Eplivanserin
Eplivanserin, also known by its former developmental code names SR-46349 and SR-46615 and by its former tentative brand names Ciltyri and Sliwens, is a serotonin 5-HT2A receptor antagonist which was under development by Sanofi Aventis for the treatment of a variety of medical conditions but was never marketed. It is taken orally.
Pharmacology
Pharmacodynamics
Eplivanserin is an inverse agonist on the serotonin receptor subtype 5-HT2A. In contrast to older sedating drugs acting on 5-HT2A receptors, eplivanserin has practically no affinity to dopamine, histamine and adrenergic receptors.Eplivanserin blocks the head-twitch response produced by the serotonin precursor 5-hydroxytryptophan, by serotonergic psychedelics like DOI, and by serotonin 5-HT1A receptor antagonists like WAY-100635 and (S)-UH-301.
The drug has been shown to upregulate serotonin 5-HT2A receptor expression, unlike many known serotonin 5-HT2A receptor antagonists, which paradoxically induce receptor downregulation. Relatedly, although eplivanserin given acutely can block the head-twitch response induced by various serotonergic drugs, it can also enhance the head-twitch response induced by 5-HTP and psychedelics like DOI when given on a sub-acute basis.
Pharmacokinetics
Eplivanserin is well-absorbed, with an absorption of more than 70%. The time to peak levels of eplivanserin is 2 to 6hours. Its elimination half-life is relatively long, with an average value of 50hours.Chemistry
Synthesis
]The condensation between 2'-Fluoroacetophenone & 4-hydroxybenzaldehyde give a chalcone intermediate, i.e. .
dimethylamine & acetone oxime are reacted together to give dimethylaminoacetoxime, .
Convergent synthesis gives the product as a mixture of isomers.