61-24-5
Chemical Structure
Cephalosporin C
- CAS No.: 61-24-5
- Formula:C16H21N3O8S
- Molecular Weight:415.42
IUPAC Name: (6R,7R)-3-(acetoxymethyl)-7-((R)-5-amino-5-carboxypentanamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
InChIKey: HOKIDJSKDBPKTQ-GLXFQSAKSA-N
SMILES: OC(C1=C(COC(C)=O)CS[C@@]([C@@H]2NC(CCC[C@@H](N)C(O)=O)=O)([H])N1C2=O)=O
Biological Activity: Cephalosporin C is an antibacterial penicillinase inhibitor. Cephalosporin C competitively inhibits penicillinase and resists hydrolysis. Cephalosporin C protects mice infected with hemolytic Streptococcus. Cephalosporin C can be used in research on bacterial infections such as hemolytic Streptococcus[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Cephalosporin C | 99.12% | Cephalosporin C is an antibacterial penicillinase inhibitor. Cephalosporin C competitively inhibits penicillinase and resists hydrolysis. Cephalosporin C protects mice infected with hemolytic Streptococcus. Cephalosporin C can be used in research on bacterial infections such as hemolytic Streptococcus. | ||||||||||||||||||||
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References
- [1]. Chen D, et al. Degradation of antibiotic cephalosporin C in aqueous solution and elimination of antimicrobial activity by gamma irradiation. Chemical Engineering Journal. 2019 Oct 15;374:1102-8.
- [2]. Newton GG, et al. Isolation of cephalosporin C, a penicillin-like antibiotic containing D-α-aminoadipic acid. Biochemical journal. 1956 Apr;62(4):651.
- [3]. Demain AL, et al. Microbial degradation of cephalosporin C. Nature. 1963 Aug 31;199(4896):909-10.
- [4]. Newton GG, et al. Cephalosporin C, a new antibiotic containing sulphur and D-α-aminoadipic acid. Nature. 1955 Mar 26;175(4456):548-.
