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Carbenicillin_Molecular_structure_CAS_)
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Carbenicillin

Catalog No. C1613 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C17H18N2O6S Telephone 1-800-521-8956
M. W. 378.39962 Fax
Purity Email
Storage Chembase ID: 460

SYNONYMS

Title
羧苄青霉素
IUPAC name
(2S,5R,6R)-6-(2-carboxy-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
IUPAC Traditional name
carbenicillin
Synonyms
α-Carboxybenzylpenicillin solution
α-Carboxybenzylpenicillin 溶液

DATABASE IDS

PubChem SID 24892425
MDL Number MFCD00242604

PROPERTIES

Concentration 100 mg/mL in ethanol/water
Empirical Formula (Hill Notation) C17H18N2O6S
Shipped in wet ice
Sterility 0.2 μm filtered
Flash Point 40 °C
Flash Point 104 °F
GHS Pictograms GHS02
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H226-H317-H334
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P280-P342 + P311
RID/ADR UN 1170 3/PG 3
Risk Statements 10-42/43
Safety Statements 23-36/37-45
Storage Temperature -20°C
Hazard Class 3
UN Number 1170
Packing Group 3
German water hazard class 2

DETAILS

Description (English)
Application
Used for selection of ampr transformed cells. Use to study the role of penicillin-sensitive transpeptidases in cell wall biosynthesis.
Biochem/physiol Actions
The antibiotic carbenicillin, an ampicillin analog, is a commonly used selection agent that binds and inhibits enzymes involved in the synthesis of the bacterial cell wall. It is active against most isolates of Pseudomonas aerogenosa and certain indole-positive Proteus strains that are resistant to ampicillin. The gene conferring resistance to ampicillin and its analogs, ampr, codes for the enzyme β-lactamase. Carbenicillin is less sensitive to β-lactamase than ampicillin. In addition it has a superior stability at low pH. Experiments have shown that the use of carbenicillin in place of ampicillin helps prevent overgrowth of satellite colonies. Effective concentration: 50 to 100 μg/ml.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Description (简体中文)
Application
Used for selection of ampr transformed cells. Use to study the role of penicillin-sensitive transpeptidases in cell wall biosynthesis.
Biochem/physiol Actions
羧苄青霉素是氨苄青霉素的类似物,是一种常用的选择剂,它可以结合并抑制细菌细胞壁合成中涉及到的酶。它对耐氨苄青霉素的大多数铜绿假单胞菌分离株以及某些吲哚阳性变形杆菌?均有效。氨苄青霉素及其类似物抗性基因 ampr 编码 β-内酰胺酶。羧苄青霉素比氨苄青霉素对 β-内酰胺酶的敏感性更弱。此外它在低 pH 下具有优异的稳定性。实验表明,用羧苄青霉素替代氨苄青霉素有助于防止卫星菌落的过度生长。有效浓度:50 至 100μg/mL。
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information

REFERENCES