Cefteram pivoxil

Description

Cefteram pivoxil is a semi-synthetic third generation cephalosporin antibacterial that is a prodrug ester of cefteram. It has been seen to express greater bactericidal predominantly against gram-negative bacteria. Cefteram pivoxil has also induced IgE antibody immune responses during in vivo immunology studies.

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
Cefteram pivoxil

Formula: C22H27N9O7S2

MW: 593.63 g/mol

Storage/Handling: Store at -20°C.

PubChem Chemical ID: 5362114

Cefteram pivoxil

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Catalog Number:
C-445-10
CAS Number:
82547-81-7
$134.00
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    Description

    Cefteram pivoxil is a semi-synthetic third generation cephalosporin antibacterial that is a prodrug ester of cefteram. It has been seen to express greater bactericidal predominantly against gram-negative bacteria. Cefteram pivoxil has also induced IgE antibody immune responses during in vivo immunology studies.

    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
    Cefteram pivoxil

    Formula: C22H27N9O7S2

    MW: 593.63 g/mol

    Storage/Handling: Store at -20°C.

    PubChem Chemical ID: 5362114

    Product Specifications

    Catalog ID: C-445
    CAS #: 82547-81-7
    MW: 593.63 g/mol
    Storage/handling: Store desiccated at -20°C.

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