Journal of Medicinal Chemistry · 2009 · 54 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryLead OptimizationStructure-activity RelationshipsChemical Library DesignDrug-receptor InteractionsLigand BindingPotency OptimizationReceptor PharmacologyStructure-activity Relationship AnalysisChemical Synthesis Of AnaloguesIn Vivo StudiesMedicinal Chemistry ApplicationsOptimization Of Drug-like PropertiesOptimization Of Pharmacodynamic PropertiesOptimization Of Pharmacokinetic PropertiesPharmacological ProfilingPharmacological Screening
In an effort to discover novel druglike NK(1) receptor antagonists a new series of suitably substituted C-phenylpiperazine derivatives was identified by an appropriate chemical exploration of related N-phenylpiperazine analogues, with the specific aim to maximize their in vitro affinity and optimize in parallel their pharmacokinetic profile. Among the compounds synthesized, 2-(S)-(4-fluoro-2-methylphenyl)piperazine-1-carboxylic acid [1-(R)-(3,5-bis-trifluoromethylphenyl)ethyl]methylamide (vestipitant) was identified as one of the most in vitro potent and selective NK(1) receptor antagonists ever discovered, showing appropriate pharmacokinetic properties and in vivo activity. On the basis of its preclinical profile, this compound was selected as a drug candidate.
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Distinct Mechanism for Antidepressant Activity by Blockade of Central Substance P Receptors
Mark S. Kramer, Neal R. Cutler, John P. Feighner et al. · Science · 1998 · 1.1K citations
Medicine, Pharmacology, Psychiatry +17