Pharmacokinetic properties of enantiomerically pure GluN2B selective NMDA receptor antagonists with 3-benzazepine scaffold-Reference-Cited by-同舟云学术

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Pharmacokinetic properties of enantiomerically pure GluN2B selective NMDA receptor antagonists with 3-benzazepine scaffold

Published:2019-08 Issue: Volume:172 Page:214-222
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Börgel Frederik,Galla Fabian,Lehmkuhl Kirstin,Schepmann Dirk,Ametamey Simon M.,Wünsch Bernhard

Funder

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference50 articles.

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2. The history of the pharmacology and cloning of ionotropic glutamate receptors and the development of idiosyncratic nomenclature;Lodge;Neuropharmacology,2009

3. Molecular basis of NMDA receptor functional diversity;Paoletti;Eur. J. Neurosci.,2011

4. Glutamate receptor ion channels: structure, Regulation, and function;Traynelis;Pharmacol. Rev.,2010

5. NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease;Paoletti;Nat. Rev. Neurosci.,2013

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