Cephalosporin C
Names | |
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IUPAC name
(6R,7R)-3-[(Acetyloxy)methyl]-7-{[(5R)-5-amino-5-carboxypentanoyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | |
Other names
7-(5-Amino-5-carboxyvaleramido)cephalosporanic acid | |
Identifiers | |
61-24-5 | |
ChEBI | CHEBI:15776 |
ChEMBL | ChEMBL482858 |
ChemSpider | 58980 |
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Jmol-3D images | Image |
PubChem | 65536 |
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Properties | |
Molecular formula |
C16H21N3O8S |
Molar mass | 415.42 g·mol−1 |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
Infobox references | |
Cephalosporin C is an antibiotic of the cephalosporin class. It was isolated from fungi of the genus Acremonium and first characterized in 1961.[1] Although not a very active antibiotic itself, synthetic analogs of cephalosporin C, such as cefalotin, became some of the first marketed cephalosporin antibiotic drugs.
References
- ↑ Abraham, E. P.; Newton, G. G. F. (1961). "Structure of cephalosporin C". Biochemical Journal 79: 377–393. PMC 1205850. PMID 13681080.