| Weight | 510.481 g/mol |
|---|---|
| Formula | C20H22N4O10S |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 9 |
cefuroxime axetil (64544-07-6)
Score:
#164 in Microbiology
,
#1757 in Biology
,
#2078 in Chemistry
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- A multicenter, randomized study comparing the efficacy and safety of intravenous and/or oral levofloxacin versus ceftriaxone and/or cefuroxime axetil in treatment of adults with community-acquired pneumonia. (Antimicrobial Agents and Chemotherapy, 1997)
- Comparison of cefuroxime axetil and doxycycline in the treatment of early Lyme disease. (Annals of Internal Medicine, 1992)
- Preparation of amorphous cefuroxime axetil nanoparticles by controlled nanoprecipitation method without surfactants. (International Journal of Pharmaceutics, 2006)
- Preparation of amorphous cefuroxime axetil nanoparticles by sonoprecipitation for enhancement of bioavailability (European Journal of Pharmaceutics and Biopharmaceutics, 2008)
- Comparison of cefuroxime axetil and doxycycline in treatment of patients with early Lyme disease associated with erythema migrans. (Antimicrobial Agents and Chemotherapy, 1995)
- Levofloxacin versus cefuroxime axetil in the treatment of acute exacerbation of chronic bronchitis: results of a randomized, double-blind study (Journal of Antimicrobial Chemotherapy, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(OC(=O)C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)C(=NOC)C3=CC=CO3)COC(=O)N
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InChIKeyKEJCWVGMRLCZQQ-UHFFFAOYSA-N
- Pubchem - cefuroxime axetil
- Wikipedia - cefuroxime axetil
Cefuroxime axetil is a second generation oral cephalosporin antibiotic. It was discovered by Glaxo now GlaxoSmithKline and introduced in 1987 as Zinnat. It was approved by FDA on Dec 28, 1987.
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cefuroxime axetil
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