Desfuroyl Ceftiofur Dimer (>90%)

For research use only. Not for therapeutic Use.

  • CAT Number: C000394
  • CAS Number: 120905-00-2
  • Molecular Formula: C₂₈H₂₈N₁₀O₁₀S₆
  • Molecular Weight: 856.97
  • Purity: ≥95%
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Desfuroyl Ceftiofur Dimer (>90%)(Cat No.:C000394)is a metabolite of Ceftiofur, a third-generation cephalosporin antibiotic used in veterinary medicine to treat bacterial infections in animals. This compound forms when Ceftiofur is metabolized in the body, typically in livestock, and is used to assess the residue levels of Ceftiofur in animal products. The dimer form, with a purity greater than 90%, is significant for its high stability and longer half-life compared to the parent drug, making it important in residue analysis and ensuring compliance with food safety regulations.


Catalog Number C000394
CAS Number 120905-00-2
Synonyms

(6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[[[(6R,7R)-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]dithio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid;

Molecular Formula C₂₈H₂₈N₁₀O₁₀S₆
Purity ≥95%
Solubility Acetone (Slightly), DMSO (Slightly), Methanol (Slightly)
Appearance Off-White to Pale Beige Solid
Storage -20°C, Hygroscopic
IUPAC Name (6R,7R)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[[[(6R,7R)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyldisulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
InChI InChI=1S/C28H28N10O10S6/c1-47-35-13(11-7-51-27(29)31-11)19(39)33-15-21(41)37-17(25(43)44)9(3-49-23(15)37)5-53-54-6-10-4-50-24-16(22(42)38(24)18(10)26(45)46)34-20(40)14(36-48-2)12-8-52-28(30)32-12/h7-8,15-16,23-24H,3-6H2,1-2H3,(H2,29,31)(H2,30,32)(H,33,39)(H,34,40)(H,43,44)(H,45,46)/b35-13+,36-14+/t15-,16-,23-,24-/m1/s1
InChIKey PYRWVZOVUOUHKK-AFQMBUBWSA-N
SMILES CO/N=C(/C(=O)N[C@@H]1C(=O)N2[C@@H]1SCC(=C2C(=O)O)CSSCC3=C(N4C(=O)[C@H]([C@H]4SC3)NC(=O)/C(=N/OC)/C5=CSC(=N5)N)C(=O)O)\C6=CSC(=N6)N
Reference

Donaldson, S.C. et al.: Appl. Environ. Microbiol., 72, 3940 (2006); Yancey, R.J. et al.: Am. J. Vet. Res., 48, 1050 (1987);

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