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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.

✍ Scribed by Andrew W. Thomas; et al. et al.


Publisher
John Wiley and Sons
Year
2006
Weight
18 KB
Volume
37
Category
Article
ISSN
0931-7597

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