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64485-93-4 分子结构
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sodium (6R,7R)-3-[(acetyloxy)methyl]-7-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

ChemBase编号:133418
分子式:C16H16N5NaO7S2
平均质量:477.44731
单一同位素质量:477.03888416
SMILES和InChIs

SMILES:
CC(=O)OCC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OC)/c2csc(n2)N)SC1)C(=O)[O-].[Na+]
Canonical SMILES:
CO/N=C(/c1csc(n1)N)\C(=O)N[C@@H]1C(=O)N2[C@@H]1SCC(=C2C(=O)[O-])COC(=O)C.[Na+]
InChI:
InChI=1S/C16H17N5O7S2.Na/c1-6(22)28-3-7-4-29-14-10(13(24)21(14)11(7)15(25)26)19-12(23)9(20-27-2)8-5-30-16(17)18-8;/h5,10,14H,3-4H2,1-2H3,(H2,17,18)(H,19,23)(H,25,26);/q;+1/p-1/b20-9-;/t10-,14-;/m1./s1
InChIKey:
AZZMGZXNTDTSME-JUZDKLSSSA-M

引用这个纪录

CBID:133418 http://www.chembase.cn/molecule-133418.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 (6R,7R)-3-[(acetyloxy)methyl]-7-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
IUPAC传统名
sodium cefotaxime(1-)
别名
Cefotaxim sodium salt 钠盐
Cefotaxime sodium salt 钠盐
Cefotaxime sodium salt
(6R,7R)-3-[(Acetyloxy)methyl]-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt
Cefotax
HR 756
Pretor
Tolycar
Cefotaxime Sodium
CAS号
64485-93-4
EC号
264-915-9
MDL号
MFCD00079073
Beilstein号
5711411
PubChem SID
162227695
24278336
24892923
PubChem CID
10695961

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 10695961 external link

理论计算性质

理论计算性质

JChem
Acid pKa 3.1773155  质子受体
质子供体 LogD (pH = 5.5) -2.9842594 
LogD (pH = 7.4) -4.1677856  Log P -1.9052299 
摩尔折射率 115.9454 cm3 极化性 39.9619 Å3
极化表面积 176.34 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: soluble (aqueous solutions of pH 4.3-6.2 are stable up to 3 weeks at 2-8 °C.) expand 查看数据来源
Methanol expand 查看数据来源
Water expand 查看数据来源
外观
White Solid expand 查看数据来源
white to yellow powder expand 查看数据来源
熔点
> 165°C (dec.) expand 查看数据来源
保存条件
-20°C Freezer, Under Inert Atmosphere expand 查看数据来源
RTECS编号
XI0250000 expand 查看数据来源
欧盟危险性物质标志
有害性(Harmful) 有害性(Harmful) (Xn) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
德国WGK号
2 expand 查看数据来源
危险公开号
42/43 expand 查看数据来源
安全公开号
22-36/37 expand 查看数据来源
GHS危险品标识
GHS08 expand 查看数据来源
GHS警示词
Danger expand 查看数据来源
GHS危险声明
H317-H334 expand 查看数据来源
GHS警示性声明
P261-P280-P342 + P311 expand 查看数据来源
个人保护装置
dust mask type N95 (US), Eyeshields, Faceshields, Gloves expand 查看数据来源
保存温度
2-8°C expand 查看数据来源
药效
916-964 μg per mg expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
适用性
plant cell culture tested expand 查看数据来源
suitable for 1694 per US EPA expand 查看数据来源

详细说明

详细说明

Sigma Aldrich Sigma Aldrich TRC TRC
Sigma Aldrich -  C7039 external link
Other Notes
Broad spectrum third generation cephalosporin antibiotic.
Biochem/physiol Actions
Cefotaxim inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls. As a result, bacteria lyse due to cell wall autolytic enzymes.
Cefotaxime, a cephalosporin antibiotic, is active against both gram-negative and gram-positive bacteria. In addition, cefotaxime blocks the division of cyanobacteria and lower plant organelles/plastids such as the photosynthetic organelles of Glaucophytes and chloroplasts of bryophytes.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  C7912 external link
Biochem/physiol Actions
Used to study the effect of expression, binding and inhibition of penicillin-binding proteins especially PBP2 on bacterial cell wall mucopeptide synthesis.
Cefotaxim inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls. As a result, bacteria lyse due to cell wall autolytic enzymes.
Other Notes
Broad spectrum third generation cephalosporin antibiotic.
Application
Cefotaxim is a broad spectrum third generation cephalosporin antibiotic that is used to study the effect of expression, binding and inhibition of penicillin-binding proteins especially PBP2 on bacterial cell wall mucopeptide synthesis. It has been used to find new residues involved in cefotaxime hydrolysis in CTX-M β-lactamases1, to study antibiotic-susceptible and -resistant Streptococcus pneumoniae infections 2, and to study pneumococcal pneumonia and the pharmokinetics of various treatments3.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Toronto Research Chemicals -  C242950 external link
Broad spectrum third generation cephalosporin antibiotic. The name Cefotaxime applies to the isomer having a syn-methoxy imino group.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Wise, R., et al.: Antimicrob. Agents Chemother., 14, 807 (1978)
  • Muhtadi, F.J., et al.: Anal. Profiles Drug Subs., 11, 139 (1978)
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专利

专利

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