CHEBI:32761 - L-tyrosinate(2−)

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ChEBI Name L-tyrosinate(2−)
ChEBI ID CHEBI:32761
ChEBI ASCII Name L-tyrosinate(2-)
Definition The L-enantiomer of tyrosinate(2−).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C9H9NO3
Net Charge -2
Average Mass 179.17270
Monoisotopic Mass 179.05934
InChI InChI=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
InChIKey OUYCCCASQSFEME-QMMMGPOBSA-L
SMILES N[C@@H](Cc1ccc([O-])cc1)C([O-])=O
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
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ChEBI Ontology
Outgoing 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 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 Sources
(2S)-2-amino-3-(4-oxidophenyl)propanoate IUPAC
L-tyrosinate(2−) JCBN
L-tyrosine dianion JCBN
Registry Numbers Types Sources
364975 Gmelin Registry Number Gmelin
5339596 Beilstein Registry Number Beilstein
5339596 Reaxys Registry Number Reaxys
Last Modified
09 July 2014