Timentin™ Ticarcillin/Clavulanate (15/1)

Description

Timentin™ is a 15:1 mixture of ticarcillin and clavulanate. Ticarcillin is a penicillin ß-lactam antibiotic, which is susceptible to ß-lactamase degradation. When combined with clavulanate, a ß-lactamase inhibitor, its efficacy is greatly increased. Timentin™ exhibits high activity against gram-negative bacteria and resistant Agrobacterium species.

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.


TESTED AGAINST BOTH SENSITIVE AND RESISTANT CELLS AT GOLD BIOTECHNOLOGY LAB.

Product Specifications
Ticarcillin Disodium
Potassium Clavulanate

USP GRADE

Formula: C15H14N2Na2O6S2 / C8H8KNO5

MW: 665.64 g/mol (combined)

Storage/Handling: Store desiccated at -20°C. Soluble in water.

PubChem Chemical ID (Ticarcillin): 470375
PubChem Chemical ID (Clavulanate): 23665591

Timentin™ Ticarcillin/Clavulanate (15/1)

View Sizes & Pricing

Catalog Number:
T-104-2
CAS Number:
4697-14-7; 61177-45-5
$51.00

Availability:
In stock
Shipping:
Shipping calculated at checkout

    Description

    Timentin™ is a 15:1 mixture of ticarcillin and clavulanate. Ticarcillin is a penicillin ß-lactam antibiotic, which is susceptible to ß-lactamase degradation. When combined with clavulanate, a ß-lactamase inhibitor, its efficacy is greatly increased. Timentin™ exhibits high activity against gram-negative bacteria and resistant Agrobacterium species.

    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.


    TESTED AGAINST BOTH SENSITIVE AND RESISTANT CELLS AT GOLD BIOTECHNOLOGY LAB.

    Product Specifications
    Ticarcillin Disodium
    Potassium Clavulanate

    USP GRADE

    Formula: C15H14N2Na2O6S2 / C8H8KNO5

    MW: 665.64 g/mol (combined)

    Storage/Handling: Store desiccated at -20°C. Soluble in water.

    PubChem Chemical ID (Ticarcillin): 470375
    PubChem Chemical ID (Clavulanate): 23665591

    Product Specifications

    Catalog ID: T-104
    CAS #: 4697-14-7; 61177-45-5
    Formula: C15H14N2Na2O6S2/C8H8KNO5
    MW: 665.64 g/mol
    Grade: MOLECULAR BIOLOGY GRADE
    Storage/handling: Store desiccated at -20°C.

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