Amalgamation of the structure-activity relationship of two series of GlyT1 inhibitors developed at Merck led to the discovery of a clinical candidate, compound 16 (DCCCyB), which demonstrated excellent in vivo occupancy of GlyT1 transporters in rhesus monkey as determined by displacement of a PET tracer ligand.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007840PMC
http://dx.doi.org/10.1021/ml1001085DOI Listing

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