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.


Product Specifications
Cefteram pivoxil

Formula: C22H27N9O7S2

MW: 593.63 g/mol

Storage/Handling: Store at -20°C.

PubChem Chemical ID: 5362114

Cefteram pivoxil

View Sizes & Pricing

Catalog Number:
C-445-10
CAS Number:
82547-81-7
$138.00

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

    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.


    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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