Clometocillin

Chemical compound
  • J01CE07 (WHO)
Identifiers
  • (2S,5R,6R)-6-([2-(3,4-dichlorophenyl)-2-methoxyacetyl]amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
CAS Number
  • 1926-49-4
PubChem CID
  • 71807
ChemSpider
  • 64831
UNII
  • YI8LL014GF
KEGG
  • D07236
ChEBI
  • CHEBI:131732
ChEMBL
  • ChEMBL2106548
CompTox Dashboard (EPA)
  • DTXSID20172859 Edit this at Wikidata
ECHA InfoCard100.016.053 Edit this at WikidataChemical and physical dataFormulaC17H18Cl2N2O5SMolar mass433.30 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(O)[C@@H]2N3C(=O)[C@@H](NC(=O)C(OC)c1ccc(Cl)c(Cl)c1)[C@H]3SC2(C)C

Clometocillin (or clometacillin) is a penicillin.[1][2]

References

  1. ^ Vanhoof R (September 1998). "Comparative in-vitro activities of amoxycillin and penicillin against Streptococcus pneumoniae isolates". The Journal of Antimicrobial Chemotherapy. 42 (3): 397–8. doi:10.1093/jac/42.3.397. PMID 9786482.
  2. ^ "Clometocillin". Pharmaceutical Manufacturing Encyclopedia (3rd ed.). Norwich, N.Y.: William Andrew Publishing. 2007. p. 1091. ISBN 978-0-8155-1856-3.
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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)
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spectrum
β-lactamase sensitive
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β-lactamase resistant
(2nd generation)
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  • Inhibits PG elongation and crosslinking: Ramoplanin§
Intracellular
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