标签归档：氯唑

氯唑西林 钠盐 一水合物

发表于由

氯唑西林 钠盐 一水合物

抗β-内酰胺酶抗生素

有货

氯唑西林 钠盐 一水合物

CAS编号 7081-44-9 | 品牌：Jinpan
Cloxacillin sodium salt monohydrate

MSDS

质检证书(CoA)

相似产品

  • 分子式 C19H17ClN3O5SNa · H2O
  • 分子量457.86(as Anhydrous)
  • Beilstein号 4103180
  • PubChem编号 23675743

货号 (SKU) 包装规格 是否现货 价格 数量
C433363-1g 1g 期货 氯唑西林 钠盐 一水合物  
C433363-5g 5g 期货 氯唑西林 钠盐 一水合物  

基本信息

产品名称 氯唑西林 钠盐 一水合物
英文名称 Cloxacillin sodium salt monohydrate
规格或纯度 抗β-内酰胺酶抗生素
运输条件 冰袋运输
生化机理 Cloxacillin is a semi-synthetic antibiotic and a chlorinated derivative of oxacillin. It inhibits the last stage of bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), which results in cell lysis. Cell lysis is mediated by bacterial cell wall autolytic enzymes. Cloxacillin is often used as AmpC β-lactamase inhibitor in combination with β-lactam antibiotics.

一般描述

General Description

Chemical structure: ß-lactam

Application

Cloxacillin is effective against infections caused by penicillin G-resistant staphylococci. It was used in studies of topical antibacterial agents for burn and crush wounds.

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

General Description

Chemical structure: ß-lactam

Application

Cloxacillin is effective against infections caused by penicillin G-resistant staphylococci. It was used in studies of topical antibacterial agents for burn and crush wounds.

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

相关属性

CAS编号 7081-44-9
比旋光度 164° (C=1,H2O)
熔点 170°C
储存温度 2-8°C储存
分子量 457.86(as Anhydrous)
分子式 C19H17ClN3O5SNa · H2O
品牌 Jinpan
PubChem CID 23675743

氯唑西林钠盐

发表于由

氯唑西林钠盐

≥95.0% (HPLC)

有货

氯唑西林钠盐

CAS编号 642-78-4 | 品牌：Jinpan
Cloxacillin sodium salt

MSDS

质检证书(CoA)

相似产品

  • 分子式 C₁₉H₁₇ClN₃NaO₅S
  • 分子量457.86
  • MDL号 MFCD00063568
  • PubChem编号 23675320

货号 (SKU) 包装规格 是否现货 价格 数量
C464035-5g 5g 期货 氯唑西林钠盐  
C464035-1g 1g 期货 氯唑西林钠盐  

基本信息

产品名称 氯唑西林钠盐
英文名称 Cloxacillin sodium salt
规格或纯度 ≥95.0% (HPLC)
运输条件 冰袋运输

一般描述

Description

Chemical structure: ß-lactamCloxacillin 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 effectiveness and how oxgall, acid, and hydrogen peroxide stress effects the susceptibility ofBifidobacteria.

Description

Chemical structure: ß-lactamCloxacillin 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 effectiveness and how oxgall, acid, and hydrogen peroxide stress effects the susceptibility ofBifidobacteria.

相关属性

CAS编号 642-78-4
熔点 170° C
储存温度 2-8°C储存
MDL号 MFCD00063568
分子量 457.86
分子式 C₁₉H₁₇ClN₃NaO₅S
品牌 Jinpan
Smiles CC1=C(C(=NO1)C2=CC=CC=C2Cl)C(=O)N[C@H]3[C@@H]4N(C3=O)[C@H](C(S4)(C)C)C(=O)[O-].[Na+]
PubChem CID 23675320

氯唑西林钠

发表于由

氯唑西林钠

抗生素
95%

有货

氯唑西林钠

CAS编号 642-78-4 | 品牌：Jinpan
Cloxacillin sodium salt

MSDS

质检证书(CoA)

相似产品

  • 分子式 C₁₉H₁₇ClN₃NaO₅S
  • 分子量457.86
  • PubChem编号 23675320

货号 (SKU) 包装规格 是否现货 价格 数量
C352143-250mg 250mg 现货 氯唑西林钠  
C352143-1g 1g 现货 氯唑西林钠  
C352143-5g 5g 现货 氯唑西林钠  

基本信息

产品名称 氯唑西林钠
英文名称 Cloxacillin sodium salt
别名 (2S;5R;6R)-3,3-二甲基-6-[5-甲基-3-(2-氯苯基)-4-异恶唑甲酰氨基]-7-氧代-4-硫杂-1-氮杂双环[3.2.0]庚烷-2-甲酸钠盐
英文别名 Sodium cloxacillin；(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 monosodium salt；3-dimethyl-7-oxo-thyl-4-isoxazolecarboxamido)-monosodiumsalt
规格或纯度 95%
运输条件 超低温冰袋运输

一般描述

氯沙西林是一种属于异恶唑基青霉素类的抗生素。氯西林用于治疗由葡萄球菌引起的感染，这种葡萄球菌由于其对β-内酰胺酶结合的抑制作用而产生β-内酰胺酶。

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.

相关属性

CAS编号 642-78-4
熔点 170° C
溶解性 Soluble in water: 50 mg/mL, clear, colorless
储存温度 -20°C储存
分子量 457.86
分子式 C₁₉H₁₇ClN₃NaO₅S
品牌 Jinpan
Smiles CC1=C(C(=NO1)C2=CC=CC=C2Cl)C(=O)N[C@H]3[C@@H]4N(C3=O)[C@H](C(S4)(C)C)C(=O)[O-].[Na+]
PubChem CID 23675320