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Journal Abstract Search

136 related items for PubMed ID: 20481572

  • 21. Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference.
    Temperini C, Cecchi A, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2009 Feb 01; 17(3):1214-21. PubMed ID: 19119014
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  • 22. Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XV.
    Di Fiore A, Monti SM, Innocenti A, Winum JY, De Simone G, Supuran CT.
    Bioorg Med Chem Lett; 2010 Jun 15; 20(12):3601-5. PubMed ID: 20472429
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  • 23. Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitors.
    Di Fiore A, Pedone C, Antel J, Waldeck H, Witte A, Wurl M, Scozzafava A, Supuran CT, De Simone G.
    Bioorg Med Chem Lett; 2008 Apr 15; 18(8):2669-74. PubMed ID: 18359629
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  • 24. S-glycosyl primary sulfonamides--a new structural class for selective inhibition of cancer-associated carbonic anhydrases.
    Lopez M, Paul B, Hofmann A, Morizzi J, Wu QK, Charman SA, Innocenti A, Vullo D, Supuran CT, Poulsen SA.
    J Med Chem; 2009 Oct 22; 52(20):6421-32. PubMed ID: 19827837
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  • 26. Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?
    Temperini C, Cecchi A, Scozzafava A, Supuran CT.
    Org Biomol Chem; 2008 Jul 21; 6(14):2499-506. PubMed ID: 18600270
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  • 27. QSAR study on carbonic anhydrase inhibitors: aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties, with topical activity as antiglaucoma agents.
    Agrawal VK, Bano S, Supuran CT, Khadikar PV.
    Eur J Med Chem; 2004 Jul 21; 39(7):593-600. PubMed ID: 15236839
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  • 30. Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II-trithiocarbonate adduct--an inhibitor mimicking the sulfonamide and urea binding to the enzyme.
    Temperini C, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2010 Jan 15; 20(2):474-8. PubMed ID: 20005709
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  • 31. A QM/MM study of fluoroaromatic interactions at the binding site of carbonic anhydrase II, using a DFT method corrected for dispersive interactions.
    Morgado CA, Hillier IH, Burton NA, McDouall JJ.
    Phys Chem Chem Phys; 2008 May 21; 10(19):2706-14. PubMed ID: 18464985
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  • 33. Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides.
    Wilkinson BL, Bornaghi LF, Houston TA, Innocenti A, Vullo D, Supuran CT, Poulsen SA.
    J Med Chem; 2007 Apr 05; 50(7):1651-7. PubMed ID: 17343373
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  • 34. Analysis of human carbonic anhydrase II: docking reliability and receptor-based 3D-QSAR study.
    Tuccinardi T, Nuti E, Ortore G, Supuran CT, Rossello A, Martinelli A.
    J Chem Inf Model; 2007 Apr 05; 47(2):515-25. PubMed ID: 17295464
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