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J Med Chem ; 53(23): 8228-40, 2010 Dec 09.
Artículo en Inglés | MEDLINE | ID: mdl-21053897

RESUMEN

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.


Asunto(s)
Imidazoles/farmacología , Quinolinas/farmacología , Antagonistas de la Serotonina/farmacología , Administración Oral , Animales , Células CHO , Cromatografía Liquida , Cricetulus , Descubrimiento de Drogas , Humanos , Imidazoles/administración & dosificación , Imidazoles/química , Espectroscopía de Resonancia Magnética , Masculino , Quinolinas/administración & dosificación , Quinolinas/química , Ratas Sprague-Dawley , Receptores de Serotonina/clasificación , Antagonistas de la Serotonina/administración & dosificación , Antagonistas de la Serotonina/química , Espectrometría de Masas en Tándem
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