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Journal Abstract Search

294 related items for PubMed ID: 22440859

  • 1. Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases.
    Čapkauskaitė E, Zubrienė A, Baranauskienė L, Tamulaitienė G, Manakova E, Kairys V, Gražulis S, Tumkevičius S, Matulis D.
    Eur J Med Chem; 2012 May; 51():259-70. PubMed ID: 22440859
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  • 3. Benzenesulfonamides with pyrimidine moiety as inhibitors of human carbonic anhydrases I, II, VI, VII, XII, and XIII.
    Čapkauskaitė E, Zubrienė A, Smirnov A, Torresan J, Kišonaitė M, Kazokaitė J, Gylytė J, Michailovienė V, Jogaitė V, Manakova E, Gražulis S, Tumkevičius S, Matulis D.
    Bioorg Med Chem; 2013 Nov 15; 21(22):6937-47. PubMed ID: 24103428
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  • 6. Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII.
    Čapkauskaitė E, Baranauskienė L, Golovenko D, Manakova E, Gražulis S, Tumkevičius S, Matulis D.
    Bioorg Med Chem; 2010 Nov 01; 18(21):7357-64. PubMed ID: 20926301
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  • 8. 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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  • 9. 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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  • 10. S-glycosyl primary sulfonamides--a new structural class for selective inhibition of cancer-associated carbonic anhydrases.
    Lopez M, Paul B, Hofmann A, Morizzi J, Wu QK, Charman SA, Innocenti A, Vullo D, Supuran CT, Poulsen SA.
    J Med Chem; 2009 Oct 22; 52(20):6421-32. PubMed ID: 19827837
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  • 12. Pyrrolidinone-bearing methylated and halogenated benzenesulfonamides as inhibitors of carbonic anhydrases.
    Vaškevičienė I, Paketurytė V, Pajanok N, Žukauskas Š, Sapijanskaitė B, Kantminienė K, Mickevičius V, Zubrienė A, Matulis D.
    Bioorg Med Chem; 2019 Jan 15; 27(2):322-337. PubMed ID: 30553625
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  • 13. Synthesis of sulfonamides with effective inhibitory action against Porphyromonas gingivalis γ-carbonic anhydrase.
    Ceruso M, Del Prete S, AlOthman Z, Osman SM, Scozzafava A, Capasso C, Supuran CT.
    Bioorg Med Chem Lett; 2014 Aug 15; 24(16):4006-10. PubMed ID: 25011913
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  • 14. Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives.
    Poulsen SA, Wilkinson BL, Innocenti A, Vullo D, Supuran CT.
    Bioorg Med Chem Lett; 2008 Aug 15; 18(16):4624-7. PubMed ID: 18644716
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  • 15. 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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