Ceftiofur Sodium

Description

Ceftiofur sodium is a third generation cephalosporin antibiotic effective against gram-positive and gram-negative bacteria. Although ceftiofur is resistant to β-lactamase degradation, there are several strains of E. coli known to be unaffected by this antibiotic. It is soluble in aqueous solution.

Cephalosporins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a six-membered dihydrothiazine ring. This two-ring system causes distortion of the β-lactam amide bond, resulting in decreased resonance stabilization and increased reactivity. β-lactams inhibit the formation of peptidoglycan cross-links within bacterial cell walls by targeting penicillin-binding proteins or PBPs. Consequently, the bacterial cell wall becomes weak and cytolysis occurs. Cephalosporins are less susceptible to β-lactamases than the penicillin β-lactam antibiotics.


Product Specifications
Ceftiofur Sodium

MOLECULAR BIOLOGY GRADE

Formula: C19H16N5NaO7S3

MW: 545.54 g/mol

Storage/Handling: Store at 2-8°C.

PubChem Chemical ID: 23671563

Ceftiofur Sodium

View Sizes & Pricing

Catalog Number:
C-770-1
CAS Number:
104010-37-9
$117.00

For research use only. Not for food, drug, household, or cosmetic use.
Availability:
2-3 Weeks
Shipping:
$14.99 Ground shipping (In continental US only.)

    Description

    Ceftiofur sodium is a third generation cephalosporin antibiotic effective against gram-positive and gram-negative bacteria. Although ceftiofur is resistant to β-lactamase degradation, there are several strains of E. coli known to be unaffected by this antibiotic. It is soluble in aqueous solution.

    Cephalosporins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a six-membered dihydrothiazine ring. This two-ring system causes distortion of the β-lactam amide bond, resulting in decreased resonance stabilization and increased reactivity. β-lactams inhibit the formation of peptidoglycan cross-links within bacterial cell walls by targeting penicillin-binding proteins or PBPs. Consequently, the bacterial cell wall becomes weak and cytolysis occurs. Cephalosporins are less susceptible to β-lactamases than the penicillin β-lactam antibiotics.


    Product Specifications
    Ceftiofur Sodium

    MOLECULAR BIOLOGY GRADE

    Formula: C19H16N5NaO7S3

    MW: 545.54 g/mol

    Storage/Handling: Store at 2-8°C.

    PubChem Chemical ID: 23671563

    Product Specifications

    Catalog ID: C-770
    CAS #: 104010-37-9
    MW: 545.54 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.

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