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Cefetamet

From Wikipedia, the free encyclopedia

Chemical compound
Pharmaceutical compound
Cefetamet
Clinical data
ATC code
Identifiers
  • (6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-
    2-methoxyiminoacetyl]amino}-3-methyl-8-oxo-
    5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.201.087Edit this at Wikidata
Chemical and physical data
FormulaC14H15N5O5S2
Molar mass397.42 g·mol−1
3D model (JSmol)
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)C(=N\OC)/c3nc(sc3)N)C)C(=O)O
  • InChI=1S/C14H15N5O5S2/c1-5-3-25-12-8(11(21)19(12)9(5)13(22)23)17-10(20)7(18-24-2)6-4-26-14(15)16-6/h4,8,12H,3H2,1-2H3,(H2,15,16)(H,17,20)(H,22,23)/b18-7-/t8-,12-/m1/s1
  • Key:MQLRYUCJDNBWMV-GHXIOONMSA-N

Cefetamet is acephalosporinantibiotic.[1][2]

References

[edit]
  1. ^Pubchem."Cefetamet".pubchem.ncbi.nlm.nih.gov. Retrieved2018-03-23.
  2. ^Bryson HM, Brogden RN (April 1993). "Cefetamet pivoxil. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use".Drugs.45 (4):589–621.doi:10.2165/00003495-199345040-00009.PMID 7684677.S2CID 264011171.
β-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
Lipopeptides
Other
  • Inhibits PG elongation and crosslinking:Ramoplanin§
Intracellular
Other


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