As a part of our ongoing research to develop novel and selective 5-HT6 receptor antagonists, a new series of 2-(4- methylpiperazin-1-yl methyl)-1-(arylsulfonyl)-1H-indole derivatives were designed to study the effect of two ionisable basic centers on the 5-HT6 receptor binding affinity. The synthesis and their in-vitro affinity towards the 5- HT6 receptor is the subject matter of this communication.
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