Antagonist properties of the stereoisomers of ifenprodil at NR1A/NR2A and NR1A/NR2B subtypes of the NMDA receptor expressed in Xenopus oocytes
Author:
Publisher
Elsevier BV
Subject
Pharmacology
Reference10 articles.
1. The NMDA receptor antagonist eliprodil (SL 82.0715) blocks Ca2+ channels in acutely dissociated neurons from rat hippocampus and cerebellum;Avenet;Neurosci. Abstr.,1994
2. The NMDA receptor antagonist eliprodil (SL 82.0715) blocks voltage-operated Ca2+ channels in rat cultured cortical neurons;Biton;Eur. J. Pharmacol.,1994
3. Non-competitive NMDA receptor antagonists acting on the polyamine site;Carter,1991
4. Separation of α1 adrenergic and N-methyl-d-aspartate antagonist activity in a series of ifenprodil compounds;Chenard;J. Med. Chem.,1991
5. Blockade by ifenprodil of high voltage-activated Ca2+ channels in rat and mouse cultured hippocampal pyramidal neurones: comparison with N-methyl-d-aspartate receptor antagonist actions;Church;Br. J. Pharmacol.,1994
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