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PRX-07034 is a potent and highly selective small-molecule antagonist of the serotonin 6 (5-HT6) receptor. It was developed primarily for the treatment of cognitive impairment associated with Alzheimer's disease and schizophrenia, as well as for obesity. Preclinical studies have shown that it enhances working memory and cognitive flexibility in animal models, likely through modulation of both acetylcholine and glutamate neurotransmitter systems. The drug demonstrates high selectivity for the 5-HT6 receptor (Ki = 4–8 nM; IC50 = 19 nM), with over 100-fold selectivity compared to most other GPCRs except D3 and 5-HT1B receptors[1][2][5]. Development was originally by Epix Pharmaceuticals.
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