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Journal Abstract Search

164 related items for PubMed ID: 11073664

  • 21. Arylfurans as potential trypanosoma cruzi trypanothione reductase inhibitors.
    de Oliveira RB, Vaz AB, Alves RO, Liarte DB, Donnici CL, Romanha AJ, Zani CL.
    Mem Inst Oswaldo Cruz; 2006 Mar; 101(2):169-73. PubMed ID: 16830710
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  • 22. Two interacting binding sites for quinacrine derivatives in the active site of trypanothione reductase: a template for drug design.
    Saravanamuthu A, Vickers TJ, Bond CS, Peterson MR, Hunter WN, Fairlamb AH.
    J Biol Chem; 2004 Jul 09; 279(28):29493-500. PubMed ID: 15102853
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  • 26. Synthesis, inhibition potency, binding mode, and antiprotozoal activities of fluorescent inhibitors of trypanothione reductase based on mepacrine-conjugated diaryl sulfide scaffolds.
    Eberle C, Burkhard JA, Stump B, Kaiser M, Brun R, Krauth-Siegel RL, Diederich F.
    ChemMedChem; 2009 Dec 09; 4(12):2034-44. PubMed ID: 19847846
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  • 27. Biological Evaluation and X-ray Co-crystal Structures of Cyclohexylpyrrolidine Ligands for Trypanothione Reductase, an Enzyme from the Redox Metabolism of Trypanosoma.
    De Gasparo R, Brodbeck-Persch E, Bryson S, Hentzen NB, Kaiser M, Pai EF, Krauth-Siegel RL, Diederich F.
    ChemMedChem; 2018 May 08; 13(9):957-967. PubMed ID: 29624890
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  • 29. Privileged structure-guided synthesis of quinazoline derivatives as inhibitors of trypanothione reductase.
    Cavalli A, Lizzi F, Bongarzone S, Brun R, Luise Krauth-Siegel R, Bolognesi ML.
    Bioorg Med Chem Lett; 2009 Jun 01; 19(11):3031-5. PubMed ID: 19414258
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  • 34. Mechanism of inhibition of trypanothione reductase and glutathione reductase by trivalent organic arsenicals.
    Cunningham ML, Zvelebil MJ, Fairlamb AH.
    Eur J Biochem; 1994 Apr 01; 221(1):285-95. PubMed ID: 8168518
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  • 37. Engineering the substrate specificity of glutathione reductase toward that of trypanothione reduction.
    Henderson GB, Murgolo NJ, Kuriyan J, Osapay K, Kominos D, Berry A, Scrutton NS, Hinchliffe NW, Perham RN, Cerami A.
    Proc Natl Acad Sci U S A; 1991 Oct 01; 88(19):8769-73. PubMed ID: 1924337
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  • 38. Polyamines with N-(3-phenylpropyl) substituents are effective competitive inhibitors of trypanothione reductase and trypanocidal agents.
    Li Z, Fennie MW, Ganem B, Hancock MT, Kobaslija M, Rattendi D, Bacchi CJ, O'Sullivan MC.
    Bioorg Med Chem Lett; 2001 Jan 22; 11(2):251-4. PubMed ID: 11206471
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  • 39. Leishmania infantum trypanothione reductase is a promiscuous enzyme carrying an NADPH:O2 oxidoreductase activity shared by glutathione reductase.
    Angiulli G, Lantella A, Forte E, Angelucci F, Colotti G, Ilari A, Malatesta F.
    Biochim Biophys Acta; 2015 Sep 22; 1850(9):1891-7. PubMed ID: 26033467
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