Home > Compound List > Product Information
Cefmetazole_Molecular_structure_CAS_56796-20-4)
Click picture or here to close

Cefmetazole

Catalog No. DB00274 Name DrugBank
CAS Number 56796-20-4 Website http://www.ualberta.ca/
M. F. C15H17N7O5S3 Telephone (780) 492-3111
M. W. 471.53438 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 159

SYNONYMS

IUPAC name
(6R,7S)-7-{2-[(cyanomethyl)sulfanyl]acetamido}-7-methoxy-3-{[(1-methyl-1H-1,2,3,4-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
IUPAC Traditional name
cefmetazole sodium
Brand Name
Zefazone
Synonyms
Cefmetazolum [INN-Latin]
Cefmetazolo [INN-Spanish]
Cefmetazole sodium

DATABASE IDS

PubChem SID 46504461
PubChem CID 42008
CAS Number 56796-20-4

PROPERTIES

Hydrophobicity(logP) -2.2
Solubility 94.2 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. [PubChem]
Indication For the treatment of infections caused by susceptible organisms.
Pharmacology Cefmetazole is a second-generation cephalosporin. The cephalosporins are bactericidal drugs with both gram-positive and gram-negative activity. They inhibit bacterial cell wall synthesis in a way similar to the penicillins. Cefmetazole is more active than 1st-generation cephalosporins against indole-positive Proteus, Serratia, anaerobic gram-negative bacilli (including B. fragilis), and some E. coli, Klebsiella, and P. mirabilis, but is less active than cefoxitin or cefotetan against most gram-negative bacilli.
Toxicity Oral LD50 in rats is 3,204 mg/kg. With other b-lactam antibiotics, adverse effects following overdosage have included nausea, vomiting, epigastric distress, diarrhea, and convulsions.
Affected Organisms
• Enteric bacteria and other eubacteria
Biotransformation No appreciable metabolism.
Absorption Bioavailability is approximately 100% following intramuscular injection.
Half Life 1.50 ±0.14 hours
External Links
• Wikipedia

REFERENCES