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Journal Abstract Search

227 related items for PubMed ID: 22181786

  • 21. 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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  • 22. Synthesis and evaluation of N-heteroarylsubstituted triazolosulfonamides as carbonic anhydrase inhibitors.
    Balci A, Arslan M, Nixha AR, Bilen C, Ergun A, Gençer N.
    J Enzyme Inhib Med Chem; 2015 Jun 15; 30(3):377-82. PubMed ID: 25068730
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  • 23. Virtual screening-driven identification of human carbonic anhydrase inhibitors incorporating an original, new pharmacophore.
    Pala N, Dallocchio R, Dessì A, Brancale A, Carta F, Ihm S, Maresca A, Sechi M, Supuran CT.
    Bioorg Med Chem Lett; 2011 Apr 15; 21(8):2515-20. PubMed ID: 21420862
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  • 27. 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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  • 31. 3D-QSAR study of benzene sulfonamide analogs as carbonic anhydrase II inhibitors.
    Sethi KK, Verma SM, Prasanthi N, Sahoo SK, Parhi RN, Suresh P.
    Bioorg Med Chem Lett; 2010 May 15; 20(10):3089-93. PubMed ID: 20443227
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  • 32. 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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  • 33. In Vitro inhibition of human carbonic anhydrase I and II isozymes with natural phenolic compounds.
    Sentürk M, Gülçin I, Beydemir S, Küfrevioğlu Oİ, Supuran CT.
    Chem Biol Drug Des; 2011 Jun 15; 77(6):494-9. PubMed ID: 21332948
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  • 34. 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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  • 35. A physically interpretable quantum-theoretic QSAR for some carbonic anhydrase inhibitors with diverse aromatic rings, obtained by a new QSAR procedure.
    Clare BW, Supuran CT.
    Bioorg Med Chem; 2005 Mar 15; 13(6):2197-211. PubMed ID: 15727872
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  • 36. Quaternary ammonium substituted thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides: Potential membrane-impermeable inhibitors of carbonic anhydrase.
    May JA, Namil A, Chen HH, Dantanarayana AP, Dupré B, Liao JC.
    Bioorg Med Chem; 2006 Mar 15; 14(6):2052-9. PubMed ID: 16297631
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  • 37. Inhibition of carbonic anhydrase isozymes I and II with natural products extracted from plants, mushrooms and honey.
    Sahin H, Can Z, Yildiz O, Kolayli S, Innocenti A, Scozzafava G, Supuran CT.
    J Enzyme Inhib Med Chem; 2012 Jun 15; 27(3):395-402. PubMed ID: 21740099
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  • 39. 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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  • 40. Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with carboxylates.
    Innocenti A, Vullo D, Scozzafava A, Casey JR, Supuran C.
    Bioorg Med Chem Lett; 2005 Feb 01; 15(3):573-8. PubMed ID: 15664815
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