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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bioorganic & medicinal chemistry letters 2011-06, Vol.21 (12), p.3682-3685
Hauptverfasser: Low, Eddy, Kim, Bum, Francavilla, Charles, Shiau, Timothy P., Turtle, Eric D., O’Mahony, Donogh J.R., Alvarez, Nichole, Houchin, Ashley, Xu, Ping, Zuck, Meghan, Celeri, Chris, Anderson, Mark B., Najafi, Ramin (Ron), Jain, Rakesh K.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
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