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Journal Abstract Search

173 related items for PubMed ID: 16902938

  • 1. Integrated approach using protein and ligand information to analyze selectivity- and affinity-determining features of carbonic anhydrase isozymes.
    Hillebrecht A, Supuran CT, Klebe G.
    ChemMedChem; 2006 Aug; 1(8):839-53. PubMed ID: 16902938
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  • 2. 3D QSAR selectivity analyses of carbonic anhydrase inhibitors: insights for the design of isozyme selective inhibitors.
    Weber A, Böhm M, Supuran CT, Scozzafava A, Sotriffer CA, Klebe G.
    J Chem Inf Model; 2006 Aug; 46(6):2737-60. PubMed ID: 17125213
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  • 3. Quantum chemical QSAR models to distinguish between inhibitory activities of sulfonamides against human carbonic anhydrases I and II and bovine IV isozymes.
    Deeb O, Goodarzi M, Khadikar PV.
    Chem Biol Drug Des; 2012 Apr; 79(4):514-22. PubMed ID: 22181786
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  • 4. Indanesulfonamides as carbonic anhydrase inhibitors. Toward structure-based design of selective inhibitors of the tumor-associated isozyme CA IX.
    Thiry A, Ledecq M, Cecchi A, Dogné JM, Wouters J, Supuran CT, Masereel B.
    J Med Chem; 2006 May 04; 49(9):2743-9. PubMed ID: 16640335
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  • 11. Homology modeling and receptor-based 3D-QSAR study of carbonic anhydrase IX.
    Tuccinardi T, Ortore G, Rossello A, Supuran CT, Martinelli A.
    J Chem Inf Model; 2007 May 04; 47(6):2253-62. PubMed ID: 17949069
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  • 12. 3D-QSAR study of sulfonamide inhibitors of human carbonic anhydrase II.
    Huang H, Pan X, Tan N, Zeng G, Ji C.
    Eur J Med Chem; 2007 Mar 04; 42(3):365-72. PubMed ID: 17118494
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  • 13. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozymes I and II and tumor-associated isozymes IX and XII with S-substituted 4-chloro-2-mercapto-5-methyl-benzenesulfonamides.
    Saczewski F, Innocenti A, Sławiński J, Kornicka A, Brzozowski Z, Pomarnacka E, Scozzafava A, Temperini C, Supuran CT.
    Bioorg Med Chem; 2008 Apr 01; 16(7):3933-40. PubMed ID: 18242998
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  • 14. A DFT-based quantum theoretic QSAR study of aromatic and heterocyclic sulfonamides as carbonic anhydrase inhibitors against isozyme, CA-II.
    Eroglu E, Türkmen H.
    J Mol Graph Model; 2007 Nov 01; 26(4):701-8. PubMed ID: 17493855
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  • 15. 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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  • 16. QSAR studies for the inhibition of the transmembrane isozymes XII and XIV of human carbonic anhydrase with a series of sulfonamides.
    Tarko L, Supuran CT.
    Bioorg Med Chem; 2007 Sep 01; 15(17):5666-71. PubMed ID: 17574422
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  • 17. Carbonic anhydrase inhibitors: 2-substituted-1,3,4-thiadiazole-5-sulfamides act as powerful and selective inhibitors of the mitochondrial isozymes VA and VB over the cytosolic and membrane-associated carbonic anhydrases I, II and IV.
    Smaine FZ, Pacchiano F, Rami M, Barragan-Montero V, Vullo D, Scozzafava A, Winum JY, Supuran CT.
    Bioorg Med Chem Lett; 2008 Dec 15; 18(24):6332-5. PubMed ID: 18990571
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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. Design, synthesis, and docking studies of new 1,3,4-thiadiazole-2-thione derivatives with carbonic anhydrase inhibitory activity.
    Abdel-Hamid MK, Abdel-Hafez AA, El-Koussi NA, Mahfouz NM, Innocenti A, Supuran CT.
    Bioorg Med Chem; 2007 Nov 15; 15(22):6975-84. PubMed ID: 17822907
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  • 20. Carbonic anhydrase inhibitors. Aromatic/heterocyclic sulfonamides incorporating phenacetyl, pyridylacetyl and thienylacetyl tails act as potent inhibitors of human mitochondrial isoforms VA and VB.
    Güzel O, Innocenti A, Scozzafava A, Salman A, Supuran CT.
    Bioorg Med Chem; 2009 Jul 15; 17(14):4894-9. PubMed ID: 19539481
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