Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: Consequences of Adding an N-3 Methylcarbamoyl Group to the Diazepine Ring of 2,3-Benzodiazepine Derivatives
Author:
Affiliation:
1. Department of Chemistry, and Center for Neuroscience Research, University at Albany, SUNY, Albany, New York 12222, United States
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi2007977
Reference26 articles.
1. Mechanism of Inhibition of the GluR2 AMPA Receptor Channel Opening by 2,3-Benzodiazepine Derivatives
2. Ritz, M., Wang, C. Z., Micale, N., Ettari, R., and Niu, L.Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: the Role of 4-Methylversus4-Carbonyl Group on the Diazepine Ring of 2,3-Benzodiazepine Derivatives.ACS Chem. Neurosci. 2011, in press.
3. Differentiation of kainate and quisqualate receptors in the cat spinal cord by selective antagonism with γ-D(and L)-glutamylglycine
4. The Molecular Pharmacology and Cell Biology of α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors
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