Tryptophan metabolism through the kynurenine pathway in rat brain and liver slices

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Human macrophages convert <scp>l</scp>-tryptophan into the neurotoxin quinolinic acid Melvyn P. Heyes, Kuniaki Saito, Sanford P. Markey Biochemical Journal Immune ActivationImmunologyNeurotoxin Quinolinic AcidNeuroinflammationInflammation	1992	448
1-methyl-dl-tryptophan, β-(3-benzofuranyl)-dl-alanine (the oxygen analog of tryptophan), and β-[3-benzo(b)thienyl]-dl-alanine (the sulfur analog of tryptophan) are competitive inhibitors for indoleamine 2,3-dioxygenase Susan G. Cady, Masanori Sono Archives of Biochemistry and Biophysics Medicinal ChemistryBiochemistryMedicineNatural SciencesCompetitive Inhibitors	1991	281
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Rat Brain Slices Produce and Liberate Kynurenic Acid upon Exposure to <scp>l</scp>‐Kynurenine Waldemar A. Turski, Jan Bert Gramsbergen, Helmut Traitler, Journal of Neurochemistry	1989	217
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