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PUBMED FOR HANDHELDS

Journal Abstract Search


185 related items for PubMed ID: 34328515

  • 1. Structure and mechanism of secondary sulfonamide binding to carbonic anhydrases.
    Baronas D, Dudutienė V, Paketurytė V, Kairys V, Smirnov A, Juozapaitienė V, Vaškevičius A, Manakova E, Gražulis S, Zubrienė A, Matulis D.
    Eur Biophys J; 2021 Oct; 50(7):993-1011. PubMed ID: 34328515
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  • 2. Thermodynamic, kinetic, and structural parameterization of human carbonic anhydrase interactions toward enhanced inhibitor design.
    Linkuvienė V, Zubrienė A, Manakova E, Petrauskas V, Baranauskienė L, Zakšauskas A, Smirnov A, Gražulis S, Ladbury JE, Matulis D.
    Q Rev Biophys; 2018 Jan; 51():e10. PubMed ID: 30912486
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  • 3. Intrinsic thermodynamics of sulfonamide inhibitor binding to human carbonic anhydrases I and II.
    Morkūnaitė V, Gylytė J, Zubrienė A, Baranauskienė L, Kišonaitė M, Michailovienė V, Juozapaitienė V, Todd MJ, Matulis D.
    J Enzyme Inhib Med Chem; 2015 Apr; 30(2):204-11. PubMed ID: 24758348
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  • 4. Intrinsic thermodynamics of high affinity inhibitor binding to recombinant human carbonic anhydrase IV.
    Mickevičiūtė A, Timm DD, Gedgaudas M, Linkuvienė V, Chen Z, Waheed A, Michailovienė V, Zubrienė A, Smirnov A, Čapkauskaitė E, Baranauskienė L, Jachno J, Revuckienė J, Manakova E, Gražulis S, Matulienė J, Di Cera E, Sly WS, Matulis D.
    Eur Biophys J; 2018 Apr; 47(3):271-290. PubMed ID: 28975383
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  • 5. Intrinsic Thermodynamics and Structures of 2,4- and 3,4-Substituted Fluorinated Benzenesulfonamides Binding to Carbonic Anhydrases.
    Zubrienė A, Smirnov A, Dudutienė V, Timm DD, Matulienė J, Michailovienė V, Zakšauskas A, Manakova E, Gražulis S, Matulis D.
    ChemMedChem; 2017 Jan 20; 12(2):161-176. PubMed ID: 28001003
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  • 6. Thiazole-substituted benzenesulfonamides as inhibitors of 12 human carbonic anhydrases.
    Čapkauskaitė E, Zubrienė A, Paketurytė V, Timm DD, Tumkevičius S, Matulis D.
    Bioorg Chem; 2018 Apr 20; 77():534-541. PubMed ID: 29459130
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  • 8. 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies.
    Leitans J, Sprudza A, Tanc M, Vozny I, Zalubovskis R, Tars K, Supuran CT.
    Bioorg Med Chem; 2013 Sep 01; 21(17):5130-8. PubMed ID: 23859774
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  • 11. Design of two-tail compounds with rotationally fixed benzenesulfonamide ring as inhibitors of carbonic anhydrases.
    Zakšauskas A, Čapkauskaitė E, Jezepčikas L, Linkuvienė V, Kišonaitė M, Smirnov A, Manakova E, Gražulis S, Matulis D.
    Eur J Med Chem; 2018 Aug 05; 156():61-78. PubMed ID: 30006175
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  • 15. Methyl 2-Halo-4-Substituted-5-Sulfamoyl-Benzoates as High Affinity and Selective Inhibitors of Carbonic Anhydrase IX.
    Zakšauskas A, Čapkauskaitė E, Paketurytė-Latvė V, Smirnov A, Leitans J, Kazaks A, Dvinskis E, Stančaitis L, Mickevičiūtė A, Jachno J, Jezepčikas L, Linkuvienė V, Sakalauskas A, Manakova E, Gražulis S, Matulienė J, Tars K, Matulis D.
    Int J Mol Sci; 2021 Dec 23; 23(1):. PubMed ID: 35008553
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  • 16. Characterization of human carbonic anhydrase XII stability and inhibitor binding.
    Jogaitė V, Zubrienė A, Michailovienė V, Gylytė J, Morkūnaitė V, Matulis D.
    Bioorg Med Chem; 2013 Mar 15; 21(6):1431-6. PubMed ID: 23159038
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