Structure stability/activity relationships of sulfone stabilized N, N-dichloroamines
This study identified a new class of solution-stable, topical, antimicrobial agents. These agents are sulfone-stabilized and possess either a quaternary ammonium or sulfonate as a water solubilizing group. Structure stability/activity relationships (SXR) of a new class of N, N-dichloroamine compound...
Gespeichert in:
Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2011-06, Vol.21 (12), p.3682-3685 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This study identified a new class of solution-stable, topical, antimicrobial agents. These agents are sulfone-stabilized and possess either a quaternary ammonium or sulfonate as a water solubilizing group.
Structure stability/activity relationships (SXR) of a new class of
N,
N-dichloroamine compounds were explored to improve antimicrobial activity against
Escherichia coli,
Staphylococcus aureus, and
Candida albicans while maintaining aqueous solution stability. This study identified a new class of solution-stable and topical antimicrobial agents. These agents are sulfone-stabilized and possess either a quaternary ammonium or sulfonate appendages as a water solubilizing group. Several unique challenges were confronted in the synthesis of these novel compounds which are highlighted in the discussion. |
---|---|
ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2011.04.084 |