Abstract
A series of N-(2-phenethyl)cinnamides was synthesized and assayed for antagonism at three N-methyl-D-asparate (NMDA) receptor subtypes (NR1A/2A-C). N-(2-(4-hydroxyphenyl)ethyl)-4-chlorocinnamide (6) was identified as a highly potent and selective antagonist of the NR1A/2B subtype.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cinnamates / chemistry
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Cinnamates / pharmacology*
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Excitatory Amino Acid Antagonists / chemistry
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Excitatory Amino Acid Antagonists / pharmacology*
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Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
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Structure-Activity Relationship
Substances
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Cinnamates
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Excitatory Amino Acid Antagonists
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N-(2-(hydroxyphenyl)ethyl)-4-chlorocinnamide
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Receptors, N-Methyl-D-Aspartate