메뉴 건너뛰기




Volumn 54, Issue 19, 2011, Pages 6936-6948

Halogenated 2′-benzoylpyridine thiosemicarbazone (XBpT) chelators with potent and selective anti-neoplastic activity: Relationship to intracellular redox activity

Author keywords

[No Author keywords available]

Indexed keywords

2' BENZOYLPYRIDINE THIOSEMICARBAZONE DERIVATIVE; ANTINEOPLASTIC AGENT; CHELATING AGENT; DICHLOROFLUORESCEIN; REACTIVE OXYGEN METABOLITE; THIOSEMICARBAZONE DERIVATIVE; UNCLASSIFIED DRUG; 2',7'-DICHLOROFLUORESCEIN; ASCORBIC ACID; COORDINATION COMPOUND; FLUORESCEIN DERIVATIVE; FLUORESCENT DYE; IRON CHELATING AGENT; PYRIDINE DERIVATIVE;

EID: 80053895153     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm200924c     Document Type: Article
Times cited : (53)

References (51)
  • 3
    • 0037733128 scopus 로고    scopus 로고
    • Multidentate pyridinones inhibit the metabolism of nontransferrin-bound iron by hepatocytes and hepatoma cells
    • DOI 10.1046/j.1432-1033.2003.03525.x
    • Chua, A. C. G.; Ingram, H. A.; Raymond, K. N.; Baker, E. Multidentate pyridinones inhibit the metabolism of nontransferrin-bound iron by hepatocytes and hepatoma cells Eur. J. Biochem. 2003, 270, 1689-1698 (Pubitemid 36532528)
    • (2003) European Journal of Biochemistry , vol.270 , Issue.8 , pp. 1689-1698
    • Chua, A.C.G.1    Ingram, H.A.2    Raymond, K.N.3    Baker, E.4
  • 4
    • 77249090271 scopus 로고    scopus 로고
    • Conjugates of desferrioxamine B (DFOB) with derivatives of adamantane or with orally available chelators as potential agents for treating iron overload
    • Liu, J.; Obando, D.; Schipanski, L. G.; Groebler, L. K.; Witting, P. K.; Kalinowski, D. S.; Richardson, D. R.; Codd, R. Conjugates of desferrioxamine B (DFOB) with derivatives of adamantane or with orally available chelators as potential agents for treating iron overload J. Med. Chem. 2010, 53, 1370-1382
    • (2010) J. Med. Chem. , vol.53 , pp. 1370-1382
    • Liu, J.1    Obando, D.2    Schipanski, L.G.3    Groebler, L.K.4    Witting, P.K.5    Kalinowski, D.S.6    Richardson, D.R.7    Codd, R.8
  • 5
    • 0038324398 scopus 로고    scopus 로고
    • The role of iron chelation in cancer therapy
    • DOI 10.2174/0929867033457638
    • Buss, J. L.; Torti, F. M.; Torti, S. V. The role of iron chelation in cancer therapy Curr. Med. Chem. 2003, 10, 1021-1034 (Pubitemid 36582246)
    • (2003) Current Medicinal Chemistry , vol.10 , Issue.12 , pp. 1021-1034
    • Buss, J.L.1    Torti, F.M.2    Torti, S.V.3
  • 7
    • 27644552326 scopus 로고    scopus 로고
    • 2 cell-cycle arrest, activates checkpoint kinases, and sensitizes cells to ionizing radiation
    • DOI 10.1182/blood-2005-03-1263
    • Turner, J.; Koumenis, C.; Kute, T. E.; Planalp, R. P.; Brechbiel, M. W.; Beardsley, D.; Cody, B.; Brown, K. D.; Torti, F. M.; Torti, S. V. Tachpyridine, a metal chelator, induces G(2) cell-cycle arrest, activates checkpoint kinases, and sensitizes cells to ionizing radiation Blood 2005, 106, 3191-3199 (Pubitemid 41565918)
    • (2005) Blood , vol.106 , Issue.9 , pp. 3191-3199
    • Turner, J.1    Koumenis, C.2    Kute, T.E.3    Planalp, R.P.4    Brechbiel, M.W.5    Beardsley, D.6    Cody, B.7    Brown, K.D.8    Torti, F.M.9    Torti, S.V.10
  • 8
    • 0018603336 scopus 로고
    • Modulation of cell surface iron transferrin receptors by cellular density and state of activation
    • Larrick, J. W.; Cresswell, P. Modulation of cell-surface iron transferrin receptors by cellular density and state of activation J. Supramol. Struct. 1979, 11, 579-586 (Pubitemid 10067168)
    • (1979) Journal of Supramolecular and Cellular Biochemistry , vol.11 , Issue.4 , pp. 579-586
    • Larrick, J.W.1    Cresswell, P.2
  • 9
    • 0037237032 scopus 로고    scopus 로고
    • Examination of the antiproliferative activity of iron chelators: Multiple cellular targets and the different mechanism of action of triapine compared with desferrioxamine and the potent pyridoxal isonicotinoyl hydrazone analogue 311
    • Chaston, T. B.; Lovejoy, D. B.; Watts, R. N.; Richardson, D. R. Examination of the antiproliferative activity of iron chelators: Multiple cellular targets and the different mechanism of action of triapine compared with desferrioxamine and the potent pyridoxal isonicotinoyl hydrazone analogue 311 Clin. Cancer Res. 2003, 9, 402-414 (Pubitemid 36109758)
    • (2003) Clinical Cancer Research , vol.9 , Issue.1 , pp. 402-414
    • Chaston, T.B.1    Lovejoy, D.B.2    Watts, R.N.3    Richardson, D.R.4
  • 10
    • 0029833706 scopus 로고    scopus 로고
    • The relationship of intracellular iron chelation to the inhibition and regeneration of human ribonucleotide reductase
    • DOI 10.1074/jbc.271.34.20291
    • Cooper, C. E.; Lynagh, G. R.; Hoyes, K. P.; Hider, R. C.; Cammack, R.; Porter, J. B. The relationship of intracellular iron chelation to the inhibition and regeneration of human ribonucleotide reductase J. Biol. Chem. 1996, 271, 20291-20299 (Pubitemid 26281794)
    • (1996) Journal of Biological Chemistry , vol.271 , Issue.34 , pp. 20291-20299
    • Cooper, C.E.1    Lynagh, G.R.2    Hoyes, K.P.3    Hider, R.C.4    Cammack, R.5    Porter, J.B.6
  • 12
    • 34547137681 scopus 로고    scopus 로고
    • Iron chelation and regulation of the cell cycle: 2 Mechanisms of posttranscriptional regulation of the universal cyclin-dependent kinase inhibitor p21CIP1/WAF1 by iron depletion
    • DOI 10.1182/blood-2007-03-076737
    • Fu, D.; Richardson, D. R. Iron chelation and regulation of the cell cycle: 2 mechanisms of posttranscriptional regulation of the universal cyclin-dependent kinase inhibitor p21(CIP1/WAF1) by iron depletion Blood 2007, 110, 752-761 (Pubitemid 47105414)
    • (2007) Blood , vol.110 , Issue.2 , pp. 752-761
    • Fu, D.1    Richardson, D.R.2
  • 13
    • 7244239197 scopus 로고    scopus 로고
    • Iron chelators with high antiproliferative activity up-regulate the expression of a growth inhibitory and metastasis suppressor gene: A link between iron metabolism and proliferation
    • DOI 10.1182/blood-2004-05-1866
    • Le, N. T. V.; Richardson, D. R. Iron chelators with high antiproliferative activity up-regulate the expression of a growth inhibitory and metastasis suppressor gene: a link between iron metabolism and proliferation Blood 2004, 104, 2967-2975 (Pubitemid 39434989)
    • (2004) Blood , vol.104 , Issue.9 , pp. 2967-2975
    • Le, N.T.V.1    Richardson, D.R.2
  • 14
    • 34247373460 scopus 로고    scopus 로고
    • Iron chelation regulates cyclin D1 expression via the proteasome: A link to iron deficiency-mediated growth suppression
    • DOI 10.1182/blood-2006-10-047753
    • Nurtjahja-Tjendraputra, E.; Fu, D.; Phang, J. M.; Richardson, D. R. Iron chelation regulates cyclin D1 expression via the proteasome: A link to iron deficiency-mediated growth suppression Blood 2007, 109, 4045-4054 (Pubitemid 46641760)
    • (2007) Blood , vol.109 , Issue.9 , pp. 4045-4054
    • Nurtjahja-Tjendraputra, E.1    Fu, D.2    Phang, J.M.3    Richardson, D.R.4
  • 16
    • 29844457587 scopus 로고    scopus 로고
    • The evolution of iron chelators for the treatment of iron overload disease and cancer
    • DOI 10.1124/pr.57.4.2
    • Kalinowski, D. S.; Richardson, D. R. The evolution of iron chelators for the treatment of iron overload disease and cancer Pharmacol. Rev. 2005, 57, 547-583 (Pubitemid 43036441)
    • (2005) Pharmacological Reviews , vol.57 , Issue.4 , pp. 547-583
    • Kalinowski, D.S.1    Richardson, D.R.2
  • 18
    • 4444248453 scopus 로고    scopus 로고
    • Novel di-2-pyridyl-derived iron chelators with marked and selective antitumor activity: In vitro and in vivo assessment
    • DOI 10.1182/blood-2004-03-0868
    • Yuan, J.; Lovejoy, D. B.; Richardson, D. R. Novel di-2-pyridyl-derived iron chelators with marked and selective antitumor activity: In vitro and in vivo assessment Blood 2004, 104, 1450-1458 (Pubitemid 39166524)
    • (2004) Blood , vol.104 , Issue.5 , pp. 1450-1458
    • Yuan, J.1    Lovejoy, D.B.2    Richardson, D.R.3
  • 19
    • 0022529172 scopus 로고
    • Oxygen free radicals and iron in relation to biology and medicine: Some problems and concepts
    • Halliwell, B.; Gutteridge, J. M. C. Oxygen free-radicals and iron in relation to biology and medicine-Some problems and concepts Arch. Biochem. Biophys. 1986, 246, 501-514 (Pubitemid 16072574)
    • (1986) Archives of Biochemistry and Biophysics , vol.246 , Issue.2 , pp. 501-514
    • Halliwell, B.1    Gutteridge, J.M.C.2
  • 20
    • 8444235919 scopus 로고    scopus 로고
    • Potent antitumor activity of novel iron chelators derived from di-2-pyridylketone isonicotinoyl hydrazone involves fenton-derived free radical generation
    • DOI 10.1158/1078-0432.CCR-04-0865
    • Chaston, T. B.; Watts, R. N.; Yuan, J.; Richardson, D. R. Potent antitumor activity of novel iron chelators derived from di-2-pyridylketone isonicotinoyl hydrazone involves fenton-derived free radical generation Clin. Cancer Res. 2004, 10, 7365-7374 (Pubitemid 39487726)
    • (2004) Clinical Cancer Research , vol.10 , Issue.21 , pp. 7365-7374
    • Chaston, T.B.1    Watts, R.N.2    Yuan, J.3    Richardson, D.R.4
  • 21
    • 0023092624 scopus 로고
    • Antineuroblastoma activity of desferoxamine in human cell lines
    • Blatt, J.; Stitely, S. Antineuroblastoma activity of desferoxamine in human cell-lines Cancer Res. 1987, 47, 1749-1750 (Pubitemid 17056669)
    • (1987) Cancer Research , vol.47 , Issue.7 , pp. 1749-1750
    • Blatt, J.1    Stitely, S.2
  • 22
    • 0026683009 scopus 로고
    • Deferoxamine, cyclophosphamide, etoposide, carboplatin, and thiotepa (D-CECAT)-A new cytoreductive chelation-chemotherapy regimen in patients with advanced neuroblastoma
    • Donfrancesco, A.; Deb, G.; Dominici, C.; Angioni, A.; Caniglia, M.; Desio, L.; Fidani, P.; Amici, A.; Helson, L. Deferoxamine, cyclophosphamide, etoposide, carboplatin, and thiotepa (D-CECAT)-A new cytoreductive chelation-chemotherapy regimen in patients with advanced neuroblastoma Am. J. Clin. Oncol.-Cancer Clin. Trials 1992, 15, 319-322
    • (1992) Am. J. Clin. Oncol.-Cancer Clin. Trials , vol.15 , pp. 319-322
    • Donfrancesco, A.1    Deb, G.2    Dominici, C.3    Angioni, A.4    Caniglia, M.5    Desio, L.6    Fidani, P.7    Amici, A.8    Helson, L.9
  • 24
    • 0023135326 scopus 로고
    • In vitro and in vivo effects of deferoxamine in neonatal acute leukemia
    • Estrov, Z.; Tawa, A.; Wang, X. H.; Dube, I. D.; Sulh, H.; Cohen, A.; Gelfand, E. W.; Freedman, M. H. In vitro and in vivo effects of deferoxamine in neonatal acute-leukemia Blood 1987, 69, 757-761 (Pubitemid 17057452)
    • (1987) Blood , vol.69 , Issue.3 , pp. 757-761
    • Estrov, Z.1    Tawa, A.2    Wang, X.-H.3
  • 26
    • 27744528421 scopus 로고    scopus 로고
    • Molecular mechanisms of iron uptake by cells and the use of iron chelators for the treatment of cancer
    • DOI 10.2174/092986705774462996
    • Richardson, D. R. Molecular mechanisms of iron uptake by cells and the use of iron chelators for the treatment of cancer Curr. Med. Chem. 2005, 12, 2711-2729 (Pubitemid 41601569)
    • (2005) Current Medicinal Chemistry , vol.12 , Issue.23 , pp. 2711-2729
    • Richardson, D.R.1
  • 27
    • 36048952046 scopus 로고    scopus 로고
    • ®) in combination with the nucleoside analog fludarabine for patients with refractory acute leukemias and aggressive myeloproliferative disorders
    • DOI 10.1016/j.leukres.2007.05.003, PII S0145212607001890
    • Karp, J. E.; Giles, F. J.; Gojo, L.; Morris, L.; Greer, J.; Johnson, B.; Thein, M.; Sznol, M.; Low, J. A phase I study of the novel ribonucleotide reductase inhibitor 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP, Triapine(R)) in combination with the nucleoside analog fludarabine for patients with refractory acute leukemias and aggressive myeloproliferative disorders Leuk. Res. 2008, 32, 71-77 (Pubitemid 350100849)
    • (2008) Leukemia Research , vol.32 , Issue.1 , pp. 71-77
    • Karp, J.E.1    Giles, F.J.2    Gojo, I.3    Morris, L.4    Greer, J.5    Johnson, B.6    Thein, M.7    Sznol, M.8    Low, J.9
  • 28
    • 40549137513 scopus 로고    scopus 로고
    • A multicenter phase II trial of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP, Triapine®) and gemcitabine in advanced non-small-cell lung cancer with pharmacokinetic evaluation using peripheral blood mononuclear cells
    • DOI 10.1007/s10637-007-9085-0
    • Ma, B.; Goh, B. C.; Tan, E. H.; Lam, K. C.; Soo, R.; Leong, S. S.; Wang, L. Z.; Mo, F.; Chan, A. T. C.; Zee, B.; Mok, T. A multicenter phase II trial of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP, Triapine (R)) and gemcitabine in advanced non-small-cell lung cancer with pharmacokinetic evaluation using peripheral blood mononuclear cells Invest. New Drugs 2008, 26, 169-173 (Pubitemid 351357710)
    • (2008) Investigational New Drugs , vol.26 , Issue.2 , pp. 169-173
    • Ma, B.1    Goh, B.C.2    Tan, E.H.3    Lam, K.C.4    Soo, R.5    Leong, S.S.6    Wang, L.Z.7    Mo, F.8    Chan, A.T.C.9    Zee, B.10    Mok, T.11
  • 29
    • 39549120057 scopus 로고    scopus 로고
    • A Phase II study of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) and gemcitabine in advanced pancreatic carcinoma. A trial of the Princess Margaret Hospital Phase II consortium
    • Mackenzie, M. J.; Saltman, D.; Hirte, H.; Low, J.; Johnson, C.; Pond, G.; Moore, M. J. A Phase II study of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) and gemcitabine in advanced pancreatic carcinoma. A trial of the Princess Margaret Hospital Phase II consortium Invest. New Drugs 2007, 25, 553-558
    • (2007) Invest. New Drugs , vol.25 , pp. 553-558
    • MacKenzie, M.J.1    Saltman, D.2    Hirte, H.3    Low, J.4    Johnson, C.5    Pond, G.6    Moore, M.J.7
  • 31
    • 33750471953 scopus 로고    scopus 로고
    • Dipyridyl thiosemicarbazone chelators with potent and selective antitumor activity form iron complexes with redox activity
    • DOI 10.1021/jm0606342
    • Richardson, D. R.; Sharpe, P. C.; Lovejoy, D. B.; Senaratne, D.; Kalinowski, D. S.; Islam, M.; Bernhardt, P. V. Dipyridyl thiosemicarbazone chelators with potent and selective antitumor activity form iron complexes with redox activity J. Med. Chem. 2006, 49, 6510-6521 (Pubitemid 44657445)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.22 , 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    Bernhardt, P.V.7
  • 32
    • 34250778335 scopus 로고    scopus 로고
    • Future of toxicology - Iron chelators and differing modes of action and toxicity: The changing face of iron chelation therapy
    • DOI 10.1021/tx700039c
    • Kalinowski, D. S.; Richardson, D. R. Future of toxicology-iron chelators and differing modes of action and toxicity: The changing face of iron chelation therapy Chem. Res. Toxicol. 2007, 20, 715-720 (Pubitemid 46953677)
    • (2007) Chemical Research in Toxicology , vol.20 , Issue.5 , pp. 715-720
    • Kalinowski, D.S.1    Richardson, D.R.2
  • 33
    • 34547562971 scopus 로고    scopus 로고
    • Design, synthesis, and characterization of novel iron chelators: Structure-activity relationships of the 2-benzoylpyridine thiosemicarbazone series and their 3-nitrobenzoyl analogues as potent antitumor agents
    • DOI 10.1021/jm070445z
    • Kalinowski, D. S.; Yu, Y.; Sharpe, P. C.; Islam, M.; Liao, Y. T.; Lovejoy, D. B.; Kumar, N.; Bernhardt, P. V.; Richardson, D. R. Design, synthesis, and characterization of novel iron chelators: Structure-activity relationships of the 2-benzoylpyridine thiosemicarbazone series and their 3-nitrobenzoyl analogues as potent antitumor agents J. Med. Chem. 2007, 50, 3716-3729 (Pubitemid 47195478)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.15 , pp. 3716-3729
    • Kalinowski, D.S.1    Yu, Y.2    Sharpe, P.C.3    Islam, M.4    Liao, Y.-T.5    Lovejoy, D.B.6    Kumar, N.7    Bernhardt, P.V.8    Richardson, D.R.9
  • 34
    • 80053926659 scopus 로고    scopus 로고
    • Bp44mT: An orally-active iron chelator of the thiosemicarbazone class with potent anti-tumor efficacy
    • June 9. DOI: 10.1111/j.1476-5381.2011.01526.x. [Epub ahead of print] PMID:21658021.
    • Yu, Y.; Suryo Rahmanto, Y.; Richardson, D. R. Bp44mT: An orally-active iron chelator of the thiosemicarbazone class with potent anti-tumor efficacy. Br. J. Pharmacol. 2011, June 9. DOI: 10.1111/j.1476-5381.2011.01526.x. [Epub ahead of print] PMID:21658021.
    • (2011) Br. J. Pharmacol.
    • Yu, Y.1    Suryo Rahmanto, Y.2    Richardson, D.R.3
  • 35
    • 0345714575 scopus 로고    scopus 로고
    • Cytotoxic iron chelators: Characterization of the structure, solution chemistry and redox activity of ligands and iron complexes of the di-2-pyridyl ketone isonicotinoyl hydrazone (HPKIH) analogues
    • DOI 10.1007/s00775-003-0486-z
    • Bernhardt, P. V.; Caldwell, L. M.; Chaston, T. B.; Chin, P.; Richardson, D. R. Cytotoxic iron chelators: Characterization of the structure, solution chemistry and redox activity of ligands and iron complexes of the di-2-pyridyl ketone isonicotinoyl hydrazone (HPKIH) analogues J. Biol. Inorg. Chem. 2003, 8, 866-880 (Pubitemid 37486501)
    • (2003) Journal of Biological Inorganic Chemistry , vol.8 , Issue.8 , pp. 866-880
    • Bernhardt, P.V.1    Caldwell, L.M.2    Chaston, T.B.3    Chin, P.4    Richardson, D.R.5
  • 36
    • 64349093037 scopus 로고    scopus 로고
    • 2-Acetylpyridine thiosemicarbazones are potent iron chelators and antiproliferative agents: Redox activity, iron complexation and characterization of their antitumor activity
    • Richardson, D. R.; Kalinowski, D. S.; Richardson, V.; Sharpe, P. C.; Lovejoy, D. B.; Islam, M.; Bernhardt, P. V. 2-Acetylpyridine thiosemicarbazones are potent iron chelators and antiproliferative agents: Redox activity, iron complexation and characterization of their antitumor activity J. Med. Chem. 2009, 52, 1459-1470
    • (2009) J. Med. Chem. , vol.52 , pp. 1459-1470
    • Richardson, D.R.1    Kalinowski, D.S.2    Richardson, V.3    Sharpe, P.C.4    Lovejoy, D.B.5    Islam, M.6    Bernhardt, P.V.7
  • 37
    • 0028891974 scopus 로고
    • The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents
    • Richardson, D. R.; Tran, E. H.; Ponka, P. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents Blood 1995, 86, 4295-4306
    • (1995) Blood , vol.86 , pp. 4295-4306
    • Richardson, D.R.1    Tran, E.H.2    Ponka, P.3
  • 38
    • 0028030463 scopus 로고
    • Iron chelators of the pyridoxal isonicotinoyl hydrazone class. Relationship of the lipophilicity of the apochelator to its ability to mobilise iron from reticulocytes in vitro
    • Ponka, P.; Richardson, D. R.; Edward, J. T.; Chubb, F. L. Iron chelators of the pyridoxal isonicotinoyl hydrazone class. Relationship of the lipophilicity of the apochelator to its ability to mobilize iron from reticulocytes in vitro Can. J. Physiol. Pharmacol. 1994, 72, 659-666 (Pubitemid 24264698)
    • (1994) Canadian Journal of Physiology and Pharmacology , vol.72 , Issue.6 , pp. 659-666
    • Ponka, P.1    Richardson, D.R.2    Edward, J.T.3    Chubb, F.L.4
  • 39
    • 0028535112 scopus 로고
    • The iron-metabolism of the human neuroblastoma cell - Lack of relationship between the efficacy of iron chelation and the inhibition of DNA-synthesis
    • Richardson, D. R.; Ponka, P. The iron-metabolism of the human neuroblastoma cell-Lack of relationship between the efficacy of iron chelation and the inhibition of DNA-synthesis J. Lab. Clin. Med. 1994, 124, 660-671
    • (1994) J. Lab. Clin. Med. , vol.124 , pp. 660-671
    • Richardson, D.R.1    Ponka, P.2
  • 40
    • 0038814301 scopus 로고    scopus 로고
    • Interactions of the pyridine-2-carboxaldehyde isonicotinoyl hydrazone class of chelators with iron and DNA: Implications for toxicity in the treatment of iron overload disease
    • Chaston, T. B.; Richardson, D. R. Interactions of the pyridine-2-carboxaldehyde isonicotinoyl hydrazone class of chelators with iron and DNA: Implications for toxicity in the treatment of iron overload disease J. Biol. Inorg. Chem. 2003, 8, 427-438 (Pubitemid 36578194)
    • (2003) Journal of Biological Inorganic Chemistry , vol.8 , Issue.4 , pp. 427-438
    • Chaston, T.B.1    Richardson, D.R.2
  • 41
    • 0037718255 scopus 로고    scopus 로고
    • Evaluation of the probes 2′,7′-dichlorofluorescin diacetate, luminol, and lucigenin as indicators of reactive species formation
    • DOI 10.1016/S0006-2952(03)00083-2
    • Myhre, O.; Andersen, J. M.; Aarnes, H.; Fonnum, F. Evaluation of the probes 2′,7′-dichlorofluorescin diacetate, luminol, and lucigenin as indicators of reactive species formation Biochem. Pharmacol. 2003, 65, 1575-1582 (Pubitemid 36581871)
    • (2003) Biochemical Pharmacology , vol.65 , Issue.10 , pp. 1575-1582
    • Myhre, O.1    Andersen, J.M.2    Aarnes, H.3    Fonnum, F.4
  • 42
    • 0023289451 scopus 로고
    • Atomic physicochemical parameters for 3-dimensional-structure-directed quantitative structure-activity-relationships. 2. Modeling dispersive and hydrophobic interactions
    • Ghose, A. K.; Crippen, G. M. Atomic physicochemical parameters for 3-dimensional-structure-directed quantitative structure-activity-relationships. 2. Modeling dispersive and hydrophobic interactions J. Chem. Inf. Comput. Sci. 1987, 27, 21-35
    • (1987) J. Chem. Inf. Comput. Sci. , vol.27 , pp. 21-35
    • Ghose, A.K.1    Crippen, G.M.2
  • 44
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for windows - A version of ORTEP-III with a graphical user interface (GUI)
    • Farrugia, L. J. ORTEP-3 for windows-A version of ORTEP-III with a graphical user interface (GUI) J. Appl. Crystallogr. 1997, 30, 565 (Pubitemid 127791756)
    • (1997) Journal of Applied Crystallography , vol.30 , Issue.5 , pp. 565
    • Farrugia, L.J.1
  • 45
    • 0141452964 scopus 로고    scopus 로고
    • WinGX suite for small-molecule single-crystal crystallography
    • Farrugia, L. J. WinGX suite for small-molecule single-crystal crystallography J. Appl. Crystallogr. 1999, 32, 837-838 (Pubitemid 129794704)
    • (1999) Journal of Applied Crystallography , vol.32 , Issue.4 , pp. 837-838
    • Farrugia, L.J.1
  • 46
    • 0030894798 scopus 로고    scopus 로고
    • The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents II: The mechanism of action of ligands derived from salicylaldehyde benzoyl hydrazone and 2-hydroxy-1- naphthylaldehyde benzoyl hydrazone
    • Richardson, D. R.; Milnes, K. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents 0.2. The mechanism of action of ligands derived from salicylaldehyde benzoyl hydrazone and 2-hydroxy-1-naphthylaldehyde benzoyl hydrazone Blood 1997, 89, 3025-3038 (Pubitemid 27172591)
    • (1997) Blood , vol.89 , Issue.8 , pp. 3025-3038
    • Richardson, D.R.1    Milnes, K.2
  • 47
    • 0026575576 scopus 로고
    • Evaluation of the iron chelation potential of hydrazones of pyridoxal, salicylaldehyde and 2-hydroxy-1-naphthylaldehyde using the hepatocyte in culture
    • Baker, E.; Richardson, D.; Gross, S.; Ponka, P. Evaluation of the iron chelation potential of hydrazones of pyridoxal, salicylaldehyde and 2-hydroxy-1-naphthylaldehyde using the hepatocyte in culture Hepatology 1992, 15, 492-501
    • (1992) Hepatology , vol.15 , pp. 492-501
    • Baker, E.1    Richardson, D.2    Gross, S.3    Ponka, P.4
  • 48
    • 0033230124 scopus 로고    scopus 로고
    • Development of novel aroylhydrazone ligands for iron chelation therapy: 2-pyridylcarboxaldehyde isonicotinoyl hydrazone analogs
    • DOI 10.1016/S0022-2143(99)90173-7
    • Becker, E.; Richardson, D. R. Development of novel aroylhydrazone ligands for iron chelation therapy: 2-Pyridylcarboxaldehyde isonicotinoyl hydrazone analogs J. Lab. Clin. Med. 1999, 134, 510-521 (Pubitemid 29530701)
    • (1999) Journal of Laboratory and Clinical Medicine , vol.134 , Issue.5 , pp. 510-521
    • Becker, E.1    Richardson, D.R.2
  • 50
    • 0026787076 scopus 로고
    • Intermediate steps in cellular iron uptake from transferrin - Detection of a cytoplasmic pool of iron, free of transferrin
    • Richardson, D. R.; Baker, E. Intermediate steps in cellular iron uptake from transferrin-Detection of a cytoplasmic pool of iron, free of transferrin J. Biol. Chem. 1992, 267, 21384-21389
    • (1992) J. Biol. Chem. , vol.267 , pp. 21384-21389
    • Richardson, D.R.1    Baker, E.2
  • 51
    • 0028215081 scopus 로고
    • The action of nine chelators on iron-dependent radical damage
    • Dean, R. T.; Nicholson, P. The action of 9 chelators on iron-dependent radical damage Free Radical Res. 1994, 20, 83-101 (Pubitemid 24103739)
    • (1994) Free Radical Research , vol.20 , Issue.2 , pp. 83-101
    • Dean, R.T.1    Nicholson, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.