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Journal Abstract Search

256 related items for PubMed ID: 22883029

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  • 4. Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.
    Vullo D, Voipio J, Innocenti A, Rivera C, Ranki H, Scozzafava A, Kaila K, Supuran CT.
    Bioorg Med Chem Lett; 2005 Feb 15; 15(4):971-6. PubMed ID: 15686895
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  • 7. Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides.
    Nishimori I, Vullo D, Innocenti A, Scozzafava A, Mastrolorenzo A, Supuran CT.
    Bioorg Med Chem Lett; 2005 Sep 01; 15(17):3828-33. PubMed ID: 16039848
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  • 10. Carbonic anhydrase inhibitors: synthesis and inhibition of the human carbonic anhydrase isoforms I, II, VII, IX and XII with benzene sulfonamides incorporating 4,5,6,7-tetrabromophthalimide moiety.
    Sethi KK, Vullo D, Verma SM, Tanç M, Carta F, Supuran CT.
    Bioorg Med Chem; 2013 Oct 01; 21(19):5973-82. PubMed ID: 23965175
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  • 14. Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs.
    Nishimori I, Minakuchi T, Morimoto K, Sano S, Onishi S, Takeuchi H, Vullo D, Scozzafava A, Supuran CT.
    J Med Chem; 2006 Mar 23; 49(6):2117-26. PubMed ID: 16539401
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  • 15. The first activation study of a bacterial carbonic anhydrase (CA). The thermostable α-CA from Sulfurihydrogenibium yellowstonense YO3AOP1 is highly activated by amino acids and amines.
    Vullo D, De Luca V, Scozzafava A, Carginale V, Rossi M, Supuran CT, Capasso C.
    Bioorg Med Chem Lett; 2012 Oct 15; 22(20):6324-7. PubMed ID: 22999416
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  • 16. Synthesis of novel acridine and bis acridine sulfonamides with effective inhibitory activity against the cytosolic carbonic anhydrase isoforms II and VII.
    Ulus R, Yeşildağ I, Tanç M, Bülbül M, Kaya M, Supuran CT.
    Bioorg Med Chem; 2013 Sep 15; 21(18):5799-805. PubMed ID: 23910989
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  • 17. 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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  • 18. Carbonic anhydrase inhibitors: inhibition of the beta-class enzyme from the yeast Saccharomyces cerevisiae with sulfonamides and sulfamates.
    Isik S, Kockar F, Aydin M, Arslan O, Guler OO, Innocenti A, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2009 Feb 01; 17(3):1158-63. PubMed ID: 19124253
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  • 19. Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides.
    Innocenti A, Firnges MA, Antel J, Wurl M, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2005 Feb 15; 15(4):1149-54. PubMed ID: 15686931
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  • 20. Biochemical properties of a novel and highly thermostable bacterial α-carbonic anhydrase from Sulfurihydrogenibium yellowstonense YO3AOP1.
    Capasso C, De Luca V, Carginale V, Cannio R, Rossi M.
    J Enzyme Inhib Med Chem; 2012 Dec 15; 27(6):892-7. PubMed ID: 22803664
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