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Volumn 13, Issue 3, 2013, Pages 365-372

Recent studies of antioxidant quinoline derivatives

Author keywords

Antioxidant activity; Free radical; Oxidative stress; Quinoline

Indexed keywords

PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE; QUINOLINE DERIVATIVE; REACTIVE OXYGEN METABOLITE; THIOSEMICARBAZONE;

EID: 84876852029     PISSN: 13895575     EISSN: 18755607     Source Type: Journal    
DOI: 10.2174/1389557511313030005     Document Type: Article
Times cited : (100)

References (79)
  • 1
    • 84876885259 scopus 로고
    • Quinoline
    • Runge, F. Quinoline. Pogg. Ann., 1834, p. 68-72.
    • (1834) Pogg. Ann , pp. 68-72
    • Runge, F.1
  • 2
    • 55949127978 scopus 로고    scopus 로고
    • Convergent, regiospecific synthesis of quinolines from o-aminophenylboronates
    • Horn, J.; Marsden, S. P.; Nelson, A.; House, D.; Weingarten, G. G. Convergent, regiospecific synthesis of quinolines from o-aminophenylboronates. Org. Lett., 2008, 10, 4117-20.
    • (2008) Org. Lett , vol.10 , pp. 4117-4120
    • Horn, J.1    Marsden, S.P.2    Nelson, A.3    House, D.4    Weingarten, G.G.5
  • 4
    • 0030235033 scopus 로고    scopus 로고
    • Isolation characterization, and substrate utilization of a quinoline degrading bacterium
    • O'Loughlin, E.J.; Kehrmeyer, S.R. and Sims. G.K. Isolation, characterization, and substrate utilization of a quinoline degrading bacterium. Int. Biodeter. Biodeg., 1996, 38(2), 107-118.
    • (1996) Int. Biodeter. Biodeg , vol.38 , Issue.2 , pp. 107-118
    • O'Loughlin, E.J.1    Kehrmeyer, S.R.2    Sims, G.K.3
  • 6
    • 0033694467 scopus 로고    scopus 로고
    • 1,8-naphthyridines IV. 9-substituted. N,N-dialkyl-5-(alkylamino or cycloalkyl amino) [1,2,4] triazolo [4,3-a] [1,8] naphthyridine -6-carboxamides, new compounds with antiaggressive and potent anti-inflammatory activities
    • Roma, G.; Braccio, M.D.; Grossi, G.; Mattioli, F.; Ghia, M. 1,8-naphthyridines IV. 9-substituted. N,N-dialkyl-5-(alkylamino or cycloalkyl amino) [1,2,4] triazolo [4,3-a] [1,8] naphthyridine -6-carboxamides, new compounds with antiaggressive and potent anti-inflammatory activities. Eur. J. Med. Chem., 2000, 35, 1021-1035.
    • (2000) Eur. J. Med. Chem , vol.35 , pp. 1021-1035
    • Roma, G.1    Braccio, M.D.2    Grossi, G.3    Mattioli, F.4    Ghia, M.5
  • 7
    • 0035811449 scopus 로고    scopus 로고
    • Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives
    • Chen, Y.L.; Fang, K.C.; Sheu, J.Y.; Hsu, S.L.; Tzeng C.C. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives. J. Med. Chem., 2001, 44, 2374-2377.
    • (2001) J. Med. Chem , vol.44 , pp. 2374-2377
    • Chen, Y.L.1    Fang, K.C.2    Sheu, J.Y.3    Hsu, S.L.4    Tzeng, C.C.5
  • 9
    • 77949908330 scopus 로고    scopus 로고
    • Biological activities of quinoline derivatives
    • Kumar, S.; Bawa, S.; Gupta, H. Biological activities of quinoline derivatives. Mini Rev Med Chem., 2009, 9(14), 1648-1654.
    • (2009) Mini Rev Med Chem , vol.9 , Issue.14 , pp. 1648-1654
    • Kumar, S.1    Bawa, S.2    Gupta, H.3
  • 10
    • 0041589305 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory evaluation of 9-phenoxyacridine and 4-phenoxyfour [2,3-b] quinoline derivaties Part-2
    • Chen, Y.; Chen, I.; Lu, C; Tzeng, C; Tsao, L. and Wang, J. Synthesis and anti-inflammatory evaluation of 9-phenoxyacridine and 4-phenoxyfour [2,3-b] quinoline derivaties Part-2. Bioorg. Med. Chem., 2003, 11, 3921-3927.
    • (2003) Bioorg. Med. Chem , vol.11 , pp. 3921-3927
    • Chen, Y.1    Chen, I.2    Lu, C.3    Tzeng, C.4    Tsao, L.5    Wang, J.6
  • 11
    • 0037140882 scopus 로고    scopus 로고
    • Synthesis and evaluation of new antimalarial analogues of quinoline alkaloids derived from Cinchona ledgerianamoens extrimen
    • Park B.; Kim D.; Rosenthal PJ.; Huh S.; Lee BJ.; Park E. Synthesis and evaluation of new antimalarial analogues of quinoline alkaloids derived from Cinchona ledgerianamoens extrimen. Bioorg. Med. Chem. Lett., 2002, 12, 1351-1355.
    • (2002) Bioorg. Med. Chem. Lett , vol.12 , pp. 1351-1355
    • Park, B.1    Kim, D.2    Rosenthal, P.J.3    Huh, S.4    Lee, B.J.5    Park, E.6
  • 12
    • 84955807304 scopus 로고
    • Synthesis of some new quinoline derivatives-potential antimalarial drugs
    • Vlabhov, R.; Parushev, S.; Vlahov, J.; Nickel, P.; Snatzke, G. Synthesis of some new quinoline derivatives-potential antimalarial drugs. Pure Appl. Chem., 1990, 62(7), 1303-1306.
    • (1990) Pure Appl. Chem , vol.62 , Issue.7 , pp. 1303-1306
    • Vlabhov, R.1    Parushev, S.2    Vlahov, J.3    Nickel, P.4    Snatzke, G.5
  • 13
    • 0021324432 scopus 로고
    • 2-Acetylpyridine Thiosemicarbazones, 8, Derivatives of 1-Acetylisoquinoline as Potential Antimalarial Agents
    • Klayman, DL. and Scovill, JP. 2-Acetylpyridine Thiosemicarbazones, 8, Derivatives of 1-Acetylisoquinoline as Potential Antimalarial Agents. J. Med. Chem., 1984, 27, 84-87.
    • (1984) J. Med. Chem , vol.27 , pp. 84-87
    • Klayman, D.L.1    Scovill, J.P.2
  • 14
    • 3042588256 scopus 로고    scopus 로고
    • DNA binding to guide the development of tetrahydroindeno[1,2-b] pyrido[4,3,2-de] quinoline derivatives as cytotoxic agents
    • Catoen-Chackal, Facompre M., Houssin, R.; Pommery, N.; Goossens, J.; Colson, P. et al. DNA binding to guide the development of tetrahydroindeno[1,2-b] pyrido[4,3,2-de] quinoline derivatives as cytotoxic agents. J. Med. Chem., 2004, 47, 3665-3673.
    • (2004) J. Med. Chem , vol.47 , pp. 3665-3673
    • Catoen-Chackal, F.M.1    Houssin, R.2    Pommery, N.3    Goossens, J.4    Colson, P.5
  • 15
    • 0017334150 scopus 로고    scopus 로고
    • Elucidation of the structure of the antineoplastic agents, 2-formylpyridine and 1-formylisoquinoline thiosemicarbazones
    • Antonini, L.; Claudi, F.; Franchetti, P.; Grifantini, M. and Martelli, S. Elucidation of the structure of the antineoplastic agents, 2-formylpyridine and 1-formylisoquinoline thiosemicarbazones. J. Med. Chem., 1997, 20(3), 447-449.
    • (1997) J. Med. Chem , vol.20 , Issue.3 , pp. 447-449
    • Antonini, L.1    Claudi, F.2    Franchetti, P.3    Grifantini, M.4    Martelli, S.5
  • 17
    • 76149127743 scopus 로고    scopus 로고
    • Antioxidant potential study of some synthesized N-heterocycles
    • Hossain, MM.; Shaha, SK. and Aziz, F. Antioxidant potential study of some synthesized N-heterocycles. Bangladesh Med Res Counc. Bull., 2009, 35, 49-52.
    • (2009) Bangladesh Med Res Counc. Bull , vol.35 , pp. 49-52
    • Hossain, M.M.1    Shaha, S.K.2    Aziz, F.3
  • 18
    • 0036009867 scopus 로고    scopus 로고
    • Synthesis of a novel quinoline derivative, 2-(2- methylquinolin-4-ylamino)-N-phenylacetamide-A potential antileishmanial agent
    • Sahu, NP.; Pal, C; Mandal, NB.; Banerjee, S.; Raha, M.; Kundu, AP. et al. Synthesis of a novel quinoline derivative, 2-(2- methylquinolin-4-ylamino)-N-phenylacetamide-A potential antileishmanial agent. Bioorg Med Chem 2002; 10: 1687-1693.
    • (2002) Bioorg Med Chem , vol.10 , pp. 1687-1693
    • Sahu, N.P.1    Pal, C.2    Mandal, N.B.3    Banerjee, S.4    Raha, M.5    Kundu, A.P.6
  • 20
    • 25144491192 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of 7-alkoxyl-4,5-dihydro-[1,2,4]triazolo [4,3-a]quinolines
    • Zie, Z.; Chai, K.; Piao, H.; Kwak, K. and Quan, Z. Synthesis and anticonvulsant activity of 7-alkoxyl-4,5-dihydro-[1,2,4]triazolo [4,3-a]quinolines. Bioorg. Med. Chem. Lett., 2005, 15, 4803-05.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 4803-4805
    • Zie, Z.1    Chai, K.2    Piao, H.3    Kwak, K.4    Quan, Z.5
  • 21
    • 84876886661 scopus 로고    scopus 로고
    • Synthesis, antimicrobial activities and cytogenetic studies of newer diazepino quinoline derivatives via vilsmeier-Haack reaction
    • Nandhakumar, R.; Suresh; Calistus Judge, AL.; Rajesh Kannan, V.; Mohan, PS. Synthesis, antimicrobial activities and cytogenetic studies of newer diazepino quinoline derivatives via vilsmeier-Haack reaction. Eur. J. Med. Chem., 2007, XX, 1-9.
    • (2007) Eur. J. Med. Chem , vol.20 , pp. 1-9
    • Nandhakumar, R.1    Suresh2    Calistus, J.A.L.3    Rajesh, K.V.4    Mohan, P.S.5
  • 22
    • 58149374012 scopus 로고    scopus 로고
    • Heterocycles[h]-Fused onto 4-oxoxquinoline-3-carbaoxylic acid'part VIII [1]. Convenient synthesis and antimicrobial properties of substituted hexahydro [1,4]diazepino[2,3-h]quinoline-9-carboxylic acid and its tetrahydrquino[7,8-b]benzodiazepine analog
    • Al-Hiari, YM.; Abu-dahab, R. and El- Abadelah, ME. Heterocycles[h]-Fused onto 4-oxoxquinoline-3-carbaoxylic acid'part VIII [1]. Convenient synthesis and antimicrobial properties of substituted hexahydro [1,4]diazepino[2,3-h]quinoline-9-carboxylic acid and its tetrahydrquino[7,8-b]benzodiazepine analog. Molecules, 2008, 13, 2880-2893.
    • (2008) Molecules , vol.13 , pp. 2880-2893
    • Al-Hiari, Y.M.1    Abu-Dahab, R.2    El-abadelah, M.E.3
  • 25
    • 0028243048 scopus 로고
    • A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives
    • Maguire, M.P.; Sheets, K.R.; McVety, K.; Spada, A.P.; Zilberstein, A. A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives. J. Med. Chem., 1994, 37, 2129-2141.
    • (1994) J. Med. Chem , vol.37 , pp. 2129-2141
    • Maguire, M.P.1    Sheets, K.R.2    McVety, K.3    Spada, A.P.4    Zilberstein, A.5
  • 26
    • 0034942474 scopus 로고    scopus 로고
    • Novel pyrrolo[3,2-f]quinolines:Synthesis and antiproliferative activity
    • Palumbo, M.; Ferlin, MG.; Gatto, B. and Chiarelotto, G. Novel pyrrolo[3,2-f]quinolines:synthesis and antiproliferative activity. Bioorg. Med. Chem., 2001, 9, 1843-1848.
    • (2001) Bioorg. Med. Chem , vol.9 , pp. 1843-1848
    • Palumbo, M.1    Ferlin, M.G.2    Gatto, B.3    Chiarelotto, G.4
  • 27
    • 11144356237 scopus 로고    scopus 로고
    • Linkermodified quinoline derivatives targeting HIV-1 integrase: Synthesis and biological activity
    • Benard, C.; Zouhiri, F.; Normand-Bayle, N.; Danet, M.; Desmaele, D.; Leh, H. et al. Linkermodified quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity. Bioorg. Med. Chem. Lett., 2004, 14, 2473-76.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 2473-2476
    • Benard, C.1    Zouhiri, F.2    Normand-Bayle, N.3    Danet, M.4    Desmaele, D.5    Leh, H.6
  • 28
    • 78449295900 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and antioxidant evaluation of quinolines and bis(indolyl)methanes
    • Praveen, C.; DheenKumar, P.; Muralidharan, D.; Perumal, P. T. Synthesis, antimicrobial and antioxidant evaluation of quinolines and bis(indolyl)methanes. Bioorg. Med. Chem. Lett., 2010, 20, 7292-7296.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , pp. 7292-7296
    • Praveen, C.1    Dheenkumar, P.2    Muralidharan, D.3    Perumal, P.T.4
  • 29
    • 70349678844 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial activity of some substituted N'-arylidene-2-(quinolin-8-yloxy) aceto hydrazides
    • Mohammed, IA.; Subrahmanyam, E.V.S. Synthesis, characterization and antimicrobial activity of some substituted N'-arylidene-2-(quinolin-8-yloxy) aceto hydrazides. Acta Pharm. Sci., 2009, 51, 163-168.
    • (2009) Acta Pharm. Sci , vol.51 , pp. 163-168
    • Mohammed, I.A.1    Subrahmanyam, E.V.S.2
  • 31
    • 0036178191 scopus 로고    scopus 로고
    • Antimicrobial activity of some new hydrazones of 4-fluorobenzoic acid hydrazide and 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines
    • Rollas, S.; Gulerman, N.; Erdeniz, H. Antimicrobial activity of some new hydrazones of 4-fluorobenzoic acid hydrazide and 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines. Farmaco, 2002, 57, 171-4.
    • (2002) Farmaco , vol.57 , pp. 171-174
    • Rollas, S.1    Gulerman, N.2    Erdeniz, H.3
  • 32
    • 45849100079 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial activity of long-chain hydrazones
    • Rauf, A.; Banday, MR.; Mattoo, RH. Synthesis, characterization and antimicrobial activity of long-chain hydrazones. Acta Chim. Slov., 2008, 55, 448-52.
    • (2008) Acta Chim. Slov , vol.55 , pp. 448-452
    • Rauf, A.1    Banday, M.R.2    Mattoo, R.H.3
  • 33
    • 28944442553 scopus 로고    scopus 로고
    • Synthesis, properties, and antimicrobial activity of 3-hydrazones of 1-aryl-5-methyl-1,5-ethoxycarbonylpyrrolidine-2,3-diones
    • Gein, VL.; Gein, LF.; Chirkova, MV.; Mikhalev, VA.; Voronina, EV. Synthesis, properties, and antimicrobial activity of 3-hydrazones of 1-aryl-5-methyl-1,5-ethoxycarbonylpyrrolidine-2,3-diones. Pharm. Chem. J., 2005, 39, 413-7.
    • (2005) Pharm. Chem. J , vol.39 , pp. 413-417
    • Gein, V.L.1    Gein, L.F.2    Chirkova, M.V.3    Mikhalev, V.A.4    Voronina, E.V.5
  • 34
    • 0029080662 scopus 로고
    • Hydrazones of [(2-benzothiazolylthio)acetyl] hydrazine: Synthesis and antimicrobial activity
    • Yildir, I.; Perçiner, H.; Sahin, MF.; Abbasaoglu, U. Hydrazones of [(2-benzothiazolylthio)acetyl] hydrazine: Synthesis and antimicrobial activity. Arch. Pharm. (Weinheim), 1995, 328, 547-9.
    • (1995) Arch. Pharm. (Weinheim) , vol.328 , pp. 547-549
    • Yildir, I.1    Perçiner, H.2    Sahin, M.F.3    Abbasaoglu, U.4
  • 35
    • 54949109391 scopus 로고    scopus 로고
    • Investigation of antimicrobial activities of indole-3-aldehyde hydrazide/hydrazone derivatives
    • Gurkok, G.; Altanlar, N.; Suzen, S. Investigation of antimicrobial activities of indole-3-aldehyde hydrazide/hydrazone derivatives. Chemotherapy, 2009, 55, 15-9.
    • (2009) Chemotherapy , vol.55 , pp. 15-19
    • Gurkok, G.1    Altanlar, N.2    Suzen, S.3
  • 36
    • 80054862119 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 2-chloro-6-methylquinoline hydrazone derivatives
    • Bawa S.; Kumar S.; Drabu S.; Kumar R. Synthesis and antimicrobial activity of 2-chloro-6-methylquinoline hydrazone derivatives. J. Pharm. Bioall Sci, 2009, 1, 27-31.
    • (2009) J. Pharm. Bioall Sci , vol.1 , pp. 27-31
    • Bawa, S.1    Kumar, S.2    Drabu, S.3    Kumar, R.4
  • 37
    • 34447508262 scopus 로고    scopus 로고
    • Synthesis of some quinoline-2 (1H)-one and 1, 2, 4 - triazolo[4, 3 -a] quinoline derivatives as potent anticonvulsants
    • Guan, LP; Jin, QH.; Tian, GR.; Chai, KY. and Quan, ZS. Synthesis of some quinoline-2 (1H)-one and 1, 2, 4 - triazolo[4, 3 -a] quinoline derivatives as potent anticonvulsants. J. Pharm. Pharmaceut. Sci. 2007, 10, 254-262.
    • (2007) J. Pharm. Pharmaceut. Sci , vol.10 , pp. 254-262
    • Guan, L.P.1    Jin, Q.H.2    Tian, G.R.3    Chai, K.Y.4    Quan, Z.S.5
  • 38
  • 39
    • 77956370311 scopus 로고    scopus 로고
    • Synthesis and in vivo Anticonvulsant Evaluation of 2-Chloroquinolinyl Hydrazon derivatives
    • Kumar, S.; Bawa, S., Drabu, S.; Kumar, R. and Machawal, L. Synthesis and in vivo Anticonvulsant Evaluation of 2-Chloroquinolinyl Hydrazon derivatives. Acta Poloniae Pharmaceutica- Drug Res., 2010, 67(5), 567-573.
    • (2010) Acta Poloniae Pharmaceutica-Drug Res , vol.67 , Issue.5 , pp. 567-573
    • Kumar, S.1    Bawa, S.2    Drabu, S.3    Kumar, R.4    Machawal, L.5
  • 40
    • 0002204357 scopus 로고    scopus 로고
    • Photosensitized oxidation and Singlet-Oxygen: Consequences in Biological Systems. In: Free Rad
    • Foote C. S. Photosensitized oxidation and Singlet-Oxygen: Consequences in Biological Systems. In: Free Rad. Biol., 1976, 2, 85-133.
    • Biol., 1976 , vol.2 , pp. 85-133
    • Foote, C.S.1
  • 41
    • 13844262622 scopus 로고    scopus 로고
    • Intracellular generation of reactive oxygen species by mitochondria
    • Nohl, H.; Gille, L.; Staniek, K. Intracellular generation of reactive oxygen species by mitochondria. Biochem. Pharmacol., 2005, 69, 719-23.
    • (2005) Biochem. Pharmacol , vol.69 , pp. 719-723
    • Nohl, H.1    Gille, L.2    Staniek, K.3
  • 43
    • 1642545540 scopus 로고    scopus 로고
    • Oxidative stress in aging and disease
    • Boveris, A.; Fraga, G.C. Oxidative stress in aging and disease. Mol. Aspects Med. 2004, 25, 1-4.
    • (2004) Mol. Aspects Med , vol.25 , pp. 1-4
    • Boveris, A.1    Fraga, G.C.2
  • 45
    • 80755159011 scopus 로고    scopus 로고
    • Synthesis and antioxidant evaluation of novel 4-arylhexahydroquinolines from lignin
    • Yang, XH.; Zhang, PH.; Zhou, YH.; Liu, CG.; Lin, XY.; Cuia, JF. Synthesis and antioxidant evaluation of novel 4-arylhexahydroquinolines from lignin. Arkivoc, 2011, 335-345.
    • (2011) Arkivoc , pp. 335-345
    • Yang, X.H.1    Zhang, P.H.2    Zhou, Y.H.3    Liu, C.G.4    Lin, X.Y.5    Cuia, J.F.6
  • 47
    • 0037213428 scopus 로고    scopus 로고
    • Antioxidant activity of the fused heterocyclic compounds, 1,2,3,4-tetrahydroquinolines, and related compounds-effect of ortho-substituents
    • Nishiyama, T.; Hashiguchi, Y.; Sakata, T.; Sakaguchi, T. Antioxidant activity of the fused heterocyclic compounds, 1,2,3,4-tetrahydroquinolines, and related compounds-effect of ortho-substituents. Polymer Deg. Stab., 2003, 79, 225-230.
    • (2003) Polymer Deg. Stab , vol.79 , pp. 225-230
    • Nishiyama, T.1    Hashiguchi, Y.2    Sakata, T.3    Sakaguchi, T.4
  • 48
    • 0034852901 scopus 로고    scopus 로고
    • Antioxidant mechanism of flavonoids. Solvent effect on rate constant for chain-breaking reaction of quercetin and epicatechin in autoxidation of methyl linoleate
    • Pedrielli, P.; Pedulci, G. F.; Skibsted, L. H. Antioxidant mechanism of flavonoids. Solvent effect on rate constant for chain-breaking reaction of quercetin and epicatechin in autoxidation of methyl linoleate. J. Agric. Food Chem. 2001, 4, 3034.
    • (2001) J. Agric. Food Chem , vol.4 , pp. 3034
    • Pedrielli, P.1    Pedulci, G.F.2    Skibsted, L.H.3
  • 49
    • 3042786057 scopus 로고    scopus 로고
    • Solvent effect on quercetin antioxidant capacity
    • Pinelo, M.; Manzocco, L.; Nunez, M. J.; Nicoli, M. C. Solvent effect on quercetin antioxidant capacity. Food Chem., 2004, 88, 201.
    • (2004) Food Chem , vol.88 , pp. 201
    • Pinelo, M.1    Manzocco, L.2    Nunez, M.J.3    Nicoli, M.C.4
  • 50
    • 84855780946 scopus 로고    scopus 로고
    • Antioxidant properties of 4-quinolones and structurally related flavones
    • Greeff, J.; Joubert, J.; Malan, SF.; Dyk, S. Antioxidant properties of 4-quinolones and structurally related flavones. Bioorg. Med. Chem., 2012, 20, 809-818.
    • (2012) Bioorg. Med. Chem , vol.20 , pp. 809-818
    • Greeff, J.1    Joubert, J.2    Malan, S.F.3    Dyk, S.4
  • 51
    • 33845372349 scopus 로고    scopus 로고
    • Novel Schiff Base Copper Complexes of Quinoline-2-Carboxaldehyde as Proteasome Inhibitors in Human Prostate Cancer Cells
    • Adsule, S.; Barve, V.; Chen, D.; Ahmed, F.; Dou, QP.; Padhye, S. and Sarkar, FH. Novel Schiff Base Copper Complexes of Quinoline-2-Carboxaldehyde as Proteasome Inhibitors in Human Prostate Cancer Cells. J. Med. Chem., 2006, 49, 7242-7246.
    • (2006) J. Med. Chem , vol.49 , pp. 7242-7246
    • Adsule, S.1    Barve, V.2    Chen, D.3    Ahmed, F.4    Dou, Q.P.5    Padhye, S.6    Sarkar, F.H.7
  • 52
    • 34547602615 scopus 로고    scopus 로고
    • Activity of mannitol and hypertonic saline therapy on the oxidant and antioxidant system during the acute term after traumatic brain injury in the rats
    • Yilmaz, N.; Dulger, H.; Kiymaz, N.; Yilmaz, C.; Gudu, B.O.; Demir, I. Activity of mannitol and hypertonic saline therapy on the oxidant and antioxidant system during the acute term after traumatic brain injury in the rats. Brain Res., 2007, 1164, 132-135.
    • (2007) Brain Res , vol.1164 , pp. 132-135
    • Yilmaz, N.1    Dulger, H.2    Kiymaz, N.3    Yilmaz, C.4    Gudu, B.O.5    Demir, I.6
  • 53
    • 0345529031 scopus 로고    scopus 로고
    • Modeling the co-antioxidant behavior of monofunctional phenols. Applications to some relevant compounds
    • Amorati, R.; Ferroni, F.; Pedulli, G.F.; Valgimigli, L. Modeling the co-antioxidant behavior of monofunctional phenols. Applications to some relevant compounds. J. Org. Chem., 2003, 68, 9654-9658.
    • (2003) J. Org. Chem , vol.68 , pp. 9654-9658
    • Amorati, R.1    Ferroni, F.2    Pedulli, G.F.3    Valgimigli, L.4
  • 54
    • 70349764463 scopus 로고    scopus 로고
    • Synthesis, crystal structure, DNA interaction and antioxidant activities of two novel water-soluble Cu(2+) complexes derivated from 2-oxo-quinoline-3-carbaldehyde Schiff-bases
    • Liu, ZC.; Wang, BD.; Yang, ZY.; Li, Y.; Qin, DD.; Li, TR. Synthesis, crystal structure, DNA interaction and antioxidant activities of two novel water-soluble Cu(2+) complexes derivated from 2-oxo-quinoline-3-carbaldehyde Schiff-bases. Eur. J. Med. Chem., 2009, 44, 4477-4484.
    • (2009) Eur. J. Med. Chem , vol.44 , pp. 4477-4484
    • Liu, Z.C.1    Wang, B.D.2    Yang, Z.Y.3    Li, Y.4    Qin, D.D.5    Li, T.R.6
  • 55
    • 79951651821 scopus 로고    scopus 로고
    • Synthesis and Free Radical Scavenging Property of Some Quinoline Derivatives
    • Subashini, R.; Ropan, SM.; Nawaz Khan, F. Synthesis and Free Radical Scavenging Property of Some Quinoline Derivatives. J. Chil. Chem. Soc., 2010, 55/3, 317-9.
    • (2010) J. Chil. Chem. Soc , vol.55 , Issue.3 , pp. 317-319
    • Subashini, R.1    Ropan, S.M.2    Nawaz, K.F.3
  • 56
    • 0027939613 scopus 로고
    • Nutrition and health aspects of free radicals and antioxidants
    • Aruoma O.I. Nutrition and health aspects of free radicals and antioxidants. Food Chem. Toxicol., 1994, 32, 671-683.
    • (1994) Food Chem. Toxicol , vol.32 , pp. 671-683
    • Aruoma, O.I.1
  • 57
    • 0032819772 scopus 로고    scopus 로고
    • Dietary flavonoids: Intake, health effects and bioavailability
    • Hollman P.C.H.; Katan M.B. Dietary flavonoids: intake, health effects and bioavailability. Food Chem. Toxicol., 1999, 37, 937-942.
    • (1999) Food Chem. Toxicol , vol.37 , pp. 937-942
    • Hollman, P.C.H.1    Katan, M.B.2
  • 58
    • 0141460591 scopus 로고    scopus 로고
    • 3,4-Dihydroxymandelic acid amides of alkylamines as antioxidants for lipids
    • Jakob P.L.; Heinz J.B. 3,4-Dihydroxymandelic acid amides of alkylamines as antioxidants for lipids. Eur. J. Lipid Sci. Technol., 2003, 105, 529-535.
    • (2003) Eur. J. Lipid Sci. Technol , vol.105 , pp. 529-535
    • Jakob, P.L.1    Heinz, J.B.2
  • 59
    • 12444259662 scopus 로고    scopus 로고
    • Antioxidative effects of flavonols and their glycosides against the free-radical-induced peroxidation of linoleic acid in solution and in micelles
    • Zhou B.; Miao Q.; Yang L.; Liu Z.L. Antioxidative effects of flavonols and their glycosides against the free-radical-induced peroxidation of linoleic acid in solution and in micelles. Chem. Eur. J., 2005, 11, 680-691.
    • (2005) Chem. Eur. J , vol.11 , pp. 680-691
    • Zhou, B.1    Miao, Q.2    Yang, L.3    Liu, Z.L.4
  • 61
    • 34447268471 scopus 로고    scopus 로고
    • Synthesis and pharmacochemical evaluation of novel aryl-acetic acid inhibitors of lipoxygenase, antioxidants, and anti-inflammatory agents
    • Pontiki E.; Hadjipavlou-Litina D. Synthesis and pharmacochemical evaluation of novel aryl-acetic acid inhibitors of lipoxygenase, antioxidants, and anti-inflammatory agents. Bioorg. Med. Chem., 2007, 15, 5819-5827.
    • (2007) Bioorg. Med. Chem , vol.15 , pp. 5819-5827
    • Pontiki, E.1    Hadjipavlou-Litina, D.2
  • 62
    • 0037063405 scopus 로고    scopus 로고
    • Antioxidative activity of heterocyclic compounds found in coffee volatiles produced by maillard reaction
    • Yanagimoto K.; Lee K.G.; Ochi H.; Shibamoto T. Antioxidative activity of heterocyclic compounds found in coffee volatiles produced by maillard reaction. J. Agric Food Chem., 2002, 50, 5480-5484.
    • (2002) J. Agric Food Chem , vol.50 , pp. 5480-5484
    • Yanagimoto, K.1    Lee, K.G.2    Ochi, H.3    Shibamoto, T.4
  • 63
    • 74549151154 scopus 로고    scopus 로고
    • 2-Induced Oxidative Stress in BMSCs
    • Wang, TT.; Zeng, GC.; Li, XC and Zeng, HP. In Vitro Studies on the Antioxidant and Protective Effect of 2-Substituted-8-Hydroxyquinoline Derivatives Against H2O2-Induced Oxidative Stress in BMSCs. Chem. Biol. Drug Des., 2010, 75, 214-222.
    • (2010) Chem. Biol. Drug Des , vol.75 , pp. 214-222
    • Wang, T.T.1    Zeng, G.C.2    Li, X.C.3    Zeng, H.P.4
  • 64
    • 0028796955 scopus 로고
    • Hydroxyl Radical scavenging by rebamipide and related compounds electron paramagnetic resonance study
    • Yuji, N.; Toshikazu, Y.T.; Tanigawa, K.; Sakura, K.; Yamasaki, M.; Motoharu, K. Hydroxyl Radical scavenging by rebamipide and related compounds electron paramagnetic resonance study. Free Rad. Biol. Med., 1995, 18(1): 117-123.
    • (1995) Free Rad. Biol. Med , vol.18 , Issue.1 , pp. 117-123
    • Yuji, N.1    Toshikazu, Y.T.2    Tanigawa, K.3    Sakura, K.4    Yamasaki, M.5    Motoharu, K.6
  • 65
    • 84868613702 scopus 로고    scopus 로고
    • Quinolines Antioxydant Activity Structure Activity Relation-Ship
    • Korrichi, L.; Dalila, B. and Dalila, S. Quinolines Antioxydant Activity Structure Activity Relation-Ship. Eu.r J. Biol. Sci., 2009, 1(3): 32-36.
    • (2009) Eu.r J. Biol. Sci , vol.1 , Issue.3 , pp. 32-36
    • Korrichi, L.1    Dalila, B.2    Dalila, S.3
  • 66
    • 0014626902 scopus 로고
    • Chemotherapy of the drug-resistant Malarias
    • Schmidt, L.H. Chemotherapy of the drug-resistant Malarias. Ann. Rev. Microbiol., 1969, 23, 427-454.
    • (1969) Ann. Rev. Microbiol , vol.23 , pp. 427-454
    • Schmidt, L.H.1
  • 67
    • 0000350263 scopus 로고
    • Synthesis and properties of 7-formyl-8-hydroxyquinoline and its transition metal complexes
    • El-Asmy, A.A.; El-Sonbati, A.Z.; Ba-Issa, A.A. and Mounir, M. Synthesis and properties of 7-formyl-8-hydroxyquinoline and its transition metal complexes. Transit. Metal. Chem., 1990, 5, 222-225.
    • (1990) Transit. Metal. Chem , vol.5 , pp. 222-225
    • El-Asmy, A.A.1    El-Sonbati, A.Z.2    Ba-Issa, A.A.3    Mounir, M.4
  • 68
    • 0014820512 scopus 로고
    • Antitumor activities of some Schiff bases
    • Hodnett, E.M. and Mooney, P.D. Antitumor activities of some Schiff bases. J. Med. Chem., 1970, 13, 786-786.
    • (1970) J. Med. Chem , vol.13 , pp. 786
    • Hodnett, E.M.1    Mooney, P.D.2
  • 69
    • 0347908578 scopus 로고
    • Cobalt derivatives of Schiff bases of aliphatic amines as antitumor agents
    • Hodnett, E.M. and Dunn, W.J. Cobalt derivatives of Schiff bases of aliphatic amines as antitumor agents. J. Med. Chem., 1972, 15, 339-339.
    • (1972) J. Med. Chem , vol.15 , pp. 339
    • Hodnett, E.M.1    Dunn, W.J.2
  • 70
    • 69249231105 scopus 로고    scopus 로고
    • Crystal structures, antioxidation and DNA binding properties of Yb(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carbaldehyde and four aroylhydrazines
    • Liu, YC. and Yang, ZY. Crystal structures, antioxidation and DNA binding properties of Yb(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carbaldehyde and four aroylhydrazines. Biometals, 2009, 22, 733-751.
    • (2009) Biometals , vol.22 , pp. 733-751
    • Liu, Y.C.1    Yang, Z.Y.2
  • 71
    • 68149123699 scopus 로고    scopus 로고
    • Synthesis, crystal structure, antioxidation and DNA binding properties of binuclear Ho(III) complexes of Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and four aroylhydrazines
    • Liu, YC. and Yang, ZY. Synthesis, crystal structure, antioxidation and DNA binding properties of binuclear Ho(III) complexes of Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and four aroylhydrazines. J. Organomet. Chem., 2009, 694, 3091-3101.
    • (2009) J. Organomet. Chem , vol.694 , pp. 3091-3101
    • Liu, Y.C.1    Yang, Z.Y.2
  • 72
    • 67549098073 scopus 로고    scopus 로고
    • Crystal structures, antioxidation and DNA binding properties of Eu(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and three aroylhydrazines
    • Liu, YC. and Yang, ZY. Crystal structures, antioxidation and DNA binding properties of Eu(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and three aroylhydrazines. J. Inorg. Biochem., 2009, 103, 1014-1022.
    • (2009) J. Inorg. Biochem , vol.103 , pp. 1014-1022
    • Liu, Y.C.1    Yang, Z.Y.2
  • 73
    • 67651204429 scopus 로고    scopus 로고
    • Antioxidation and DNA binding properties of binuclear Nd(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and four aroylhydrazides
    • Liu, YC. and Yang, ZY. Antioxidation and DNA binding properties of binuclear Nd(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxyaldehyde and four aroylhydrazides. Inorg. Chem. Commun., 2009, 12, 704-706.
    • (2009) Inorg. Chem. Commun , vol.12 , pp. 704-706
    • Liu, Y.C.1    Yang, Z.Y.2
  • 74
    • 77249145893 scopus 로고    scopus 로고
    • Antioxidation and DNA-binding properties of binuclear Er(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxaldehyde and four aroylhydrazines
    • Liu, YC. and Yang, ZY. Antioxidation and DNA-binding properties of binuclear Er(III) complexes with Schiff-base ligands derived from 8-hydroxyquinoline-2-carboxaldehyde and four aroylhydrazines. J. Biochem., 2010, 147(3), 381-391.
    • (2010) J. Biochem , vol.147 , Issue.3 , pp. 381-391
    • Liu, Y.C.1    Yang, Z.Y.2
  • 75
    • 78149284098 scopus 로고    scopus 로고
    • Synthesis, antioxidant and toxicological study of novel pyrimido quinoline derivatives from 4-hydroxy-3-acyl quinolin-2-one
    • Sankaran, M.; Kumarasamy, C; Chokkalingam, U.; Mohan, PS. Synthesis, antioxidant and toxicological study of novel pyrimido quinoline derivatives from 4-hydroxy-3-acyl quinolin-2-one. Bioorg. Med. Chem. Lett., 2010, 20, 7147-7151.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , pp. 7147-7151
    • Sankaran, M.1    Kumarasamy, C.2    Chokkalingam, U.3    Mohan, P.S.4
  • 76
    • 84860634004 scopus 로고    scopus 로고
    • Four component one-pot synthesis of novel 7,8-dihydroquinolin-5(1H,4H,6H)-one derivatives containing an ionone unit and in vitro antioxidant activity
    • Findik, E.; Ceylan, M. and Elmasta, M. Four component one-pot synthesis of novel 7,8-dihydroquinolin-5(1H,4H,6H)-one derivatives containing an ionone unit and in vitro antioxidant activity. J. Heterocyc. Chem., 2012, 49(2), 253-260.
    • (2012) J. Heterocyc. Chem , vol.49 , Issue.2 , pp. 253-260
    • Findik, E.1    Ceylan, M.2    Elmasta, M.3
  • 77
    • 0000209774 scopus 로고
    • Studies on products of browning reaction prepared from glucosamine
    • Oyaizu M. Studies on products of browning reaction prepared from glucosamine. Jpn. J. Nutr., 1986, 44, 307-315.
    • (1986) Jpn. J. Nutr , vol.44 , pp. 307-315
    • Oyaizu, M.1
  • 78
    • 0842323018 scopus 로고    scopus 로고
    • Amplification of antioxidant activity of catechin by polycondensation with acetaldehyde
    • Chung, JE.; Kurisawa M.; Kim YJ.; Uyama H.; Kobayashi, S. Amplification of antioxidant activity of catechin by polycondensation with acetaldehyde. Biomacromol, 2004, 5, 113-118.
    • (2004) Biomacromol , vol.5 , pp. 113-118
    • Chung, J.E.1    Kurisawa, M.2    Kim, Y.J.3    Uyama, H.4    Kobayashi, S.5
  • 79
    • 84861213476 scopus 로고    scopus 로고
    • Structure-activity relationship study of copper(II) complexes with 2-oxo-1,2-dihydroquinoline-3-carbaldehyde (4'-methylbenzoyl) hydrazone: Synthesis, structures, DNA and protein interaction studies, antioxidative and cytotoxic activity
    • Raja, DS.; Bhuvanesh, NSP.; Natarajan, K. Structure-activity relationship study of copper(II) complexes with 2-oxo-1,2-dihydroquinoline-3-carbaldehyde (4'-methylbenzoyl) hydrazone: synthesis, structures, DNA and protein interaction studies, antioxidative and cytotoxic activity. J. Biol. Inorg. Chem., 2012, 17, 223-237.
    • (2012) J. Biol. Inorg. Chem , vol.17 , pp. 223-237
    • Raja, D.S.1    Bhuvanesh, N.S.P.2    Natarajan, K.3


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