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Journal Abstract Search

116 related items for PubMed ID: 21369613

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  • 4. Carbonic anhydrase activators: design of high affinity isozymes I, II, and IV activators, incorporating tri-/tetrasubstituted-pyridinium-azole moieties.
    Ilies M, Banciu MD, Ilies MA, Scozzafava A, Caproiu MT, Supuran CT.
    J Med Chem; 2002 Jan 17; 45(2):504-10. PubMed ID: 11784154
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  • 5. Mono- and di-halogenated histamine, histidine and carnosine derivatives are potent carbonic anhydrase I, II, VII, XII and XIV activators.
    Saada MC, Vullo D, Montero JL, Scozzafava A, Supuran CT, Winum JY.
    Bioorg Med Chem; 2014 Sep 01; 22(17):4752-8. PubMed ID: 25082511
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  • 6. Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides derived from 4-isothiocyanato-benzolamide.
    Cecchi A, Winum JY, Innocenti A, Vullo D, Montero JL, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2004 Dec 06; 14(23):5775-80. PubMed ID: 15501039
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  • 8. 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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  • 9. Carbonic anhydrase activators: X-ray crystal structure of the adduct of human isozyme II with L-histidine as a platform for the design of stronger activators.
    Temperini C, Scozzafava A, Puccetti L, Supuran CT.
    Bioorg Med Chem Lett; 2005 Dec 01; 15(23):5136-41. PubMed ID: 16214338
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  • 10. Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library.
    Davis RA, Innocenti A, Poulsen SA, Supuran CT.
    Bioorg Med Chem; 2010 Jan 01; 18(1):14-8. PubMed ID: 19962903
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  • 12. Carbonic anhydrase inhibitors: 2-substituted-1,3,4-thiadiazole-5-sulfamides act as powerful and selective inhibitors of the mitochondrial isozymes VA and VB over the cytosolic and membrane-associated carbonic anhydrases I, II and IV.
    Smaine FZ, Pacchiano F, Rami M, Barragan-Montero V, Vullo D, Scozzafava A, Winum JY, Supuran CT.
    Bioorg Med Chem Lett; 2008 Dec 15; 18(24):6332-5. PubMed ID: 18990571
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  • 14. 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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  • 16. 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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  • 18. New Histamine-Related Five-Membered N-Heterocycle Derivatives as Carbonic Anhydrase I Activators.
    Chiaramonte N, Gabellini A, Angeli A, Bartolucci G, Braconi L, Dei S, Teodori E, Supuran CT, Romanelli MN.
    Molecules; 2022 Jan 15; 27(2):. PubMed ID: 35056859
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  • 19. Quantum chemical QSAR models to distinguish between inhibitory activities of sulfonamides against human carbonic anhydrases I and II and bovine IV isozymes.
    Deeb O, Goodarzi M, Khadikar PV.
    Chem Biol Drug Des; 2012 Apr 15; 79(4):514-22. PubMed ID: 22181786
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  • 20. 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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