Product Information
- (6R,7R)-3-(Aminocarbonyl)oxymethyl-7-(2Z)-2-(2-furanyl)-2-(methoxyimino)acetylamino-8-oxo-5-thia-1-azabicyclo4.2.0oct-3-en e-2-carb oxylic acid
- (6R,7R)-3-[(carbamoyloxy)methyl]-7-{[(2Z)-2-furan-2-yl-2-(methoxyimino)acetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- (6R,7R)-3-[(carbamoyloxy)methyl]-7-{[furan-2-yl(methoxyimino)acetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- (6R,7R)-3-[[(Aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- 1-(acetyloxy)ethyl (6R,7R)-3-[(carbamoyloxy)methyl]-7-{[(2Z)-2-furan-2-yl-2-(methoxyimino)acetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, [6R-[6α,7β(Z)]]-
- Biofuroksym
- Biofuroxim
- See more synonyms
- Cefaloxime
- Cefasyn
- Cefuroxime Acid
- Cefuroxime,Free Acid
- Cefuroximo
- Cephuroxime
- Ketocef
- Maxalac
- Multisef
Cefuroxime is a third-generation cephalosporin antibiotic that inhibits bacterial growth by binding to the penicillin-binding proteins in the bacterial cell wall. Cefuroxime has a concentration-time curve that can be described by a linear relationship with an effect constant of 0.077/hr and a rate constant of 0.016/hr. Its pharmacokinetic properties are similar to those of cefprozil, which is an active inhibitor of cefuroxime. The optical sensor used for this study was based on a streptococcal pharyngitis therapy group experiment and used microdialysis probes to detect changes in the skin’s pH following treatment with various doses of cefuroxime or placebo. This drug had minimal toxicity, low-dose groups showed no change in their skin pH, and high dose groups showed significant increases in their skin pH within 24 hours after treatment.
Chemical properties
Technical inquiry about: 3D-FA19881 Cefuroxime
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