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Journal Abstract Search

294 related items for PubMed ID: 9865942

  • 1. Structural analysis of inhibitor binding to human carbonic anhydrase II.
    Boriack-Sjodin PA, Zeitlin S, Chen HH, Crenshaw L, Gross S, Dantanarayana A, Delgado P, May JA, Dean T, Christianson DW.
    Protein Sci; 1998 Dec; 7(12):2483-9. PubMed ID: 9865942
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  • 2. Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor celecoxib.
    Di Fiore A, Pedone C, D'Ambrosio K, Scozzafava A, De Simone G, Supuran CT.
    Bioorg Med Chem Lett; 2006 Jan 15; 16(2):437-42. PubMed ID: 16290146
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  • 7. Structural study of the location of the phenyl tail of benzene sulfonamides and the effect on human carbonic anhydrase inhibition.
    Güzel-Akdemir O, Biswas S, Lastra K, McKenna R, Supuran CT.
    Bioorg Med Chem; 2013 Nov 01; 21(21):6674-80. PubMed ID: 24012377
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  • 9. Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme II.
    Menchise V, De Simone G, Alterio V, Di Fiore A, Pedone C, Scozzafava A, Supuran CT.
    J Med Chem; 2005 Sep 08; 48(18):5721-7. PubMed ID: 16134940
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  • 11. Kinetic and X-ray crystallographic investigations on carbonic anhydrase isoforms I, II, IX and XII of a thioureido analog of SLC-0111.
    Lomelino CL, Mahon BP, McKenna R, Carta F, Supuran CT.
    Bioorg Med Chem; 2016 Mar 01; 24(5):976-81. PubMed ID: 26810836
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  • 13. Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studies.
    Gitto R, Agnello S, Ferro S, De Luca L, Vullo D, Brynda J, Mader P, Supuran CT, Chimirri A.
    J Med Chem; 2010 Mar 25; 53(6):2401-8. PubMed ID: 20170095
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  • 14. Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms.
    Biswas S, Aggarwal M, Güzel Ö, Scozzafava A, McKenna R, Supuran CT.
    Bioorg Med Chem; 2011 Jun 15; 19(12):3732-8. PubMed ID: 21620713
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  • 18. Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studies.
    Güzel O, Temperini C, Innocenti A, Scozzafava A, Salman A, Supuran CT.
    Bioorg Med Chem Lett; 2008 Jan 01; 18(1):152-8. PubMed ID: 18024029
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  • 19. Phosphorus versus Sulfur: Discovery of Benzenephosphonamidates as Versatile Sulfonamide-Mimic Chemotypes Acting as Carbonic Anhydrase Inhibitors.
    Nocentini A, Gratteri P, Supuran CT.
    Chemistry; 2019 Jan 24; 25(5):1188-1192. PubMed ID: 30411821
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