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Vancomycin hydrochloride

Catalog No.
B1223
glycopeptide antibacterial agent
Grouped product items
SizePriceStock Qty
10mM (in 1mL DMSO)
$61.00
In stock
250mg
$57.00
In stock
1g
$74.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

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Background

Vancomycin hydrochloride (CAS 1404-93-9) is a glycopeptide antibacterial agent, commonly employed in microbiological and drug resistance research due to its specific inhibitory activity. Its antibacterial function derives from the inhibition of bacterial cell wall synthesis through binding directly to D-alanyl-D-alanine terminal residues of peptidoglycan precursors, consequently disrupting cell-wall assembly in Gram-positive bacteria. Typically, vancomycin hydrochloride serves as a positive control in assays evaluating antibiotic resistance profiles, bacterial susceptibility tests, and screening studies related to novel glycopeptide-derivatives. Reported inhibitory concentrations (IC50) vary based on bacterial strains tested, generally ranging from approximately 0.5 μg/mL to 2.0 μg/mL under standard laboratory assay conditions.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt1485.72
Cas No.1404-93-9
FormulaC66H76Cl3N9O24
Solubility≥55.8 mg/mL in DMSO with gentle warming; insoluble in EtOH; ≥22.15 mg/mL in H2O
SDFDownload SDF
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.

Protocol

Animal experiment:[1]

Animal models

C57BL/6 mice challenged with Clostridium difficile (C. difficile) strain VPI 10463

Dosage form

20 mg/kg

Once daily by oral gavage for 5 days

Applications

Vancomycin treatment of infected mice was associated with improved clinical, diarrhea, and histopathology scores and survival during treatment. However, after discontinuation of the drug, clinical scores and histopathology were worse in treated mice than in untreated infected controls. Decreasing the duration of vancomycin treatment from 5 days to 1 day decreased recurrence and deaths in C. difficile infection.

Note

The technical data provided above is for reference only.

References:

1. Warren CA, van Opstal EJ, Riggins MS, et al. Vancomycin treatment's association with delayed intestinal tissue injury, clostridial overgrowth, and recurrence of Clostridium difficile infection in mice. Antimicrobial Agents and Chemotherapy, 2013, 57(2): 689-696.

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