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Journal Abstract Search

725 related items for PubMed ID: 20889345

  • 61. 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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  • 67. Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI.
    Alp C, Özsoy Ş, Alp NA, Erdem D, Gültekin MS, Küfrevioğlu Öİ, Şentürk M, Supuran CT.
    J Enzyme Inhib Med Chem; 2012 Dec 05; 27(6):818-24. PubMed ID: 22188522
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  • 68. 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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  • 70. Fluorinated pyrrolidines and piperidines incorporating tertiary benzenesulfonamide moieties are selective carbonic anhydrase II inhibitors.
    Le Darz A, Mingot A, Bouazza F, Castelli U, Karam O, Tanc M, Supuran CT, Thibaudeau S.
    J Enzyme Inhib Med Chem; 2015 Jan 15; 30(5):737-45. PubMed ID: 25431145
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  • 72. Synthesis and carbonic anhydrase inhibitory properties of new spiroindoline-substituted sulphonamide compounds.
    Güleç Ö, Arslan M, Gencer N, Ergun A, Bilen C, Arslan O.
    Arch Physiol Biochem; 2017 Dec 15; 123(5):306-312. PubMed ID: 28562072
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  • 73. Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library.
    Davis RA, Innocenti A, Poulsen SA, Supuran CT.
    Bioorg Med Chem; 2010 Jan 01; 18(1):14-8. PubMed ID: 19962903
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  • 74. Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: structure-based drug design, synthesis, and biological evaluation.
    Vernier W, Chong W, Rewolinski D, Greasley S, Pauly T, Shaw M, Dinh D, Ferre RA, Meador JW, Nukui S, Ornelas M, Paz RL, Reyner E.
    Bioorg Med Chem; 2010 May 01; 18(9):3307-19. PubMed ID: 20363633
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  • 75. Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.
    Cincinelli A, Martellini T, Innocenti A, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2011 Mar 15; 19(6):1847-51. PubMed ID: 21377369
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  • 76. 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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  • 78. 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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  • 79. Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes.
    Yenikaya C, Sari M, Bülbül M, Ilkimen H, Cinar B, Büyükgüngör O.
    J Enzyme Inhib Med Chem; 2011 Feb 01; 26(1):104-14. PubMed ID: 20860527
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