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Journal Abstract Search


725 related items for PubMed ID: 20889345

  • 1. 4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII.
    Sūdžius J, Baranauskienė L, Golovenko D, Matulienė J, Michailovienė V, Torresan J, Jachno J, Sukackaitė R, Manakova E, Gražulis S, Tumkevičius S, Matulis D.
    Bioorg Med Chem; 2010 Nov 01; 18(21):7413-21. PubMed ID: 20889345
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 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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  • 4. 4-Substituted-2,3,5,6-tetrafluorobenzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, XII, and XIII.
    Dudutienė V, Zubrienė A, Smirnov A, Gylytė J, Timm D, Manakova E, Gražulis S, Matulis D.
    Bioorg Med Chem; 2013 Apr 01; 21(7):2093-106. PubMed ID: 23394791
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  • 5. Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies.
    Carta F, Garaj V, Maresca A, Wagner J, Avvaru BS, Robbins AH, Scozzafava A, McKenna R, Supuran CT.
    Bioorg Med Chem; 2011 May 15; 19(10):3105-19. PubMed ID: 21515057
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  • 6. Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety.
    Sethi KK, Verma SM, Tanç M, Carta F, Supuran CT.
    Bioorg Med Chem; 2013 Sep 01; 21(17):5168-74. PubMed ID: 23867389
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  • 7. 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 01; 51():259-70. PubMed ID: 22440859
    [Abstract] [Full Text] [Related]

  • 8. Benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulfonamides as inhibitors of carbonic anhydrase.
    Dudutiene V, Baranauskiene L, Matulis D.
    Bioorg Med Chem Lett; 2007 Jun 15; 17(12):3335-8. PubMed ID: 17442568
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  • 10. Inhibition and binding studies of carbonic anhydrase isozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides.
    Baranauskienė L, Hilvo M, Matulienė J, Golovenko D, Manakova E, Dudutienė V, Michailovienė V, Torresan J, Jachno J, Parkkila S, Maresca A, Supuran CT, Gražulis S, Matulis D.
    J Enzyme Inhib Med Chem; 2010 Dec 15; 25(6):863-70. PubMed ID: 20166809
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  • 11. In vitro inhibition of α-carbonic anhydrase isozymes by some phenolic compounds.
    Oztürk Sarikaya SB, Topal F, Sentürk M, Gülçin I, Supuran CT.
    Bioorg Med Chem Lett; 2011 Jul 15; 21(14):4259-62. PubMed ID: 21669522
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  • 12. Effects of dopaminergic compounds on carbonic anhydrase isozymes I, II, and VI.
    Sentürk M, Ekinci D, Göksu S, Supuran CT.
    J Enzyme Inhib Med Chem; 2012 Jun 15; 27(3):365-9. PubMed ID: 21699374
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  • 14. Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studies.
    Gitto R, Agnello S, Ferro S, De Luca L, Vullo D, Brynda J, Mader P, Supuran CT, Chimirri A.
    J Med Chem; 2010 Mar 25; 53(6):2401-8. PubMed ID: 20170095
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  • 15. Functionalization of fluorinated benzenesulfonamides and their inhibitory properties toward carbonic anhydrases.
    Dudutienė V, Zubrienė A, Smirnov A, Timm DD, Smirnovienė J, Kazokaitė J, Michailovienė V, Zakšauskas A, Manakova E, Gražulis S, Matulis D.
    ChemMedChem; 2015 Apr 25; 10(4):662-87. PubMed ID: 25758852
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  • 16. Carbonic anhydrase inhibitors. Aromatic/heterocyclic sulfonamides incorporating phenacetyl, pyridylacetyl and thienylacetyl tails act as potent inhibitors of human mitochondrial isoforms VA and VB.
    Güzel O, Innocenti A, Scozzafava A, Salman A, Supuran CT.
    Bioorg Med Chem; 2009 Jul 15; 17(14):4894-9. PubMed ID: 19539481
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  • 18. Carbonic anhydrase inhibitors: novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX.
    Garaj V, Puccetti L, Fasolis G, Winum JY, Montero JL, Scozzafava A, Vullo D, Innocenti A, Supuran CT.
    Bioorg Med Chem Lett; 2005 Jun 15; 15(12):3102-8. PubMed ID: 15905091
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  • 19. 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
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