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Journal Abstract Search
407 related items for PubMed ID: 19303173
21. Predictive QSAR modeling of HIV reverse transcriptase inhibitor TIBO derivatives. Mandal AS, Roy K. Eur J Med Chem; 2009 Apr; 44(4):1509-24. PubMed ID: 18760864 [Abstract] [Full Text] [Related]
22. TOMOCOMD-CARDD descriptors-based virtual screening of tyrosinase inhibitors: evaluation of different classification model combinations using bond-based linear indices. Casañola-Martín GM, Marrero-Ponce Y, Khan MT, Ather A, Sultan S, Torrens F, Rotondo R. Bioorg Med Chem; 2007 Feb 01; 15(3):1483-503. PubMed ID: 17110117 [Abstract] [Full Text] [Related]
23. Carbonic anhydrase inhibitors. Inhibition of isoforms I, II, IV, VA, VII, IX, and XIV with sulfonamides incorporating fructopyranose-thioureido tails. Winum JY, Thiry A, Cheikh KE, Dogné JM, Montero JL, Vullo D, Scozzafava A, Masereel B, Supuran CT. Bioorg Med Chem Lett; 2007 May 15; 17(10):2685-91. PubMed ID: 17376683 [Abstract] [Full Text] [Related]
24. QSAR study on topically acting sulfonamides incorporating GABA moieties: a molecular connectivity approach. Agrawal VK, Singh J, Khadikar PV, Supuran CT. Bioorg Med Chem Lett; 2006 Apr 01; 16(7):2044-51. PubMed ID: 16458003 [Abstract] [Full Text] [Related]
25. Novel use of chemical shift in NMR as molecular descriptor: a first report on modeling carbonic anhydrase inhibitory activity and related parameters. Khadikar PV, Sharma V, Karmarkar S, Supuran CT. Bioorg Med Chem Lett; 2005 Feb 15; 15(4):931-6. PubMed ID: 15686889 [Abstract] [Full Text] [Related]
26. QSAR study on carbonic anhydrase inhibitors: water-soluble sulfonamides incorporating beta-alanyl moieties, possessing long lasting-intra ocular pressure lowering properties--a molecular connectivity approach. Agrawal VK, Banerji M, Gupta M, Singh J, Khadikar PV, Supuran CT. Eur J Med Chem; 2005 Oct 15; 40(10):1002-12. PubMed ID: 15961191 [Abstract] [Full Text] [Related]
28. Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. Wilkinson BL, Bornaghi LF, Houston TA, Innocenti A, Vullo D, Supuran CT, Poulsen SA. J Med Chem; 2007 Apr 05; 50(7):1651-7. PubMed ID: 17343373 [Abstract] [Full Text] [Related]
29. Correlation analyses on binding affinity of substituted benzenesulfonamides with carbonic anhydrase using ab initio MO calculations on their complex structures (II). Munei Y, Shimamoto K, Harada M, Yoshida T, Chuman H. Bioorg Med Chem Lett; 2011 Jan 01; 21(1):141-4. PubMed ID: 21130650 [Abstract] [Full Text] [Related]
30. New aromatic/heteroaromatic propanesulfonylhydrazone compounds: synthesis, physical properties and inhibition studies against carbonic anhydrase II (CAII) enzyme. Özmen Özdemir Ü, Altuntaş A, Gündüzalp AB, Arslan F, Hamurcu F. Spectrochim Acta A Mol Biomol Spectrosc; 2014 Jul 15; 128():452-60. PubMed ID: 24682061 [Abstract] [Full Text] [Related]
31. QSAR studies on the activation of the human carbonic anhydrase cytosolic isoforms I and II and secretory isozyme VI with amino acids and amines. Singh J, Shaik B, Singh S, Sikhima S, Agrawal VK, Khadikar PV, Supuran CT. Bioorg Med Chem; 2007 Oct 15; 15(20):6501-9. PubMed ID: 17689086 [Abstract] [Full Text] [Related]
32. QSTR with extended topochemical atom (ETA) indices. 12. QSAR for the toxicity of diverse aromatic compounds to Tetrahymena pyriformis using chemometric tools. Roy K, Ghosh G. Chemosphere; 2009 Nov 15; 77(7):999-1009. PubMed ID: 19709717 [Abstract] [Full Text] [Related]
33. Quaternary ammonium substituted thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides: Potential membrane-impermeable inhibitors of carbonic anhydrase. May JA, Namil A, Chen HH, Dantanarayana AP, Dupré B, Liao JC. Bioorg Med Chem; 2006 Mar 15; 14(6):2052-9. PubMed ID: 16297631 [Abstract] [Full Text] [Related]
34. Carbonic anhydrase inhibitors: binding of indanesulfonamides to the human isoform II. D'Ambrosio K, Masereel B, Thiry A, Scozzafava A, Supuran CT, De Simone G. ChemMedChem; 2008 Mar 15; 3(3):473-7. PubMed ID: 18161740 [Abstract] [Full Text] [Related]
35. Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference. Temperini C, Cecchi A, Scozzafava A, Supuran CT. Bioorg Med Chem; 2009 Feb 01; 17(3):1214-21. PubMed ID: 19119014 [Abstract] [Full Text] [Related]
36. Topological modeling of lipophilicity, diuretic activity, and carbonic inhibition activity of benzene sulfonamides: a molecular connectivity approach. Jaiswal M, Khadikar PV, Supuran CT. Bioorg Med Chem Lett; 2004 Nov 15; 14(22):5661-6. PubMed ID: 15482943 [Abstract] [Full Text] [Related]
37. Inhibition of carbonic anhydrase II by thioxolone: a mechanistic and structural study. Barrese AA, Genis C, Fisher SZ, Orwenyo JN, Kumara MT, Dutta SK, Phillips E, Kiddle JJ, Tu C, Silverman DN, Govindasamy L, Agbandje-McKenna M, McKenna R, Tripp BC. Biochemistry; 2008 Mar 11; 47(10):3174-84. PubMed ID: 18266323 [Abstract] [Full Text] [Related]
38. Quantitative structure-activity relationship modeling of juvenile hormone mimetic compounds for Culex pipiens larvae, with a discussion of descriptor-thinning methods. Basak SC, Natarajan R, Mills D, Hawkins DM, Kraker JJ. J Chem Inf Model; 2006 Mar 11; 46(1):65-77. PubMed ID: 16426041 [Abstract] [Full Text] [Related]
39. 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 [Abstract] [Full Text] [Related]