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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

725 related items for PubMed ID: 20889345

  • 21.
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  • 22. Pyridazinone substituted benzenesulfonamides as potent carbonic anhydrase inhibitors.
    Yaseen R, Ekinci D, Senturk M, Hameed AD, Ovais S, Rathore P, Samim M, Javed K, Supuran CT.
    Bioorg Med Chem Lett; 2016 Feb 15; 26(4):1337-41. PubMed ID: 26804228
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  • 23. Inhibition pattern of sulfamide-related compounds in binding to carbonic anhydrase isoforms I, II, VII, XII and XIV.
    Gavernet L, Gonzalez Funes JL, Palestro PH, Bruno Blanch LE, Estiu GL, Maresca A, Barrios I, Supuran CT.
    Bioorg Med Chem; 2013 Mar 15; 21(6):1410-8. PubMed ID: 23266178
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  • 29. Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides.
    Mete E, Comez B, Inci Gul H, Gulcin I, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Mar 15; 31(sup2):1-5. PubMed ID: 27435177
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  • 30. Facile synthesis and characterization of novel pyrazole-sulfonamides and their inhibition effects on human carbonic anhydrase isoenzymes.
    Balseven H, Mustafa İşgör M, Mert S, Alım Z, Beydemir S, Ok S, Kasımoğulları R.
    Bioorg Med Chem; 2013 Jan 01; 21(1):21-7. PubMed ID: 23218470
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  • 31. Effects of new 5-amino-1,3,4-thiadiazole-2-sulfonamide derivatives on human carbonic anhydrase isozymes.
    Kasimoğullari R, Bülbül M, Günhan H, Güleryüz H.
    Bioorg Med Chem; 2009 May 01; 17(9):3295-301. PubMed ID: 19362844
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  • 34. Synthesis and carbonic anhydrase isoenzymes I and II inhibitory effects of novel benzylamine derivatives.
    Çetinkaya Y, Göçer H, Göksu S, Gülçin İ.
    J Enzyme Inhib Med Chem; 2014 Apr 01; 29(2):168-74. PubMed ID: 23391138
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  • 35. Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency.
    Pacchiano F, Aggarwal M, Avvaru BS, Robbins AH, Scozzafava A, McKenna R, Supuran CT.
    Chem Commun (Camb); 2010 Nov 28; 46(44):8371-3. PubMed ID: 20922253
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  • 37. New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII.
    Meleddu R, Maccioni E, Distinto S, Bianco G, Melis C, Alcaro S, Cottiglia F, Ceruso M, Supuran CT.
    Bioorg Med Chem Lett; 2015 Aug 15; 25(16):3281-4. PubMed ID: 26073006
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  • 39. Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors.
    Güzel O, Innocenti A, Scozzafava A, Salman A, Supuran CT.
    Bioorg Med Chem Lett; 2009 Jun 15; 19(12):3170-3. PubMed ID: 19435663
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