Page last updated: 2024-08-21

8-hydroxy-2-methylquinoline and chloroxine

8-hydroxy-2-methylquinoline has been researched along with chloroxine in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Barlow, DJ; Benoni, G; Bompiani, KM; Caglič, D; Dickerson, TJ; Houseknecht, KL; Krutein, MC; Lairson, LL; Pelletier, JC; Reitz, AB; Smith, GR1
Brunst, S; Burgers, LD; Frank, D; Fürst, R; Gobec, S; Martinelli, G; Proschak, A; Proschak, E; Rotter, MJ; Sosič, I; Weizel, L; Wichelhaus, TA1

Other Studies

2 other study(ies) available for 8-hydroxy-2-methylquinoline and chloroxine

ArticleYear
Identification of clinically viable quinolinol inhibitors of botulinum neurotoxin A light chain.
    Journal of medicinal chemistry, 2014, Feb-13, Volume: 57, Issue:3

    Topics: Animals; Botulinum Toxins, Type A; Catalytic Domain; Humans; Hydrogen-Ion Concentration; Hydroxyquinolines; In Vitro Techniques; Microsomes, Liver; Rats; Rats, Sprague-Dawley; Solubility; Structure-Activity Relationship

2014
Nitroxoline and its derivatives are potent inhibitors of metallo-β-lactamases.
    European journal of medicinal chemistry, 2022, Jan-15, Volume: 228

    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