학술논문
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
Document Type
Short Communication
Author
Source
In Bioorganic & Medicinal Chemistry Letters 2006 16(16):4305-4310
Subject
Language
ISSN
0960-894X