<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">3534</id>
  <title>T3D3492</title>
  <common-name>Cephalosporin </common-name>
  <description>Ceftibuten is a third-generation cephalosporin antibiotic. It is an orally-administered agent. Cefalexin is used to treat acute bacterial exacerbations of chronic bronchitis (ABECB), acute bacterial otitis media, pharyngitis, and tonsilitis.</description>
  <cas>97519-39-6</cas>
  <pubchem-id>5282242</pubchem-id>
  <chemical-formula>C15H14N4O6S2</chemical-formula>
  <weight></weight>
  <appearance>White powder.</appearance>
  <melting-point></melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility></solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Rapidly absorbed following oral administration.</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Ceftibuten exerts its bactericidal action by binding to essential target proteins of the bacterial cell wall. This binding leads to inhibition of cell-wall synthesis.</mechanism-of-toxicity>
  <metabolism>A study with radiolabeled ceftibuten administered to 6 healthy adult male volunteers demonstrated that cis-ceftibuten is the predominant component in both plasma and urine. About 10% of ceftibuten is converted to the trans-isomer is approximately 1/8 as antimicrobially potent as the cis-isomer.Route of Elimination: Ceftibuten is excreted in the urine; 95% of the administered radioactivity was recovered either in urine or feces.</metabolism>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>Used to treat acute bacterial exacerbations of chronic bronchitis (ABECB), acute bacterial otitis media, pharyngitis, and tonsilitis. It is also indicated for pneumonia, infections of the urinary tract, enteritis and gastroenteritis. [Wikipedia]</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms>Overdosage of cephalosporins can cause cerebral irritation leading to convulsions.</symptoms>
  <treatment nil="true"/>
  <created-at type="dateTime">2009-07-30T17:58:46Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:07Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Ceftibuten</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C08117</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>3510</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id>Cephalosporin </stitch-id>
  <drugbank-id>DB01415</drugbank-id>
  <pdb-id></pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>[H]\C(CC(O)=O)=C(\C(O)=N[C@]1([H])C(=O)N2C(=CCS[C@]12[H])C(O)=O)C1=CSC(=N)N1</moldb-smiles>
  <moldb-formula>C15H14N4O6S2</moldb-formula>
  <moldb-inchi>InChI=1S/C15H14N4O6S2/c16-15-17-7(5-27-15)6(1-2-9(20)21)11(22)18-10-12(23)19-8(14(24)25)3-4-26-13(10)19/h1,3,5,10,13H,2,4H2,(H2,16,17)(H,18,22)(H,20,21)(H,24,25)/b6-1-/t10-,13-/m1/s1</moldb-inchi>
  <moldb-inchikey>InChIKey=UNJFKXSSGBWRBZ-BJCIPQKHSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">410.425</moldb-average-mass>
  <moldb-mono-mass type="decimal">410.03547558</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id>CHEMBL1605</chembl-id>
  <chemspider-id>4445418</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
