Design, synthesis, and evaluation of polyamine-memantine hybrids as NMDA channel blockers

[Display omitted] N-Methyl-d-aspartate (NMDA) receptors have been implicated in learning and memory, and may also play a central role in various conditions leading to neuronal degradation. NMDA receptor antagonists could therefore be of therapeutic benefit for a number of neurological disorders. We...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2018-02, Vol.26 (3), p.603-608
Hauptverfasser: Kumamoto, Takuya, Nakajima, Marie, Uga, Reina, Ihayazaka, Naoko, Kashihara, Haruna, Katakawa, Kazuaki, Ishikawa, Tsutomu, Saiki, Ryotaro, Nishimura, Kazuhiro, Igarashi, Kazuei
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Sprache:eng
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Zusammenfassung:[Display omitted] N-Methyl-d-aspartate (NMDA) receptors have been implicated in learning and memory, and may also play a central role in various conditions leading to neuronal degradation. NMDA receptor antagonists could therefore be of therapeutic benefit for a number of neurological disorders. We have designed hybrid compounds of polyamines and memantine, both of which function as NMDA channel blockers. The triamine derivative with a guanidine moiety showed more potent antagonistic activity than memantine.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2017.12.021