U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H15N7O5S4
Molecular Weight 513.594
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFUZONAM

SMILES

CO\N=C(/C(=O)N[C@H]1[C@H]2SCC(CSC3=CN=NS3)=C(N2C1=O)C(O)=O)C4=CSC(N)=N4

InChI

InChIKey=CXHKZHZLDMQGFF-ZSDSSEDPSA-N
InChI=1S/C16H15N7O5S4/c1-28-21-9(7-5-31-16(17)19-7)12(24)20-10-13(25)23-11(15(26)27)6(4-30-14(10)23)3-29-8-2-18-22-32-8/h2,5,10,14H,3-4H2,1H3,(H2,17,19)(H,20,24)(H,26,27)/b21-9-/t10-,14-/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/3322588

Cefuzoname (CZON, L-105) is a second-generation cephalosporin antibiotic, has broad spectrum on Gram-positive or -negative bacteria and may also be effective against Staphylococcus aureus against which third generation cephalosporins are largely ineffective.

CNS Activity

Curator's Comment: CNS penetrant in rabbits and humans http://www.ncbi.nlm.nih.gov/pubmed/3613085

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Klebsiella pneumoniae growth
Target ID: Escherichia coli growth
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Clinical studies on cefuzonam for acute peritonitis due to perforated appendicitis. Tissue concentration and clinical efficacy].
1991-09
Bone cement not weakened by cefuzonam powder.
1991-06
[Clinical evaluation of cefuzonam (CZON) for bacterial pneumonia and lung abscess: comparative study with cefotiam (CTM)].
1991-04
[Fundamental and clinical studies on cefuzoname in the pediatric field].
1987-04
Patents

Sample Use Guides

In Vivo Use Guide
Cefuzonam in a dose of 1 g was administered by intravenous bolus injection or intravenous drip infusion for 60 minutes.
Route of Administration: Intravenous
In Vitro Use Guide
Curator's Comment: The MIC80's against Serratia marcescens and Enterobacter aerogenes were both 6.25 ug/ml, and that against Pseudomonas aeruginosa was 100 ug/ml. The MIC80's against Staphy-lococcus epidermidis were 25 and 6.25 ug/ml, respectively. Approximately 70% of strains of S. aureus were inhibited at concentrations less than 1.56 ug/ml.
The MIC80's of cefuzonam against Streptococcus pneumoniae, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Proteus vulgaris, Haemophilus influenzae and Citrobacter spp. were less than 0.20 ug/ml.
Name Type Language
CEFUZONAM [MI]
Preferred Name English
CEFUZONAM
INN   MART.   MI   WHO-DD  
INN  
Official Name English
cefuzonam [INN]
Common Name English
CEFUZONAM [MART.]
Common Name English
Cefuzonam [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C357
Created by admin on Wed Apr 02 06:51:45 GMT 2025 , Edited by admin on Wed Apr 02 06:51:45 GMT 2025
Code System Code Type Description
INN
5888
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SMS_ID
100000082043
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FDA UNII
860MT00T7T
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MERCK INDEX
m1062
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MESH
C049934
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EPA CompTox
DTXSID8048282
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CAS
82219-78-1
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NCI_THESAURUS
C76179
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WIKIPEDIA
CEFUZONAM
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CHEBI
55488
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PUBCHEM
6336505
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ChEMBL
CHEMBL1689069
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EVMPD
SUB07434MIG
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DRUG CENTRAL
3077
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