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
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
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/3613097Curator's Comment: Description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/3322588
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3613097
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
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3530123
Curator's Comment: CNS penetrant in rabbits and humans http://www.ncbi.nlm.nih.gov/pubmed/3613085
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: Klebsiella pneumoniae growth Sources: http://www.ncbi.nlm.nih.gov/pubmed/3613094 |
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Target ID: Escherichia coli growth Sources: http://www.ncbi.nlm.nih.gov/pubmed/3613094 |
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Target ID: map00550 Sources: http://www.kegg.jp/dbget-bin/www_bget?dr:D03432 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Curative | Unknown Approved UseUnknown |
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Curative | Unknown Approved UseUnknown |
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Curative | Unknown Approved UseUnknown |
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Curative | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
[Fundamental and clinical studies on cefuzoname in the pediatric field]. | 1987 Apr |
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Bone cement not weakened by cefuzonam powder. | 1991 Jun |
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[Clinical studies on cefuzonam for acute peritonitis due to perforated appendicitis. Tissue concentration and clinical efficacy]. | 1991 Sep |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/1960860
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
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3204654
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.
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NCI_THESAURUS |
C357
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DTXSID40231634
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SUB01141MIG
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23663965
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6SOU25L22C
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100000084685
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C98232
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82219-81-6
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CHEMBL1689069
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ACTIVE MOIETY
SUBSTANCE RECORD