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Journal Abstract Search

110 related items for PubMed ID: 25468040

  • 1. Inhibition studies of new ureido-substituted sulfonamides incorporating a GABA moiety against human carbonic anhydrase isoforms I-XIV.
    Ceruso M, Antel S, Vullo D, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2014 Dec 15; 22(24):6768-75. PubMed ID: 25468040
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  • 3. Synthesis and inhibition potency of novel ureido benzenesulfonamides incorporating GABA as tumor-associated carbonic anhydrase IX and XII inhibitors.
    Ceruso M, Antel S, Scozzafava A, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Dec 15; 31(2):205-11. PubMed ID: 25792500
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  • 12. Design, synthesis and biological evaluation of novel ureido benzenesulfonamides incorporating 1,3,5-triazine moieties as potent carbonic anhydrase IX inhibitors.
    Lolak N, Akocak S, Bua S, Supuran CT.
    Bioorg Chem; 2019 Feb 15; 82():117-122. PubMed ID: 30312866
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  • 13. Carbonic anhydrase inhibitors: inhibition of the human transmembrane isozyme XIV with a library of aromatic/heterocyclic sulfonamides.
    Ozensoy O, Nishimori I, Vullo D, Puccetti L, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2005 Nov 15; 13(22):6089-93. PubMed ID: 16006130
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  • 19. Benzenesulfonamide bearing 1,2,4-triazole scaffolds as potent inhibitors of tumor associated carbonic anhydrase isoforms hCA IX and hCA XII.
    SitaRam, Celik G, Khloya P, Vullo D, Supuran CT, Sharma PK.
    Bioorg Med Chem; 2014 Mar 15; 22(6):1873-82. PubMed ID: 24560737
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  • 20. 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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