Design and Synthesis of a Novel Water-Soluble NMDA Receptor Antagonist with a 1,4,7,10-Tetraazacyclododecane Group
Author:
Affiliation:
1. College of Pharmacy, Nihon University
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/53/4/53_4_444/_pdf
Reference10 articles.
1. Glutamate neurotoxicity and diseases of the nervous system
2. The NMDA Receptor, NMDA Antagonists and Epilepsy Therapy
3. Interactions of polyamines with ion channels
4. Spider toxins as tools for dissecting elements of excitatory amino acid transmission
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1. Synthesis of Water-Soluble Polyamine Derivatives Effective as N-Methyl-D-aspartate Receptor Antagonists;Chemical and Pharmaceutical Bulletin;2010
2. Synthesis of Two Novel Water-soluble Cleft-Type Cyclophanes Effective as N-Methyl-D-aspartate Receptor Antagonist;HETEROCYCLES;2009
3. Synthesis of a Novel Water-Soluble Cleft-Type Cyclophane as an N-Methyl-D-aspartate Receptor Antagonist;Chemical and Pharmaceutical Bulletin;2009
4. Differential effects of linear and cyclic polyamines on NMDA receptor activities;Neurochemistry International;2008-07
5. Synthesis of a novel water‐soluble NMDA receptor antagonist;Journal of Heterocyclic Chemistry;2008-03
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