Oritavancin

Oritavancin

Catalog Number:
M001341888TOK
Mfr. No.:
TOK-O043
Price:
$274
  • Size:
    Quantity:
    Add to Cart:
      • Overview
        • Oritavancin is a semi-synthetic glycopeptide antibiotic that is an analog of vancomycin. It has bactericidal activity against Gram-positive bacteria.

          Please contact us at for specific academic pricing.

          Background

          Like other glycopeptides and lipoglycopeptides, Oritavancin inhibits transglycosylation to stop peptidoglycan synthesis.
          Its secondary mode of action is to interact directly with the cell membranes, causing depolarization which permeabilizes the membrane and causes cell death. This is attributable to the 4'-chlorobiphenylmethyl group.

      • Properties
        • CAS Number
          171099-57-3
          Molecular Formula
          C86H97Cl3N10O26
          Molecular Weight
          1793.1
          Appearance
          White or off-white powder
          Other Properties
          Source: Semi-synthetic
          Storage
          -20 °C

          * For research use only

      • Applications
        • Application Description
          Spectrum: Effective against Gram-positive bacteria. It is effective at killing biofilm-producing pathogens like methicillin-resistant S. aureus (MRSA) and vancomycin-resistant enterococci (VRE).

          Microbiology Applications: Oritavancin is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (panels, discs, and MIC strips) against Gram -positive isolates. Medical microbiologists use AST results to recommend antibiotic treatment options. Representative MIC values include: S. aureus: 0.12 µ/ml - 4 µg/ml MRSA: 0.25 µg/mL – 4 µg/mL Researchers studied the effect of polysorbate 80 on oritavancin binding to plastic surfaces and found it was rapidly lost from solution in susceptibility assay test plates. Greater losses were observed at lower concentrations suggesting saturable binding to surfaces. The inclusion of 0.002% Polysorbate 80 permitted the recovery of 80-100 % oritavancin, and it is suggested to use it in broth microdilution. It putatively blocks the nonspecific binding sites on he surfaces of the test vessels. The 16- to 32-fold reductions in the oritavancin MICs for the staphylococci and enterococci in the presence of polysorbate 80 are likely a result of polysorbate 80 inhibition of the binding of oritavancin to plastic surfaces. Investigators should use caution during in vitro and in vivo experiments to ensure proper assessment of the intended concentration. (Arhin et al, 2008).

    Documents

    MSDS-EU

    Note: If you don't receive our verification email, do the following:

  • Copyright © Amerigo Scientific. All rights reserved.