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Cefuroxime

产品号 DB01112 公司名称 DrugBank
CAS号 55268-75-2 公司网站 http://www.ualberta.ca/
分子式 C16H16N4O8S 电 话 (780) 492-3111
分子量 424.38524 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 983

产品价格信息

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产品别名

标题
Cefuroxime
IUPAC标准名
(6R,7R)-3-[(carbamoyloxy)methyl]-7-[(2E)-2-(furan-2-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
IUPAC传统名
cefuroxime
商标名
Sharox
Cedax
Cephuroxime
Kefzol
Cefotan
Ceftin
Cefuril
Cepazine
Elobact
Mandol
Maxipime
Velosef
Zinacef
Zinat
Zinnat
Ancef
Biofuroksym
Cefizox
Cefobid
Cefurax
Cefzil
Duricef
Kefurox
Kerurox
Mefoxin
Monocid
Oraxim
Rocephin
别名
Cefuroximum [INN-Latin]
Cefuroxime [USAN:BAN:INN]
Cefuroximo [INN-Spanish]
Cefuroxim

产品登记号

CAS号 55268-75-2

产品性质

疏水性(logP) -0.8
溶解度 Freely soluble as sodium salt (145 mg/L)

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Broad-spectrum cephalosporin antibiotic resistant to beta-lactamase. It has been proposed for infections with gram-negative and gram-positive organisms, gonorrhea, and haemophilus. [PubChem]
Indication For the treatment of many different types of bacterial infections such as bronchitis, sinusitis, tonsillitis, ear infections, skin infections, gonorrhea, and urinary tract infections.
Pharmacology Cefuroxime is a β-lactam type antibiotic. More specifically, it is a second-generation cephalosporin. Cephalosporins work the same way as penicillins: they interfere with the peptidoglycan synthesis of the bacterial wall by inhibiting the final transpeptidation needed for the cross-links. This effect is bactericidal. Cefuroxime is effective against the following organisms: Aerobic Gram-positive Microorganisms: Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes. Aerobic Gram-negative Microorganisms: Escherichia coli, Haemophilus influenzae (including beta-lactamase-producing strains), Haemophilus parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis (including beta-lactamase-producing strains), Neisseria gonorrhoeae (including beta-lactamase-producing strains). Spirochetes: Borrelia burgdorferi. Cefuroxime axetil is the prodrug
Toxicity Allergic reactions might be expected, including rash, nasal congestion, cough, dry throat, eye irritation, or anaphylactic shock. Overdosage of cephalosporins can cause cerebral irritation leading to convulsions.
Affected Organisms
Enteric bacteria and other eubacteria
Biotransformation The axetil moiety is metabolized to acetaldehyde and acetic acid.
Absorption Absorbed from the gastrointestinal tract. Absorption is greater when taken after food (absolute bioavailability increases from 37% to 52%).
Half Life Approximately 80 minutes following intramuscular or intravenous injection.
Protein Binding 50% to serum protein
References
Perry CM, Brogden RN: Cefuroxime axetil. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1996 Jul;52(1):125-58. [Pubmed]
External Links
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参考文献

  • Perry CM, Brogden RN: Cefuroxime axetil. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1996 Jul;52(1):125-58. Pubmed