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58-71-9 分子结构
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sodium (6R,7R)-3-[(acetyloxy)methyl]-8-oxo-7-[2-(thiophen-2-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

ChemBase编号:105794
分子式:C16H15N2NaO6S2
平均质量:418.41987
单一同位素质量:418.02692249
SMILES和InChIs

SMILES:
[Na+].O=C1N2C(=C(CS[C@@H]2[C@@H]1NC(=O)Cc1sccc1)COC(=O)C)C(=O)[O-]
Canonical SMILES:
CC(=O)OCC1=C(C(=O)[O-])N2[C@H](SC1)[C@@H](C2=O)NC(=O)Cc1cccs1.[Na+]
InChI:
InChI=1S/C16H16N2O6S2.Na/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10;/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23);/q;+1/p-1/t12-,15-;/m1./s1
InChIKey:
VUFGUVLLDPOSBC-XRZFDKQNSA-M

引用这个纪录

CBID:105794 http://www.chembase.cn/molecule-105794.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]-8-oxo-7-[2-(thiophen-2-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
IUPAC传统名
sodium cefalotin(1-)
别名
(6R,7R)-3-[(Acetyloxy)methyl]-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid
7-(2-Thienylacetamido)cephalosporanic Acid
7-(Thiophene-2-acetamido)cephalosporin
7-[2-(2-Thienyl)acetylamido]cephalosporanic Acid
CT
Cefalotin
Cephalotin
Cephalothin
7-(2-Thienylacetamido)cephalosporanic acid sodium salt
Cephalotin sodium salt
Cephalothin sodium salt
7-[2-Thienylacetamido]-cephalosporanic acid
CEPHALOTHIN SODIUM SALT
CAS号
58-71-9
EC号
200-394-6
MDL号
MFCD00072025
Beilstein号
4120706
PubChem SID
162094211
24278314
24892330
PubChem CID
23675321

理论计算性质

理论计算性质

JChem
Acid pKa 3.625907  质子受体
质子供体 LogD (pH = 5.5) -1.8540871 
LogD (pH = 7.4) -3.3175669  Log P 0.016272906 
摩尔折射率 104.6311 cm3 极化性 36.26567 Å3
极化表面积 115.84 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, faintly yellow expand 查看数据来源
熔点
204-205 expand 查看数据来源
保存条件
0°C expand 查看数据来源
RTECS编号
XI0388300 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
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
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
纯度
≥99.0% (TLC) expand 查看数据来源
96.0-101.0% 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
适用性
suitable for cell culture expand 查看数据来源
Empirical Formula (Hill Notation)
C16H15N2NaO6S2 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 -  02194155 external link
Sodium Salt
Sigma Aldrich -  C4520 external link
Biochem/physiol Actions
Cephalothin is a first-generation cephalosporin antibiotic that disrupts the synthesis of the peptidoglycan layer of bacterial cell walls. It is effective against gram-positive and gram-negative bacteria. Mode of Resistance: Cephalosporinase production.
Mode of Action: Inhibits cell wall synthesis.Antimicrobial spectrum: Gram-positive cocci.Mode of Resistance: Cephalosporinase production.
Other Notes
First generation cephalosporin antibiotic.
Application
Cephalothis is used to study the mechanism of liposome encapsulated antibiotics 1, strategies for co-opting β-lactamases of Gram-negative bacteria for treatment of antibiotics 2, and for immunology studies in relation to antibiotics 3. It is used to study the effect of expression, binding and inhibition of penicillin-binding proteins especially PBP6 on bacterial cell wall mucopeptide synthesis.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  C3050 external link
Biochem/physiol Actions
Mode of Action: Inhibits cell wall synthesis.Antimicrobial spectrum: Gram-positive cocci.Mode of Resistance: Cephalosporinase production.
Mode of Action: Inhibits cell wall synthesis.Antimicrobial spectrum: Gram-positive cocci.Mode of Resistance: Cephalosporinase production.
Other Notes
First generation cephalosporin antibiotic.
General description
Cephalotin is a first generation cephalosporin antibiotic.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich -  22241 external link
Biochem/physiol Actions
Mode of Action: Inhibits cell wall synthesis.Antimicrobial spectrum: Gram-positive cocci.Mode of Resistance: Cephalosporinase production.
Other Notes
First generation cephalosporin antibiotic.
Toronto Research Chemicals -  C261150 external link
A first generation cephalosporin antibiotic with a wide range antibacterial activity. It is effective against gram-positive and gram-negative bacteria, and has been tested in respiratory disease and neuromuscular junction studies.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Shibata, K., et al.: J. Antibiot., 50, 135 (1997)
  • Farra, A., et al.: Int. J. Antimicrob. Agents., 31, 427 (1997)
  • Pichardo, C., et al.: Eur. J. Clin. Microbiol. Infect. Dis., 30, 289 (1997)
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专利

专利

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