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A review of chromatographic methods for bioactive tryptophan metabolites, kynurenine, kynurenic acid, quinolinic acid, and others, in biological fluids.

Biomedical chromotography, 2022
sKynurenine (KYN) is synthesized from an essential amino acid, tryptophan by tryptophan 2,3-dioxygenase or indoleamine 2,3-dioxygenase via N-formyl- KYN in vivo. Subsequently, KYN acts as a precursor of some neuroactive metabolites such as kynurenic acid,
T. Fukushima   +3 more
semanticscholar   +1 more source

Quinoline-4-carboxylic Acid [PDF]

open access: possibleActa Crystallographica Section C Crystal Structure Communications, 1998
The title acid, C10H7NO2, crystallized in the centrosymmetric space group P2(1)/c with one molecule in the asymmetric unit. There is a single hydrogen bond. O-H...N, with a donor-acceptor distance of 2.596 (1) A. The carboxylic H atom is ordered. The dihedral angle between the best-fit quinoline core plane and the carboxyl plane is 45.9 (1) degrees ...
Amonette, Allison J., Gerkin, Roger E.
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A radioenzymatic assay for quinolinic acid

Analytical Biochemistry, 1986
A new and rapid method for the determination of the excitotoxic tryptophan metabolite quinolinic acid is based on its enzymatic conversion to nicotinic acid mononucleotide and, in a second step utilizing [3H]ATP, further to [3H] deamido-NAD. Specificity of the assay is assured by using a highly purified preparation of the specific quinolinic acid ...
Daniel S. Brougher   +3 more
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Brain quinolinic acid in Alzheimer's dementia

European Archives of Psychiatry and Neurological Sciences, 1989
Quinolinic acid (QA) content was measured in postmortem frontal and temporal cortex, putamen and cerebellum obtained from patients with senile dementia of Alzheimer type (SDAT), Huntington's disease (HD) and controls, using a gas chromatography/mass spectrometry method.
Peter Riederer   +6 more
openaire   +4 more sources

Inhibition of quinolinate phosphoribosyl transferase by pyridine analogs of quinolinic acid

Biochemical and Biophysical Research Communications, 1988
The enzyme quinolinate phosphoribosyl transferase was purified from ATCC strain 23269. An HPLC method was developed for the analysis of the product of the enzyme reaction, nicotinate mononucleotide. Steady state kinetics in the forward reaction demonstrated a sequential mechanism for the enzyme. In order to gain more information on the mechanism of the
Linda Kalikin, K.C. Calvo
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The Crystal Structure of Quinolinic Acid

Bulletin of the Chemical Society of Japan, 1973
Abstract The crystal structure of quinolinic acid (2,3-pyridinedicarboxylic acid) has been determined by the method of X-ray diffraction. The crystal is monoclinic, with a space group of P21/c and with cell dimensions of a=7.421, b=12.729, c=7.850 Å, and β=116.96°.
Akira Shimada   +2 more
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ChemInform Abstract: Bromodecarboxylation of Quinoline Salicylic Acids: Increasing the Diversity of Accessible Substituted Quinolines. [PDF]

open access: possibleChemInform, 2009
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Neelu Kaila, Kristin Janz
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