Ceftibuten dihydrate

Ceftibuten dihydrate
  • CAS No.:118081-34-8
Other grades of this product :
Ceftibuten dihydrate Basic information
Product Name:Ceftibuten dihydrate
Synonyms:Cedax dihydrate;CEDAX DIHYDRATE;SCH-39720 DIHYDRATE;Sch-39720 dihydrate;(+)-(6r,7r)-7-[2-(2-amino-1,3-thiazol-4-yl)-4-carboxy-2-butenamide]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid dihydrate;Cedax;Cedax (tn);Ceftibuten (jp15);Cetb
CAS:118081-34-8
MF:C15H16N4O7S2
MW:428.43
EINECS:
Product Categories:Intermediates & Fine Chemicals;Pharmaceuticals;Chiral Reagents;Heterocycles;Sulfur & Selenium Compounds
Mol File:118081-34-8.mol
Ceftibuten dihydrate Chemical Properties
Melting point >180°C (dec.)
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility DMSO (Slightly), Water (Slightly)
form Solid
color Pale Yellow to Light Orange
Stability:Hygroscopic
Safety Information
MSDS Information
Ceftibuten dihydrate Usage And Synthesis
Chemical PropertiesLight-Yellow Solid
UsesCeftibuten dihydrate, one of the third-generation cephalosporin antibiotic is effectively used in curing several infectious diseases.
UsesCeftibuten Dihydrate is used in preparation of Ceftibuten crystal.
DefinitionChEBI: Ceftibuten dihydrate is the dihydrate of ceftibuten. It is used as an orally administered treatment for urinary-tract and respiratory-tract infections. It has a role as an antibacterial drug. It contains a ceftibuten.
Biological ActivityCeftibuten is an orally bioavailable broad-spectrum cephalosporin antibiotic that inhibits the growth of B. catarrhalis, H. influenzae, pathogenic Neisseria, Streptococcus, penicillin-susceptible S. pneumoniae, and eleven Enterobacteriaceae strains (MICs = 0.25, ≤0.06, ≤0.06, 0.5-1, 4, and ≤0.06-0.5 μg/ml, respectively).1,2 Ceftibuten is also active against E. coli expressing β-lactamase type I, III, and V and K. oxytoca expressing β-lactamase type IV (MICs = 8, 0.25, 0.5, and ≤0.06 μg/ml, respectively) as well as a panel of eight bacterial stains expressing plasmid-encoded extended spectrum β-lactamases, including E. coli CTX-M and K. pneumoniae SHV-2 (MICs = 1 and 0.25 μg/ml, respectively). In vivo, ceftibuten reduces the number of mice killed within 6 days of a K. pneumoniae, E. coli, S. pneumoniae, or S. aureus infection by 50% when administered subcutaneously at doses of 0.125, 2, 1,024, and >512 mg/kg, respectively.3 Formulations containing ceftibuten have been used in the treatment of bacterial infections including bronchitis, pneumonia, and enteritis.
PharmacokineticsCeftibuten Dihydrate is the dihydrate form of ceftibuten, a semisynthetic, beta-lactamase-stable, third-generation cephalosporin with antibacterial activity. Ceftibuten binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis.
Ceftibuten dihydrate Preparation Products And Raw materials

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