N-Hydroxypyrazolyl Glycine Derivatives as Selective N-Methyl-d-aspartic Acid Receptor Ligands-Reference-Cited by-同舟云学术

N-Hydroxypyrazolyl Glycine Derivatives as Selective N-Methyl-d-aspartic Acid Receptor Ligands

Published:2008-06-25 Issue:14 Volume:51 Page:4179-4187
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Clausen Rasmus P.¹,Christensen Caspar¹,Hansen Kasper B.¹,Greenwood Jeremy R.¹,Micale Nicola¹,Madsen Jens Christian¹,Nielsen Birgitte¹,Egebjerg Jan¹,Bräuner-Osborne Hans¹,Traynelis Stephen F.¹,Kristensen Jesper L.¹

Affiliation:

1. Department of Medicinal Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, 2 Universitetsparken, DK-2100 Copenhagen, Denmark, Department of Pharmacology, Emory University School of Medicine, Rollins Research Center, Atlanta, Georgia, Department of Medicinal Chemistry and Department of Molecular Neurobiology, H. Lundbeck A/S, 9 Ottiliavej, DK-2500 Valby, Denmark

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm800025e

Reference39 articles.

1. Ligands for Glutamate Receptors: Design and Therapeutic Prospects

2. Glutamate Receptor Gating

3. Glutamate receptor function in learning and memory

4. Glutamate as a therapeutic target in psychiatric disorders

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Electrocatalytic three-component synthesis of 4-halopyrazoles with sodium halide as the halogen source;Organic & Biomolecular Chemistry;2022

2. A convenient approach for the electrochemical bromination and iodination of pyrazoles;Zeitschrift für Naturforschung B;2021-12-10

3. Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels;Pharmacological Reviews;2021-10

4. Recent Developments in the Practical Application of Novel Carboxylic Acid Bioisosteres;Current Medicinal Chemistry;2021-08-20

5. Stereoselective synthesis of novel 2′-(S)-CCG-IV analogues as potent NMDA receptor agonists;European Journal of Medicinal Chemistry;2021-02