Synthesis of Tricyclic Indole-2-caboxylic Acids as Potent NMDA-Glycine Antagonists
Author:
Affiliation:
1. Research Division, Sumitomo Pharmaceuticals Co., Ltd, 1−98 Kasugadenaka 3-chome, Konohana-ku, Osaka 554-0022, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo010002h
Reference34 articles.
1. Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders
2. Attenuation of nociceptive responses by ACEA-1021, a competitive NMDA receptor/glycine site antagonist, in the mice
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