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Supuran CT 55
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Display all abstracts from Supuran CT98238 Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitorsKumar R
Archiv der Pharmazie 2022; 355: e2100241
98385 2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activityChiaramonte N
European Journal of Medicinal Chemistry 2022; 228: 114026
99065 A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII InhibitorsBanoglu E
ChemMedChem 2022; 0: e202200056
98416 One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase EnzymesVannozzi G
Journal of Medicinal Chemistry 2022; 65: 824-837
99337 Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitorsKumar A
Bioorganic chemistry 2022; 123: 105764
99065 A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII InhibitorsErcanlı T
ChemMedChem 2022; 0: e202200056
98416 One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase EnzymesVullo D
Journal of Medicinal Chemistry 2022; 65: 824-837
98238 Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitorsKumar A
Archiv der Pharmazie 2022; 355: e2100241
99337 Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitorsSiwach K
Bioorganic chemistry 2022; 123: 105764
98385 2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activityAngeli A
European Journal of Medicinal Chemistry 2022; 228: 114026
99337 Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitorsRom T
Bioorganic chemistry 2022; 123: 105764
98385 2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activitySgambellone S
European Journal of Medicinal Chemistry 2022; 228: 114026
99065 A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII InhibitorsGür Maz T
ChemMedChem 2022; 0: e202200056
98238 Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitorsRam S
Archiv der Pharmazie 2022; 355: e2100241
98416 One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase EnzymesAngeli A
Journal of Medicinal Chemistry 2022; 65: 824-837
99337 Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitorsKumar R
Bioorganic chemistry 2022; 123: 105764
99065 A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII InhibitorsVullo D
ChemMedChem 2022; 0: e202200056
98385 2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activityBonardi A
European Journal of Medicinal Chemistry 2022; 228: 114026
98238 Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitorsAngeli A
Archiv der Pharmazie 2022; 355: e2100241
98416 One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase EnzymesFerraroni M
Journal of Medicinal Chemistry 2022; 65: 824-837
99065 A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII InhibitorsBonardi A
ChemMedChem 2022; 0: e202200056
98385 2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activityNocentini A
European Journal of Medicinal Chemistry 2022; 228: 114026
98416 One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase EnzymesCombs J
Journal of Medicinal Chemistry 2022; 65: 824-837
98238 Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitorsBonardi A
Archiv der Pharmazie 2022; 355: e2100241
99337 Tail-approach based design and synthesis of Arylthiazolylhydrazono-1,2,3-triazoles incorporating sulfanilamide and metanilamide as human carbonic anhydrase I, II, IV and IX inhibitorsAngeli A
Bioorganic chemistry 2022; 123: 105764
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