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Journal Abstract Search

760 related items for PubMed ID: 21669522

  • 21. 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; 29(2):168-74. PubMed ID: 23391138
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  • 22. 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 Apr; 31(sup2):1-5. PubMed ID: 27435177
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  • 23. Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols and their derivatives including natural products: vidalol B.
    Balaydın HT, Şentürk M, Göksu S, Menzek A.
    Eur J Med Chem; 2012 Aug; 54():423-8. PubMed ID: 22687439
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  • 24. 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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  • 25. In vitro inhibition effects of some new sulfonamide inhibitors on human carbonic anhydrase I and II.
    Cakir U, Uğraş HI, Ozensoy O, Sinan S, Arslan O.
    J Enzyme Inhib Med Chem; 2004 Jun 15; 19(3):257-61. PubMed ID: 15499997
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  • 26. Carbonic anhydrase inhibitors: inhibition of human and bovine isoenzymes by benzenesulphonamides, cyclitols and phenolic compounds.
    Ekinci D, Kurbanoglu NI, Salamci E, Şentürk M, Supuran CT.
    J Enzyme Inhib Med Chem; 2012 Dec 15; 27(6):845-8. PubMed ID: 21999604
    [Abstract] [Full Text] [Related]

  • 27. 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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  • 28. Mono-/dihydroxybenzoic acid esters and phenol pyridinium derivatives as inhibitors of the mammalian carbonic anhydrase isoforms I, II, VII, IX, XII and XIV.
    Carta F, Vullo D, Maresca A, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2013 Mar 15; 21(6):1564-9. PubMed ID: 22668600
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  • 29. Carbonic anhydrase inhibitors. Inhibition of cytosolic isozymes I and II and transmembrane, cancer-associated isozyme IX with lipophilic sulfonamides.
    Franchi M, Vullo D, Gallori E, Pastorek J, Russo A, Scozzafava A, Pastorekova S, Supuran CT.
    J Enzyme Inhib Med Chem; 2003 Aug 15; 18(4):333-8. PubMed ID: 14567548
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  • 30. Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.
    Sentürk M, Gülçin I, Daştan A, Küfrevioğlu OI, Supuran CT.
    Bioorg Med Chem; 2009 Apr 15; 17(8):3207-11. PubMed ID: 19231207
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  • 31. Synthesis and biological evaluation of novel bromophenol derivatives as carbonic anhydrase inhibitors.
    Akbaba Y, Balaydın HT, Menzek A, Göksu S, Şahin E, Ekinci D.
    Arch Pharm (Weinheim); 2013 Jun 15; 346(6):447-54. PubMed ID: 23649517
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  • 32. In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II.
    Bayram E, Senturk M, Kufrevioglu OI, Supuran CT.
    Bioorg Med Chem; 2008 Oct 15; 16(20):9101-5. PubMed ID: 18819808
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  • 33. 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 15; 79(4):514-22. PubMed ID: 22181786
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  • 34. The synthesis of novel pyrazole-3,4-dicarboxamides bearing 5-amino-1,3,4-thiadiazole-2-sulfonamide moiety with effective inhibitory activity against the isoforms of human cytosolic carbonic anhydrase I and II.
    Mert S, Alım Z, İşgör MM, Beydemir Ş, Kasımoğulları R.
    Bioorg Chem; 2016 Oct 15; 68():64-71. PubMed ID: 27454619
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  • 35. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives.
    Innocenti A, Antel J, Wurl M, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2004 Nov 15; 14(22):5703-7. PubMed ID: 15482952
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  • 36. Carbonic anhydrase inhibitors. DNA cloning, characterization, and inhibition studies of the human secretory isoform VI, a new target for sulfonamide and sulfamate inhibitors.
    Nishimori I, Minakuchi T, Onishi S, Vullo D, Scozzafava A, Supuran CT.
    J Med Chem; 2007 Jan 25; 50(2):381-8. PubMed ID: 17228881
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  • 37. Synthesis and carbonic anhydrase inhibitory properties of novel cyclohexanonyl bromophenol derivatives.
    Balaydın HT, Sentürk M, Menzek A.
    Bioorg Med Chem Lett; 2012 Feb 01; 22(3):1352-7. PubMed ID: 22230050
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  • 38. Synthesis and biological evaluation of novel aromatic and heterocyclic bis-sulfonamide Schiff bases as carbonic anhydrase I, II, VII and IX inhibitors.
    Akocak S, Lolak N, Nocentini A, Karakoc G, Tufan A, Supuran CT.
    Bioorg Med Chem; 2017 Jun 15; 25(12):3093-3097. PubMed ID: 28400084
    [Abstract] [Full Text] [Related]

  • 39. Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors.
    Mishra CB, Kumari S, Angeli A, Monti SM, Buonanno M, Prakash A, Tiwari M, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Jun 15; 31(sup2):174-179. PubMed ID: 27314170
    [Abstract] [Full Text] [Related]

  • 40. Carbonic anhydrase inhibitors: inhibition of cytosolic carbonic anhydrase isozymes II and VII with simple aromatic sulfonamides and some azo dyes.
    Carta F, Pothen B, Maresca A, Tiwari M, Singh V, Supuran CT.
    Chem Biol Drug Des; 2009 Aug 15; 74(2):196-202. PubMed ID: 19549076
    [Abstract] [Full Text] [Related]

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