Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: The Role of 4-Methyl versus 4-Carbonyl Group on the Diazepine Ring of 2,3-Benzodiazepine Derivatives-Reference-Cited by-同舟云学术

Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: The Role of 4-Methyl versus 4-Carbonyl Group on the Diazepine Ring of 2,3-Benzodiazepine Derivatives

Published:2011-05-25 Issue:9 Volume:2 Page:506-513
ISSN:1948-7193
Container-title:ACS Chemical Neuroscience
language:en
Short-container-title:ACS Chem. Neurosci.

Author:

Ritz Mark¹,Wang Congzhou¹,Micale Nicola²,Ettari Roberta²,Niu Li¹

Affiliation:

1. Department of Chemistry, and Center for Neuroscience Research, University at Albany, SUNY, Albany, New York 12222, United States

2. Dipartimento Farmaco-Chimico, Università di Messina, viale Annunziata, 98168 Messina, Italy

Publisher

American Chemical Society (ACS)

Subject

Cell Biology,Cognitive Neuroscience,Physiology,Biochemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/cn200033j

Reference28 articles.

1. The Molecular Pharmacology and Cell Biology of α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors

2. Quinoxalinediones: Potent Competitive Non-NMDA Glutamate Receptor Antagonists

3. ZK200775: A phosphonate quinoxalinedione AMPA antagonist for neuroprotection in stroke and trauma

4. synthesis and Structure-Activity Relationships of 2,3-Benzodiazepines as AMPA Receptor Antagonists

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