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

J Med Chem. 2019 Jan 10;62(1):3-23. doi: 10.1021/acs.jmedchem.7b01640. Epub 2018 Mar 5.

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.

Publication types

  • Review

MeSH terms

  • Allosteric Regulation
  • Benzenesulfonamides
  • Binding Sites
  • Cholesterol / analogs & derivatives
  • Cholesterol / metabolism
  • Humans
  • Neurotransmitter Agents / chemistry
  • Neurotransmitter Agents / metabolism
  • Phenanthrenes / chemistry
  • Phenanthrenes / metabolism
  • Protein Isoforms / chemistry
  • Protein Isoforms / metabolism
  • Receptors, N-Methyl-D-Aspartate / chemistry
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Structure-Activity Relationship
  • Sulfonamides / chemistry
  • Sulfonamides / metabolism

Substances

  • Neurotransmitter Agents
  • Phenanthrenes
  • Protein Isoforms
  • Receptors, N-Methyl-D-Aspartate
  • Sulfonamides
  • phenanthrene
  • Cholesterol