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KYNURENIC ACID — II. PHOTOSENSITIZING PROPERTIES

Photochemistry and Photobiology, 1979
Abstract— The photosensitizing properties of kynurenic acid have been studied by 353 nm laser flash spectroscopy and steady state irradiations. Laser flash spectroscopy indicates that the kynurenic acid triplet is reduced by amino acids and nucleic acid bases. Photoreactions implying singlet oxygen formation are shown to occur.
Michel Giraud   +2 more
openaire   +2 more sources

Synthesis of New Substituted Kynurenic Acids

Organic Preparations and Procedures International, 2017
Kynurenic acid (4-hydroxyquinoline-2-carboxylic acid) and its derivatives play a crucial role in maintaining normal brain function.1 Several kynurenic acid derivatives containing halo, amino, hydro...
Ajoy K. Banerjee, William J. Vera
openaire   +2 more sources

Developmental changes in brain kynurenic acid concentrations

Developmental Brain Research, 1992
The cerebral distribution and regulation of excitatory amino acid levels may play a crucial role in neuronal development. In the present study we examined concentrations of the endogenous excitatory amino acid antagonist kynurenic acid and related substances during development in fetal and neonatal rat brain and fetal non-human primate cerebral cortex.
M. Flint Beal   +2 more
openaire   +3 more sources

Distribution, Synthesis, and Absorption of Kynurenic Acid in Plants

Planta Medica, 2010
Kynurenic acid (KYNA) is an endogenous antagonist of the ionotropic glutamate receptors and the α7 nicotinic acetylcholine receptor as well as an agonist of the G-protein-coupled receptor GPR35. In this study, KYNA distribution and synthesis in plants as well as its absorption was researched.
Michal P. Turski   +5 more
openaire   +2 more sources

Time-course of kynurenic acid concentration in mouse serum following the administration of a novel kynurenic acid analog

Journal of Pharmaceutical and Biomedical Analysis, 2011
The changes in concentration of kynurenic acid (KYNA) in different biological samples are of great interest in the pathomechanism and medication of several disorders, and especially those affecting the nervous system. Besides the recent pharmaceutical advances targeting the kynurenine pathway, there is a constant need for further drug development ...
Zádori Dénes   +7 more
openaire   +4 more sources

Tautomeric polymorphism of the neuroactive inhibitor kynurenic acid

Acta Crystallographica Section C Structural Chemistry, 2019
Kynurenic acid (KYN; systematic name: 4-hydroxyquinoline-2-carboxylic acid, C10H7NO3) displays a therapeutic effect in the treatment of some neurological diseases and is used as a broad-spectrum neuroprotective agent. However, it is understudied with respect to its solid-state chemistry and only one crystal form (α-KYN·H2O) has been reported up to now.
Jan Janczak   +4 more
openaire   +3 more sources

Neuroprotective potency of kynurenic acid against excitotoxicity

NeuroReport, 2000
The aim of this study was to determine in vivo which extracellular levels of kynurenic acid (KYNA) are required to control excessive NMDA receptor activation in the rat cortex. As excitotoxicity is coupled to marked ion movements, local depolarisations induced by perfusion of NMDA or quinolinic acid (QUIN) through microdialysis probes were recorded at ...
Jutta Urenjak, Tihomir P. Obrenovitch
openaire   +2 more sources

ON THE EXCRETION OF KYNURENIC ACID

American Journal of Physiology-Legacy Content, 1898
Holmes C. Jackson, Lafayette B. Mendel
openaire   +2 more sources

Kynurenic acid in ALS patients

Acta Neurologica Scandinavica, 2004
Joe Aoyagi   +10 more
openaire   +2 more sources

Endogenous Kynurenic Acid and Neurotoxicity

2014
Ewa M. Urbańska   +4 more
openaire   +3 more sources

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