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279 related items for PubMed ID: 17407273

  • 1. Density functional theory study of the reaction mechanism and energetics of the reduction of hydrogen peroxide by ebselen, ebselen diselenide, and ebselen selenol.
    Pearson JK, Boyd RJ.
    J Phys Chem A; 2007 Apr 26; 111(16):3152-60. PubMed ID: 17407273
    [Abstract] [Full Text] [Related]

  • 2. Modeling the reduction of hydrogen peroxide by glutathione peroxidase mimics.
    Pearson JK, Boyd RJ.
    J Phys Chem A; 2006 Jul 20; 110(28):8979-85. PubMed ID: 16836462
    [Abstract] [Full Text] [Related]

  • 3. Reduction of hydrogen peroxide by glutathione peroxidase mimics: reaction mechanism and energetics.
    Heverly-Coulson GS, Boyd RJ.
    J Phys Chem A; 2010 Feb 04; 114(4):1996-2000. PubMed ID: 20039711
    [Abstract] [Full Text] [Related]

  • 4. Modeling the oxidation of ebselen and other organoselenium compounds using explicit solvent networks.
    Bayse CA, Antony S.
    J Phys Chem A; 2009 May 14; 113(19):5780-5. PubMed ID: 19374403
    [Abstract] [Full Text] [Related]

  • 5. Effect of substituents on the GPx-like activity of ebselen: steric versus electronic.
    Pearson JK, Boyd RJ.
    J Phys Chem A; 2008 Feb 07; 112(5):1013-7. PubMed ID: 18197644
    [Abstract] [Full Text] [Related]

  • 6. Mechanism of the reaction of ebselen with endogenous thiols: dihydrolipoate is a better cofactor than glutathione in the peroxidase activity of ebselen.
    Haenen GR, De Rooij BM, Vermeulen NP, Bast A.
    Mol Pharmacol; 1990 Mar 07; 37(3):412-22. PubMed ID: 2107391
    [Abstract] [Full Text] [Related]

  • 7. A novel antioxidant mechanism of ebselen involving ebselen diselenide, a substrate of mammalian thioredoxin and thioredoxin reductase.
    Zhao R, Holmgren A.
    J Biol Chem; 2002 Oct 18; 277(42):39456-62. PubMed ID: 12177067
    [Abstract] [Full Text] [Related]

  • 8. Glutathione peroxidase (GPx)-like antioxidant activity of the organoselenium drug ebselen: unexpected complications with thiol exchange reactions.
    Sarma BK, Mugesh G.
    J Am Chem Soc; 2005 Aug 17; 127(32):11477-85. PubMed ID: 16089478
    [Abstract] [Full Text] [Related]

  • 9. An ebselen like catalyst with enhanced GPx activity via a selenol intermediate.
    Balkrishna SJ, Kumar S, Azad GK, Bhakuni BS, Panini P, Ahalawat N, Tomar RS, Detty MR, Kumar S.
    Org Biomol Chem; 2014 Feb 28; 12(8):1215-9. PubMed ID: 24448734
    [Abstract] [Full Text] [Related]

  • 10. Determination of the relative contributions of the diselenide and selenol forms of ebselen in the mechanism of its glutathione peroxidase-like activity.
    Morgenstern R, Cotgreave IA, Engman L.
    Chem Biol Interact; 1992 Sep 14; 84(1):77-84. PubMed ID: 1394617
    [Abstract] [Full Text] [Related]

  • 11. Synthesis, characterization, and antioxidant activity of some ebselen analogues.
    Bhabak KP, Mugesh G.
    Chemistry; 2007 Sep 14; 13(16):4594-601. PubMed ID: 17299817
    [Abstract] [Full Text] [Related]

  • 12. Time-resolved study on the reactions of organic selenides with hydroxyl and oxide radicals, hydrated electrons, and H-atoms in aqueous solution, and DFT calculations of transients in comparison with sulfur analogues.
    Tobien T, Bonifacić M, Naumov S, Asmus KD.
    Phys Chem Chem Phys; 2010 Jul 07; 12(25):6750-8. PubMed ID: 20431832
    [Abstract] [Full Text] [Related]

  • 13. Antioxidant activity of the anti-inflammatory compound ebselen: a reversible cyclization pathway via selenenic and seleninic acid intermediates.
    Sarma BK, Mugesh G.
    Chemistry; 2008 Jul 07; 14(34):10603-14. PubMed ID: 18932179
    [Abstract] [Full Text] [Related]

  • 14. Can the ebselen derivatives catalyze the isomerization of peroxynitrite to nitrate?
    Musaev DG, Geletii YV, Hill CL, Hirao K.
    J Am Chem Soc; 2003 Apr 02; 125(13):3877-88. PubMed ID: 12656622
    [Abstract] [Full Text] [Related]

  • 15. Theoretical investigations on the reaction of monosubstituted tertiary-benzylamine selenols with hydrogen peroxide.
    Heverly-Coulson GS, Boyd RJ.
    J Phys Chem A; 2010 Oct 07; 114(39):10706-11. PubMed ID: 20836530
    [Abstract] [Full Text] [Related]

  • 16. Stereoelectronic interaction effects on the conformational properties of hydrogen peroxide and its analogues containing S and Se atoms: an ab initio, hybrid-DFT study and NBO analysis.
    Nori-Shargh D, Yahyaei H, Boggs JE.
    J Mol Graph Model; 2010 Jun 07; 28(8):807-13. PubMed ID: 20207563
    [Abstract] [Full Text] [Related]

  • 17. Ebselen: a thioredoxin reductase-dependent catalyst for alpha-tocopherol quinone reduction.
    Fang J, Zhong L, Zhao R, Holmgren A.
    Toxicol Appl Pharmacol; 2005 Sep 01; 207(2 Suppl):103-9. PubMed ID: 15979675
    [Abstract] [Full Text] [Related]

  • 18. Characterisation and quantitation of a selenol intermediate in the reaction of ebselen with thiols.
    Cotgreave IA, Morgenstern R, Engman L, Ahokas J.
    Chem Biol Interact; 1992 Sep 14; 84(1):69-76. PubMed ID: 1394616
    [Abstract] [Full Text] [Related]

  • 19. Modeling the mechanism of the glutathione peroxidase mimic ebselen.
    Antony S, Bayse CA.
    Inorg Chem; 2011 Dec 05; 50(23):12075-84. PubMed ID: 22059718
    [Abstract] [Full Text] [Related]

  • 20. Mechanistic aspects of propene epoxidation by hydrogen peroxide. Catalytic role of water molecules, external electric field, and zeolite framework of TS-1.
    Stare J, Henson NJ, Eckert J.
    J Chem Inf Model; 2009 Apr 05; 49(4):833-46. PubMed ID: 19267473
    [Abstract] [Full Text] [Related]

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