The synthesis and antiviral activity of original dibromoimidazo[1,2-a]pyrid
ines bearing a thioether side chain are reported.
Molecular modeling was used to identify biophoric structural patterns that
are common to 16 compounds. Structure-activity relationship (SAR) studies i
dentified hydrophobicity (logP) as the most important factor for activity.
From these SAR studies, the antiviral activity could be predicted.