CP-101,606, a potent neuroprotectant selective for forebrain neurons
- 1 July 1997
- journal article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 331 (2-3) , 117-126
- https://doi.org/10.1016/s0014-2999(97)10092-9
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Interactions between Ifenprodil and the NR2B Subunit of the N-Methyl-D-aspartate ReceptorJournal of Biological Chemistry, 1996
- The effects of ifenprodil and eliprodil on voltage-dependent Ca2+ channels and in gerbil global cerebral ischaemiaEuropean Journal of Pharmacology, 1996
- Block of P-type Ca2+ channels by the NMDA receptor antagonist eliprodil in acutely dissociated rat Purkinje cellsEuropean Journal of Pharmacology, 1995
- (1S,2S)-1-(4-Hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol: A Potent New Neuroprotectant Which Blocks N-Methyl-D-Aspartate ResponsesJournal of Medicinal Chemistry, 1995
- The NMDA receptor antagonist eliprodil (SL 82.0715) blocks voltage-operated Ca2+ channels in rat cultured cortical neuronsEuropean Journal of Pharmacology, 1994
- The neuroprotective properties of ifenprodil, a novel NMDA receptor antagonist, in neuronal cell culture toxicity studiesEuropean Journal of Pharmacology: Molecular Pharmacology, 1992
- Pharmacological characterisation and autoradiographic distribution of polyamine-sensitive [3H]ifenprodil binding sites in the rat brainNeuroscience Letters, 1991
- Ifenprodil and SL 82.0715 potently inhibit binding of [3H](+)-3-PPP to σ binding sites in rat brainNeuroscience Letters, 1990
- Pharmacology of glutamate neurotoxicity in cortical cell culture: attenuation by NMDA antagonistsJournal of Neuroscience, 1988
- The Role of Glutamate in Neurotransmission and in Neurologic DiseaseArchives of Neurology, 1986