Cefadroxil (hydrate)

Cefadroxil (hydrate)

Catalog Number:
A004364346APE
Mfr. No.:
APE-C3991
Price:
$175
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          Background

          Cefadroxil is a new semisynthetic cephalosporin with a broad antibacterial spectrum and a high chemotherapeutic potential [1]. In vitro: The inhibitory activity of this compound was similar to that of cephalexin and cephradine when tested against 602 clinical isolates on Mueller-Hinton medium. In the oral treatment of experimental infections of mice, cefadroxil was more effective than cephalexin against Streptococcus pyogenes, and comparably effective against Streptococcus pneumoniae, Staphylococcus aureus, and several gram-negative species [1].In vivo: In mice, oral administration of cefadroxil at doses ranging from 25 to 100 mg/kg attained peak concentrations in the blood. Higher peak levels were noted with cefadroxil than with cephalexin at a dose of 200 mg/kg [1].Clinical trials: A single daily dose of cefadroxil appeared to be as effective in the treatment of patients with A β-hemolytic streptococcal (GABHS) pharyngitis [2].

          [1] Buck R E, Price K E. Cefadroxil, a new broad-spectrum cephalosporin[J]. Antimicrobial agents and chemotherapy, 1977, 11(2): 324-330.
          [2] Gerber M A, Randolph M F, Chanatry J, et al. Once daily therapy for streptococcal pharyngitis with cefadroxil[J]. The Journal of pediatrics, 1986, 109(3): 531-537.

      • Properties
        • Categories
          broad-spectrum antibiotic
          Alternative Name
          Duricef,Bidocel; (6R,7R)-7-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, monohydrate
          CAS Number
          66592-87-8
          Molecular Formula
          C16H17N3O5S·H2O
          Molecular Weight
          381.4
          Purity
          98.00%
          Solubility
          insoluble in EtOH; insoluble in H2O; ≥5.8 mg/mL in DMSO with gentle warming
          Storage
          Store at -20°C
          SMILES
          OC1=CC=C([[email protected]@H](N)C(N[[email protected]@H]2C(N3[[email protected]]2([H])SCC(C)=C3C(O)=O)=O)=O)C=C1.O

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