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pubmed-article:18547807pubmed:abstractTextStrategic replacement of the nitrogen of the lead compound 1 in the original cyclic urea series with a carbon resulted in the discovery of a novel, potent and orally more efficacious gamma-lactam series of selective NK(1) antagonists. Optimization of the lactam series culminated in the identification of compounds with high binding affinity and excellent oral CNS activity.lld:pubmed
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pubmed-article:18547807pubmed:articleTitleDiscovery of a novel, potent and orally active series of gamma-lactams as selective NK1 antagonists.lld:pubmed
pubmed-article:18547807pubmed:affiliationChemical Research Department, Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA. sunil.paliwal@spcorp.comlld:pubmed
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