Dalbavancin

Biochem/physiol Actions Dalbavancin is a semisynthetic, vancomycin class lipoglycopeptide with antibacterial activity against a variety of gram-positive pathogens, including methicillin-resistant S. aureus &amp: S.

Dalbavancin is a semi-synthetic glycopeptide prepared from A40926 by introducing a positively charged lipophilic moiety in a previously unexplored region of the natural glycopeptide. This modification provides a longer in vitro half life, and

Dalbavancin is a semi-synthetic glycopeptide prepared from A40926 by introducing a positively charged lipophilic moiety in a previously unexplored region of the natural glycopeptide. This modification provides a longer in vitro half life, and

Dalbavancin is a semi-synthetic glycopeptide prepared from A40926 by introducing a positively charged lipophilic moiety in a previously unexplored region of the natural glycopeptide. This modification provides a longer in vitro half life, and

Dalbavancin is a semi-synthetic glycopeptide prepared from A40926 by introducing a positively charged lipophilic moiety in a previously unexplored region of the natural glycopeptide. This modification provides a longer in vitro half life, and

Dalbavancin Impurity is a glycopeptide antibiotic structurally similar to teicoplanin and vancomycin. It is used as precursor for synthesis of dalbavancin and inhibits peptidoglycan synthesis in the cell wall of gram-positive bacteria.

Dalbavancin Impurity is a glycopeptide antibiotic structurally similar to teicoplanin and vancomycin. It is used as precursor for synthesis of dalbavancin and inhibits peptidoglycan synthesis in the cell wall of gram-positive bacteria.

Dalbavancin Impurity is a glycopeptide antibiotic structurally similar to teicoplanin and vancomycin. It is used as precursor for synthesis of dalbavancin and inhibits peptidoglycan synthesis in the cell wall of gram-positive bacteria.

Dalbavancin Impurity is a glycopeptide antibiotic structurally similar to teicoplanin and vancomycin. It is used as precursor for synthesis of dalbavancin and inhibits peptidoglycan synthesis in the cell wall of gram-positive bacteria.

Dalbavancin Impurity is a glycopeptide antibiotic structurally similar to teicoplanin and vancomycin. It is used as precursor for synthesis of dalbavancin and inhibits peptidoglycan synthesis in the cell wall of gram-positive bacteria.