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amifloxacin
structure in UD
Also Known As:
6-fluoro-1-methylamino-7-(4-methylpiperazin-1-yl)-1,4-dihydroquinolin-4-one-3-carboxylic acid; Win 49375; Win-49375
Networked:
10
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
Fused-Ring Heterocyclic Compounds
2-Ring Heterocyclic Compounds
Quinolines: 146
Quinolones: 2938
Fluoroquinolones: 5348
Ciprofloxacin: 6260
amifloxacin: 10
Related Diseases
1.
Urinary Tract Infections (Urinary Tract Infection)
06/01/1990 - "
Clinical and pharmacokinetic data suggest that orally administered amifloxacin may have utility in the treatment of urinary tract infections.
"
04/01/1990 - "
We conducted a randomized controlled trial of orally administered amifloxacin versus trimethoprimsulfamethoxazole (TMP-SMX) as treatments of acute uncomplicated urinary tract infection in women.
"
04/01/1990 - "
Randomized, controlled trial of a 10-day course of amifloxacin versus trimethoprim-sulfamethoxazole in the treatment of acute, uncomplicated urinary tract infection.
"
04/01/1985 - "
The in vitro activity of amifloxacin (WIN 49375), a new fluoroquinolone, was compared with the activities of antimicrobial agents that are commonly used for the treatment of urinary tract infection (cinoxacin, cephalexin, gentamicin, amoxicillin, trimethoprim, and trimethoprim-sulfamethoxazole) against 25 strains of Staphylococcus saprophyticus and 28 strains of Escherichia coli.
"
2.
Neoplasms (Cancer)
09/01/1984 - "
In vitro activity of WIN 49375 compared with those of other antibiotics in isolates from cancer patients.
"
08/01/1986 - "
The in-vitro activity of Sch 34343, a new penam antibiotic, was tested against 257 Gram-positive isolates from cancer patients, and compared with that of imipenem and amifloxacin.
"
04/01/1986 - "
In-vitro activity of cefpirome (HR-810), WIN-49375, BMY-28142 and other antibiotics against nosocomially important isolates from cancer patients.
"
04/01/1986 - "
The activity of three new antimicrobial agents [cefpirome (HR 810), BMY 28142, WIN 49375], and imipenem was compared to that of four currently available agents, ceftazidime, aztreonam, timentin and piperacillin, against 253 bacterial isolates from cancer patients.
"
3.
Infections
01/01/1985 - "
WIN 49548, the major piperazinyl-N-desmethyl metabolite of WIN 49375, was aa effective as the parent drug against experimental infections in mice when given parenterally.
"
11/01/1984 - "
Amifloxacin joins other newly developed DNA gyrase inhibitors as potentially useful agents for infections due to aminoglycoside-resistant gram-negative bacilli.
"
4.
Gram-Negative Bacterial Infections
01/01/1985 - "
WIN 49375 was more active in vitro than carbenicillin and mezlocillin against Pseudomonas aeruginosa isolates and showed moderate activity against Staphylococcus aureus, with MICs of less than or equal to 2 micrograms/ml. The in vitro activity of WIN 49375 was not markedly affected by the presence of human serum, the size of the bacterial inoculum, or changes in pH between 6 and 8. Against systemic, gram-negative bacterial infections in mice, WIN 49375 was generally less active than cefotaxime but more active than gentamicin.
"
5.
Prostatitis
01/01/1985 - "
The concentrations of amifloxacin in PS, PIF, and prostatic tissue were above the minimal inhibitory concentration values of most gram-positive bacteria causing chronic bacterial prostatitis.
"
Related Drugs and Biologics
1.
Anti-Bacterial Agents (Antibiotics)
2.
Sulfamethoxazole Drug Combination Trimethoprim (Co-Trimoxazole)
3.
Imipenem
4.
Gentamicins (Gentamicin)
5.
Anti-Infective Agents (Microbicides)
6.
amifloxacin
7.
Topoisomerase II Inhibitors
8.
Fluoroquinolones
9.
Trimethoprim (Proloprim)
10.
Piperacillin