CHEBI:32716 - D-tryptophanate

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ChEBI Name D-tryptophanate ChEBI ID CHEBI:32716 ChEBI ASCII Name D-tryptophanate Definition The D-enantiomer of tryptophanate. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C11H11N2O2 Net Charge -1 Average Mass 203.21732 Monoisotopic Mass 203.08260 InChI InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/p-1/t9-/m1/s1 InChIKey QIVBCDIJIAJPQS-SECBINFHSA-M SMILES N[C@H](Cc1c[nH]c2ccccc12)C([O-])=O Roles Classification Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing D-tryptophanate (CHEBI:32716) has role bacterial metabolite (CHEBI:76969) D-tryptophanate (CHEBI:32716) is a tryptophanate (CHEBI:32727) D-tryptophanate (CHEBI:32716) is conjugate base of D-tryptophan (CHEBI:16296) D-tryptophanate (CHEBI:32716) is enantiomer of L-tryptophanate (CHEBI:32702) Incoming N-acetyl-D-tryptophanate (CHEBI:57877) has functional parent D-tryptophanate (CHEBI:32716) D-tryptophan (CHEBI:16296) is conjugate acid of D-tryptophanate (CHEBI:32716) L-tryptophanate (CHEBI:32702) is enantiomer of D-tryptophanate (CHEBI:32716) IUPAC Name D-tryptophanate Synonyms Sources (2R)-2-amino-3-(1H-indol-3-yl)propanoate IUPAC D-tryptophan anion JCBN Registry Numbers Types Sources 331344 Gmelin Registry Number Gmelin 6847890 Beilstein Registry Number Beilstein Last Modified 09 July 2014