ChemicalBook--->CAS DataBase List--->1426397-23-0

1426397-23-0

1426397-23-0 Structure

1426397-23-0 Structure
IdentificationBack Directory
[Name]

Cefsulodin Sodium Salt Hydrate
[CAS]

1426397-23-0
[Synonyms]

CefsulodinSodiumSalt>
[Molecular Formula]

C22H19N4NaO8S2.xH2O
[MDL Number]

MFCD29472517
[MOL File]

1426397-23-0.mol
[Molecular Weight]

574.55
Chemical PropertiesBack Directory
[Melting point ]

175℃
[RTECS ]

UU1785000
[storage temp. ]

-20°C
[solubility ]

DMSO: 0.1 mg/ml,PBS (pH 7.2): 10 mg/ml
[form ]

Powder
[color ]

White to Yellow
[Water Solubility ]

Freely soluble in water
[Merck ]

14,1945
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H315-H317-H319-H334-H335
[Precautionary statements ]

P261-P280a-P284-P305+P351+P338-P405-P501a
[TSCA ]

Yes
[HS Code ]

2934.99.4400
Hazard InformationBack Directory
[Uses]

Cefsulodin is most commonly used in CIN agar to select for Yersinia microorganisms. The compound displays a mechanism of action like many β lactam antibiotics through inhibition of cell wall synthesis by competitively inhibiting penicillin binding protein (PBP) crosslinking of peptidoglycan resulting in inhibition of the final transpeptidation step. Through the inability for Cefsulodin sodium salt hydrate to inhibit cefsulodin-resistant mutants of Pseudomonas aeruginosa PAO4089 growth displayed that Cefsulodin sodium salt hydrate may compete with PBP3 in addition to PBP1A and PBP1B.
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