Glycine and N-methyl-D-aspartate receptors: physiological significance and possible therapeutic applications

W Danysz, CG Parsons - Pharmacological reviews, 1998 - ASPET
Since the finding by Johnson and Ascher (1987) demonstrating that glycine enhances
electrophysiological responses mediated by N-methyl-D-aspartate (NMDA) b

Quinoxalines, Volume 61, Spplement 2

DJ Brown, EC Taylor, JA Ellman - 2004 - books.google.com
This volume in the Chemistry of Heterocyclic Compounds series presents a comprehensive
review of the quinoxaline literature from 1975 to the present (2002), updating Volumes 5 and …

Effect of plasma protein binding on in vivo activity and brain penetration of glycine/NMDA receptor antagonists

M Rowley, JJ Kulagowski, AP Watt… - Journal of medicinal …, 1997 - ACS Publications
A major issue in designing drugs as antagonists at the glycine site of the NMDA receptor has
been to achieve good in vivo activity. A series of 4-hydroxyquinolone glycine antagonists …

Synthesis, Antimicrobial and Antibiofilm Activities, and Molecular Docking Investigations of 2-(1H-Indol-3-yl)-1H-benzo[d]imidazole Derivatives

EY Mendogralo, LY Nesterova, ER Nasibullina… - Molecules, 2023 - mdpi.com
The treatment of many bacterial and fungal infections remains a problem due to increasing
antibiotic resistance and biofilm formation by pathogens. In the present article, a …

Synthesis, ionisation potentials and electron affinities of hexaazatrinaphthylene derivatives

S Barlow, Q Zhang, BR Kaafarani… - … A European Journal, 2007 - Wiley Online Library
Several hexaazatrinaphthylene derivatives and a tris (thieno) hexaazatriphenylene
derivative have been synthesised by reaction of the appropriate diamines with …

A review on multipurpose potential of bioactive heterocycle quinoxaline

G Chawla, O Gupta, T Pradhan - ChemistrySelect, 2023 - Wiley Online Library
In last few decades, nitrogen‐containing heterocycles have maintained their status as an
important core of FDA‐approved drugs and medicinally active compounds. Quinoxaline is …

Structure−Activity Relationships of 1,4-Dihydro-(1H,4H)-quinoxaline-2,3-diones as N-Methyl-d-aspartate (Glycine Site) Receptor Antagonists. 1. Heterocyclic …

MJ Fray, DJ Bull, CL Carr, ECL Gautier… - Journal of medicinal …, 2001 - ACS Publications
A series of 6, 7-dichloro-1, 4-dihydro-(1H, 4H)-quinoxaline-2, 3-diones (1− 17) were
prepared in which the 5-position substituent was a heterocyclylmethyl or 1-(heterocyclyl)-1 …

Antinociceptive effects of NMDA and non-NMDA receptor antagonists in the tail flick test in mice

K Lutfy, SX Cai, RM Woodward, E Weber - Pain, 1997 - Elsevier
Inhibition of spinal glutamate receptors induces antinociceptive effects in numerous animal
models of pain. The present study compares the effects of intrathecally administered N …

Preventing neuronal degeneration in Alzheimer's disease

JW Olney, NB Farber - US Patent 5,877,173, 1999 - Google Patents
US5877173A - Preventing neuronal degeneration in Alzheimer's disease - Google Patents
US5877173A - Preventing neuronal degeneration in Alzheimer's disease - Google Patents …

Long‐Wavelength‐Absorbing and‐Emitting Carbostyrils with High Fluorescence Quantum Yields

G Uray, KS Niederreiter, F Belaj… - Helvetica Chimica …, 1999 - Wiley Online Library
Synthesis, absorption and fluorescence spectra, as well as quantum yields of a series of
donor‐acceptor‐substituted carbostyrils (= quinolin‐2 (1H)‐ones), are reported …