Cefpiramide

Cefpiramide

Clinical data
Routes of administration	Intravenous, intramuscular
ATC code	J01DD11 (WHO)
Pharmacokinetic data
Protein binding	93% to 99.3%
Elimination half-life	4.44 hours
Excretion	Renal and fecal
Identifiers
IUPAC name (6R)-7-{[(2R)-2-(4-hydroxyphenyl)-2-[(6-methyl- 4-oxo-1H-pyridine-3-carbonyl)amino]acetyl]amino}- 3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo- 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS Number	70797-11-4
PubChem CID	107654
DrugBank	APRD00856
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}
Chemical and physical data
Formula	C25H24N8O7S2
Molar mass	612.64 g/mol

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Cefpiramide is a third-generation cephalosporin antibiotic.

                    ==References==

External links

• Wang H, Yu Y, Xie X, Wang C, Zhang Y, Yuan Y, Zhang X, Liu J, Wang P, Chen M (2000). "In-vitro antibacterial activities of cefpiramide and other broad-spectrum antibiotics against 440 clinical isolates in China". J Infect Chemother. 6 (2): 81–5. PMID 11810540.CS1 maint: Multiple names: authors list (link)
• Iakovlev V, Vishnevskiĭ V, Khlebnikov E, Khadin I, Plavlova M, Elagina L, Izotova G (1995). "[Cefpiramide (Tamicin) in the treatment of purulent complications of abdominal surgery]". Antibiot Khimioter. 40 (9): 30–4. PMID 8651827.CS1 maint: Multiple names: authors list (link)
• Sampi K, Hattori M (1992). "[Comparative study of cefpiramide + amikacin versus piperacillin + amikacin in granulocytopenic patients: a randomized, prospective study]". Gan To Kagaku Ryoho. 19 (9): 1315–20. PMID 1503486.

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