Cefalotin

Cefalotin

Clinical data
AHFS/Drugs.com	International Drug Names
MedlinePlus	a682860
Pregnancy category	AU: A US: B (No risk in non-human studies)
Routes of administration	Intravenous
ATC code	J01DB03 (WHO)
Legal status
Legal status	AU: S4 (Prescription only) UK: POM (Prescription only)
Pharmacokinetic data
Bioavailability	n/a
Protein binding	65 to 80%
Metabolism	Hepatic
Biological half-life	30 minutes to 1 hour
Excretion	Renal
Identifiers
IUPAC name (6R,7R)-3-[(acetoxy)methyl]-8-oxo-7-[(2-thienylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS Number	153-61-7
PubChem (CID)	6024
DrugBank	DB00456
ChemSpider	5802
UNII	R72LW146E6
KEGG	D07635
ChEBI	CHEBI:124991
ChEMBL	CHEMBL617
ECHA InfoCard	100.005.288
Chemical and physical data
Formula	C16H16N2O6S2
Molar mass	396.44 g/mol
3D model (Jmol)	Interactive image
SMILES O=C2N1/C(=C(\CS[C@@H]1[C@@H]2NC(=O)Cc3sccc3)COC(=O)C)C(=O)O
InChI InChI=1S/C16H16N2O6S2/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23)/t12-,15-/m1/s1 Key:XIURVHNZVLADCM-IUODEOHRSA-N
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Cefalotin (INN) /ˌsɛfəˈloʊtᵻn/ or cephalothin (USAN) /ˌsɛfəˈloʊθᵻn/ is a first-generation cephalosporin antibiotic.^[1] It was the first cephalosporin marketed (1964) and continues to be widely used.^[2] It is an intravenously administered agent with a similar antimicrobial spectrum to cefazolin and the oral agent cefalexin. Cefalotin sodium is marketed as Keflin (Lilly) and under other trade names.^[3]

References

1. Hameed, T. K.; Robinson, J. L. (2002). "Review of the use of cephalosporins in children with anaphylactic reactions from penicillins". The Canadian journal of infectious diseases = Journal canadien des maladies infectieuses. 13 (4): 253–8. PMC 2094874. PMID 18159398.
2. David Greenwood (21 February 2008). Antimicrobial Drugs: Chronicle of a Twentieth Century Medical Triumph. OUP Oxford. pp. 128–. ISBN 978-0-19-953484-5.
3. International Drug Names: Cefalotin