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CHEBI:32761 - L-tyrosinate(2−)

ChEBI IDCHEBI:32761
ChEBI NameL-tyrosinate(2−)
Stars
ASCII NameL-tyrosinate(2-)
DefinitionThe L-enantiomer of tyrosinate(2−).
Last Modified9 July 2014
SubmitterKirill Degtyarenko
DownloadsMolfile
FormulaC9H9NO3
Net Charge-2
Average Mass179.175
Monoisotopic Mass179.05934
SMILESN[C@@H](Cc1ccc([O-])cc1)C(=O)[O-]
InChIInChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/p-2/t8-/m0/s1
InChIKeyOUYCCCASQSFEME-QMMMGPOBSA-L
Roles Classification
Biological Role:
fundamental metabolite  Any metabolite produced by all living cells.
ChEBI Ontology
Outgoing Relation(s)
L-tyrosinate(2−) (CHEBI:32761) has role fundamental metabolite (CHEBI:78675)
L-tyrosinate(2−) (CHEBI:32761) is a tyrosinate(2−) (CHEBI:32785)
L-tyrosinate(2−) (CHEBI:32761) is conjugate base of L-tyrosinate(1−) (CHEBI:32760)
L-tyrosinate(2−) (CHEBI:32761) is enantiomer of D-tyrosinate(2−) (CHEBI:32774)
Incoming Relation(s)
disodium L-tyrosinate (CHEBI:53696) has part L-tyrosinate(2−) (CHEBI:32761)
L-tyrosinate(1−) (CHEBI:32760) is conjugate acid of L-tyrosinate(2−) (CHEBI:32761)
D-tyrosinate(2−) (CHEBI:32774) is enantiomer of L-tyrosinate(2−) (CHEBI:32761)
IUPAC Name 
L-tyrosinate
Synonyms  Source
L-tyrosinate(2−)JCBN
L-tyrosine dianionJCBN
(2S)-2-amino-3-(4-oxidophenyl)propanoateIUPAC
Registry NumbersSources
Gmelin:364975Gmelin
Reaxys:5339596Reaxys