42798 <common-name>Kynurenine</common-name> <description>Kynurenine is an organic compound with the chemical formula C10H12N2O3 and an average molecular weight of 208.21 g/mol. Kynurenine belongs to the carbonyl compounds, a subclass of organooxygen compounds within the organic compounds. It is categorized under the superclass of organic oxygen compounds and the class of organooxygen compounds. This substance is found in or released from one recorded source, which is electrical and electronic equipment specifically antennas.</description> <cas>2922-83-0</cas> <pubchem-id>846</pubchem-id> <chemical-formula>C10H12N2O3</chemical-formula> <weight nil="true"/> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2016-05-27T01:39:19Z</created-at> <updated-at type="dateTime">2026-05-14T17:26:20Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id>DB02070</drugbank-id> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>NC(CC(=O)C1=CC=CC=C1N)C(O)=O</moldb-smiles> <moldb-formula>C10H12N2O3</moldb-formula> <moldb-inchi>InChI=1S/C10H12N2O3/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15/h1-4,8H,5,11-12H2,(H,14,15)</moldb-inchi> <moldb-inchikey>YGPSJZOEDVAXAB-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">208.2139</moldb-average-mass> <moldb-mono-mass type="decimal">208.08479226</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>-1.9</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM041693</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00074151</susdat-id> <iupac>(2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid</iupac> <moldb-polar-surface-area>106.41000000000001</moldb-polar-surface-area> <moldb-refractivity>55.050200000000004</moldb-refractivity> <moldb-polarizability>20.591144970696817</moldb-polarizability> <moldb-rotatable-bond-count>4</moldb-rotatable-bond-count> <moldb-acceptor-count>5</moldb-acceptor-count> <moldb-donor-count>3</moldb-donor-count> <moldb-pka-strongest-acidic>1.193089749657625</moldb-pka-strongest-acidic> <moldb-pka-strongest-basic>8.96449885088756</moldb-pka-strongest-basic> <moldb-physiological-charge>0</moldb-physiological-charge> <moldb-number-of-rings>1</moldb-number-of-rings> <moldb-alogps-logp>-1.93</moldb-alogps-logp> <moldb-alogps-logs>-2.10</moldb-alogps-logs> <moldb-alogps-solubility>1.67e+00 g/l</moldb-alogps-solubility> <kingdom>Organic compounds</kingdom> <superklass>Organic oxygen compounds</superklass> <klass>Organooxygen compounds</klass> <subklass>Carbonyl compounds</subklass> <paper-count type="integer">35881</paper-count> <sync-id>CED0001665</sync-id> <structure-inchikey>YGPSJZOEDVAXAB-UHFFFAOYSA-N</structure-inchikey> 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type="dateTime">2026-09-19T04:11:22Z</structure-indexed-at> </compound>