|
|
| | Cefozopran Basic information |
| | Cefozopran Chemical Properties |
| | Cefozopran Usage And Synthesis |
| Chemical Properties | White To Pale-Yellow Powder | | Uses | Antibacterial | | Definition | ChEBI: Cefozopran is a fourth-generation cephalosporin antibiotic having imidazo[1,2-b]pyridazin-1-ium-1-ylmethyl and [(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino side groups located at positions 3 and 7 respectively. It is a cephalosporin, a member of thiadiazoles and an imidazopyridazine. | | Antimicrobial activity | An aminothiazole cephalosporin formulated as the hydrochloride.
Activity is similar to that of ceftazidime, but it is more
active against methicillin-susceptible staphylococci (MIC 1
mg/L). Representative MICs against Gram-negative species
are: Esch coli 0.25 mg/L; K. pneumoniae 1 mg/L; Ps. aeruginosa
1–8 mg/L. Activity against Acinetobacter spp., Sten. maltophilia
and B. fragilis group is poor.
A 20-min infusion of 1.5 g achieved a plasma concentration
of around 125 mg/L at the end of infusion. Almost 90%
of the dose was excreted in the urine over 24 h. The mean terminal
half-life was around 2 h. Adverse reactions appear to be
typical of those of other group 6 cephalosporins.
It is available in Japan. |
| | Cefozopran Preparation Products And Raw materials |
|