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Synthesis, in vitro pharmacology, and structure–activity relationships of 2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid derivatives as mGluR2 antagonists

Molecular PharmacologyDerivativesBiochemistryMedicineMglur2 AntagonistsPharmacological AgentPharmacotherapyVitro PharmacologyStructure–activity RelationshipsPharmacologyPharmaceutical Chemistry