Cloxacillin Sodium

Description

Cloxacillin sodium is a sodium salt formed from a chlorinated semisynthetic derivative of penicillin. It has been shown to exhibit significant bactericidal activity against penicillin G-resistant staphylococci.

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.

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
Cloxacillin sodium

Formula: C19H17ClN3NaO5S ∙ H2O

MW: 475.88 g/mol

Storage/Handling: Store at 4°C.

PubChem Chemical ID: 23675743

Cloxacillin Sodium

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Catalog Number:
C-805-1
CAS Number:
7081-44-9
$59.00

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    Description

    Cloxacillin sodium is a sodium salt formed from a chlorinated semisynthetic derivative of penicillin. It has been shown to exhibit significant bactericidal activity against penicillin G-resistant staphylococci.

    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.

    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
    Cloxacillin sodium

    Formula: C19H17ClN3NaO5S ∙ H2O

    MW: 475.88 g/mol

    Storage/Handling: Store at 4°C.

    PubChem Chemical ID: 23675743

    Product Specifications

    Catalog ID: C-805
    CAS #: 7081-44-9
    MW: 475.88 g/mol
    Storage/handling: Store at 4°C.

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