Cefdaloxime

Cefdaloxime
Clinical data
ATC code
  • None
Identifiers
CAS Number
PubChem CID
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-generation cephalosporin antibiotic.[1] Developed in the late 1980's by Hoechst-Roussel Pharmaceuticals Inc.,[2] it was never brought to market.[3]

References

  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): 105–110. doi:10.1016/0732-8893(94)00148-p. PMID 7628189.
  2. ↑ Jones RN, Erwin ME (May 1992). "Preliminary disk diffusion susceptibility testing criteria for cefdaloxime (RU29246, HR-916 metabolite), a new orally administered cephalosporin". Journal of Clinical Microbiology. 30 (5): 1297–1300. doi:10.1128/jcm.30.5.1297-1300.1992. PMC 265269. PMID 1583135.
  3. ↑ Zagursky RJ, Pichichero ME (2018). "Cross-reactivity in β-Lactam Allergy". The Journal of Allergy and Clinical Immunology. In Practice. 6 (1): 72–81.e1. doi:10.1016/j.jaip.2017.08.027. PMID 29017833.