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[1. The product of the oxidative cleavage of the indole ring in l-tryptophan; the intermediate first formed in l-tryptophan catabolism.
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pre_formula( "InChI=1/C11H12N2O4/c12-8(11(16)17)5-10(15)7-3-1-2-4-9(7)13-6-14/h1-4,6,8H,5,12H2,(H,13,14)(H,16,17)/t8-/m0/s1/f/h13,16H", "jqp067/439788.html" ); ?>
Molecular Formula:
C11H12N2O4
InChI: InChI=1/C11H12N2O4/c12-8(11(16)17)5-10(15)7-3-1-2-4-9(7)13-6-14/h1-4,6,8H,5,12H2,(H,13,14)(H,16,17)/t8-/m0/s1/f/h13,16H
InChIKey: InChIKey=BYHJHXPTQMMKCA-YXZQDHJZDZ
SMILES: [H]C(=O)Nc1ccccc1C(=O)C[C@H](N)C(O)=O
Names:
L-Formylkynurenine
L-formylkynurenine
N'-formylkynurenine
N-Formylkynurenine
N-formylkynurenine
N-Formyl-L-kynurenine
N-formyl-L-kynurenine
(2S)-2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid
3-(2-formamidobenzoyl)-L-alanine
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Registries:
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PubChem CID 439788
ChEBI 30249
Kegg C02700
PubChem ID 10298469
PubChem ID 5664
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