Abstract
Novel (E)-N(1)-(benzyl)cinnamamidines were prepared and evaluated as NR2B subtype NMDA receptor ligands. Excellent affinity was achieved by appropriate substitution of either phenyl ring. The 2-methoxybenzyl compound 1h had approximately 1,000-fold lower IC(50) in NR2B than NR2A-containing cells. Replacement of the styryl unit by 2-naphthyl was well tolerated.
MeSH terms
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Amidines / chemical synthesis*
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Amidines / metabolism
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Benzamidines / chemical synthesis
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Benzamidines / metabolism
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Drug Evaluation, Preclinical
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Humans
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Naphthalenes / chemical synthesis
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Naphthalenes / metabolism
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Protein Binding
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Radioligand Assay
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Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
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Receptors, N-Methyl-D-Aspartate / metabolism
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Structure-Activity Relationship
Substances
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Amidines
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Benzamidines
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NR2B NMDA receptor
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Naphthalenes
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Receptors, N-Methyl-D-Aspartate
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beta-naphthamidine