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Journal Abstract Search

254 related items for PubMed ID: 9108424

  • 1. 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 DR, Milnes K.
    Blood; 1997 Apr 15; 89(8):3025-38. PubMed ID: 9108424
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  • 2. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents.
    Richardson DR, Tran EH, Ponka P.
    Blood; 1995 Dec 01; 86(11):4295-306. PubMed ID: 7492790
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  • 3. Development of novel aroylhydrazone ligands for iron chelation therapy: 2-pyridylcarboxaldehyde isonicotinoyl hydrazone analogs.
    Becker E, Richardson DR.
    J Lab Clin Med; 1999 Nov 01; 134(5):510-21. PubMed ID: 10560945
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  • 4. The potential of iron chelators of the pyridoxal isonicotinoyl hydrazone class as effective antiproliferative agents III: the effect of the ligands on molecular targets involved in proliferation.
    Darnell G, Richardson DR.
    Blood; 1999 Jul 15; 94(2):781-92. PubMed ID: 10397746
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  • 5. The iron metabolism of the human neuroblastoma cell: lack of relationship between the efficacy of iron chelation and the inhibition of DNA synthesis.
    Richardson DR, Ponka P.
    J Lab Clin Med; 1994 Nov 15; 124(5):660-71. PubMed ID: 7964124
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  • 6. Mobilization of iron from neoplastic cells by some iron chelators is an energy-dependent process.
    Richardson DR.
    Biochim Biophys Acta; 1997 May 16; 1320(1):45-57. PubMed ID: 9186779
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  • 7. 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.
    Hepatology; 1992 Mar 16; 15(3):492-501. PubMed ID: 1544632
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  • 10. The effect of the iron(III) chelator, desferrioxamine, on iron and transferrin uptake by the human malignant melanoma cell.
    Richardson D, Ponka P, Baker E.
    Cancer Res; 1994 Feb 01; 54(3):685-9. PubMed ID: 8306330
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  • 13. Mode of action of iron (III) chelators as antimalarials. IV. Potentiation of desferal action by benzoyl and isonicotinoyl hydrazone derivatives.
    Tsafack A, Loyevsky M, Ponka P, Cabantchik ZI.
    J Lab Clin Med; 1996 Jun 01; 127(6):574-82. PubMed ID: 8648262
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  • 14. Lipophilicity of analogs of pyridoxal isonicotinoyl hydrazone (PIH) determines the efflux of iron complexes and toxicity in K562 cells.
    Buss JL, Arduini E, Shephard KC, Ponka P.
    Biochem Pharmacol; 2003 Feb 01; 65(3):349-60. PubMed ID: 12527328
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  • 15. Biliary iron excretion in rats following treatment with analogs of pyridoxal isonicotinoyl hydrazone.
    Bláha K, Cikrt M, Nerudová J, Ponka HF.
    Blood; 1998 Jun 01; 91(11):4368-72. PubMed ID: 9596686
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  • 18. Pyridoxal isonicotinoyl hydrazone analogs induce apoptosis in hematopoietic cells due to their iron-chelating properties.
    Buss JL, Neuzil J, Gellert N, Weber C, Ponka P.
    Biochem Pharmacol; 2003 Jan 15; 65(2):161-72. PubMed ID: 12504792
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  • 19. Methyl and ethyl ketone analogs of salicylaldehyde isonicotinoyl hydrazone: novel iron chelators with selective antiproliferative action.
    Macková E, Hrušková K, Bendová P, Vávrová A, Jansová H, Hašková P, Kovaříková P, Vávrová K, Simůnek T.
    Chem Biol Interact; 2012 May 30; 197(2-3):69-79. PubMed ID: 22521999
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  • 20. Analogues of pyridoxal isonicotinoyl hydrazone (PIH) as potential iron chelators for the treatment of neoplasia.
    Richardson DR.
    Leuk Lymphoma; 1998 Sep 30; 31(1-2):47-60. PubMed ID: 9720714
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