Cefepime

Description

Cefepime is a fourth generation cephalosporin antibiotic effective against gram-negative and gram-positive bacteria. It is resistant to a variety of β-lactamases, and is effective against some naturally resistant bacterial species such as Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae. Cefepime is slightly 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
Cefepime

MOLECULAR BIOLOGY GRADE

Formula: C19H24N6O5S2

MW: 480.56 g/mol

Storage/Handling: Store at 2-8 °C.

PubChem Chemical ID: 5479537

Cefepime

View Sizes & Pricing

Catalog Number:
C-610-10
CAS Number:
88040-23-7
$155.00

Availability:
2-3 Weeks
Shipping:
Shipping calculated at checkout

    Description

    Cefepime is a fourth generation cephalosporin antibiotic effective against gram-negative and gram-positive bacteria. It is resistant to a variety of β-lactamases, and is effective against some naturally resistant bacterial species such as Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pneumoniae. Cefepime is slightly 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
    Cefepime

    MOLECULAR BIOLOGY GRADE

    Formula: C19H24N6O5S2

    MW: 480.56 g/mol

    Storage/Handling: Store at 2-8 °C.

    PubChem Chemical ID: 5479537

    Product Specifications

    Catalog ID: C-610
    CAS #: 88040-23-7
    MW: 480.56 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.

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