Amoxicillin Sodium Salt

Description

Amoxicillin is an extended-spectrum ß-lactam antibiotic with a structure similar to that of ampicillin. It is effective against a variety of ß-lactamase negative bacteria including E. coli and various Streptococcus and Staphylococcus bacteria. It is also effective against a variety of other gram-negative and gram-positive bacteria. Amoxicillin sodium salt is freely soluble in aqueous solution.

Penicillins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a five-membered thiazolidine 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. Resistance to β-lactam antibiotics occurs in the presence of cells containing plasmid encoded extended spectrum β-lactamases or ESBLs.


Product Specifications
Amoxicillin Sodium Salt

MOLECULAR BIOLOGY GRADE

Formula: C16H18N3NaO5S

MW: 387.39 g/mol

Storage/Handling: Store at 2-8°C.

PubChem Chemical ID: 23663126

Amoxicillin Sodium Salt

View Sizes & Pricing

Catalog Number:
A-551-1
CAS Number:
34642-77-8
$69.00

For research use only. Not for food, drug, household, or cosmetic use.
Availability:
In stock
Shipping:
$14.99 Ground shipping (In continental US only.)

    Description

    Amoxicillin is an extended-spectrum ß-lactam antibiotic with a structure similar to that of ampicillin. It is effective against a variety of ß-lactamase negative bacteria including E. coli and various Streptococcus and Staphylococcus bacteria. It is also effective against a variety of other gram-negative and gram-positive bacteria. Amoxicillin sodium salt is freely soluble in aqueous solution.

    Penicillins are a type of β-lactam antibiotic consisting of a four-membered β-lactam ring bound to a five-membered thiazolidine 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. Resistance to β-lactam antibiotics occurs in the presence of cells containing plasmid encoded extended spectrum β-lactamases or ESBLs.


    Product Specifications
    Amoxicillin Sodium Salt

    MOLECULAR BIOLOGY GRADE

    Formula: C16H18N3NaO5S

    MW: 387.39 g/mol

    Storage/Handling: Store at 2-8°C.

    PubChem Chemical ID: 23663126

    Product Specifications

    Catalog ID: A-551
    CAS #: 34642-77-8
    MW: 387.39 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.

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