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642-78-4 分子结构
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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

ChemBase编号:103129
分子式:C19H17ClN3NaO5S
平均质量:457.86315
单一同位素质量:457.04751362
SMILES和InChIs

SMILES:
[Na+].O=C([O-])[C@@H]1N2C(=O)[C@@H](NC(=O)c3c(onc3c3ccccc3Cl)C)[C@H]2SC1(C)C
Canonical SMILES:
[O-]C(=O)[C@@H]1N2C(=O)[C@H]([C@H]2SC1(C)C)NC(=O)c1c(C)onc1c1ccccc1Cl.[Na+]
InChI:
InChI=1S/C19H18ClN3O5S.Na/c1-8-11(12(22-28-8)9-6-4-5-7-10(9)20)15(24)21-13-16(25)23-14(18(26)27)19(2,3)29-17(13)23;/h4-7,13-14,17H,1-3H3,(H,21,24)(H,26,27);/q;+1/p-1/t13-,14+,17-;/m1./s1
InChIKey:
SCLZRKVZRBKZCR-SLINCCQESA-M

引用这个纪录

CBID:103129 http://www.chembase.cn/molecule-103129.html

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名称和登记号

名称和登记号

名称 登记号
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-)
别名
Cloxacillin sodium salt
5-Methyl-3-(o-chlorophenyl)-4-isoxazolyl] pencillin
CLOXACILLIN SODIUM SALT
Sodium Cloxacillin
6-[3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt
Staphybiotic
(2S,5R,6R)-6-[[[3-(2-Chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt
Ankerbin
3-(o-Chlorophenyl)-5-methyl-4-isoxazolylpenicillin Sodium Salt
Austrastaph
BRL 1621 Sodium Salt
Cloxapen
Ekvacillin
Gelstaph
Orbenin
Orbenin Sodium
Prevencilina P
Prostaphilin A
Prostaphlin A
Syntarpen Sodium Salt
Tegopen
Sodium 3-(O-Chlorophenyl)-5-methyl-4-isoxazolylpenicillin
CAS号
642-78-4
7081-44-9
EC号
211-390-9
MDL号
MFCD00063568
Beilstein号
4103180
PubChem SID
162102916
24856654
PubChem CID
23675320

理论计算性质

理论计算性质

JChem
Acid pKa 3.7497845  质子受体
质子供体 LogD (pH = 5.5) 0.55099535 
LogD (pH = 7.4) -0.9830029  Log P 2.3017397 
摩尔折射率 117.4742 cm3 极化性 41.823692 Å3
极化表面积 115.57 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
H2O: soluble50 mg/mL, clear, colorless expand 查看数据来源
保存条件
2-8°C expand 查看数据来源
RTECS编号
XH8750000 expand 查看数据来源
XH8920000 expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
2 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
保存温度
2-8°C expand 查看数据来源
纯度
≥97.0% (HPLC) expand 查看数据来源
成盐信息
Na+ expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
杂质
≤5% water expand 查看数据来源
Empirical Formula (Hill Notation)
C19H17ClN3NaO5S expand 查看数据来源
分类
Derivatives & analogs of Natural Compounds expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich TRC TRC
MP Biomedicals -  02150702 external link
Sodium Salt
White micro-crystalline powder
pH 6.0-7.5
Antibacterial
Sigma Aldrich -  27555 external link
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.
Toronto Research Chemicals -  C587460 external link
Cloxacillin is an antibiotic that belongs to the group of the isoxazolylpenicillins. Cloxacillin is used to treat infections caused by species of staphylococci that produce beta-lactamase due to its inhibitory effects on beta-lactamase binding.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Gibbs, D.L. et al.: Curr. Microbiol., 2, 239 (1979)
  • Dmitrova, D. et al.: Farmat., 48, 28 (1979)
  • CRaven, N. et al.: Res. Vet. Sci., 29, 57 (1979)
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专利

专利

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