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Volumn 44, Issue 1-2, 2011, Pages 158-163

Ferrocenyl Schiff base as novel antioxidant to protect DNA against the oxidation damage

Author keywords

Antioxidant; Ferrocene; Oxidation of DNA; Prooxidant; Schiff base

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; 2 (1 FERROCENYLETHYLIDENEAMINO)PHENOL; 2,2' AZINOBIS(3 ETHYLBENZOTHIAZOLINE 6 SULFONIC ACID); 2,2' AZOBIS(2 AMIDINOPROPANE); 3 (1 FERROCENYLETHYLIDENEAMINO)PHENOL; 4 (1 FERROCENYLETHYLIDENEAMINO)PHENOL; ANTIOXIDANT; COPPER ION; FERROCENYL SCHIFF BASE; GLUTATHIONE; HYDROXYL RADICAL; SCHIFF BASE; UNCLASSIFIED DRUG;

EID: 80052036317     PISSN: 09280987     EISSN: 18790720     Source Type: Journal    
DOI: 10.1016/j.ejps.2011.07.001     Document Type: Conference Paper
Times cited : (41)

References (33)
  • 1
    • 34250807671 scopus 로고    scopus 로고
    • Synthesis and physico-analytical studies of some novel ferrocenyl Schiff base derivatives
    • DOI 10.1016/j.jorganchem.2007.03.034, PII S0022328X07002008
    • Z. Akhter, A. Nigar, M.Y. Razzaq, and H.M. Siddiqi Synthesis and physico-analytical studies of some novel ferrocenyl Schiff base derivatives J. Organomet. Chem. 692 2007 3542 3546 (Pubitemid 46976931)
    • (2007) Journal of Organometallic Chemistry , vol.692 , Issue.16 , pp. 3542-3546
    • Akhter, Z.1    Nigar, A.2    Razzaq, M.Y.3    Siddiqi, H.M.4
  • 3
    • 34548120539 scopus 로고    scopus 로고
    • Metallocene-based antimalarials: An exploration into the influence of the ferrocenyl moiety on in vitro antimalarial activity in chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum
    • DOI 10.1016/j.bmc.2007.07.012, PII S0968089607006281
    • M.A.L. Blackie, P. Beagley, S.L. Croft, H. Kendrick, J.R. Mossa, and K. Chibale Metallocene-based antimalarials: an exploration into the influence of the ferrocenyl moiety on in vitro antimalarial activity in chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum Bioorg. Med. Chem. 15 2007 6510 6516 (Pubitemid 47302316)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.20 , pp. 6510-6516
    • Blackie, M.A.L.1    Beagley, P.2    Croft, S.L.3    Kendrick, H.4    Moss, J.R.5    Chibale, K.6
  • 4
    • 0027213625 scopus 로고
    • Tocopherol-mediated peroxidation. The prooxidant effect of vitamin E on the radical-initiated oxidation of human low-density lipoprotein
    • V.W. Bowry, and R. Stocker Tocopherol-mediated peroxidation: the prooxidation effect of vitamin E on the radical-initiated oxidation of human low-density lipoprotein J. Am. Chem. Soc. 115 1993 6029 6044 (Pubitemid 23278118)
    • (1993) Journal of the American Chemical Society , vol.115 , Issue.14 , pp. 6029-6044
    • Bowry, V.W.1    Stocker, R.2
  • 7
    • 65449142517 scopus 로고    scopus 로고
    • Photoinduced DNA and protein cleavage activity of ferrocene-appended l-methionine reduced Schiff base copper(II) complexes of phenanthroline bases
    • T.K. Goswami, M. Roy, M. Nethaji, and A.R. Chakravarty Photoinduced DNA and protein cleavage activity of ferrocene-appended l-methionine reduced Schiff base copper(II) complexes of phenanthroline bases Organometallics 28 2009 1992 1994
    • (2009) Organometallics , vol.28 , pp. 1992-1994
    • Goswami, T.K.1    Roy, M.2    Nethaji, M.3    Chakravarty, A.R.4
  • 8
    • 59249102083 scopus 로고    scopus 로고
    • The wanderings of a free radical
    • B. Halliwell The wanderings of a free radical Free Radical Biol. Med. 46 2009 531 542
    • (2009) Free Radical Biol. Med. , vol.46 , pp. 531-542
    • Halliwell, B.1
  • 9
    • 70449555098 scopus 로고    scopus 로고
    • Ferrocenyl quinone methides as strong antiproliferative agents: Formation by metabolic and chemical oxidation of ferrocenyl phenols
    • D. Hamels, P.M. Dansette, E.A. Hillard, S. Top, A. Vessiéres, P. Herson, G. Jaouen, and D. Mansuy Ferrocenyl quinone methides as strong antiproliferative agents: formation by metabolic and chemical oxidation of ferrocenyl phenols Angew. Chem. Int. Ed. 48 2009 9124 9126
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9124-9126
    • Hamels, D.1    Dansette, P.M.2    Hillard, E.A.3    Top, S.4    Vessiéres, A.5    Herson, P.6    Jaouen, G.7    Mansuy, D.8
  • 10
    • 33646790053 scopus 로고    scopus 로고
    • Ferrocene-mediated proton-coupled electron transfer in a series of ferrocifen-type breast-cancer drug candidates
    • E. Hillard, A. Vessiéres, L. Thouin, G. Jaouen, and C. Amatore Ferrocene-mediated proton-coupled electron transfer in a series of ferrocifen-type breast-cancer drug candidates Angew. Chem. 118 2006 291 296
    • (2006) Angew. Chem. , vol.118 , pp. 291-296
    • Hillard, E.1    Vessiéres, A.2    Thouin, L.3    Jaouen, G.4    Amatore, C.5
  • 11
    • 35548950864 scopus 로고    scopus 로고
    • The influence of phenolic hydroxy substitution on the electron transfer and anti-cancer properties of compounds based on the 2-ferrocenyl-1-phenyl-but- 1- ene motif
    • DOI 10.1039/b705030e
    • E.A. Hillard, P. Pigeon, A. Vessires, C. Amatore, and G. Jaouen The influence of phenolic hydroxy substitution on the electron transfer and anti-cancer properties of compounds based on the 2-ferrocenyl-1-phenyl-but-1-ene motif Dalton Trans. 2007 5073 5081 (Pubitemid 350015429)
    • (2007) Dalton Transactions , Issue.43 , pp. 5073-5081
    • Hillard, E.A.1    Pigeon, P.2    Vessieres, A.3    Amatore, C.4    Jaouen, G.5
  • 13
    • 0022429763 scopus 로고
    • Malondialdehyde precursors in gamma-irradiated DNA, deoxynucleotides and deoxynucleosides
    • M.F. Janicek, W.A. Haseltine, and W.D. Henner Malondialdehyde precursors in gamma-irradiated DNA, deoxynucleotides and deoxynucleosides Nucleic Acids Res. 13 1985 9011 9029
    • (1985) Nucleic Acids Res. , vol.13 , pp. 9011-9029
    • Janicek, M.F.1    Haseltine, W.A.2    Henner, W.D.3
  • 14
    • 70449520200 scopus 로고    scopus 로고
    • Oxidative risk for atherothrombotic cardiovascular disease
    • J.A. Leopold, and J. Loscalzo Oxidative risk for atherothrombotic cardiovascular disease Free Radical Biol. Med. 47 2009 1673 1706
    • (2009) Free Radical Biol. Med. , vol.47 , pp. 1673-1706
    • Leopold, J.A.1    Loscalzo, J.2
  • 15
    • 70449674891 scopus 로고    scopus 로고
    • Captopril and 6-mercaptopurine: Whose SH possesses higher antioxidant ability?
    • G.-X. Li, and Z.-Q. Liu Captopril and 6-mercaptopurine: whose SH possesses higher antioxidant ability? Eur. J. Med. Chem. 44 2009 4841 4847
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 4841-4847
    • Li, G.-X.1    Liu, Z.-Q.2
  • 16
    • 77950646263 scopus 로고    scopus 로고
    • Properties of synthetic homoisoflavonoids to reduce oxidants and to protect linoleic acid and DNA against oxidations
    • Y.-F. Li, Z.-Q. Liu, and X.-Y. Luo Properties of synthetic homoisoflavonoids to reduce oxidants and to protect linoleic acid and DNA against oxidations J. Agric. Food Chem. 58 2010 4126 4131
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 4126-4131
    • Li, Y.-F.1    Liu, Z.-Q.2    Luo, X.-Y.3
  • 17
    • 65949106342 scopus 로고    scopus 로고
    • How many peroxyl radicals can be scavenged by hydroxyl-substituted Schiff bases in the oxidation of linoleic acid?
    • Z.-Q. Liu, and D. Wu How many peroxyl radicals can be scavenged by hydroxyl-substituted Schiff bases in the oxidation of linoleic acid? J. Phys. Org. Chem. 22 2009 308 312
    • (2009) J. Phys. Org. Chem. , vol.22 , pp. 308-312
    • Liu, Z.-Q.1    Wu, D.2
  • 19
    • 65649152371 scopus 로고    scopus 로고
    • Synthesis and biological evaluations of some Schiff-base esters of ferrocenyl aniline and simple aniline
    • H. Nawaz, Z. Akhter, S. Yameen, H.M. Siddiq, B. Mirza, and A. Rifat Synthesis and biological evaluations of some Schiff-base esters of ferrocenyl aniline and simple aniline J. Organomet. Chem. 694 2009 2198 2203
    • (2009) J. Organomet. Chem. , vol.694 , pp. 2198-2203
    • Nawaz, H.1    Akhter, Z.2    Yameen, S.3    Siddiq, H.M.4    Mirza, B.5    Rifat, A.6
  • 20
    • 63249102554 scopus 로고    scopus 로고
    • Evaluation of new thiadiazoles and benzothiazoles as potential radioprotectors: Free radical scavenging activity in vitro and theoretical studies (QSAR, DFT)
    • C. Prouillac, P. Vicendo, J.-C. Garrigues, R. Poteau, and G. Rima Evaluation of new thiadiazoles and benzothiazoles as potential radioprotectors: free radical scavenging activity in vitro and theoretical studies (QSAR, DFT) Free Radical Biol. Med. 46 2009 1139 1148
    • (2009) Free Radical Biol. Med. , vol.46 , pp. 1139-1148
    • Prouillac, C.1    Vicendo, P.2    Garrigues, J.-C.3    Poteau, R.4    Rima, G.5
  • 21
    • 0028024324 scopus 로고
    • Interaction between glutathione and Cu(II) in the vicinity of nucleic acids
    • W.A. Prutz Interaction between glutathione and Cu(II) in the vicinity of nucleic acids Biochem. J. 302 1994 373 382 (Pubitemid 24280087)
    • (1994) Biochemical Journal , vol.302 , Issue.2 , pp. 373-382
    • Prutz, W.A.1
  • 22
    • 0032982508 scopus 로고    scopus 로고
    • Antioxidant activity applying an improved ABTS radical cation decolorization assay
    • DOI 10.1016/S0891-5849(98)00315-3, PII S0891584998003153
    • R. Re, N. Pellegrini, A. Proteggente, A. Pannala, M. Yang, and C. Rice-Evans Antioxidant activity applying an improved ABTS radical cation decolorization assay Free Radical Biol. Med. 26 1999 1231 1237 (Pubitemid 29262709)
    • (1999) Free Radical Biology and Medicine , vol.26 , Issue.9-10 , pp. 1231-1237
    • Re, R.1    Pellegrini, N.2    Proteggente, A.3    Pannala, A.4    Yang, M.5    Rice-Evans, C.6
  • 23
    • 0025755263 scopus 로고
    • Chemical cleavage of plasmid DNA by glutathione in the presence of Cu(II) ions. The Cu(II)-thiol system for DNA strand scission
    • C.J. Reed, and K.T. Douglas Chemical cleavage of plasmid DNA by glutathione in the presence of Cu(II) ions. The Cu(II)-thiol system for DNA strand scission Biochem. J. 275 1991 601 608
    • (1991) Biochem. J. , vol.275 , pp. 601-608
    • Reed, C.J.1    Douglas, K.T.2
  • 25
    • 40649106476 scopus 로고    scopus 로고
    • Quantitative structure - Activity relationship of hydroxyl-substituent Schiff bases in radical-induced hemolysis of human erythrocytes
    • DOI 10.1002/cbf.1426
    • Y.-Z. Tang, and Z.-Q. Liu Quantitative structure-activity relationship of hydroxyl-substituent Schiff bases in radical-induced hemolysis of human erythrocytes Cell Biochem. Funct. 26 2008 185 191 (Pubitemid 351373965)
    • (2008) Cell Biochemistry and Function , vol.26 , Issue.2 , pp. 185-191
    • Tang, Y.-Z.1    Liu, Z.-Q.2
  • 26
    • 11144333768 scopus 로고    scopus 로고
    • Bioorganometallic chemistry of ferrocene
    • DOI 10.1021/cr0101510
    • D.R. van Staveren, and N. Metzler-Nolte Bioorganometallic chemistry of ferrocene Chem. Rev. 104 2004 5931 5985 (Pubitemid 40034049)
    • (2004) Chemical Reviews , vol.104 , Issue.12 , pp. 5931-5985
    • Van Staveren, D.R.1    Metzler-Nolte, N.2
  • 27
    • 77950690724 scopus 로고    scopus 로고
    • A ferrocenyl derivative of hydroxytamoxifen elicits an estrogen receptor-independent mechanism of action in breast cancer cell lines
    • A. Vessires, C. Corbet, J.M. Heldt, N. Lories, N. Jouy, I. Laïos, G. Leclercq, G. Jaouen, and R.-A. Toillon A ferrocenyl derivative of hydroxytamoxifen elicits an estrogen receptor-independent mechanism of action in breast cancer cell lines J. Inorg. Biochem. 104 2010 503 511
    • (2010) J. Inorg. Biochem. , vol.104 , pp. 503-511
    • Vessires, A.1    Corbet, C.2    Heldt, J.M.3    Lories, N.4    Jouy, N.5    Laïos, I.6    Leclercq, G.7    Jaouen, G.8    Toillon, R.-A.9
  • 28
    • 16644381761 scopus 로고    scopus 로고
    • A continuous spectrophotometric assay for NADPH-cytochrome P450 reductase activity using 1,1-diphenyl-2-picrylhydrazyl
    • S.-K. Yim, S.-J. Yun, and C.-H. Yun A continuous spectrophotometric assay for NADPH-cytochrome P450 reductase activity using 1,1-diphenyl-2- picrylhydrazyl J. Biochem. Mol. Biol. 37 2004 629 633 (Pubitemid 43160264)
    • (2004) Journal of Biochemistry and Molecular Biology , vol.37 , Issue.5 , pp. 629-633
    • Yim, S.-K.1    Yun, S.-J.2    Yun, C.-H.3
  • 29
    • 34248588757 scopus 로고    scopus 로고
    • A method to evaluate capacity and efficiency of water soluble antioxidants as peroxyl radical scavengers
    • DOI 10.1016/j.abb.2007.03.017, PII S0003986107001245
    • L. Zennaro, M. Rossetto, P. Vanzani, V.D. Marco, M. Scarpa, L. Battistin, and A. Rigo A method to evaluate capacity and efficiency of water soluble antioxidants as peroxyl radical scavengers Arch. Biochem. Biophys. 462 2007 38 46 (Pubitemid 46755136)
    • (2007) Archives of Biochemistry and Biophysics , vol.462 , Issue.1 , pp. 38-46
    • Zennaro, L.1    Rossetto, M.2    Vanzani, P.3    De Marco, V.4    Scarpa, M.5    Battistin, L.6    Rigo, A.7
  • 30
    • 0035087948 scopus 로고    scopus 로고
    • DNA strand breakage and oxygen tension: Effects of β-carotene, α-tocopherol and ascorbic acid
    • DOI 10.1016/S0278-6915(00)00131-9, PII S0278691500001319
    • P. Zhang, and S.T. Omaye DNA strand breakage and oxygen tension: effects of β-carotene, α-tocopherol and ascorbic acid Food Chem. Toxicol. 39 2001 239 246 (Pubitemid 32244131)
    • (2001) Food and Chemical Toxicology , vol.39 , Issue.3 , pp. 239-246
    • Zhang, P.1    Omaye, S.T.2
  • 31
    • 68949219463 scopus 로고    scopus 로고
    • The protective effect of hydroxyl-substituted Schiff bases on the radical-induced oxidation of DNA
    • F. Zhao, and Z.-Q. Liu The protective effect of hydroxyl-substituted Schiff bases on the radical-induced oxidation of DNA J. Phys. Org. Chem. 22 2009 791 798
    • (2009) J. Phys. Org. Chem. , vol.22 , pp. 791-798
    • Zhao, F.1    Liu, Z.-Q.2
  • 32
    • 36849028123 scopus 로고    scopus 로고
    • Prooxidant activity of hydroxycinnamic acids on DNA damage in the presence of Cu(II) ions: Mechanism and structure-activity relationship
    • DOI 10.1016/j.fct.2007.07.010, PII S027869150700258X
    • L.-F. Zheng, F. Dai, B. Zhou, L. Yang, and Z.-L. Liu Prooxidant activity of hydroxycinnamic acids on DNA damage in the presence of Cu(II) ions: mechanism and structure-activity relationship Food Chem. Toxicol. 46 2008 149 156 (Pubitemid 350235761)
    • (2008) Food and Chemical Toxicology , vol.46 , Issue.1 , pp. 149-156
    • Zheng, L.-F.1    Dai, F.2    Zhou, B.3    Yang, L.4    Liu, Z.-L.5
  • 33
    • 0034696796 scopus 로고    scopus 로고
    • Evidence for production of hydroxyl radicals by pentachlorophenol metabolites and hydrogen peroxide: A metal-independent organic Fenton reaction
    • DOI 10.1006/bbrc.2000.2539
    • B.-Z. Zhu, N. Kitrossky, and M. Chevion Evidence for production of hydroxyl radicals by pentachlorophenol metabolites and hydrogen peroxide: a metal-independent organic Fenton reaction Biochem. Biophys. Res. Commun. 270 2000 942 946 (Pubitemid 30444811)
    • (2000) Biochemical and Biophysical Research Communications , vol.270 , Issue.3 , pp. 942-946
    • Zhu, B.-Z.1    Kitrossky, N.2    Chevion, M.3


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