ceftibuten

Known as: Ceftibuteno, 7-(2-(2-amino-4-thiazolyl)-4-carboxy-2-butenoylamino)-3-cephem-4-carboxylic acid, cis-Ceftibuten 
A semisynthetic, beta-lactamase-stable, third-generation cephalosporin with antibacterial activity. Ceftibuten binds to and inactivates penicillin… (More)
National Institutes of Health

Papers overview

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2008
2008
Neisseria gonorrhoeae infections have been empirically treated in Hong Kong with a single oral 400-mg dose of ceftibuten since… (More)
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2003
2003
We previously demonstrated that H+/peptide cotransporter PEPT1 shows a diurnal rhythm in the rat small intestine. In the present… (More)
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2001
2001
The available oral third generation of cephalosporin, "ceftibuten" was used to substitute the intravenous drug after… (More)
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1997
1997
BACKGROUND Infections caused by Enterobacteriaceae producing extended-spectrum beta-lactamases (ESBLs) are a growing clinical… (More)
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Highly Cited
1995
Highly Cited
1995
A complementary DNA (cDNA) encoding the rat H+/peptide cotransporter (PepT1) was isolated, and the transport characteristics of… (More)
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Review
1995
Review
1995
The bioavailability and pharmacokinetics of ceftibuten administered as an oral suspension were characterized by several studies… (More)
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1994
1994
The characteristics of ceftibuten uptake into Caco-2 cells grown in a collagen-coated dish were examined. Ceftibuten showed… (More)
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1991
1991
The pharmacokinetics of ceftibuten, a new oral cephalosporin, has been studied in humans. Ceftibuten is very well absorbed in… (More)
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1991
1991
The in vitro activity of a new oral cephalosporin, ceftibuten, was determined against 837 clinical isolates by agar dilution… (More)
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1990
1990
The pharmacokinetics of the cephalosporin ceftibuten were determined after the fifth and final dose of 200 mg given every 12 h… (More)
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