Positive and Negative Allosteric Modulators of N-Methyl-d-aspartate (NMDA) Receptors: Structure-Activity Relationships and Mechanisms of Action.

Erica S Burnell, Mark Irvine, Guangyu Fang, Kiran Sapkota, David E Jane, Daniel T Monaghan

Journal: Journal of medicinal chemistry 2019;62(1):3-23

PMID: 29446949

Abstract

Excitatory activity in the CNS is predominately mediated by l-glutamate through several families of l-glutamate neurotransmitter receptors. Of these, the N-methyl-d-aspartate receptor (NMDAR) family has many critical roles in CNS function and in various neuropathological and psychiatric conditions. Until recently, the types of compounds available to regulate NMDAR function have been quite limited in terms of mechanism of action, subtype selectivity, and biological effect. However, several new classes of NMDAR agents have now been identified that are positive or negative allosteric modulators (PAMs and NAMs, respectively) with various patterns of NMDAR subtype selectivity. These new agents act at several newly recognized binding sites on the NMDAR complex and offer significantly greater pharmacological control over NMDAR activity than previously available agents. The purpose of this review is to summarize the structure-activity relationships for these new NMDAR modulator drug classes and to describe the current understanding of their mechanisms of action.

Address: Centre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience , University of Bristol , Bristol BS8 1TD , U.K.; School of Chemistry , National University of Ireland Galway , Galway H91TK33 , Ireland.; Centre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience , University of Bristol , Bristol BS8 1TD , U.K.; Department of Pharmacology and Experimental Neuroscience , University of Nebraska Medical Center , Omaha , Nebraska 68198 , United States.

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