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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H14N7O5S4.Na
Molecular Weight 535.576
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFUZONAM SODIUM

SMILES

[Na+].[H][C@]12SCC(CSC3=CN=NS3)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C4=CSC(N)=N4)C([O-])=O

InChI

InChIKey=BCMSQWPLFBUUKW-IXLPVNPSSA-M
InChI=1S/C16H15N7O5S4.Na/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);/q;+1/p-1/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
[Fundamental and clinical studies on cefuzoname in the pediatric field].
1987 Apr
Bone cement not weakened by cefuzonam powder.
1991 Jun
[Clinical studies on cefuzonam for acute peritonitis due to perforated appendicitis. Tissue concentration and clinical efficacy].
1991 Sep
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 SODIUM
JAN   WHO-DD  
Common Name English
SODIUM CEFUZONAM
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2Z)-2-(2-AMINO-4-THIAZOLYL)-2-(METHOXYIMINO)ACETYL)AMINO)-8-OXO-3-((1,2,3-THIADIAZOL-5-YLTHIO)METHYL)-, SODIUM SALT (1:1), (6R,7R)-
Common Name English
Cefuzonam sodium [WHO-DD]
Common Name English
CEFUZONAM SODIUM [JAN]
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2-AMINO-4-THIAZOLYL)(METHOXYIMINO)ACETYL)AMINO)-8-OXO-3-((1,2,3-THIADIAZOL-5- YLTHIO)METHYL)-, SODIUM SALT, (6R-(6-ALPHA,7-BETA(Z)))-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C357
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID40231634
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
PRIMARY
EVMPD
SUB01141MIG
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
PRIMARY
PUBCHEM
23663965
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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FDA UNII
6SOU25L22C
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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SMS_ID
100000084685
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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NCI_THESAURUS
C98232
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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CAS
82219-81-6
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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ChEMBL
CHEMBL1689069
Created by admin on Fri Dec 15 18:36:30 GMT 2023 , Edited by admin on Fri Dec 15 18:36:30 GMT 2023
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