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Results: 1-25/77
Authors:
Casini, A
Mincione, F
Ilies, MA
Menabuoni, L
Scozzafava, A
Supuran, CT
Citation: A. Casini et al., Carbonic anhydrase inhibitors: Synthesis and inhibition against isozymes I, II and IV of topically acting antiglaucoma sulfonamides incorporating cis-5-norbornene-endo-3-carboxy-2-carboxamido moieties, J ENZ INHIB, 16(2), 2001, pp. 113-123
Authors:
Chazalette, C
Riviere-Baudet, M
Scozzafava, A
Abbate, F
Ben Maarouf, Z
Supuran, CT
Citation: C. Chazalette et al., Carbonic anhydrase inhibitors, interaction of boron derivatives with isozymes I and II: A new binding site for hydrophobic inhibitors at the entranceof the active site as shown by docking studies, J ENZ INHIB, 16(2), 2001, pp. 125
Authors:
Clare, BW
Scozzafava, A
Supuran, CT
Citation: Bw. Clare et al., Protease inhibitors, part 13: Specific, weakly basic thrombin inhibitors incorporating sulfonyl dicyandiamide moieties in their structure, J ENZ INHIB, 16(1), 2001, pp. 1-13
Authors:
Scozzafava, A
Mastrolorenzo, A
Supuran, CT
Citation: A. Scozzafava et al., Arylsulfonyl-N,N-dialkyl-dithiocarbamates as tumor cell growth inhibitors:Novel agents targeting beta-tubulin?, J ENZ INHIB, 16(1), 2001, pp. 55-63
Authors:
Mastrolorenzo, A
Scozzafava, A
Supuran, CT
Citation: A. Mastrolorenzo et al., Small molecule antagonists of chemokine receptors as emerging anti-HIV agents, EXPERT OP T, 11(8), 2001, pp. 1245-1252
Authors:
Scozzafava, A
Mastrolorenzo, A
Supuran, CT
Citation: A. Scozzafava et al., Agents that target cysteine residues of biomolecules and their therapeuticpotential, EXPERT OP T, 11(5), 2001, pp. 765-787
Authors:
Supuran, CT
Scozzafava, A
Mastrolorenzo, A
Citation: Ct. Supuran et al., Bacterial proteases: current therapeutic use and future prospects for the development of new antibiotics, EXPERT OP T, 11(2), 2001, pp. 221-259
Authors:
Supuran, CT
Briganti, F
Tilli, S
Chegwidden, WR
Scozzafava, A
Citation: Ct. Supuran et al., Carbonic anhydrase inhibitors: Sulfonamides as antitumor agents?, BIO MED CH, 9(3), 2001, pp. 703-714
Authors:
Scozzafava, A
Menabuoni, L
Mincione, F
Mincione, G
Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors: Synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties, BIOORG MED, 11(4), 2001, pp. 575-582
Authors:
Scozzafava, A
Mastrolorenzo, A
Supuran, CT
Citation: A. Scozzafava et al., Antimycobacterial activity of 9-sulfonylated/sulfenylated-6-mercaptopurinederivatives, BIOORG MED, 11(13), 2001, pp. 1675-1678
Authors:
Mincione, F
Starnotti, M
Menabuoni, L
Scozzafava, A
Casini, A
Supuran, CT
Citation: F. Mincione et al., Carbonic anhydrase inhibitors: 4-sulfamoyl-benzenecarboxamides and 4-chloro-3-sulfamoyl-benzenecarboxamides with strong topical antiglaucoma properties, BIOORG MED, 11(13), 2001, pp. 1787-1791
Authors:
Baldi, F
Minacci, A
Pepi, M
Scozzafava, A
Citation: F. Baldi et al., Gel sequestration of heavy metals by Klebsiella oxytoca isolated from ironmat, FEMS MIC EC, 36(2-3), 2001, pp. 169-174
Authors:
Scozzafava, A
Supuran, CT
Citation: A. Scozzafava et Ct. Supuran, Carbonic anhydrase and matrix metalloproteinase inhibitors: Sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit boththese zinc enzymes (vol 43, pg 3680, 2000), J MED CHEM, 44(6), 2001, pp. 1016-1016
Authors:
Clare, BW
Scozzafava, A
Supuran, CT
Citation: Bw. Clare et al., Protease inhibitors: Synthesis of a series of bacterial collagenase inhibitors of the sulfonyl amino acyl hydroxamate type, J MED CHEM, 44(13), 2001, pp. 2253-2258
Authors:
Perticone, F
Ceravolo, R
Pujia, A
Ventura, G
Iacopino, S
Scozzafava, A
Ferraro, A
Chello, M
Mastroroberto, P
Verdecchia, P
Schillaci, G
Citation: F. Perticone et al., Prognostic significance of endothelial dysfunction in hypertensive patients, CIRCULATION, 104(2), 2001, pp. 191-196
Authors:
Randazzo, D
Berti, D
Briganti, F
Baglioni, P
Scozzafava, A
Di Gennaro, P
Galli, E
Bestetti, G
Citation: D. Randazzo et al., Efficient polycyclic aromatic hydrocarbons dihydroxylation in direct micellar systems, BIOTECH BIO, 74(3), 2001, pp. 240-248
Authors:
Mastrolorenzo, A
Scozzafava, A
Supuran, CT
Citation: A. Mastrolorenzo et al., Antifungal activity of Ag(I) and Zn(II) complexes of aminobenzolamide (5-sulfanilylamido-1,3,4-thiadiazole-2-sulfonamide) derivatives, J ENZ INHIB, 15(6), 2000, pp. 517-531
Authors:
Scozzafava, A
Banciu, MD
Popescu, A
Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors: Synthesis of Schiff bases of hydroxybenzaldehydes with aromatic sulfonamides and their reactions with arylsulfonyl isocyanates - Part 90, J ENZ INHIB, 15(6), 2000, pp. 533-546
Authors:
Mastrolorenzo, A
Scozzafava, A
Supuran, CT
Citation: A. Mastrolorenzo et al., The antifungal activity of sulfonylated/carboxylated derivatives of dibenzo-1,4-dioxine-2-acetyloxime may be due to inhibition of lanosterol-14 alpha-demethylase, J ENZ INHIB, 15(6), 2000, pp. 557-569
Authors:
Supuran, CT
Scozzafava, A
Citation: Ct. Supuran et A. Scozzafava, Carbonic anhydrase inhibitors: Aromatic sulfonamides and disulfonamides act as efficient tumor growth inhibitors - Part 95, J ENZ INHIB, 15(6), 2000, pp. 597-610
Authors:
Scozzafava, A
Banciu, MD
Popescu, A
Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors: Inhibition of isozymes I, II and IV by sulfamide and sulfamic acid derivatives, J ENZ INHIB, 15(5), 2000, pp. 443-453
Authors:
Supuran, CT
Scozzafava, A
Citation: Ct. Supuran et A. Scozzafava, Carbonic anhydrase activators: Synthesis of high affinity isozymes I, II and IV activators, derivatives of 4-(arylsulfonylureido-amino acyl)ethyl-1H-imidazole, J ENZ INHIB, 15(5), 2000, pp. 471-486
Authors:
Supuran, CT
Briganti, F
Scozzafava, A
Ilies, MA
Citation: Ct. Supuran et al., Protease inhibitors: Part 4. Synthesis of weakly basic thrombin inhibitorsincorporating pyridinium-sulfanilylaminoguanidine moieties, J ENZ INHIB, 15(4), 2000, pp. 335-356
Authors:
Supuran, CT
Scozzafava, A
Ilies, MA
Briganti, F
Citation: Ct. Supuran et al., Carbonic anhydrase inhibitors: Synthesis of sulfonamides incorporating 2,4,6-trisubstituted-pyridinium-ethylcarboxamido moieties possessing membrane-impermeability and in vivo selectivity for the membrane-bound (CA IV) versus the cytosolic (CA I and CA II) isozymes, J ENZ INHIB, 15(4), 2000, pp. 381-401
Authors:
Clare, BW
Scozzafava, A
Briganti, F
Iorga, B
Supuran, CT
Citation: Bw. Clare et al., Protease inhibitors. Part 2. Weakly basic thrombin inhibitors incorporating sulfonyl-aminoguanidine moieties as S1 anchoring groups: Synthesis and structure-activity correlations, J ENZ INHIB, 15(3), 2000, pp. 235-264