catechol has been researched along with acetazolamide in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (23.08) | 29.6817 |
| 2010's | 10 (76.92) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bellows, DS; Clarke, ID; Diamandis, P; Dirks, PB; Graham, J; Jamieson, LG; Ling, EK; Sacher, AG; Tyers, M; Ward, RJ; Wildenhain, J | 1 |
| Hilvo, M; Innocenti, A; Parkkila, S; Scozzafava, A; Supuran, CT | 1 |
| Innocenti, A; Scozzafava, A; Supuran, CT; Vullo, D | 1 |
| Beyza Öztürk Sarıkaya, S; Gülçin, İ; Innocenti, A; Supuran, CT | 1 |
| Gülçin, I; Oztürk Sarikaya, SB; Sentürk, M; Supuran, CT; Topal, F | 1 |
| Ekinci, D; Kurbanoglu, NI; Salamci, E; Şentürk, M; Supuran, CT | 1 |
| Güney, M; Kazancioğlu, EA; Şentürk, M; Supuran, CT | 1 |
| Ekinci, D; Karagoz, L; Senturk, M; Supuran, CT | 1 |
| Cavdar, H; Durdagi, S; Ekinci, D; Sentürk, M; Supuran, CT; Talaz, O | 1 |
| Alankuş-Çalişkan, Ö; Bedir, E; Ekinci, D; Koz, Ö; Perrone, A; Piacente, S; Supuran, CT | 1 |
| Çavdar, H; Ekinci, D; Güney, M; Şentürk, M | 1 |
| Çetin, A; Durdagi, S; Ekinci, D; Işık, S; Şentürk, E; Şentürk, M; Supuran, CT; Vullo, D | 1 |
| Bua, S; Capasso, C; Del Prete, S; Entezari Heravi, Y; Gratteri, P; Nocentini, A; Saboury, AA; Sereshti, H; Supuran, CT | 1 |
13 other study(ies) available for catechol and acetazolamide
| Article | Year |
|---|---|
Chemical genetics reveals a complex functional ground state of neural stem cells.
Topics: Animals; Cell Survival; Cells, Cultured; Mice; Molecular Structure; Neoplasms; Neurons; Pharmaceutical Preparations; Sensitivity and Specificity; Stem Cells | 2007 |
Carbonic anhydrase inhibitors: Inhibition of the new membrane-associated isoform XV with phenols.
Topics: Animals; Binding Sites; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Hydrogen Bonding; Isoenzymes; Mice; Molecular Structure; Phenols; Stereoisomerism; Structure-Activity Relationship | 2008 |
Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid.
Topics: Acetaminophen; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Molecular Structure; Protein Isoforms; Salicylic Acid; Structure-Activity Relationship | 2008 |
Carbonic anhydrase inhibitors. Inhibition of mammalian isoforms I-XIV with a series of natural product polyphenols and phenolic acids.
Topics: Animals; Biological Factors; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Flavonoids; Humans; Hydroxybenzoates; Isoenzymes; Mice; Molecular Structure; Phenols; Polyphenols; Stereoisomerism; Structure-Activity Relationship | 2010 |
In vitro inhibition of α-carbonic anhydrase isozymes by some phenolic compounds.
Topics: Animals; Bass; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Fish Proteins; Humans; Isoenzymes; Phenols; Sulfonamides; Sulfonic Acids | 2011 |
Carbonic anhydrase inhibitors: inhibition of human and bovine isoenzymes by benzenesulphonamides, cyclitols and phenolic compounds.
Topics: Animals; Benzenesulfonates; Carbonic Anhydrases; Cattle; Cyclitols; Electrophoresis, Polyacrylamide Gel; Enzyme Assays; Erythrocytes; Humans; Isoenzymes; Kinetics; Molecular Structure; Muscle, Skeletal; Phenols; Structure-Activity Relationship; Substrate Specificity; Sulfonamides | 2012 |
Simple methanesulfonates are hydrolyzed by the sulfatase carbonic anhydrase activity.
Topics: Carbonic Anhydrases; Electrophoresis, Polyacrylamide Gel; Enzyme Assays; Humans; Hydrolysis; Isoenzymes; Kinetics; Mesylates; Nitrobenzenes; Phenols; Substrate Specificity; Sulfatases | 2012 |
Carbonic anhydrase inhibitors: in vitro inhibition of α isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids.
Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Flavonoids; Humans; Molecular Structure; Protein Isoforms; Structure-Activity Relationship | 2013 |
Structure-activity relationships for the interaction of 5,10-dihydroindeno[1,2-b]indole derivatives with human and bovine carbonic anhydrase isoforms I, II, III, IV and VI.
Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cattle; Humans; Indoles; Models, Molecular; Protein Isoforms; Structure-Activity Relationship | 2012 |
Analysis of saponins and phenolic compounds as inhibitors of α-carbonic anhydrase isoenzymes.
Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Molecular Structure; Phenols; Protein Isoforms; Saponins; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids | 2013 |
Synthesis and carbonic anhydrase inhibitory properties of novel uracil derivatives.
Topics: Binding, Competitive; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Erythrocytes; Humans; Isoenzymes; Kinetics; Molecular Conformation; Structure-Activity Relationship; Uracil | 2015 |
Interaction of carbonic anhydrase isozymes I, II, and IX with some pyridine and phenol hydrazinecarbothioamide derivatives.
Topics: Antigens, Neoplasm; Binding Sites; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase IX; Carbonic Anhydrases; Humans; Hydrazines; Isoenzymes; Molecular Structure; Pyridines; Thioamides | 2015 |
Inhibition of Malassezia globosa carbonic anhydrase with phenols.
Topics: Acetazolamide; Carbonic Anhydrase I; Carbonic Anhydrase Inhibitors; Dandruff; Humans; Hydrogen Bonding; Malassezia; Molecular Docking Simulation; Phenols; Structure-Activity Relationship | 2017 |