Page last updated: 2024-08-25

trifluoromethylsulfonamide and acetazolamide

trifluoromethylsulfonamide has been researched along with acetazolamide in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's4 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Graham, SL; Mallorga, PJ; Randall, WC; Scholz, TH; Schwam, H; Sondey, JM; Sugrue, MF; Thompson, WJ1
Grüneberg, S; Klebe, G; Stubbs, MT1
Benfodda, Z; Blancou, H; Dahmani, A; Guillen, F; Romestand, B1
Baranauskienė, L; Golovenko, D; Gražulis, S; Jachno, J; Manakova, E; Matulienė, J; Matulis, D; Michailovienė, V; Sūdžius, J; Sukackaitė, R; Torresan, J; Tumkevičius, S1
Abbas, G; al-Rashida, M; Ashraf, M; Hussain, B; Nagra, SA1
Gylytė, J; Jogaitė, V; Matulis, D; Michailovienė, V; Morkūnaitė, V; Zubrienė, A1

Other Studies

6 other study(ies) available for trifluoromethylsulfonamide and acetazolamide

ArticleYear
Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase.
    Journal of medicinal chemistry, 1993, Jul-23, Volume: 36, Issue:15

    Topics: Animals; Binding, Competitive; Carbonic Anhydrase Inhibitors; Humans; Rabbits; Structure-Activity Relationship; Sulfonamides

1993
Successful virtual screening for novel inhibitors of human carbonic anhydrase: strategy and experimental confirmation.
    Journal of medicinal chemistry, 2002, Aug-15, Volume: 45, Issue:17

    Topics: Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Crystallography, X-Ray; Databases, Factual; Humans; Isoenzymes; Ligands; Models, Molecular; Protein Binding; Quantitative Structure-Activity Relationship

2002
Synthesis and investigation of inhibition effect of fluorinated sulfonamide derivatives on carbonic anhydrase.
    European journal of medicinal chemistry, 2010, Volume: 45, Issue:3

    Topics: Ammonia; Animals; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cattle; Enzyme Activation; Gases; Humans; Molecular Structure; Sheep; Sulfonamides

2010
4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII.
    Bioorganic & medicinal chemistry, 2010, Nov-01, Volume: 18, Issue:21

    Topics: Benzenesulfonamides; Binding Sites; Calorimetry; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Crystallography, X-Ray; Humans; Protein Structure, Tertiary; Pyrimidines; Recombinant Proteins; Structure-Activity Relationship; Sulfonamides

2010
Discovery of new chromone containing sulfonamides as potent inhibitors of bovine cytosolic carbonic anhydrase.
    Bioorganic & medicinal chemistry, 2011, Jun-01, Volume: 19, Issue:11

    Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cattle; Chromones; Drug Evaluation, Preclinical; Hydrogen Bonding; Molecular Conformation; Sulfonamides

2011
Characterization of human carbonic anhydrase XII stability and inhibitor binding.
    Bioorganic & medicinal chemistry, 2013, Mar-15, Volume: 21, Issue:6

    Topics: Calorimetry; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalytic Domain; Humans; Hydrogen-Ion Concentration; Protein Binding; Protein Stability; Salts; Sulfonamides; Temperature; Thermodynamics

2013