Cefminox Sodium Heptahydrate

Description

Cefminox sodium is a second generation β-lactam cephalosporin antibiotic that also a sodium salt. Additionally, cefminox sodium has exhibited a high degree of activity towards gram-negative and anaerobic bacteria. Cefminox has also been used to observe the effects of antibiotics on immunosuppressor and human serum albumin complexes.

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
Cefminox Sodium Heptahydrate
Cefminox Sodium Salt

Formula: C16H20N7NaO7S3 • 7H2O

MW: 667.66 g/mol

Storage/Handling: Store at -20°C.

PubChem Chemical ID: 45356840

Cefminox Sodium Heptahydrate

View Sizes & Pricing

Catalog Number:
C-465-500
CAS Number:
1351813-81-4
$165.00

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

    Description

    Cefminox sodium is a second generation β-lactam cephalosporin antibiotic that also a sodium salt. Additionally, cefminox sodium has exhibited a high degree of activity towards gram-negative and anaerobic bacteria. Cefminox has also been used to observe the effects of antibiotics on immunosuppressor and human serum albumin complexes.

    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
    Cefminox Sodium Heptahydrate
    Cefminox Sodium Salt

    Formula: C16H20N7NaO7S3 • 7H2O

    MW: 667.66 g/mol

    Storage/Handling: Store at -20°C.

    PubChem Chemical ID: 45356840

    Product Specifications

    Catalog ID: C-465
    CAS #: 1351813-81-4
    MW: 667.66 g/mol
    Storage/handling: Store at -20°C.

    Login

    Forgot your password?

    Don't have an account yet?
    Create account