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Results: 1-25 | 26-50 | 51-75 | 76-77
Results: 26-50/77
Carbonic anhydrase inhibitors; Phosphoryl-sulfonamides - A new class of high affinity inhibitors of isozymes I and II
Authors: Fenesan, I Popescu, R Scozzafava, A Crucin, V Mateiciuc, E Bauer, R Ilies, MA Supuran, CT
Citation: I. Fenesan et al., Carbonic anhydrase inhibitors; Phosphoryl-sulfonamides - A new class of high affinity inhibitors of isozymes I and II, J ENZ INHIB, 15(3), 2000, pp. 297-310
Protease inhibitors: Synthesis of L-alanine hydroxamate sulfonylated derivatives as inhibitors of Clostridium histolyticum collagenase
Authors: Supuran, CT Briganti, F Mincione, G Scozzafava, A
Citation: Ct. Supuran et al., Protease inhibitors: Synthesis of L-alanine hydroxamate sulfonylated derivatives as inhibitors of Clostridium histolyticum collagenase, J ENZ INHIB, 15(2), 2000, pp. 111-128
Carbonic anhydrase activators: Synthesis of high affinity isozymes I, II and IV activators, derivatives of 4-(4-tosylureido-amino acyl)ethyl-1H-imidazole (histamine derivatives)
Authors: Scozzafava, A Iorga, B Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase activators: Synthesis of high affinity isozymes I, II and IV activators, derivatives of 4-(4-tosylureido-amino acyl)ethyl-1H-imidazole (histamine derivatives), J ENZ INHIB, 15(2), 2000, pp. 139-161
Carbonic anhydrase inhibitors and their therapeutic potential
Authors: Supuran, CT Scozzafava, A
Citation: Ct. Supuran et A. Scozzafava, Carbonic anhydrase inhibitors and their therapeutic potential, EXPERT OP T, 10(5), 2000, pp. 575-600
Carbonic anhydrase inhibitors: Sulfonamides incorporating furan-, thiophene- and pyrrole-carboxamido groups possess strong topical intraocular pressure lowering properties as aqueous suspensions
Authors: Ilies, M Supuran, CT Scozzafava, A Casini, A Mincione, F Menabuoni, L Caproiu, MT Maganu, M Banciu, MD
Citation: M. Ilies et al., Carbonic anhydrase inhibitors: Sulfonamides incorporating furan-, thiophene- and pyrrole-carboxamido groups possess strong topical intraocular pressure lowering properties as aqueous suspensions, BIO MED CH, 8(8), 2000, pp. 2145-2155
Protease inhibitors. Part 8: Synthesis of potent Clostridium histolyticum collagenase inhibitors incorporating sulfonylated L-alanine hydroxamate moieties
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Protease inhibitors. Part 8: Synthesis of potent Clostridium histolyticum collagenase inhibitors incorporating sulfonylated L-alanine hydroxamate moieties, BIO MED CH, 8(3), 2000, pp. 637-645
Carbonic anhydrase inhibitors: Topical sulfonamide antiglaucoma agents incorporating secondary amine moieties
Authors: Renzi, G Scozzafava, A Supuran, CT
Citation: G. Renzi et al., Carbonic anhydrase inhibitors: Topical sulfonamide antiglaucoma agents incorporating secondary amine moieties, BIOORG MED, 10(7), 2000, pp. 673-676
Protease inhibitors: Synthesis of Clostridium histolyticum collagenase inhibitors incorporating sulfonyl-L-alanine hydroxamate moieties
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Protease inhibitors: Synthesis of Clostridium histolyticum collagenase inhibitors incorporating sulfonyl-L-alanine hydroxamate moieties, BIOORG MED, 10(5), 2000, pp. 499-502
Arylsulfonyl-N,N-diethyl-dithiocarbamates: A novel class of antitumor agents
Authors: Scozzafava, A Mastrolorenzo, A Supuran, CT
Citation: A. Scozzafava et al., Arylsulfonyl-N,N-diethyl-dithiocarbamates: A novel class of antitumor agents, BIOORG MED, 10(16), 2000, pp. 1887-1891
Carbonic anhydrase inhibitors: Synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Carbonic anhydrase inhibitors: Synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV, BIOORG MED, 10(10), 2000, pp. 1117-1120
4-toluenesulfonylureido derivatives of amines, amino acids and dipeptides:a novel class of potential antitumor agents
Authors: Mastrolorenzo, A Scozzafava, A Supuran, CT
Citation: A. Mastrolorenzo et al., 4-toluenesulfonylureido derivatives of amines, amino acids and dipeptides:a novel class of potential antitumor agents, EUR J PH SC, 11(4), 2000, pp. 325-332
Antifungal activity of silver and zinc complexes of sulfadrug derivatives incorporating arylsulfonylureido moieties
Authors: Mastrolorenzo, A Scozzafava, A Supuran, CT
Citation: A. Mastrolorenzo et al., Antifungal activity of silver and zinc complexes of sulfadrug derivatives incorporating arylsulfonylureido moieties, EUR J PH SC, 11(2), 2000, pp. 99-107
Protease inhibitors - Part 12. Synthesis of potent matrix metalloproteinase and bacterial collagenase inhibitors incorporating sulfonylated N-4-nitrobenzyl-beta-alanine hydroxamate moieties
Authors: Scozzafava, A Ilies, MA Manole, G Supuran, CT
Citation: A. Scozzafava et al., Protease inhibitors - Part 12. Synthesis of potent matrix metalloproteinase and bacterial collagenase inhibitors incorporating sulfonylated N-4-nitrobenzyl-beta-alanine hydroxamate moieties, EUR J PH SC, 11(1), 2000, pp. 69-79
Carbonic anhydrase activators Part 24. High affinity isozymes I, II and IVactivators, derivatives of 4-(4-chlorophenylsulfonylureido-amino acyl)ethyl-1H-imidazole
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Carbonic anhydrase activators Part 24. High affinity isozymes I, II and IVactivators, derivatives of 4-(4-chlorophenylsulfonylureido-amino acyl)ethyl-1H-imidazole, EUR J PH SC, 10(1), 2000, pp. 29-41
Protease inhibitors. Part 7 Inhibition of Clostridium histolyticum collagenase with sulfonylated derivatives of L-valine hydroxamate
Authors: Supuran, CT Scozzafava, A
Citation: Ct. Supuran et A. Scozzafava, Protease inhibitors. Part 7 Inhibition of Clostridium histolyticum collagenase with sulfonylated derivatives of L-valine hydroxamate, EUR J PH SC, 10(1), 2000, pp. 67-76
Purification and catalytic properties of two catechol 1,2-dioxygenase isozymes from benzoate-grown cells of Acinetobacter radioresistens
Authors: Briganti, F Pessione, E Giunta, C Mazzoli, R Scozzafava, A
Citation: F. Briganti et al., Purification and catalytic properties of two catechol 1,2-dioxygenase isozymes from benzoate-grown cells of Acinetobacter radioresistens, J PROTEIN C, 19(8), 2000, pp. 709-716
Carbonic anhydrase inhibitors - Part 94. 1,3,4-thiadiazole-2-sulfonamide derivatives as antitumor agents?
Authors: Supuran, CT Scozzafava, A
Citation: Ct. Supuran et A. Scozzafava, Carbonic anhydrase inhibitors - Part 94. 1,3,4-thiadiazole-2-sulfonamide derivatives as antitumor agents?, EUR J MED C, 35(9), 2000, pp. 867-874
Protease inhibitors - Part 5. Alkyl/arylsulfonyl- and arylsulfonylureido-/arylureido- glycine hydroxamate inhibitors of Clostridium histolyticum collagenase
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Protease inhibitors - Part 5. Alkyl/arylsulfonyl- and arylsulfonylureido-/arylureido- glycine hydroxamate inhibitors of Clostridium histolyticum collagenase, EUR J MED C, 35(3), 2000, pp. 299-307
Carbonic anhydrase inhibitors - Part 78. Synthesis of water-soluble sulfonamides incorporating beta-alanyl moieties, possessing long lasting-intraocular pressure lowering properties via the topical route
Authors: Supuran, CT Briganti, F Menabuoni, L Mincione, G Mincione, F Scozzafava, A
Citation: Ct. Supuran et al., Carbonic anhydrase inhibitors - Part 78. Synthesis of water-soluble sulfonamides incorporating beta-alanyl moieties, possessing long lasting-intraocular pressure lowering properties via the topical route, EUR J MED C, 35(3), 2000, pp. 309-321
Carbonic anhydrase activators - Part 21. Novel activators of isozymes I, II and IV incorporating carboxamido and ureido histamine moieties
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Carbonic anhydrase activators - Part 21. Novel activators of isozymes I, II and IV incorporating carboxamido and ureido histamine moieties, EUR J MED C, 35(1), 2000, pp. 31-39
Direct micellar systems as a tool to improve the efficiency of aromatic substrate conversion for fine chemicals production
Authors: Berti, D Randazzo, D Briganti, F Baglioni, P Scozzafava, A Di Gennaro, P Galli, E Bestetti, G
Citation: D. Berti et al., Direct micellar systems as a tool to improve the efficiency of aromatic substrate conversion for fine chemicals production, J INORG BIO, 79(1-4), 2000, pp. 103-108
Carbonic anhydrase inhibitors. Part 89 - Metal complexes of benzolamide with strong enzyme inhibitory and putative antiulcer properties
Authors: Scozzafava, A Ilies, MA Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors. Part 89 - Metal complexes of benzolamide with strong enzyme inhibitory and putative antiulcer properties, REV RO CHIM, 45(7-8), 2000, pp. 771-778
Protease inhibitors: Synthesis and QSAR study of novel classes of nonbasicthrombin inhibitors incorporating sulfonylguanidine and O-methylsulfonylisourea moieties at p1
Authors: Supuran, CT Scozzafava, A Briganti, F Clare, BW
Citation: Ct. Supuran et al., Protease inhibitors: Synthesis and QSAR study of novel classes of nonbasicthrombin inhibitors incorporating sulfonylguanidine and O-methylsulfonylisourea moieties at p1, J MED CHEM, 43(9), 2000, pp. 1793-1806
Protease inhibitors: Synthesis of potent bacterial collagenase and matrix metalloproteinase inhibitors incorporating N-4-nitrobenzylsulfonylglycine hydroxamate moieties
Authors: Scozzafava, A Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Protease inhibitors: Synthesis of potent bacterial collagenase and matrix metalloproteinase inhibitors incorporating N-4-nitrobenzylsulfonylglycine hydroxamate moieties, J MED CHEM, 43(9), 2000, pp. 1858-1865
Carbonic anhydrase inhibitors: Water-soluble 4-sulfamoylphenylthioureas astopical intraocular pressure-lowering agents with long-lasting effects
Authors: Casini, A Scozzafava, A Mincione, F Menabuoni, L Ilies, MA Supuran, CT
Citation: A. Casini et al., Carbonic anhydrase inhibitors: Water-soluble 4-sulfamoylphenylthioureas astopical intraocular pressure-lowering agents with long-lasting effects, J MED CHEM, 43(25), 2000, pp. 4884-4892
Risultati: 1-25 | 26-50 | 51-75 | 76-77