Cephalexin hydrate

Description

Cephalexin is a first generation cephalosporin antibiotic most effective against gram-positive cocci. However, it also exhibits efficacy against some gram-negative bacilli. In addition, cephalexin has been used to study the penicillin binding proteins, especially PBP3. Cephalexin hydrate 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
Cephalexin hydrate

Formula: C16H17N3O4S · H2O

MW: 365.40 g/mol

Storage/Handling: Store at 4°C.

PubChem Chemical ID: 27447

Cephalexin hydrate

View Sizes & Pricing

Catalog Number:
C-818-250
CAS Number:
23325-78-2,15686-71-2
$445.00

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

    Cephalexin is a first generation cephalosporin antibiotic most effective against gram-positive cocci. However, it also exhibits efficacy against some gram-negative bacilli. In addition, cephalexin has been used to study the penicillin binding proteins, especially PBP3. Cephalexin hydrate 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
    Cephalexin hydrate

    Formula: C16H17N3O4S · H2O

    MW: 365.40 g/mol

    Storage/Handling: Store at 4°C.

    PubChem Chemical ID: 27447

    Product Specifications

    Catalog ID: C-818
    CAS #: 23325-78-2,15686-71-2
    MW: 365.40 g/mol
    Storage/handling: Store at 4°C.

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