Substance

ID:186

Names and Identifiers
Brand Name
FlucloxSesamolFloxapen
IUPAC name
(2S,5R,6R)-6-[3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-amido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Synonyms
FlucloxacillinFlucloxacillin SodiumFlucloxacilina [INN-Spanish]Flucloxacillin-SodiumFlucloxacillinum [INN-Latin]Flucloxacilline [INN-French]Floxacillin
IUPAC Traditional name
(2S,5R,6R)-6-[3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-amido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Registration numbers
PubChem CID
CAS Number
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
3.2
Molecule Details
Drug Groups
approved
Description
Antibiotic analog of cloxacillin. [PubChem]
Indication
Used to treat bacterial infection by susceptible microorganisms.
Pharmacology
Flucloxacillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Flucloxacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of Flucloxacillin results from the inhibition of cell wall synthesis and is mediated through flucloxacillin binding to penicillin binding proteins (PBPs). Flucloxacillin is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases.
Affected Organisms
Enteric bacteria and other eubacteria
Biotransformation
Hepatic.
Absorption
Bioavailability is 50–70% following oral administration.
Half Life
0.75–1 hour
External Links
Molecular Spectra
No Data Available
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References
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