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EntityQ3664175· pop 17· linked from 188 articles

cefditoren

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Also known as CDTR-PI, Cefditoren Pivoxil, Cefditoren Pivaloyloxymethyl Ester

Research

345 papers

via PubMed

Wikidata facts

Mass
506.050081
Show 5 more facts
chemical formula
C₁₉H₁₈N₆O₅S₃
isomeric SMILES
CC1=C(SC=N1)/C=C\C2=C(N3[C@@H]([C@@H](C3=O)NC(=O)/C(=N\OC)/C4=CSC(=N4)N)SC2)C(=O)O
canonical SMILES
CC1=C(SC=N1)C=CC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)O
World Health Organisation international non-proprietary name
cefditoren
defined daily dose
0.4
Sources (3)

via Wikidata · CC0

~11 min read

Article

24 sections
Contents
  • Structure
  • Antimicrobial activity
  • Pharmacokinetics
  • Absorption
  • Distribution
  • Metabolism and Excretion
  • Medical uses
  • Spectrum of bacterial susceptibility
  • Dosage and administration
  • Adults and Adolescents (≥12 Years)
  • Children (2 months to 12 years of age)
  • Pregnancy
  • Pregnancy Category B
  • Geriatric use
  • International approvals
  • Proprietary Preparations and Countries
  • Contraindications
  • Safety and tolerability
  • Guidelines
  • Japanese Guidelines
  • A panel of 70 pulmonologists, coordinated by 9 experts in respiratory care recommendations
  • Ideal for switch therapy
  • References
  • External links

Cefditoren, also known as cefditoren pivoxil is an antibiotic used to treat infections caused by Gram-positive and Gram-negative bacteria that are resistant to other antibiotics. It is mainly used for treatment of community acquired pneumonia. It is taken by mouth and is in the cephalosporin family of antibiotics, which is part of the broader beta-lactam group of antibiotics.

== Structure == Like other cephalosporins, cefditoren has a β-lactam ring at the 7 position of cephalosporin ring that is responsible for its inhibitory action on bacterial cell wall synthesis. In addition to the cephem nucleus common to all cephalosporins, cefditoren has an aminothiazole group that enhances its activity against Gram-negative organisms, a methylthiazole group that enhances its activity against Gram-positive organisms, a methoxyimino group that gives it stability against β-lactamases, and a pivoxil ester group that enhances oral bioavailability.

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