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Results: 1-25 | 26-36
Results: 1-25/36
Carbonic anhydrase inhibitors: Sulfonamides as antitumor agents?
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
Dural arteriovenous malformation associated with recurrent subdural haematoma and intracranial hypertension
Authors: Maiuri, F Iaconetta, G Sardo, L Briganti, F
Citation: F. Maiuri et al., Dural arteriovenous malformation associated with recurrent subdural haematoma and intracranial hypertension, BR J NEUROS, 15(3), 2001, pp. 273-276
Efficient polycyclic aromatic hydrocarbons dihydroxylation in direct micellar systems
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
Pseudoaneurysm of the intracavernous carotid artery following endoscopic endonasal transsphenoidal surgery, treated by endovascular approach
Authors: Cappabianca, P Briganti, F Cavallo, LM de Divitiis, E
Citation: P. Cappabianca et al., Pseudoaneurysm of the intracavernous carotid artery following endoscopic endonasal transsphenoidal surgery, treated by endovascular approach, ACT NEUROCH, 143(1), 2001, pp. 95-96
Protease inhibitors: Part 4. Synthesis of weakly basic thrombin inhibitorsincorporating pyridinium-sulfanilylaminoguanidine moieties
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
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
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
Protease inhibitors. Part 2. Weakly basic thrombin inhibitors incorporating sulfonyl-aminoguanidine moieties as S1 anchoring groups: Synthesis and structure-activity correlations
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
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 inhibitors. Metal complexes of 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide with topical intraocular pressure lowering properties: The influence of metal ions upon the pharmacological activity
Authors: Briganti, F Tilli, S Mincione, G Mincione, F Menabuoni, L Supuran, CT
Citation: F. Briganti et al., Carbonic anhydrase inhibitors. Metal complexes of 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide with topical intraocular pressure lowering properties: The influence of metal ions upon the pharmacological activity, J ENZ INHIB, 15(2), 2000, pp. 185-200
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 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
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
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
Carbonic anhydrase inhibitors: Perfluoroalkyl/aryl-substituted derivativesof aromatic/heterocyclic sulfonamides as topical intraocular pressure-lowering agents with prolonged duration of action
Authors: Scozzafava, A Menabuoni, L Mincione, F Briganti, F Mincione, G Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors: Perfluoroalkyl/aryl-substituted derivativesof aromatic/heterocyclic sulfonamides as topical intraocular pressure-lowering agents with prolonged duration of action, J MED CHEM, 43(23), 2000, pp. 4542-4551
Carbonic anhydrase inhibitors: Synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes
Authors: Scozzafava, A Briganti, F Ilies, MA Supuran, CT
Citation: A. Scozzafava et al., Carbonic anhydrase inhibitors: Synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes, J MED CHEM, 43(2), 2000, pp. 292-300
Winter androgen levels and wattle size in male Common Pheasants
Authors: Papeschi, A Briganti, F Dessi-Fulgheri, F
Citation: A. Papeschi et al., Winter androgen levels and wattle size in male Common Pheasants, CONDOR, 102(1), 2000, pp. 193-197
Mechanism of cyanamide hydration catalyzed by carbonic anhydrase II suggested by cryogenic X-ray diffraction
Authors: Guerri, A Briganti, F Scozzafava, A Supuran, CT Mangani, S
Citation: A. Guerri et al., Mechanism of cyanamide hydration catalyzed by carbonic anhydrase II suggested by cryogenic X-ray diffraction, BIOCHEM, 39(40), 2000, pp. 12391-12397
Effect of androgens on structure and rate of growing in the Japanese quail(Coturnix Japonica)
Authors: Beani, L Briganti, F Campanella, G Lupo, C Dessi-Fulgheri, F
Citation: L. Beani et al., Effect of androgens on structure and rate of growing in the Japanese quail(Coturnix Japonica), BEHAVIOUR, 137, 2000, pp. 417-435
Carbonic anhydrase inhibitors. Synthesis of topically effective intraocular pressure lowering agents derived from 5-(omega-aminoalkylcarboxamido)-1,3,4-thiadiazole-2-sulfonamide
Authors: Barboiu, M Supuran, CT Menabuoni, L Scozzafava, A Mincione, F Briganti, F Mincione, G
Citation: M. Barboiu et al., Carbonic anhydrase inhibitors. Synthesis of topically effective intraocular pressure lowering agents derived from 5-(omega-aminoalkylcarboxamido)-1,3,4-thiadiazole-2-sulfonamide, J ENZ INHIB, 15(1), 1999, pp. 23-46
Carbonic anhydrase inhibitors. Schiff bases of some aromatic sulfonamides and their metal complexes: Towards more selective inhibitors of carbonic anhydrase isozyme IV
Authors: Popescu, A Simion, A Scozzafava, A Briganti, F Supuran, CT
Citation: A. Popescu et al., Carbonic anhydrase inhibitors. Schiff bases of some aromatic sulfonamides and their metal complexes: Towards more selective inhibitors of carbonic anhydrase isozyme IV, J ENZ INHIB, 14(6), 1999, pp. 407-423
Carbonic anhydrase inhibitors. Water-soluble, topically effective intraocular pressure lowering agents derived from isonicotinic acid and aromatic/heterocyclic sulfonamides: Is the tail more important than the ring?
Authors: Menabuoni, L Scozzafava, A Mincione, F Briganti, F Mincione, G Supuran, CT
Citation: L. Menabuoni et al., Carbonic anhydrase inhibitors. Water-soluble, topically effective intraocular pressure lowering agents derived from isonicotinic acid and aromatic/heterocyclic sulfonamides: Is the tail more important than the ring?, J ENZ INHIB, 14(6), 1999, pp. 457-474
Carbonic anhydrase inhibitors: N-cyanosulfonamides, a new class of high affinity isozyme II and IV inhibitors
Authors: Supuran, CT Scozzafava, A Briganti, F
Citation: Ct. Supuran et al., Carbonic anhydrase inhibitors: N-cyanosulfonamides, a new class of high affinity isozyme II and IV inhibitors, J ENZ INHIB, 14(4), 1999, pp. 289-306
Characterization of the biological conversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene in direct micellar systems
Authors: Briganti, F Randazzo, D Scozzafava, A Berti, D Baglioni, P Di Gennaro, P Galli, E Bestetti, G
Citation: F. Briganti et al., Characterization of the biological conversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene in direct micellar systems, J MOL CAT B, 7(5-6), 1999, pp. 263-272
Carbonic anhydrase inhibitors: Synthesis of water-soluble, topically effective intraocular pressure lowering aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties: Is the tail more important than the ring?
Authors: Borras, J Scozzafava, A Menabuoni, L Mincione, F Briganti, F Mincione, G Supuran, CT
Citation: J. Borras et al., Carbonic anhydrase inhibitors: Synthesis of water-soluble, topically effective intraocular pressure lowering aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties: Is the tail more important than the ring?, BIO MED CH, 7(11), 1999, pp. 2397-2406
Novel carbonic anhydrase isozymes I, II and IV activators incorporating sulfonyl-histamino moieties
Authors: Briganti, F Scozzafava, A Supuran, CT
Citation: F. Briganti et al., Novel carbonic anhydrase isozymes I, II and IV activators incorporating sulfonyl-histamino moieties, BIOORG MED, 9(14), 1999, pp. 2043-2048
Risultati: 1-25 | 26-36