
pmid: 16178732
This article describes recent medicinal chemistry progress toward selective potentiators of the metabotropic glutamate receptor 2 (mGluR2). Groups at Lilly and Merck have identified new classes of potentiators that exhibit selectivity for mGluR2 over the seven other subtypes of mGluRs. Structure-activity relationships as well as pharmacokinetic properties and in vivo activity are reviewed.
Structure-Activity Relationship, Allosteric Regulation, Drug Design, Excitatory Amino Acid Agonists, Animals, Humans, Receptors, Metabotropic Glutamate
Structure-Activity Relationship, Allosteric Regulation, Drug Design, Excitatory Amino Acid Agonists, Animals, Humans, Receptors, Metabotropic Glutamate
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