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Design and synthesis of 4-substituted-8-(2-phenyl-cyclohexyl)-2,8-diaza-spiro[4.5]decan-1-one as a novel class of GlyT1 inhibitors: Achieving selectivity against the μ opioid and nociceptin/orphanin FQ peptide (NOP) receptors |
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期刊:Bioorganic & Medicinal Chemistry Letters 作者:Daniela Alberati; Simona M. Ceccarelli; Synèse Jolidon; Eva A. Krafft; Anke Kurt; et al 出版日期:2006-08-01 |
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(2025-6-4)