Structural correlation between lipophilicity and lipopolysaccharide-sequestering activity in spermine-sulfonamide
Mark R Burns1, Scott A Jenkins, Nicolas M Vermeulen
1MediQuest Therapeutics, Inc., 22322 20th Ave. SE, Bothell, WA 98021, USA.
Abstract:
Lipopolysaccharides (LPS), otherwise termed 'endotoxins', are outer-membrane constituents of Gram-negative bacteria, and play a key role in the pathogenesis of 'Septic Shock', a major cause of mortality in the critically ill patient. We had previously defined the pharmacophore necessary for small molecules to specifically bind and neutralize this complex carbohydrate. A series of aryl and aliphatic spermine-sulfonamide analogs were synthesized and tested in a series of binding and cell-based assays in order to probe the effect of lipophilicity on sequestration ability. A strong correlation was indeed found, supporting the hypothesis that endotoxin-neutralizing ability involves a lipophilic or membrane attachment event. The research discussed herein may be useful for the design of additional carbohydrate recognizing molecules and endotoxin-neutralizing drugs.
More Related Videos
Related Concept Videos
Surface Active Agents
Biosynthesis of Lipids
Formation of Lipopolysaccharides
Antifungal Agents
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Structure and Nomenclature of Thiols and Sulfides


