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Journal Abstract Search

230 related items for PubMed ID: 11456617

  • 1. Glutathione peroxidase-like antioxidant activity of diaryl diselenides: a mechanistic study.
    Mugesh G, Panda A, Singh HB, Punekar NS, Butcher RJ.
    J Am Chem Soc; 2001 Feb 07; 123(5):839-50. PubMed ID: 11456617
    [Abstract] [Full Text] [Related]

  • 2. Functional mimics of glutathione peroxidase: bioinspired synthetic antioxidants.
    Bhabak KP, Mugesh G.
    Acc Chem Res; 2010 Nov 16; 43(11):1408-19. PubMed ID: 20690615
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and structure-activity correlation studies of secondary- and tertiary-amine-based glutathione peroxidase mimics.
    Bhabak KP, Mugesh G.
    Chemistry; 2009 Sep 28; 15(38):9846-54. PubMed ID: 19551790
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Introduction of a catalytic triad increases the glutathione peroxidase-like activity of diaryl diselenides.
    Bhowmick D, Mugesh G.
    Org Biomol Chem; 2015 Sep 14; 13(34):9072-82. PubMed ID: 26220806
    [Abstract] [Full Text] [Related]

  • 6. A simple and efficient strategy to enhance the antioxidant activities of amino-substituted glutathione peroxidase mimics.
    Bhabak KP, Mugesh G.
    Chemistry; 2008 Sep 14; 14(28):8640-51. PubMed ID: 18668498
    [Abstract] [Full Text] [Related]

  • 7. Synthesis, structure, and glutathione peroxidase-like activity of amino acid containing ebselen analogues and diaryl diselenides.
    Selvakumar K, Shah P, Singh HB, Butcher RJ.
    Chemistry; 2011 Nov 04; 17(45):12741-55. PubMed ID: 21956838
    [Abstract] [Full Text] [Related]

  • 8. Amide-based glutathione peroxidase mimics: effect of secondary and tertiary amide substituents on antioxidant activity.
    Bhabak KP, Mugesh G.
    Chem Asian J; 2009 Jun 02; 4(6):974-983. PubMed ID: 19378298
    [Abstract] [Full Text] [Related]

  • 9. Tuning the activity of glutathione peroxidase mimics through intramolecular Se···N,O interactions: a DFT study incorporating solvent-assisted proton exchange (SAPE).
    Bayse CA, Pavlou A.
    Org Biomol Chem; 2011 Dec 07; 9(23):8006-15. PubMed ID: 21989570
    [Abstract] [Full Text] [Related]

  • 10. Biomimetic studies on selenoenzymes: modeling the role of proximal histidines in thioredoxin reductases.
    Sarma BK, Mugesh G.
    Inorg Chem; 2006 Jul 10; 45(14):5307-14. PubMed ID: 16813393
    [Abstract] [Full Text] [Related]

  • 11. Biomimetic studies on iodothyronine deiodinase intermediates: modeling the reduction of selenenyl iodide by thiols.
    Mugesh G, du Mont WW, Wismach C, Jones PG.
    Chembiochem; 2002 May 03; 3(5):440-7. PubMed ID: 12007178
    [Abstract] [Full Text] [Related]

  • 12. Aromatic ring strain in arylselenenyl bromides: role in facile synthesis of selenenate esters via intramolecular cyclization.
    Selvakumar K, Singh HB, Butcher RJ.
    Chemistry; 2010 Sep 10; 16(34):10576-91. PubMed ID: 20648486
    [Abstract] [Full Text] [Related]

  • 13. Anti-thyroid drugs and thyroid hormone synthesis: effect of methimazole derivatives on peroxidase-catalyzed reactions.
    Roy G, Mugesh G.
    J Am Chem Soc; 2005 Nov 02; 127(43):15207-17. PubMed ID: 16248663
    [Abstract] [Full Text] [Related]

  • 14. Antioxidant activity of the anti-inflammatory compound ebselen: a reversible cyclization pathway via selenenic and seleninic acid intermediates.
    Sarma BK, Mugesh G.
    Chemistry; 2008 Nov 02; 14(34):10603-14. PubMed ID: 18932179
    [Abstract] [Full Text] [Related]

  • 15. Design, synthesis and glutathione peroxidase-like properties of ovothiol-derived diselenides.
    Bailly F, Azaroual N, Bernier JL.
    Bioorg Med Chem; 2003 Oct 15; 11(21):4623-30. PubMed ID: 14527559
    [Abstract] [Full Text] [Related]

  • 16. Glutathione peroxidase-like activity of simple selenium compounds. Peroxides and the heterocyclic N-oxide resazurin acting as O-atom donors.
    Prütz WA.
    Z Naturforsch C J Biosci; 1995 Oct 15; 50(3-4):209-19. PubMed ID: 7766257
    [Abstract] [Full Text] [Related]

  • 17. Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenides.
    Back TG, Moussa Z.
    J Am Chem Soc; 2003 Nov 05; 125(44):13455-60. PubMed ID: 14583041
    [Abstract] [Full Text] [Related]

  • 18. Synthesis, structure and reactivity of [o-(2,6-diisopropylphenyliminomethinyl)phenyl]selenenyl selenocyanate (RSeSeCN) and related derivatives.
    Rakesh P, Singh HB, Jasinski JP, Golen JA.
    Dalton Trans; 2014 Jul 07; 43(25):9431-7. PubMed ID: 24671344
    [Abstract] [Full Text] [Related]

  • 19. Disubstituted diaryl diselenides as potential atheroprotective compounds: Involvement of TrxR and GPx-like systems.
    Straliotto MR, de Oliveira J, Mancini G, Bainy AC, Latini A, Deobald AM, Rocha JB, de Bem AF.
    Eur J Pharm Sci; 2013 Mar 12; 48(4-5):717-25. PubMed ID: 23348152
    [Abstract] [Full Text] [Related]

  • 20. 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]

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