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626 related items for PubMed ID: 18024029
1. Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studies. Güzel O, Temperini C, Innocenti A, Scozzafava A, Salman A, Supuran CT. Bioorg Med Chem Lett; 2008 Jan 01; 18(1):152-8. PubMed ID: 18024029 [Abstract] [Full Text] [Related]
2. Carbonic anhydrase inhibitors. Interaction of 2-N,N-dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studies. Temperini C, Cecchi A, Boyle NA, Scozzafava A, Cabeza JE, Wentworth P, Blackburn GM, Supuran CT. Bioorg Med Chem Lett; 2008 Feb 01; 18(3):999-1005. PubMed ID: 18162396 [Abstract] [Full Text] [Related]
3. Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. Güzel O, Innocenti A, Scozzafava A, Salman A, Parkkila S, Hilvo M, Supuran CT. Bioorg Med Chem; 2008 Oct 15; 16(20):9113-20. PubMed ID: 18819811 [Abstract] [Full Text] [Related]
14. Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors. Güzel O, Innocenti A, Scozzafava A, Salman A, Supuran CT. Bioorg Med Chem Lett; 2009 Jun 15; 19(12):3170-3. PubMed ID: 19435663 [Abstract] [Full Text] [Related]
17. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition. Weber A, Casini A, Heine A, Kuhn D, Supuran CT, Scozzafava A, Klebe G. J Med Chem; 2004 Jan 29; 47(3):550-7. PubMed ID: 14736236 [Abstract] [Full Text] [Related]
18. 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]
19. 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]
20. 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies. Leitans J, Sprudza A, Tanc M, Vozny I, Zalubovskis R, Tars K, Supuran CT. Bioorg Med Chem; 2013 Sep 01; 21(17):5130-8. PubMed ID: 23859774 [Abstract] [Full Text] [Related] Page: [Next] [New Search]