Cefpodoxime, Free acid

Description

Cefpodoxime is a third generation cephalosporin antibiotic. It targets gram-positive and gram-negative bacteria, especially those responsible for otitis media and pharyngitis.

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.

Antibiotics are often used in clinical in vitro tests known as antimicrobial susceptibility tests or ASTs to determine their efficacy against certain bacterial species. They are tested against gram-negative and gram-positive bacteria using panels, discs, and MIC strips by medical microbiologists. ASTs decrease the risk of using an antibiotic against bacteria exhibiting resistance to it, and the results are used in clinical settings to determine which antibiotic(s) to prescribe for various infections.

Product Specifications
Cefpodoxime, Free Acid

MOLECULAR BIOLOGY GRADE

Formula: C15H17N5O6S2

MW: 427.46 g/mol

Storage/Handling: Store at -20°C.
Product is light sensitive. Soluble in DMSO

PubChem Chemical ID: 6335986

Cefpodoxime, Free acid

View Sizes & Pricing

Catalog Number:
C-712-100
CAS Number:
80210-62-4
$280.00
Availability:
In Stock
Shipping:
Shipping calculated at checkout

    Description

    Cefpodoxime is a third generation cephalosporin antibiotic. It targets gram-positive and gram-negative bacteria, especially those responsible for otitis media and pharyngitis.

    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.

    Antibiotics are often used in clinical in vitro tests known as antimicrobial susceptibility tests or ASTs to determine their efficacy against certain bacterial species. They are tested against gram-negative and gram-positive bacteria using panels, discs, and MIC strips by medical microbiologists. ASTs decrease the risk of using an antibiotic against bacteria exhibiting resistance to it, and the results are used in clinical settings to determine which antibiotic(s) to prescribe for various infections.

    Product Specifications
    Cefpodoxime, Free Acid

    MOLECULAR BIOLOGY GRADE

    Formula: C15H17N5O6S2

    MW: 427.46 g/mol

    Storage/Handling: Store at -20°C.
    Product is light sensitive. Soluble in DMSO

    PubChem Chemical ID: 6335986

    Product Specifications

    Catalog ID: C-712
    CAS #: 80210-62-4
    MW: 427.46 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at -20°C.

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