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Journal Abstract Search
192 related items for PubMed ID: 15599912
1. In situ click chemistry: enzyme-generated inhibitors of carbonic anhydrase II. Mocharla VP, Colasson B, Lee LV, Röper S, Sharpless KB, Wong CH, Kolb HC. Angew Chem Int Ed Engl; 2004 Dec 17; 44(1):116-20. PubMed ID: 15599912 [No Abstract] [Full Text] [Related]
2. Carbonic anhydrase II-induced selection of inhibitors from a dynamic combinatorial library of Schiff's bases. Nasr G, Petit E, Supuran CT, Winum JY, Barboiu M. Bioorg Med Chem Lett; 2009 Nov 01; 19(21):6014-7. PubMed ID: 19796939 [Abstract] [Full Text] [Related]
3. Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: structure-based drug design, synthesis, and biological evaluation. Vernier W, Chong W, Rewolinski D, Greasley S, Pauly T, Shaw M, Dinh D, Ferre RA, Meador JW, Nukui S, Ornelas M, Paz RL, Reyner E. Bioorg Med Chem; 2010 May 01; 18(9):3307-19. PubMed ID: 20363633 [Abstract] [Full Text] [Related]
4. QSAR study on para-substituted aromatic sulfonamides as carbonic anhydrase II inhibitors using topological information indices. Melagraki G, Afantitis A, Sarimveis H, Igglessi-Markopoulou O, Supuran CT. Bioorg Med Chem; 2006 Feb 15; 14(4):1108-14. PubMed ID: 16213737 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. Nitric oxide-donating carbonic anhydrase inhibitors for the treatment of open-angle glaucoma. Steele RM, Benedini F, Biondi S, Borghi V, Carzaniga L, Impagnatiello F, Miglietta D, Chong WK, Rajapakse R, Cecchi A, Temperini C, Supuran CT. Bioorg Med Chem Lett; 2009 Dec 01; 19(23):6565-70. PubMed ID: 19854054 [Abstract] [Full Text] [Related]
7. A new synthesis of difluoromethanesulfonamides--a novel pharmacophore for carbonic anhydrase inhibition. Boyle NA, Chegwidden WR, Blackburn GM. Org Biomol Chem; 2005 Jan 21; 3(2):222-4. PubMed ID: 15632962 [Abstract] [Full Text] [Related]
8. 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]
9. Synthesis, in vitro antibacterial and carbonic anhydrase II inhibitory activities of N-acylsulfonamides using silica sulfuric acid as an efficient catalyst under both solvent-free and heterogeneous conditions. Massah AR, Adibi H, Khodarahmi R, Abiri R, Majnooni MB, Shahidi S, Asadi B, Mehrabi M, Zolfigol MA. Bioorg Med Chem; 2008 May 15; 16(10):5465-72. PubMed ID: 18439830 [Abstract] [Full Text] [Related]
10. 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]
11. Carbonic anhydrase-encoded dynamic constitutional libraries: toward the discovery of isozyme-specific inhibitors. Nasr G, Petit E, Vullo D, Winum JY, Supuran CT, Barboiu M. J Med Chem; 2009 Aug 13; 52(15):4853-9. PubMed ID: 19580287 [Abstract] [Full Text] [Related]
12. Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency. Pacchiano F, Aggarwal M, Avvaru BS, Robbins AH, Scozzafava A, McKenna R, Supuran CT. Chem Commun (Camb); 2010 Nov 28; 46(44):8371-3. PubMed ID: 20922253 [Abstract] [Full Text] [Related]
13. Fragment-based drug discovery of carbonic anhydrase II inhibitors by dynamic combinatorial chemistry utilizing alkene cross metathesis. Poulsen SA, Bornaghi LF. Bioorg Med Chem; 2006 May 15; 14(10):3275-84. PubMed ID: 16431113 [Abstract] [Full Text] [Related]
14. 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]
15. 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 [Abstract] [Full Text] [Related]
16. 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 15; 74(2):196-202. PubMed ID: 19549076 [Abstract] [Full Text] [Related]
18. 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]