Page last updated: 2024-09-03

ulifloxacin and gatifloxacin

ulifloxacin has been researched along with gatifloxacin in 3 studies

Compound Research Comparison

Studies
(ulifloxacin)
Trials
(ulifloxacin)
Recent Studies (post-2010)
(ulifloxacin)
Studies
(gatifloxacin)
Trials
(gatifloxacin)
Recent Studies (post-2010) (gatifloxacin)
503151,047131268

Protein Interaction Comparison

ProteinTaxonomyulifloxacin (IC50)gatifloxacin (IC50)
DNA gyrase subunit AEscherichia coli K-120.5
DNA gyrase subunit BEscherichia coli K-120.5
DNA topoisomerase 4 subunit AStaphylococcus aureus1.2
DNA gyrase subunit AMycobacterium tuberculosis H37Rv9.4

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Araake, M; Hara, T; Nishino, T; Watabe, H1
Araake, M; Hara, T; Nishino, T; Shimizu, M; Tabata, M; Watabe, H1
Araake, M; Maebashi, K; Tani, M; Watabe, H1

Other Studies

3 other study(ies) available for ulifloxacin and gatifloxacin

ArticleYear
[In vitro antibacterial activity of prulifloxacin, a new oral fluoroquinolone].
    The Japanese journal of antibiotics, 2002, Volume: 55, Issue:6

    Topics: Anti-Infective Agents; Ciprofloxacin; Dioxolanes; Dosage Forms; Dose-Response Relationship, Drug; Drug Resistance, Bacterial; Fleroxacin; Fluoroquinolones; Gatifloxacin; Gram-Negative Bacteria; Gram-Positive Bacteria; Humans; Levofloxacin; Naphthyridines; Ofloxacin; Piperazines; Prodrugs; Quinolones

2002
[In vitro short-term bactericidal activity and accumulation of NM394, the active metabolite of prulifloxacin, for Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa: comparison with ciprofloxacin, levofloxacin, and gatifloxacin].
    The Japanese journal of antibiotics, 2002, Volume: 55, Issue:6

    Topics: Anti-Infective Agents; Ciprofloxacin; Dioxolanes; Dose-Response Relationship, Drug; Drug Resistance, Bacterial; Escherichia coli; Fluoroquinolones; Gatifloxacin; Levofloxacin; Ofloxacin; Piperazines; Prodrugs; Pseudomonas aeruginosa; Quinolones; Staphylococcus aureus; Time Factors

2002
[Inhibitory activity of NM394, the active form of prodrug prulifloxacin against type II topoisomerase from Pseudomonas aeruginosa].
    The Japanese journal of antibiotics, 2002, Volume: 55, Issue:6

    Topics: Anti-Infective Agents; Ciprofloxacin; Dioxolanes; DNA Topoisomerase IV; Dose-Response Relationship, Drug; Fluoroquinolones; Gatifloxacin; Levofloxacin; Ofloxacin; Piperazines; Prodrugs; Pseudomonas aeruginosa; Quinolones; Topoisomerase II Inhibitors

2002