Tricyclic Indole-2-carboxylic Acids: Highly in Vivo Active and Selective Antagonists for the Glycine Binding Site of the NMDA Receptor-Reference-Cited by-同舟云学术

Tricyclic Indole-2-carboxylic Acids: Highly in Vivo Active and Selective Antagonists for the Glycine Binding Site of the NMDA Receptor

Published:2003-01-24 Issue:5 Volume:46 Page:691-701
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Katayama Seiji¹,Ae Nobuyuki¹,Kodo Toru¹,Masumoto Shuji¹,Hourai Shinji¹,Tamamura Chika¹,Tanaka Hiroyasu¹,Nagata Ryu¹

Affiliation:

1. Research Division, Sumitomo Pharmaceuticals Co., Ltd, 1-98 Kasugadenaka 3-chome, Konohana-ku, Osaka 554-0022, Japan, and Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd, 4-2-1 Takatsukasa, Takarazuka, Hyogo 665-8555, Japan

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm020239l

Reference50 articles.

1. British higher education in the 1990s

2. Requirement for Glycine in Activation of NMDA-Receptors Expressed in Xenopus Oocytes

3. Therapeutic potential of excitatory amino acid antagonists: channel blockers and 2,3-benzodiazepines

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