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Ceftazidime pentahydrate

Catalog No.
B8669
A broad-spectrum antibiotic effective against Gram-positive and Gram-negative aerobic bacteria.
Grouped product items
SizePriceStock Qty
Evaluation Sample
$30.00
In stock
500mg
$50.00
In stock
1g
$77.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

Ceftazidime pentahydrate (CAS No.: 78439-06-2) is a third-generation cephalosporin antibiotic widely utilized in biomedical research for its broad-spectrum activity against Gram-positive and Gram-negative aerobic bacteria. It exerts its antibacterial effects by binding to penicillin-binding proteins, thereby inhibiting the final stages of bacterial cell wall synthesis and leading to cell lysis. Notably, it demonstrates strong activity against members of the Enterobacteriaceae family, including β-lactamase-producing strains, due to its resistance to hydrolysis by many β-lactamases. In vitro studies have shown potent antibacterial activity across a range of clinically relevant species, with efficacy typically observed in the low micromolar to sub-micromolar range depending on the organism and assay conditions. Ceftazidime pentahydrate is frequently employed in cell-based assays and animal infection models to investigate antimicrobial resistance mechanisms, evaluate β-lactamase inhibition strategies, and assess combination therapies targeting multidrug-resistant pathogens. Experimental concentrations or dosing regimens vary according to specific study designs and microbial susceptibility profiles, making it a valuable reference compound in antibacterial drug discovery and translational research.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt636.65
Cas No.78439-06-2
FormulaC22H32N6O12S2
Solubilityinsoluble in EtOH; insoluble in H2O; ≥46 mg/mL in DMSO
Chemical Name(6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate pentahydrate
Canonical SMILESO=C1N2[C@]([C@@H]1NC(/C(C3=CSC(N)=N3)=N\OC(C)(C(O)=O)C)=O)([H])SCC(C[N+]4=CC=CC=C4)=C2C([O-])=O.O.O.O.O.O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

User Guide