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Journal of Enzyme Inhibition|October 28, 1999
Carbonic anhydrase inhibitors. Schiff bases of some aromatic sulfonamides and their metal complexes: towards more selective inhibitors of carbonic anhydrase isozyme IVA Popescu, A Simion, A Scozzafava, et al.Journal of Enzyme Inhibition|October 31, 1998
Sulfonylamido derivatives of 2-aminophenoxathiin-10,10-dioxide and related compounds possess antifungal action due to the possible inhibition of lanosterol-14-alpha-demethylaseC T Supuran, A Scozzafava, F Briganti, et al.Journal of Enzyme Inhibition|August 8, 2002
Carbonic anhydrase inhibitors: metal complexes of a sulfanilamide derived Schiff base and their interaction with isozymes I, II and IVM Ul-Hassan, A Scozzafava, Z H Chohan, et al.Biochemistry|October 4, 2000
Mechanism of cyanamide hydration catalyzed by carbonic anhydrase II suggested by cryogenic X-ray diffractionA Guerri, F Briganti, A Scozzafava, et al.Journal of Enzyme Inhibition|October 16, 1999
The antifungal activity of 2,2'-diamino-4,4'-dithiazole derivatives is due to the possible inhibition of lanosterol-14-alpha-demethylaseA Scozzafava, A Nicolae, O Maior, et al.Biological & Pharmaceutical Bulletin|November 1, 1996
Carbonic anhydrase activators. XV. A kinetic study of the interaction of bovine isozyme II with pyrazoles, bis- and tris-azolyl-methanesC T Supuran, R M Claramunt, J L Lavandera, et al.Metal-Based Drugs|January 1, 1996
Complexes With Biologically Active Ligands. Part 7 Synthesis and Fungitoxic Activity of Metal Complexes Containing 1,3,5-tris-(8-Hydroxyquinolino)- Trichlorocyclo-TriphosphazatrieneM Barboiu, C Guran, I Jitaru, et al.Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|November 7, 1999
Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction?F Briganti, S Mangani, A Scozzafava, et al.Bioorganic & Medicinal Chemistry Letters|March 7, 2001
Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma propertiesA Scozzafava, L Menabuoni, F Mincione, et al.Journal of Enzyme Inhibition|May 16, 2000
Protease inhibitors. Part 2. Weakly basic thrombin inhibitors incorporating sulfonyl-aminoguanidine moieties as S1 anchoring groups: synthesis and structure-activity correlationsB W Clare, A Scozzafava, F Briganti, et al.Pageof 13