ChemicalBook--->CAS DataBase List--->9012-26-4

9012-26-4

9012-26-4 Structure

9012-26-4 Structure
IdentificationBack Directory
[Name]

PENICILLINASE
[CAS]

9012-26-4
[Synonyms]

3.5.2.6
EC 3.5.2.6
EC: 3.5.2.6
BETA-LACTAMASE I
EC 3.5.2.6 TYPE I
EC 3.5.2.6 TYPE II
EC 3.5.2.6 TYPE IV
EC 3.5.2.6 TYPE III
PENICILLINASE TYPE I
PENICILLINASE TYPE II
PENICILLINASE TYPE IV
PENICILLINASE TYPE III
BETA LACTAMASE I TYPE I
CEPHALOSPORINASE TYPE I
CEPHALOSPORINASE TYPE II
BETA-LACTAMASE I TYPE IV
CEPHALOSPORINASE TYPE IV
BETA-LACTAMASE I TYPE II
BETA-LACTAMASE II TYPE I
BETA-LACTAMASE II TYPE II
BETA-LACTAMASE I TYPE III
BETA-LACTAMASE II TYPE IV
CEPHALOSPORINASE TYPE III
BETA-LACTAMASE II TYPE III
Cephalosporinase (1*104units)
PENICILLIN AMIDO-BETA-LACTAMHYDROLASE
BETA-LACTAMASE, BACILLUS CEREUS 569/H9
β-Lactamase from Pseudomonas fluorescens
PENICILLIN AMIDO-BETA-LACTAM HYDROLASE TYPE I
PENICILLIN AMIDO-BETA-LACTAM HYDROLASE TYPE II
PENICILLIN AMIDO-BETA-LACTAM HYDROLASE TYPE IV
Cephalosporinase from Bacillus(10000unit/vial)
PENICILLIN AMIDO-BETA-LACTAM HYDROLASE TYPE III
Cephalosporinase from Bacillus(1000000unit/vial)
Cephalosporinase from Bacillus (1*10^6units/vial)
Cephalosporinase from Bacillus (1*10^4units/vial)
[EINECS(EC#)]

232-728-1
[MDL Number]

MFCD00131819
Chemical PropertiesBack Directory
[Melting point ]

121-126 °C
[storage temp. ]

2-8°C
[form ]

powder
[color ]

white
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

42/43
[Safety Statements ]

22-36/37
[WGK Germany ]

3
[F ]

10-21
[HS Code ]

3507.90.7000
Hazard InformationBack Directory
[Uses]

Cephalosporinase, bacillus are enzymes produced by bacillus, inactivated and degrade the ability of the cephalosporin class of antibiotics. Cephalosporins are a class of β-lactam antibiotics that are widely used to treat bacterial infections[1].
[References]

[1] Colque CA, et al. Longitudinal Evolution of the Pseudomonas-Derived Cephalosporinase (PDC) Structure and Activity in a Cystic Fibrosis Patient Treated with β-Lactams. mBio. 2022 Oct 26;13(5):e0166322. DOI:10.1128/mbio.01663-22
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