BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 23116520)

  • 21. Salen and tetrahydrosalen derivatives act as effective inhibitors of the tumor-associated carbonic anhydrase XII--a new scaffold for designing isoform-selective inhibitors.
    Carradori S; De Monte C; D'Ascenzio M; Secci D; Celik G; Ceruso M; Vullo D; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2013 Dec; 23(24):6759-63. PubMed ID: 24189056
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations.
    Carta F; Aggarwal M; Maresca A; Scozzafava A; McKenna R; Supuran CT
    Chem Commun (Camb); 2012 Feb; 48(13):1868-70. PubMed ID: 22218610
    [TBL] [Abstract][Full Text] [Related]  

  • 23. (3,4-Dihydroxyphenyl)(2,3,4-trihydroxyphenyl)methanone and its derivatives as carbonic anhydrase isoenzymes inhibitors.
    Nar M; Çetinkaya Y; Gülçin İ; Menzek A
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):402-6. PubMed ID: 22468746
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Inhibitory effect of novel pyrazole carboxamide derivatives on human carbonic anhydrase enzyme.
    Şen E; Alim Z; Duran H; İşgör MM; Beydemir Ş; Kasimoğullari R; Ok S
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):328-36. PubMed ID: 22299586
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three β-class carbonic anhydrases from Mycobacterium tuberculosis.
    Maresca A; Scozzafava A; Vullo D; Supuran CT
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):384-7. PubMed ID: 22214209
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms I and II.
    Alp C; Maresca A; Alp NA; Gültekin MS; Ekinci D; Scozzafava A; Supuran CT
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):294-8. PubMed ID: 22380772
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Synthesis and characterization of metal complexes of heterocyclic sulfonamide as carbonic anhydrase inhibitors.
    Büyükkidan N; Bülbül M; Kasimoğullari R; Büyükkidan B
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):311-5. PubMed ID: 22957724
    [TBL] [Abstract][Full Text] [Related]  

  • 28. QSAR studies for the inhibition of the transmembrane isozymes XII and XIV of human carbonic anhydrase with a series of sulfonamides.
    Tarko L; Supuran CT
    Bioorg Med Chem; 2007 Sep; 15(17):5666-71. PubMed ID: 17574422
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Quantitative structure-activity relationship (QSAR) studies on a series of 1,3,4-thiadiazole-2-thione derivatives as tumor-associated carbonic anhydrase IX inhibitors.
    Abdel-Hamid MK; Abdel-Hafez AA; El-Koussi NA; Mahfouz NM
    J Enzyme Inhib Med Chem; 2009 Jun; 24(3):722-9. PubMed ID: 18720193
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inhibition of α-class cytosolic human carbonic anhydrases I, II, IX and XII, and β-class fungal enzymes by carboxylic acids and their derivatives: new isoform-I selective nanomolar inhibitors.
    Sechi M; Innocenti A; Pala N; Rogolino D; Carcelli M; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2012 Sep; 22(18):5801-6. PubMed ID: 22901388
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A DFT-based quantum theoretic QSAR study of aromatic and heterocyclic sulfonamides as carbonic anhydrase inhibitors against isozyme, CA-II.
    Eroglu E; Türkmen H
    J Mol Graph Model; 2007 Nov; 26(4):701-8. PubMed ID: 17493855
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozymes I and II and tumor-associated isozymes IX and XII with S-substituted 4-chloro-2-mercapto-5-methyl-benzenesulfonamides.
    Saczewski F; Innocenti A; Sławiński J; Kornicka A; Brzozowski Z; Pomarnacka E; Scozzafava A; Temperini C; Supuran CT
    Bioorg Med Chem; 2008 Apr; 16(7):3933-40. PubMed ID: 18242998
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Synthesis and characterization of phenolic Mannich bases and effects of these compounds on human carbonic anhydrase isozymes I and II.
    Büyükkidan N; Büyükkidan B; Bülbül M; Özer S; Gonca Yalçin H
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):337-42. PubMed ID: 22994608
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Recent advances in the discovery of zinc-binding motifs for the development of carbonic anhydrase inhibitors.
    Winum JY; Supuran CT
    J Enzyme Inhib Med Chem; 2015 Apr; 30(2):321-4. PubMed ID: 24939097
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Homology modeling and receptor-based 3D-QSAR study of carbonic anhydrase IX.
    Tuccinardi T; Ortore G; Rossello A; Supuran CT; Martinelli A
    J Chem Inf Model; 2007; 47(6):2253-62. PubMed ID: 17949069
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Carbonic anhydrase inhibitors. Regioselective synthesis of novel series 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer-associated isozymes IX and XII.
    Brzozowski Z; Sławiński J; Vullo D; Supuran CT
    Eur J Med Chem; 2012 Oct; 56():282-91. PubMed ID: 22910138
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Inhibition of the alpha- and beta-carbonic anhydrases from the gastric pathogen Helycobacter pylori with anions.
    Maresca A; Vullo D; Scozzafava A; Supuran CT
    J Enzyme Inhib Med Chem; 2013 Apr; 28(2):388-91. PubMed ID: 22299578
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 27(3):365-9. PubMed ID: 21699374
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dithiocarbamates effectively inhibit the α-carbonic anhydrase from
    Giovannuzzi S; Abutaleb NS; Hewitt CS; Carta F; Nocentini A; Seleem MN; Flaherty DP; Supuran CT
    J Enzyme Inhib Med Chem; 2022 Dec; 37(1):1-8. PubMed ID: 34894954
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Homology modeling and QSAR analysis of 1,3,4-thiadiazole and 1,3,4-triazole derivatives as carbonic anhydrase inhibitors.
    Akula NV; Kumar S; Singh V; Tiwari M
    Indian J Biochem Biophys; 2010 Aug; 47(4):234-42. PubMed ID: 21174951
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.