cloxyquin has been researched along with 8-hydroxy-2-methylquinoline in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 6 (85.71) | 24.3611 |
2020's | 1 (14.29) | 2.80 |
Authors | Studies |
---|---|
Cohen, SM; Fullagar, JL; Jacobsen, JA; Miller, MT | 1 |
Byrd, MS; Campos, CG; Clare, M; Cotter, PA; Hagen, TJ; Henderson, MW; Horn, JR; Masoudi, A; Myler, PJ; Wangtrakuldee, P; Zhang, Z | 1 |
Aoki, S; Ariyasu, S; Hanaya, K; Hoshi, M; Morita, A; Sawa, A; Takahashi, I; Wang, B | 1 |
Aoki, S; Ariyasu, S; Hanaya, K; Shoji, M; Sugai, T; Yoshioka, S | 1 |
Campbell, Y; Cardellina, JH; Eccard, VS; Ensel, SM; Guernieri, R; Harrell, WA; Montgomery, V; Roxas-Duncan, V; Smith, LA; Vieira, RC; Webb, RP | 1 |
Abendroth, J; Audia, JP; Chen, C; Edwards, TE; Hagen, TJ; Helgren, TR; Horn, JR; Housley, NA; Myler, PJ; Sankaran, B; Staker, BL; Wangtrakuldee, P | 1 |
Brunst, S; Burgers, LD; Frank, D; Fürst, R; Gobec, S; Martinelli, G; Proschak, A; Proschak, E; Rotter, MJ; Sosič, I; Weizel, L; Wichelhaus, TA | 1 |
7 other study(ies) available for cloxyquin and 8-hydroxy-2-methylquinoline
Article | Year |
---|---|
Identifying chelators for metalloprotein inhibitors using a fragment-based approach.
Topics: Antigens, Bacterial; Bacterial Toxins; Chelating Agents; Copper; Drug Design; Humans; Hydroxyquinolines; Iron; Ligands; Lipoxygenase Inhibitors; Matrix Metalloproteinase Inhibitors; Matrix Metalloproteinases; Monophenol Monooxygenase; Nitric Oxide Synthase Type II; Recombinant Proteins; Small Molecule Libraries; Structure-Activity Relationship; Sulfonamides; Zinc | 2011 |
Discovery of Inhibitors of
Topics: | 2013 |
Design and synthesis of 8-hydroxyquinoline-based radioprotective agents.
Topics: Apoptosis; Cell Line, Tumor; Drug Design; Electrophoretic Mobility Shift Assay; Gamma Rays; Humans; Oxyquinoline; Radiation-Protective Agents; Tumor Suppressor Protein p53; Zinc | 2014 |
Development of a novel sulfonate ester-based prodrug strategy.
Topics: Aeromonas; Alkanesulfonates; Aminopeptidases; Animals; Chloroquinolinols; Cyclization; Humans; Hydrolysis; Leucine; Liver; Mice; Prodrugs; Propylamines; Rats; Sulfonamides | 2016 |
A matrix-focused structure-activity and binding site flexibility study of quinolinol inhibitors of botulinum neurotoxin serotype A.
Topics: Animals; Binding Sites; Botulinum Toxins, Type A; Hydroxyquinolines; Inhibitory Concentration 50; Mice; Phrenic Nerve; Protein Binding; Serogroup; Structure-Activity Relationship | 2017 |
Rickettsia prowazekii methionine aminopeptidase as a promising target for the development of antibacterial agents.
Topics: Animals; Anti-Bacterial Agents; Cell Survival; Cells, Cultured; Dose-Response Relationship, Drug; Endothelial Cells; Enzyme Inhibitors; Methionyl Aminopeptidases; Microbial Sensitivity Tests; Molecular Docking Simulation; Molecular Structure; Pulmonary Artery; Rats; Rickettsia prowazekii; Structure-Activity Relationship | 2017 |
Nitroxoline and its derivatives are potent inhibitors of metallo-β-lactamases.
Topics: Anti-Bacterial Agents; beta-Lactamase Inhibitors; beta-Lactamases; Cell Survival; Cells, Cultured; Dose-Response Relationship, Drug; Gram-Negative Bacteria; Humans; Microbial Sensitivity Tests; Molecular Structure; Nitroquinolines; Recombinant Proteins; Structure-Activity Relationship | 2022 |