaving agents: Effects of intercalation, side chains, and substituent groups
    • Li, Z.; Yang, G.; Qian, X. Novel thiazonaphthalimides as efficient antitumor and DNA photocleaving agents: Effects of intercalation, side chains, and substituent groups. Bioorg. Med. Chem., 2005, 13, 4864-4870.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 4864-4870
    • Li, Z.1    Yang, G.2    Qian, X.3
  • 10
    • 34249939072 scopus 로고    scopus 로고
    • Molecular design, chemical synthesis, and biological evaluation of '4-1' pentacyclic aryl/heteroaryl-imidazonaphthalimides
    • Li, F.; Cui, J.; Guo, L.; Qian, X.; Ren, W.; Wang, K.; Liu, F. Molecular design, chemical synthesis, and biological evaluation of '4-1' pentacyclic aryl/heteroaryl-imidazonaphthalimides. Bioorg. Med. Chem., 2007, 15, 5114-5121.
    • (2007) Bioorg. Med. Chem , vol.15 , pp. 5114-5121
    • Li, F.1    Cui, J.2    Guo, L.3    Qian, X.4    Ren, W.5    Wang, K.6    Liu, F.7
  • 11
    • 16244392102 scopus 로고    scopus 로고
    • Five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains: Intercalation and photocleavage to DNA
    • Xu, Y.; Qu, B.; Qian, X.; Li, Y. Five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains: Intercalation and photocleavage to DNA. Bioorg. Med. Chem. Lett., 2005, 15, 1139-1142.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 1139-1142
    • Xu, Y.1    Qu, B.2    Qian, X.3    Li, Y.4
  • 12
    • 1942502386 scopus 로고    scopus 로고
    • Highly-efficient DNA photocleavers with long wavelength absorptions: Thio-heterocyclic fused naphthalimides containing aminoalkyl side chains
    • Quian, X.; Li, Y.; Xu, Y.; Liu, Y.; Qu, B. Highly-efficient DNA photocleavers with long wavelength absorptions: Thio-heterocyclic fused naphthalimides containing aminoalkyl side chains. Bioorg. Med. Chem. Lett., 2004, 14, 2665-2668.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 2665-2668
    • Quian, X.1    Li, Y.2    Xu, Y.3    Liu, Y.4    Qu, B.5
  • 13
    • 33947595807 scopus 로고    scopus 로고
    • Novel N-oxides of naphthalimides as prodrug leads against hypoxic solid tumor: Synthesis and biological evaluation
    • Yin, H.; Xu, Y.; Qian, X.; Li, Y.; Liu, J. Novel N-oxides of naphthalimides as prodrug leads against hypoxic solid tumor: Synthesis and biological evaluation. Bioorg. Med. Chem. Lett., 2007, 17, 2166-2170.
    • (2007) Bioorg. Med. Chem. Lett , vol.17 , pp. 2166-2170
    • Yin, H.1    Xu, Y.2    Qian, X.3    Li, Y.4    Liu, J.5
  • 14
    • 0141670379 scopus 로고    scopus 로고
    • Evaluation of naphthalmustine, a nitrogen mustard derivative of naphthalimide as a rationally-designed anticancer agent
    • Pain, A.; Samanta, S.; Dutta, S.; Saxena, A. K.; Shanmugavel, M.; Kampasi, H.; Qazi, G. N.; Sanyal. U. Evaluation of naphthalmustine, a nitrogen mustard derivative of naphthalimide as a rationally-designed anticancer agent. J. Exp. Clin. Cancer Res., 2003, 22, 411-418.
    • (2003) J. Exp. Clin. Cancer Res , vol.22 , pp. 411-418
    • Pain, A.1    Samanta, S.2    Dutta, S.3    Saxena, A.K.4    Shanmugavel, M.5    Kampasi, H.6    Qazi, G.N.7    Sanyal, U.8
  • 16
    • 65649107140 scopus 로고    scopus 로고
    • Naphthalimide derivatives for the treatment of cancer
    • Patent EP1593672
    • Van Quaquebeke, E.; Simon, G.; Van Den Hove, L.; Kiss, R.; Darro, F. Naphthalimide derivatives for the treatment of cancer. Patent EP1593672, 2005.
    • (2005)
    • Van Quaquebeke, E.1    Simon, G.2    Van Den Hove, L.3    Kiss, R.4    Darro, F.5
  • 18
    • 65649104913 scopus 로고    scopus 로고
    • Van Quaquebeke, E.; Simon, G.; El Yazidi, M.; Van den Hove, L.; Darro, F.; Kiss, R. 5-urea substituted naphthalimide derivatives, methods of production and pharmaceutical compositions for treating cancer. Patent WO2007128538, 2007.
    • Van Quaquebeke, E.; Simon, G.; El Yazidi, M.; Van den Hove, L.; Darro, F.; Kiss, R. 5-urea substituted naphthalimide derivatives, methods of production and pharmaceutical compositions for treating cancer. Patent WO2007128538, 2007.
  • 20
    • 65649083965 scopus 로고
    • Basically substituted bis-naphthalimides and their production
    • Patent GB1069337
    • Bayer, A.G. Basically substituted bis-naphthalimides and their production. Patent GB1069337, 1967.
    • (1967)
    • Bayer, A.G.1
  • 21
    • 65649107941 scopus 로고
    • Ethynyl-substituted bis-naphthalimides
    • Patent US4151358
    • Arnold, F. E.; Hedberg, F. L. Ethynyl-substituted bis-naphthalimides. Patent US4151358, 1979.
    • (1979)
    • Arnold, F.E.1    Hedberg, F.L.2
  • 22
    • 65649137166 scopus 로고
    • Bis-naphthalimides, their preparation and use
    • Patent EP0281902
    • Braña, M. F.; Castellano, J. M.; Keilhauer, G.; Schlick, E. Bis-naphthalimides, their preparation and use. Patent EP0281902, 1988.
    • (1988)
    • Braña, M.F.1    Castellano, J.M.2    Keilhauer, G.3    Schlick, E.4
  • 27
    • 65649119533 scopus 로고
    • Bis-naphthalimides as anticancer agents
    • Patent US5086059
    • Patten, A. D.; Sun, J.-H, Ardecky, R. J. Bis-naphthalimides as anticancer agents. Patent US5086059, 1992.
    • (1992)
    • Patten, A.D.1    Sun, J.-H.2    Ardecky, R.J.3
  • 31
    • 65649120254 scopus 로고    scopus 로고
    • Sun, J.-H (The DuPont Merck Pharm. Co) Bis-naphthalimides containing amino-acid derived linkers as anticancer agents. Patents EP506008, EP 577753, JP 94506229, US5206249, WO9217453, 1992
    • Sun, J.-H (The DuPont Merck Pharm. Co) Bis-naphthalimides containing amino-acid derived linkers as anticancer agents. Patents EP506008, EP 577753, JP 94506229, US5206249, WO9217453, 1992.
  • 32
    • 0029945099 scopus 로고    scopus 로고
    • Casey; Robinson, P.; Robinson, K. A.; Castañoner, J. Bisnafide mesylate: Antineoplastic. Drugs Future, 1996, 21, 239-244.
    • Casey; Robinson, P.; Robinson, K. A.; Castañoner, J. Bisnafide mesylate: Antineoplastic. Drugs Future, 1996, 21, 239-244.
  • 33
    • 0027474538 scopus 로고
    • 2-substituted 1,2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones. A new class of antitumor agent
    • Sami, S. M.; Dorr, R. T.; Remers, W. A. 2-substituted 1,2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones. A new class of antitumor agent. J. Med. Chem., 1993, 36, 765-770.
    • (1993) J. Med. Chem , vol.36 , pp. 765-770
    • Sami, S.M.1    Dorr, R.T.2    Remers, W.A.3
  • 34
    • 0028965599 scopus 로고
    • Amino-substituted 2-[2'-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz [de,h]isoquinoline-1, 3-diones. Synthesis, antitumor activity, and quantitative structure - activity relationship
    • Sami, S. M.; Dorr, R. T.; Solyom, A. M.; Alberts, D. S.; Remers, W. A. Amino-substituted 2-[2'-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz [de,h]isoquinoline-1, 3-diones. Synthesis, antitumor activity, and quantitative structure - activity relationship. J. Med. Chem., 1995, 38, 983-993.
    • (1995) J. Med. Chem , vol.38 , pp. 983-993
    • Sami, S.M.1    Dorr, R.T.2    Solyom, A.M.3    Alberts, D.S.4    Remers, W.A.5
  • 35
    • 0029862703 scopus 로고    scopus 로고
    • 6- and 7-substituted 2-[2'-(dimethylamino) ethyl]-1,2-dihydro-3H-dibenz[de,h] isoquinoline-1,3-diones: Synthesis, nucleophilic displacements, antitumor activity, and quantitative structure-activity relationships
    • Sami, S. M.; Dorr, R. T.; Solyom A. M.; Alberts, D. S.; Iyengar B. S.; Remers, W. A. 6- and 7-substituted 2-[2'-(dimethylamino) ethyl]-1,2-dihydro-3H-dibenz[de,h] isoquinoline-1,3-diones: Synthesis, nucleophilic displacements, antitumor activity, and quantitative structure-activity relationships. J. Med. Chem., 1996, 39, 1609-1618.
    • (1996) J. Med. Chem , vol.39 , pp. 1609-1618
    • Sami, S.M.1    Dorr, R.T.2    Solyom, A.M.3    Alberts, D.S.4    Iyengar, B.S.5    Remers, W.A.6
  • 36
    • 0029753267 scopus 로고    scopus 로고
    • Sami, S. M.; Dorr, R. T.; Alberts, D. S.; Solyom A. M.; Remers, W. A. 2-[2'-(Dimethylamino)ethyl]-1,2-dihydro- 3H-dibenz[de,h] isoquinoline-1,3-diones with substituents at positions 4, 8, 9, 10, and 11. Synthesis, antitumor activity, and quantitative structure-activity relationships. J. Med. Chem., 1996, 39, 4978-4987.
    • Sami, S. M.; Dorr, R. T.; Alberts, D. S.; Solyom A. M.; Remers, W. A. 2-[2'-(Dimethylamino)ethyl]-1,2-dihydro- 3H-dibenz[de,h] isoquinoline-1,3-diones with substituents at positions 4, 8, 9, 10, and 11. Synthesis, antitumor activity, and quantitative structure-activity relationships. J. Med. Chem., 1996, 39, 4978-4987.
  • 37
  • 40
    • 39749089553 scopus 로고    scopus 로고
    • Chau, M.; Christensen, J. L.; Ajami, A. M; Capizzi, R. L. Amonafide, a topoisomerase II inhibitor, is unaffected by P-glycoprotein-mediated efflux. Leuk. Res., 2008, 32, 465-473.
    • Chau, M.; Christensen, J. L.; Ajami, A. M; Capizzi, R. L. Amonafide, a topoisomerase II inhibitor, is unaffected by P-glycoprotein-mediated efflux. Leuk. Res., 2008, 32, 465-473.
  • 43
    • 0035065265 scopus 로고    scopus 로고
    • Preclinical antitumor activity of the azonafide series of anthracene-based DNA intercalators
    • Dorr, R. T.; Liddil, J. D.; Sami, S. M.; Remers, W.; Hersh, E. M.; Alberts, D. S. Preclinical antitumor activity of the azonafide series of anthracene-based DNA intercalators. Anticancer Drugs, 2001, 12, 213-220.
    • (2001) Anticancer Drugs , vol.12 , pp. 213-220
    • Dorr, R.T.1    Liddil, J.D.2    Sami, S.M.3    Remers, W.4    Hersh, E.M.5    Alberts, D.S.6
  • 45
    • 34248578176 scopus 로고    scopus 로고
    • Ethonafide-induced cytotoxicity is mediated by topoisomerase II inhibition in prostate cancer cells
    • Pourpak, A.; Landowski, T. H.; Dorr, R. T. Ethonafide-induced cytotoxicity is mediated by topoisomerase II inhibition in prostate cancer cells. J. Pharmacol. Exp. Ther., 2007, 321, 1109-1117.
    • (2007) J. Pharmacol. Exp. Ther , vol.321 , pp. 1109-1117
    • Pourpak, A.1    Landowski, T.H.2    Dorr, R.T.3
  • 46
    • 0028123489 scopus 로고    scopus 로고
    • McRipley, R. J.; Burns-Horwitz, P. E.; Czerniak, P. M.; Diamond, R. J.; Diamond, M. A.; Miller, J. L.; Page, R. J.; Dexter, D. L.; Chen, S. F.; Sun,J. H.; Behrens, C. H.; Seitz, S. P.; Gross, J. L. Efficacy of DMP 840: A novel bis-naphthalimide cytotoxic agent with human solid tumor xenograft selectivity. Cancer Res., 1994, 54, 159-164.
    • McRipley, R. J.; Burns-Horwitz, P. E.; Czerniak, P. M.; Diamond, R. J.; Diamond, M. A.; Miller, J. L.; Page, R. J.; Dexter, D. L.; Chen, S. F.; Sun,J. H.; Behrens, C. H.; Seitz, S. P.; Gross, J. L. Efficacy of DMP 840: A novel bis-naphthalimide cytotoxic agent with human solid tumor xenograft selectivity. Cancer Res., 1994, 54, 159-164.
  • 47
    • 15844386050 scopus 로고
    • Magnitude and duration of anti-tumor response caused by DMP 840, a novel bis-naphthalimide anti-tumor agent, against human solid tumor xenografts in vivo
    • Abstract 2289
    • Czerniak, P.; McRipley, R.; Behrens, C. H.; et al. Magnitude and duration of anti-tumor response caused by DMP 840, a novel bis-naphthalimide anti-tumor agent, against human solid tumor xenografts in vivo. Proc. Amer. Assoc. Cancer Res., 1993, 34, Abstract 2289.
    • (1993) Proc. Amer. Assoc. Cancer Res , vol.34
    • Czerniak, P.1    McRipley, R.2    Behrens, C.H.3
  • 50
    • 15844368731 scopus 로고
    • Preclinical toxicity of the anticancer agent DMP 840 in mice, rats and dog
    • Abstract 2290
    • Arthaud, L.E; Springer, J. K. Preclinical toxicity of the anticancer agent DMP 840 in mice, rats and dog. Proc. Amer. Assoc. Cancer Res., 1993, 34, Abstract 2290.
    • (1993) Proc. Amer. Assoc. Cancer Res , vol.34
    • Arthaud, L.E.1    Springer, J.K.2
  • 51
    • 0028174984 scopus 로고
    • DNA topoisomerases: Essential enzymes and lethal targets
    • Chen, A. Y.; Liu, L.F. DNA topoisomerases: Essential enzymes and lethal targets. Annu. Rev. Pharmacol. Toxicol., 1994, 34, 191-218.
    • (1994) Annu. Rev. Pharmacol. Toxicol , vol.34 , pp. 191-218
    • Chen, A.Y.1    Liu, L.F.2
  • 52
    • 0036085460 scopus 로고    scopus 로고
    • Cellular roles of DNA topoisomerases: A molecular perspective
    • Wang, J. C. Cellular roles of DNA topoisomerases: A molecular perspective. Nat. Rev. Mol. Cell Biol., 2002, 3, 430-440.
    • (2002) Nat. Rev. Mol. Cell Biol , vol.3 , pp. 430-440
    • Wang, J.C.1
  • 53
    • 0024316466 scopus 로고
    • DNA topoisomerase poisons as antitumor drugs
    • Liu, L. F. DNA topoisomerase poisons as antitumor drugs. Annu. Rev. Biochem., 1989, 58, 351-375.
    • (1989) Annu. Rev. Biochem , vol.58 , pp. 351-375
    • Liu, L.F.1
  • 54
    • 0032189962 scopus 로고    scopus 로고
    • Catalytic inhibitors of DNA topoisomerase II
    • Andoh, T.; Ishida, R. Catalytic inhibitors of DNA topoisomerase II. Biochim. Biophys. Acta, 1998, 1400, 155-171.
    • (1998) Biochim. Biophys. Acta , vol.1400 , pp. 155-171
    • Andoh, T.1    Ishida, R.2
  • 55
    • 0024469320 scopus 로고
    • Topoisomerase II-mediated DNA cleavage by amonafide and its structural analogs
    • Hsiang, Y. H.; Jiang, J. B.; Liu, L. F. Topoisomerase II-mediated DNA cleavage by amonafide and its structural analogs. Mol. Pharmacol., 1989, 36, 371-376.
    • (1989) Mol. Pharmacol , vol.36 , pp. 371-376
    • Hsiang, Y.H.1    Jiang, J.B.2    Liu, L.F.3
  • 56
    • 0030123920 scopus 로고    scopus 로고
    • Computer simulation of the binding of amonafide and azonafide to DNA
    • Bear, S.; Remers, W. A. Computer simulation of the binding of amonafide and azonafide to DNA. J. Comput. Aided Mol. Des., 1996, 10, 165-175.
    • (1996) J. Comput. Aided Mol. Des , vol.10 , pp. 165-175
    • Bear, S.1    Remers, W.A.2
  • 57
    • 0035844288 scopus 로고    scopus 로고
    • Atp-bound topoisomerase II as a target for antitumor drugs
    • Wang, H.; Mao, Y.; Zhou, N.; Hu, T.; Hsieh, T. S; Liu, L. F. Atp-bound topoisomerase II as a target for antitumor drugs. J. Biol. Chem., 2001, 276, 15990-15995.
    • (2001) J. Biol. Chem , vol.276 , pp. 15990-15995
    • Wang, H.1    Mao, Y.2    Zhou, N.3    Hu, T.4    Hsieh, T.S.5    Liu, L.F.6
  • 58
    • 0030933706 scopus 로고    scopus 로고
    • In vitro cytotoxicity and DNA damage production in Chinese hamster ovary cells and topoisomerase II inhibition by 2-[2-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz[de,h] isoquinoline-1,3-diones with substitutions at the 6-and 7- positions (azonafides)
    • Mayr, C. A.; Sami, S. A.; Dorr, R. T. In vitro cytotoxicity and DNA damage production in Chinese hamster ovary cells and topoisomerase II inhibition by 2-[2-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz[de,h] isoquinoline-1,3-diones with substitutions at the 6-and 7- positions (azonafides). Anti-Cancer Drugs, 1997, 8, 245-256.
    • (1997) Anti-Cancer Drugs , vol.8 , pp. 245-256
    • Mayr, C.A.1    Sami, S.A.2    Dorr, R.T.3
  • 59
    • 0032478137 scopus 로고    scopus 로고
    • The bis(naphthalimide) DMP-840 causes cytotoxicity by its action against eukaryotic topoisomerase II
    • Nitiss, J. L.; Zhou, J.; Rose, A.; Hsiung, Y.; Gale, K. C.; Osheroff, N. The bis(naphthalimide) DMP-840 causes cytotoxicity by its action against eukaryotic topoisomerase II. Biochemistry, 1998, 37, 3078-3085.
    • (1998) Biochemistry , vol.37 , pp. 3078-3085
    • Nitiss, J.L.1    Zhou, J.2    Rose, A.3    Hsiung, Y.4    Gale, K.C.5    Osheroff, N.6
  • 60
    • 0033576252 scopus 로고    scopus 로고
    • Solution structure and dynamics of a complex between DNA and the antitumor bisnaphthalimide LU-79553: Intercalated ring flipping on the millisecond time scale
    • Gallego, J.; Reid, B. R. Solution structure and dynamics of a complex between DNA and the antitumor bisnaphthalimide LU-79553: Intercalated ring flipping on the millisecond time scale. Biochemistry, 1999, 38, 15104-15115.
    • (1999) Biochemistry , vol.38 , pp. 15104-15115
    • Gallego, J.1    Reid, B.R.2
  • 61
    • 0029797006 scopus 로고    scopus 로고
    • Sequence-selective intercalation of antitumour bis-naphthalimides into DNA. Evidence for an approach via the major groove
    • Bailly, C.; Braña, M.; Waring, M. J. Sequence-selective intercalation of antitumour bis-naphthalimides into DNA. Evidence for an approach via the major groove. Eur. J. Biochem., 1996, 240, 195-208.
    • (1996) Eur. J. Biochem , vol.240 , pp. 195-208
    • Bailly, C.1    Braña, M.2    Waring, M.J.3
  • 65
    • 0027234007 scopus 로고    scopus 로고
    • Chen, S. F.; Behrens, D. L; Behrens, C. H.; Czerniak, P.M.; Dexter, D. L.; Dusak, B. L.; Fredericks, J. R.; Gale, K. C.; Gross, J. L.; Jiang, J. B.; Kirshenbaum, M. R.; McRipley, R., J.; Papp, L. M.; Patten, A. D.; Perrella, F. W.; Seitz, S. P.; Stafford, M. P.; Sun, J. H.; Sun, T.; Wuonola, M. A.; Von Hoff, D. D. XB596, a promising bis-naphthalimide anti-cancer agent. Anticancer Drugs, 1993, 4, 447-457.
    • Chen, S. F.; Behrens, D. L; Behrens, C. H.; Czerniak, P.M.; Dexter, D. L.; Dusak, B. L.; Fredericks, J. R.; Gale, K. C.; Gross, J. L.; Jiang, J. B.; Kirshenbaum, M. R.; McRipley, R., J.; Papp, L. M.; Patten, A. D.; Perrella, F. W.; Seitz, S. P.; Stafford, M. P.; Sun, J. H.; Sun, T.; Wuonola, M. A.; Von Hoff, D. D. XB596, a promising bis-naphthalimide anti-cancer agent. Anticancer Drugs, 1993, 4, 447-457.
  • 66
    • 0035083626 scopus 로고    scopus 로고
    • Reactive oxygen-dependent production of novel photo-chemotherapeutic agents
    • Pervaiz, S. Reactive oxygen-dependent production of novel photo-chemotherapeutic agents. FASEB J., 2001, 15, 612-617.
    • (2001) FASEB J , vol.15 , pp. 612-617
    • Pervaiz, S.1
  • 67
    • 21144447742 scopus 로고    scopus 로고
    • Suzuki, K.; Nagasawa, H.; Uto, Y.; Sugimoto, Y.; Noguchi, K.; Wakida, M; Wierzba, K.; Terada, T.; Asao, T.; Yamada, Y.; Kitazato, K.; Hori, H. Naphthalimidobenzamide DB-51630: A novel DNA binding agent inducing p300 gene expression and exerting a potent anti-cancer activity. Bioorg, Med. Chem., 2005, 13, 4014-4021
    • Suzuki, K.; Nagasawa, H.; Uto, Y.; Sugimoto, Y.; Noguchi, K.; Wakida, M; Wierzba, K.; Terada, T.; Asao, T.; Yamada, Y.; Kitazato, K.; Hori, H. Naphthalimidobenzamide DB-51630: A novel DNA binding agent inducing p300 gene expression and exerting a potent anti-cancer activity. Bioorg, Med. Chem., 2005, 13, 4014-4021
  • 68
    • 0032928476 scopus 로고    scopus 로고
    • 4-Amino-1,8-naphthalimide: A novel inhibitor of poly(ADP-ribose) polymerase and radiation sensitizer
    • Schlicker, A.; Peschke, P.; Bürkle, A.; Hahn, E. W.; Kim, J. H. 4-Amino-1,8-naphthalimide: A novel inhibitor of poly(ADP-ribose) polymerase and radiation sensitizer. Int. J. Radiat. Biol., 1999, 75, 91-100.
    • (1999) Int. J. Radiat. Biol , vol.75 , pp. 91-100
    • Schlicker, A.1    Peschke, P.2    Bürkle, A.3    Hahn, E.W.4    Kim, J.H.5
  • 69
    • 33645469913 scopus 로고    scopus 로고
    • Radiosensitization by the poly(ADP-ribose) polymerase inhibitor 4-amino-1,8-naphthalimide is specific of the S phase of the cell cycle and involves arrest of DNA synthesis
    • Noël, G.; Godon, C.; Fernet, M.; Giocanti, N.; Mégnin-Chanet, F.; Favaudon, V. Radiosensitization by the poly(ADP-ribose) polymerase inhibitor 4-amino-1,8-naphthalimide is specific of the S phase of the cell cycle and involves arrest of DNA synthesis. Mol. Cancer Ther., 2006, 5, 564-574.
    • (2006) Mol. Cancer Ther , vol.5 , pp. 564-574
    • Noël, G.1    Godon, C.2    Fernet, M.3    Giocanti, N.4    Mégnin-Chanet, F.5    Favaudon, V.6
  • 71
    • 26444615468 scopus 로고    scopus 로고
    • Perinucleolar compartment and transformation
    • Kopp, K.; Huang, S. Perinucleolar compartment and transformation. J. Cell Biochem., 2005, 95, 217-225.
    • (2005) J. Cell Biochem , vol.95 , pp. 217-225
    • Kopp, K.1    Huang, S.2
  • 73
    • 50249088917 scopus 로고    scopus 로고
    • Perinucleolar compartment prevalence is a phenotypic pancancer marker of malignancy
    • Norton, J.T.; Pollock, C. B.; Wang, C.; Schink, J. C.; Kim, J. J.; Huang, S. Perinucleolar compartment prevalence is a phenotypic pancancer marker of malignancy. Cancer, 2008, 113, 861-869.
    • (2008) Cancer , vol.113 , pp. 861-869
    • Norton, J.T.1    Pollock, C.B.2    Wang, C.3    Schink, J.C.4    Kim, J.J.5    Huang, S.6
  • 78
    • 0029919926 scopus 로고    scopus 로고
    • Individualized dosing of amonafide based on a pharmacodynamic model incorporating acetylator phenotype and gender
    • Ratain, M. J.; Mick, R.; Janish, L.; Berezin, F.; Schilsky, R. L.; Vogelzang, N. J.; Kut, M. Individualized dosing of amonafide based on a pharmacodynamic model incorporating acetylator phenotype and gender. Pharmacogenetics, 1996, 6, 93-101.
    • (1996) Pharmacogenetics , vol.6 , pp. 93-101
    • Ratain, M.J.1    Mick, R.2    Janish, L.3    Berezin, F.4    Schilsky, R.L.5    Vogelzang, N.J.6    Kut, M.7
  • 79
    • 0028641646 scopus 로고
    • Phase I study of mitonafide with a 3-day administration schedule: Early interruption due to severe central nervous system toxicity
    • Díaz-Rubio, E.; Martín, M.; López-Vega, J. M.; Casado, A.; Benavides, A. Phase I study of mitonafide with a 3-day administration schedule: Early interruption due to severe central nervous system toxicity. Invest. New Drugs, 1994, 12, 277-281.
    • (1994) Invest. New Drugs , vol.12 , pp. 277-281
    • Díaz-Rubio, E.1    Martín, M.2    López-Vega, J.M.3    Casado, A.4    Benavides, A.5
  • 83
    • 0347926533 scopus 로고    scopus 로고
    • EORTC-ECSG phase I study. An EORTC-ECSG phase I study of LU 79553 administered every 21 or 42 days in patients with solid tumours
    • Awada, A.; Thödtmann, R.; Piccart, M. J.; Wanders, J.; Schrijvers, A. H.; Von Broen, I. M.; Hanauske, A. R. EORTC-ECSG phase I study. An EORTC-ECSG phase I study of LU 79553 administered every 21 or 42 days in patients with solid tumours. Eur. J. Cancer, 2003, 39, 742-747.
    • (2003) Eur. J. Cancer , vol.39 , pp. 742-747
    • Awada, A.1    Thödtmann, R.2    Piccart, M.J.3    Wanders, J.4    Schrijvers, A.H.5    Von Broen, I.M.6    Hanauske, A.R.7
  • 91
    • 0036223432 scopus 로고    scopus 로고
    • Evaluation of naphthal-NU, a 2-chloroethylnitrosourea derivative of naphthalimide, as a mixed-function anticancer agent
    • Samanta, S.; Pain, A.; Dutta, S.; Sanyal, U. Evaluation of naphthal-NU, a 2-chloroethylnitrosourea derivative of naphthalimide, as a mixed-function anticancer agent. J. Exp. Clin. Cancer Res., 2002, 21, 87-93.
    • (2002) J. Exp. Clin. Cancer Res , vol.21 , pp. 87-93
    • Samanta, S.1    Pain, A.2    Dutta, S.3    Sanyal, U.4
  • 92
    • 0031896592 scopus 로고    scopus 로고
    • There are no bad anticancer agents, only bad clinical trial designs - Twenty-first Richard and Hinda Rosenthal Foundation Award Lecture
    • Von Hoff, D. D. There are no bad anticancer agents, only bad clinical trial designs - Twenty-first Richard and Hinda Rosenthal Foundation Award Lecture. Clin. Cancer Res., 1998, 4, 1079-1086.
    • (1998) Clin. Cancer Res , vol.4 , pp. 1079-1086
    • Von Hoff, D.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.