Pivampicillin

From Wikipedia, the free encyclopedia

Pivampicillin chemical structure
Pivampicillin
Systematic (IUPAC) name
2,2-dimethylpropanoyloxymethyl (2S,5R,6R)-
6-{[(2R)-2-amino-2-phenyl-acetyl]amino}-3,3-
dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]
heptane-2-carboxylate
Identifiers
CAS number 33817-20-8
ATC code J01CA02
PubChem 33478
Chemical data
Formula C22H29N3O6S 
Mol. weight 463.548 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion Renal (76%)
Therapeutic considerations
Pregnancy cat.

?

Legal status
Routes Oral

Pivampicillin is a pivaloyloxymethylester of ampicillin. It is a prodrug, which is thought to enhance the oral bioavailability of ampicillin because of its greater lipophilicity compared to that of ampicillin.

Penicillins (J01C) edit

Amoxicillin, Ampicillin, Azlocillin, Carbenicillin, Cloxacillin, Dicloxacillin, Flucloxacillin, Mezlocillin, Nafcillin, Piperacillin, Pivampicillin, Ticarcillin