物质信息

ID:186

名称和标识
商标名
FlucloxSesamolFloxapen
IUPAC标准名
(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
别名
FlucloxacillinFlucloxacillin SodiumFlucloxacilina [INN-Spanish]Flucloxacillin-SodiumFlucloxacillinum [INN-Latin]Flucloxacilline [INN-French]Floxacillin
IUPAC传统名
(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
数据登录号
PubChem CID
CAS号
PubChem SID
化合物性质
理化性质
疏水性(logP)
3.2
描述信息
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
分子图谱
暂无数据
点击上传数据
参考文献
暂无数据
点击上传数据