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trovafloxacin

Known as: 7-(6-amino-3-azabicyclo[3.1.0]hex-3-yl)- 1-(2,4-difluorophenyl)- 6-fluoro-4-oxo-[1,8] naphthyridine-3-carboxylic acid, trovafloxacin [Chemical/Ingredient] 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Current 2-dimensional hepatic model systems often fail to predict chemically induced hepatotoxicity due to the loss of a… Expand
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Highly Cited
2006
Highly Cited
2006
Idiosyncratic drug toxicity refers to toxic reactions occurring in a small subset of patients and usually cannot be predicted… Expand
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Highly Cited
2002
Highly Cited
2002
A selective, sensitive and accurate liquid chromatographic method with UV and fluorescence detection was developed, validated and… Expand
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Highly Cited
2001
Highly Cited
2001
As part of the SENTRY Antimicrobial Surveillance Program, a total of 1078 Acinetobacter species and 842 Stenotrophomonas… Expand
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Highly Cited
2000
Highly Cited
2000
In an open, randomized, six-period crossover study, the pharmacokinetics of ciprofloxacin, gatifloxacin, grepafloxacin… Expand
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Review
2000
Review
2000
The history of the development of the quinolones is described from the first quinolone, nalidixic acid, via the first 6… Expand
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2000
2000
Gatifloxacin, grepafloxacin, moxifloxacin and trovafloxacin are fluoroquinolones with enhanced Gram-positive activity while… Expand
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Highly Cited
1999
Highly Cited
1999
Successful treatment of Helicobacter pylori infection is becoming compromised by emerging resistance. We report the prevalence… Expand
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Highly Cited
1997
Highly Cited
1997
The in-vitro activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin and… Expand
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Highly Cited
1996
Highly Cited
1996
The MICs of trovafloxacin, ciprofloxacin, ofloxacin, and sparfloxacin at which 90% of isolates are inhibited for 55 isolates of… Expand
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