Ceftazidime Pentahydrate

Description

Ceftazidime pentahydrate is a third generation cephalosporin antibiotic. It has been used to study the penicillin binding proteins, especially PBP3. It has also been used as a selection tool for mutant colonies. Ceftazidime targets gram-negative bacteria, including Pseudomonas aeruginosa and is less effective against gram-positive cocci. It is soluble in acidic and alkali solvents.

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.

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
Ceftazidime Pentahydrate

MOLECULAR BIOLOGY GRADE

Formula: C22H22N6O7S2 ∙ 5H2O

MW: 636.65 g/mol

Storage/Handling: Store at 2-8 °C.

PubChem Chemical ID: 6536864

Ceftazidime Pentahydrate

View Sizes & Pricing

Catalog Number:
C-740-1
CAS Number:
78439-06-2
$78.00

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    Description

    Ceftazidime pentahydrate is a third generation cephalosporin antibiotic. It has been used to study the penicillin binding proteins, especially PBP3. It has also been used as a selection tool for mutant colonies. Ceftazidime targets gram-negative bacteria, including Pseudomonas aeruginosa and is less effective against gram-positive cocci. It is soluble in acidic and alkali solvents.

    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.

    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
    Ceftazidime Pentahydrate

    MOLECULAR BIOLOGY GRADE

    Formula: C22H22N6O7S2 ∙ 5H2O

    MW: 636.65 g/mol

    Storage/Handling: Store at 2-8 °C.

    PubChem Chemical ID: 6536864

    Product Specifications

    Catalog ID: C-740
    CAS #: 78439-06-2
    MW: 636.65 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store at 4°C.

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