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J Med Chem ; 53(23): 8228-40, 2010 Dec 09.
Article in English | MEDLINE | ID: mdl-21053897

ABSTRACT

In an effort to identify selective drug like pan-antagonists of the 5-HT1 autoreceptors, studies were conducted to elaborate a previously reported dual acting 5-HT1 antagonist/SSRI structure. A novel series of compounds was identified showing low intrinsic activities and potent affinities across the 5-HT1A, 5-HT1B, and 5-HT1D receptors as well as high selectivity against the serotonin transporter. From among these compounds, 1-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)-2-imidazolidinone (36) was found to combine potent in vivo activity with a strong preclinical developability profile, and on this basis it was selected as a drug candidate with the aim of assessing its potential as a fast-onset antidepressant/anxiolytic.


Subject(s)
Imidazoles/pharmacology , Quinolines/pharmacology , Serotonin Antagonists/pharmacology , Administration, Oral , Animals , CHO Cells , Chromatography, Liquid , Cricetulus , Drug Discovery , Humans , Imidazoles/administration & dosage , Imidazoles/chemistry , Magnetic Resonance Spectroscopy , Male , Quinolines/administration & dosage , Quinolines/chemistry , Rats, Sprague-Dawley , Receptors, Serotonin/classification , Serotonin Antagonists/administration & dosage , Serotonin Antagonists/chemistry , Tandem Mass Spectrometry
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