Parallel Synthesis Of A Series Of Subtype-Selective Nmda Receptor Antagonists

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS(2000)

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摘要
A series of 1-(heteroarylthioalkyl)-4-benzylpiperidines was rapidly synthesized through the use of parallel synthesis to investigate the binding affinity for the NR1A/2B receptor subtype. (C) 2000 Published by Elsevier Science Ltd. All rights reserved.
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关键词
nmda receptor antagonist,binding affinity
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