Antagonist properties of the stereoisomers of ifenprodil at NR1A/NR2A and NR1A/NR2B subtypes of the NMDA receptor expressed in Xenopus oocytes

Author:

Avenet Patrick,Léonardon Jacques,Besnard François,Graham David,Frost Jonathan,Depoortere Henri,Langer Salomon Z.,Scatton Bernard

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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