Abstract
Since the 1990s, ionotropic glutamate receptors have served as an outstanding target for drug discovery research aimed at the discovery of new neurotherapeutic agents. With the recent approval of perampanel, the first marketed non-competitive antagonist of AMPA receptors, particular interest has been directed toward ‘non-NMDA’ (AMPA and kainate) receptor inhibitors. Although the role of AMPA receptors in the development of neurological or psychiatric disorders has been well recognized and characterized, progress in understanding the function of kainate receptors (KARs) has been hampered, mainly due to the lack of specific and selective pharmacological tools. The latest findings in the biology of KA receptors indicate that they are involved in neurophysiological activity and play an important role in both health and disease, including conditions such as anxiety, schizophrenia, epilepsy, neuropathic pain, and migraine. Therefore, we reviewed recent advances in the field of competitive and non-competitive kainate receptor antagonists and their potential therapeutic applications. Due to the high level of structural divergence among the compounds described here, we decided to divide them into seven groups according to their overall structure, presenting a total of 72 active compounds.
Funder
NATIONAL SCIENCE CENTRE POLAND
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis
Reference227 articles.
1. Glutamate, glutamate receptors, and downstream signaling pathways;Willard;Int. J. Biol. Sci.,2013
2. Structure, function, and pharmacology of glutamate receptor ion channels;Hansen;Pharmacol. Rev.,2021
3. Glutamate receptor ion channels: Structure, regulation, and function;Traynelis;Pharmacol. Rev.,2010
4. Non-canonical signaling, the hidden life of ligand-gated ion channels;Valbuena;Neuron,2016
5. Non-canonical mechanisms of presynaptic kainate receptors controlling glutamate release;Sihra;Front. Mol. Neurosci.,2018
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献