| Weight | 424.391 g/mol |
|---|---|
| Formula | C16H16N4O8S |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
cefuroxime (55268-75-2)
Zinacef · Cephuroxime · Ketocef
Score:
#383 in Microbiology
,
#1187 in Biochemistry
,
#2995 in Biology
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#3743 in Chemistry
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- Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens (Infection, 1983)
- 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)
- Protective effect of intravenously administered cefuroxime against nosocomial pneumonia in patients with structural coma. (American Journal of Respiratory and Critical Care Medicine, 1997)
- Prophylactic intracameral cefuroxime: Efficacy in preventing endophthalmitis after cataract surgery (Journal of Cataract and Refractive Surgery, 2002)
- A Comparison of Ceftriaxone and Cefuroxime for the Treatment of Bacterial Meningitis in Children (The New England Journal of Medicine, 1990)
- Prophylactic intracameral cefuroxime Evaluation of safety and kinetics in cataract surgery (Journal of Cataract and Refractive Surgery, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Zinacef
- Cephuroxime
- Ketocef
-
SMILESCON=C(C1=CC=CO1)C(=O)NC2C3N(C2=O)C(=C(CS3)COC(=O)N)C(=O)O
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InChIKeyJFPVXVDWJQMJEE-UHFFFAOYSA-N
- Pubchem - cefuroxime
- Wikipedia - cefuroxime
Cefuroxime is an enteral second-generation cephalosporin antibiotic. It was discovered by Glaxo, now GlaxoSmithKline, and first marketed in 1978 as Zinacef. It received approval from the U.S.
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