Using solid phase synthesis techniques, we have rapidly obtained a series o
f eight aryl sulphonamides derived from putrescine. These conjugates with v
arious aryl groups were evaluated for their affinity towards 5-HT6 receptor
s in man. This evaluation revealed the interest of two compounds which pres
ent the same activity level, in the submicromolar range, as two reference d
erivatives. The most potent will be considered as a new lead for further in
vestigations.