跳转至内容
Merck
CN

SML3854

Sigma-Aldrich

Potassium clavulanate cellulose (1:1)

≥97% (NMR)

别名:

(2R,3Z,5R)-3-(2-Hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid potassium clavulanate cellulose (1:1), Z-(3R,5R)-2-(β-Hydroxyethylidene)clavam-3-carboxylic acid potassium clavulanate cellulose (1:1)

登录查看公司和协议定价


About This Item

线性分子式:
(C6H10O5)n
分子量:
237.25
UNSPSC代码:
51111800
UNSPSC代码:
12352200
NACRES:
NA.21

质量水平

方案

≥97% (NMR)

表单

powder

储存条件

desiccated

颜色

white to beige

储存温度

-10 to -25°C

生化/生理作用

Clavulanic acid is an orally available and potent mechanism-based β-lactamase inhibitor. In combination with β-lactam antibiotic clavulanic acid can overcome antibiotic resistance in bacteria that produce β-lactamase. Clavulanic acid is produced by Streptomyces clavuligerus.

注意

Hygroscopic

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

抱歉,我们目前尚未线上提供该产品的COA。

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

In vitro Antibacterial Activity and Resistance Prevention of Antimicrobial Combinations for Dihydropteroate Synthase-Carrying Stenotrophomonas maltophilia
Infection and Drug Resistance, 15, 3039-3046 (2022)
Penicillin-Binding Proteins, ?-Lactamases, and ?-Lactamase Inhibitors in ?-Lactam-Producing Actinobacteria: Self-Resistance Mechanisms
International Journal of Molecular Sciences, 23(10), 5662-5662 (2022)
C Reading et al.
Antimicrobial agents and chemotherapy, 11(5), 852-857 (1977-05-01)
A novel beta-lactamase inhibitor has been isolated from Streptomyces clavuligerus ATCC 27064 and given the name clavulanic acid. Conditions for the cultivation of the organism and detection and isolation of clavulanic acid are described. This compound resembles the nucleus of

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门