Cefalonium

Chemical compound
  • QJ51DB90 (WHO)
Legal statusLegal status
  • Veterinary use only
Identifiers
  • (6R,7R)-3-[(4-carbamoylpyridin-1-ium-1-yl)methyl]-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
CAS Number
  • 5575-21-3
PubChem CID
  • 21743
ChemSpider
  • 20438
UNII
  • K2P920217W
KEGG
  • D07634
ChEMBL
  • ChEMBL2105567
CompTox Dashboard (EPA)
  • DTXSID5045388 Edit this at Wikidata
ECHA InfoCard100.024.499 Edit this at WikidataChemical and physical dataFormulaC20H18N4O5S2Molar mass458.51 g·mol−13D model (JSmol)
  • Interactive image
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)Cc3sccc3)C[n+]4ccc(C(=O)N)cc4)C([O-])=O

Cefalonium (INN) is a first-generation cephalosporin antibiotic.[1]

References

  1. ^ Boothe DN (2008). "Principles of Antibacterial Therapy". In Maddison JE, Page SW, Church DB (eds.). Small animal clinical pharmacology (Second ed.). [Edinburgh]: Elsevier Health Sciences. p. 167. ISBN 978-0-7020-2858-8.
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Antibacterials active on the cell wall and envelope (J01C-J01D)
Beta-lactams
(inhibit synthesis
of peptidoglycan
layer of bacterial
cell wall by binding
to and inhibiting
PBPs, a group of
D-alanyl-D-alanine
transpeptidases)
Penicillins (Penams)
Narrow
spectrum
β-lactamase sensitive
(1st generation)
β-lactamase resistant
(2nd generation)
Extended
spectrum
Aminopenicillins (3rd generation)
Carboxypenicillins (4th generation)
Ureidopenicillins (4th generation)
Other
Carbapenems / Penems
Cephems
Cephalosporins
Cephamycins
Carbacephems
1st generation
2nd generation
3rd generation
4th generation
5th generation
Siderophore
Veterinary
Monobactams
β-lactamase inhibitors
Combinations
Polypeptides
Glycopeptides
Lipoglycopeptides
Lipopeptides
Polymyxins
Other
  • Inhibits PG elongation and crosslinking: Ramoplanin§
Intracellular
Other


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