An impaired signaling capacity of the serotonin (5-HT) 5-HT receptor (5-HTR) has been implicated in the neurobehavioral processes that promote relapse vulnerability in cocaine use disorder (CUD). Restoration of the diminished 5-HTR signaling through positive allosteric modulation presents a novel therapeutic approach. Several new molecules with the 4-alkylpiperidine-2-carboxamide scaffold were designed, synthesized, and pharmacologically evaluated, leading to the discovery of selective 5-HTR positive allosteric modulators (PAMs). Compound 16 (CYD-1-79) potentiated 5-HT-evoked intracellular calcium release in cells stably expressing the human 5-HTR but not the 5-HTR cells. A topographically distinct allosteric site was identified based on the newly solved 5-HTR structure. Compound 16 modulated 5-HTR-mediated spontaneous ambulation, partially substituted for the training dose of the 5-HTR agonist WAY163909, synergized with a low dose of WAY163909 to substitute fully for the stimulus effects of WAY163909, and attenuated relapse vulnerability as assessed in a rodent self-administration model, indicating its therapeutic promise for CUD.
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| http://dx.doi.org/10.1021/acs.jmedchem.8b00401 | DOI Listing |
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