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Cloxacillin sodium salt

产品号 27555 公司名称 Sigma Aldrich
CAS号 642-78-4 公司网站 http://www.sigmaaldrich.com
分子式 C19H17ClN3NaO5S 电 话 1-800-521-8956
分子量 457.86315 传 真
纯 度 ≥97.0% (HPLC) 电子邮件
保 存 Chembase数据库ID: 103129

产品价格信息

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产品别名

标题
Cloxacillin sodium salt
IUPAC标准名
sodium (2S,5R,6R)-6-[3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-amido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
IUPAC传统名
sodium cloxacillin(1-)

产品登记号

CAS号 642-78-4
EC号 211-390-9
PubChem SID 24856654
MDL号 MFCD00063568
Beilstein号 4103180

产品性质

Empirical Formula (Hill Notation) C19H17ClN3NaO5S
杂质 ≤5% water
纯度 ≥97.0% (HPLC)
溶解度 H2O: soluble50 mg/mL, clear, colorless
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS编号 XH8750000
保存温度 2-8°C
德国WGK号 2

产品详细信息

详细说明 (English)
Biochem/physiol Actions
Cloxacillin interferes with the last stage of bacterial cell wall synthesis by binding to penicillin-binding proteins. This inhibits the necessary cross-linking and leads to autolysis of the bacteria by autolysins.
Application
Cloxacillin is a semisynthetic antibiotic in the same class as penicillin. Cloxacillin is used against staphylococci that produce β-lactamase. It is used to study the role of pH in antibiotic effectiveness1 and how oxgall, acid, and hydrogen peroxide stress effects the susceptibility of Bifidobacteria2.
详细说明 (简体中文)
Biochem/physiol Actions
Cloxacillin interferes with the last stage of bacterial cell wall synthesis by binding to penicillin-binding proteins. This inhibits the necessary cross-linking and leads to autolysis of the bacteria by autolysins.
Application
Cloxacillin is a semisynthetic antibiotic in the same class as penicillin. Cloxacillin is used against staphylococci that produce β-lactamase. It is used to study the role of pH in antibiotic effectiveness1 and how oxgall, acid, and hydrogen peroxide stress effects the susceptibility of Bifidobacteria2.

参考文献