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CHEBI:32511 - L-histidinate(2−)

ChEBI IDCHEBI:32511
ChEBI NameL-histidinate(2−)
Stars
ASCII NameL-histidinate(2-)
DefinitionThe L-enantiomer of histidinate(2−).
Last Modified11 November 2014
SubmitterKirill Degtyarenko
DownloadsMolfile
FormulaC6H7N3O2
Net Charge-2
Average Mass153.141
Monoisotopic Mass153.05492
SMILESN[C@@H](Cc1c[n-]cn1)C(=O)[O-]
InChIInChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H2,8,9,10,11)/p-2/t5-/m0/s1
InChIKeyTWRZMXZXJKNOLO-YFKPBYRVSA-L
Species of MetaboliteComponentSourceComments
Escherichia coli (ncbitaxon:562) - PubMed (8852895)
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (8852895)
Roles Classification
Biological Roles:
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
ChEBI Ontology
Outgoing Relation(s)
L-histidinate(2−) (CHEBI:32511) has role Escherichia coli metabolite (CHEBI:76971)
L-histidinate(2−) (CHEBI:32511) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-histidinate(2−) (CHEBI:32511) is a histidinate(2−) (CHEBI:32530)
L-histidinate(2−) (CHEBI:32511) is conjugate base of L-histidinate(1−) (CHEBI:32510)
L-histidinate(2−) (CHEBI:32511) is enantiomer of D-histidinate(2−) (CHEBI:32524)
Incoming Relation(s)
L-histidinate(1−) (CHEBI:32510) is conjugate acid of L-histidinate(2−) (CHEBI:32511)
D-histidinate(2−) (CHEBI:32524) is enantiomer of L-histidinate(2−) (CHEBI:32511)
IUPAC Name 
L-histidinate
Synonyms  Source
(2S)-2-amino-3-imidazol-1-id-4-ylpropanoateIUPAC
L-histidinate(2−)JCBN
L-histidine dianionJCBN
Registry NumbersSources
Gmelin:364419Gmelin
Reaxys:5436298Reaxys