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538 related items for PubMed ID: 19269822

  • 1. Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anions.
    Innocenti A, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2009 Apr 01; 19(7):1855-7. PubMed ID: 19269822
    [Abstract] [Full Text] [Related]

  • 2. Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamate.
    Innocenti A, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2010 Mar 01; 20(5):1548-50. PubMed ID: 20137947
    [Abstract] [Full Text] [Related]

  • 3. Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV).
    Innocenti A, Vullo D, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2008 Mar 01; 18(5):1583-7. PubMed ID: 18242985
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  • 4. Carbonic anhydrase inhibitors: inhibition of cytosolic carbonic anhydrase isozymes II and VII with simple aromatic sulfonamides and some azo dyes.
    Carta F, Pothen B, Maresca A, Tiwari M, Singh V, Supuran CT.
    Chem Biol Drug Des; 2009 Aug 01; 74(2):196-202. PubMed ID: 19549076
    [Abstract] [Full Text] [Related]

  • 5. Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II-trithiocarbonate adduct--an inhibitor mimicking the sulfonamide and urea binding to the enzyme.
    Temperini C, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2010 Jan 15; 20(2):474-8. PubMed ID: 20005709
    [Abstract] [Full Text] [Related]

  • 6. 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
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  • 7. QSAR study on carbonic anhydrase inhibitors: aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties, with topical activity as antiglaucoma agents.
    Agrawal VK, Bano S, Supuran CT, Khadikar PV.
    Eur J Med Chem; 2004 Jul 01; 39(7):593-600. PubMed ID: 15236839
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.
    Innocenti A, Lehtonen JM, Parkkila S, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2004 Nov 01; 14(21):5435-9. PubMed ID: 15454240
    [Abstract] [Full Text] [Related]

  • 11. Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid.
    Innocenti A, Vullo D, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2008 Aug 01; 16(15):7424-8. PubMed ID: 18579385
    [Abstract] [Full Text] [Related]

  • 12. New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II.
    Carta F, Vullo D, Maresca A, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2012 Mar 15; 22(6):2182-5. PubMed ID: 22365761
    [Abstract] [Full Text] [Related]

  • 13. Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?
    Temperini C, Cecchi A, Scozzafava A, Supuran CT.
    Org Biomol Chem; 2008 Jul 21; 6(14):2499-506. PubMed ID: 18600270
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  • 17. Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.
    Cincinelli A, Martellini T, Innocenti A, Scozzafava A, Supuran CT.
    Bioorg Med Chem; 2011 Mar 15; 19(6):1847-51. PubMed ID: 21377369
    [Abstract] [Full Text] [Related]

  • 18. Anion inhibition studies of an α-carbonic anhydrase from the living fossil Astrosclera willeyana.
    Ohradanova A, Vullo D, Pastorekova S, Pastorek J, Jackson DJ, Wörheide G, Supuran CT.
    Bioorg Med Chem Lett; 2012 Feb 01; 22(3):1314-6. PubMed ID: 22227210
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  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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