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Cefdaloxime

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Cefdaloxime
Clinical data
ATC code
  • None
Identifiers
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H15N5O6S2
Molar mass413.42 g·mol−1
3D model (JSmol)
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)C(=N\O)/c3nc(sc3)N)COC)C(=O)O
  • InChI=1S/C14H15N5O6S2/c1-25-2-5-3-26-12-8(11(21)19(12)9(5)13(22)23)17-10(20)7(18-24)6-4-27-14(15)16-6/h4,8,12,24H,2-3H2,1H3,(H2,15,16)(H,17,20)(H,22,23)/b18-7-/t8-,12-/m1/s1
  • Key:HOGISBSFFHDTRM-GHXIOONMSA-N
  (verify)

Cefdaloxime (INN) is a third-generationcephalosporinantibiotic.[1]

References

[edit]
  1. ^Sader HS, Runyon BA, Erwin ME, Jones RN (February 1995). "Antimicrobial activity of 11 newer and investigational drugs tested against aerobic isolates from spontaneous bacterial peritonitis".Diagnostic Microbiology and Infectious Disease.21 (2):105–10.doi:10.1016/0732-8893(94)00148-p.PMID 7628189.
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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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