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Journal Abstract Search

83 related items for PubMed ID: 20386818

  • 1. Chimeric microtubule disruptors.
    Leese MP, Jourdan F, Kimberley MR, Cozier GE, Thiyagarajan N, Stengel C, Regis-Lydi S, Foster PA, Newman SP, Acharya KR, Ferrandis E, Purohit A, Reed MJ, Potter BV.
    Chem Commun (Camb); 2010 May 07; 46(17):2907-9. PubMed ID: 20386818
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  • 2. Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents.
    Leese MP, Jourdan FL, Gaukroger K, Mahon MF, Newman SP, Foster PA, Stengel C, Regis-Lydi S, Ferrandis E, Di Fiore A, De Simone G, Supuran CT, Purohit A, Reed MJ, Potter BV.
    J Med Chem; 2008 Mar 13; 51(5):1295-308. PubMed ID: 18260615
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  • 3. 2-substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity.
    Leese MP, Leblond B, Smith A, Newman SP, Di Fiore A, De Simone G, Supuran CT, Purohit A, Reed MJ, Potter BV.
    J Med Chem; 2006 Dec 28; 49(26):7683-96. PubMed ID: 17181151
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  • 4. Design, synthesis and anticancer evaluation of novel tetrahydroquinoline derivatives containing sulfonamide moiety.
    Ghorab MM, Ragab FA, Hamed MM.
    Eur J Med Chem; 2009 Oct 28; 44(10):4211-7. PubMed ID: 19540022
    [Abstract] [Full Text] [Related]

  • 5. Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitors.
    Di Fiore A, Pedone C, Antel J, Waldeck H, Witte A, Wurl M, Scozzafava A, Supuran CT, De Simone G.
    Bioorg Med Chem Lett; 2008 Apr 15; 18(8):2669-74. PubMed ID: 18359629
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  • 6. Out of the active site binding pocket for carbonic anhydrase inhibitors.
    D'Ambrosio K, Carradori S, Monti SM, Buonanno M, Secci D, Vullo D, Supuran CT, De Simone G.
    Chem Commun (Camb); 2015 Apr 15; 51(2):302-5. PubMed ID: 25407638
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  • 7. Protein surface-assisted enhancement in the binding affinity of an inhibitor for recombinant human carbonic anhydrase-II.
    Banerjee AL, Swanson M, Roy BC, Jia X, Haldar MK, Mallik S, Srivastava DK.
    J Am Chem Soc; 2004 Sep 08; 126(35):10875-83. PubMed ID: 15339172
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  • 8. Thermodynamic optimisation in drug discovery: a case study using carbonic anhydrase inhibitors.
    Scott AD, Phillips C, Alex A, Flocco M, Bent A, Randall A, O'Brien R, Damian L, Jones LH.
    ChemMedChem; 2009 Dec 08; 4(12):1985-9. PubMed ID: 19882701
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  • 13. Synthesis, characterization and antiglaucoma activity of a novel proton transfer compound and a mixed-ligand Zn(II) complex.
    Yenikaya C, Sari M, Bülbül M, Ilkimen H, Celik H, Büyükgüngör O.
    Bioorg Med Chem; 2010 Jan 15; 18(2):930-8. PubMed ID: 20006931
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  • 14. 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 15; 39(7):593-600. PubMed ID: 15236839
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  • 19. Analysis of human carbonic anhydrase II: docking reliability and receptor-based 3D-QSAR study.
    Tuccinardi T, Nuti E, Ortore G, Supuran CT, Rossello A, Martinelli A.
    J Chem Inf Model; 2007 Jul 15; 47(2):515-25. PubMed ID: 17295464
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  • 20. Benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulfonamides as inhibitors of carbonic anhydrase.
    Dudutiene V, Baranauskiene L, Matulis D.
    Bioorg Med Chem Lett; 2007 Jun 15; 17(12):3335-8. PubMed ID: 17442568
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