CHEBI:32510 - L-histidinate(1−)

ChEBI IDCHEBI:32510
ChEBI NameL-histidinate(1−)
Stars
ASCII NameL-histidinate(1-)
DefinitionThe L-enantiomer of histidinate(1−),
Last Modified11 November 2014
SubmitterKirill Degtyarenko
DownloadsMolfile
FormulaC6H8N3O2
Net Charge-1
Average Mass154.149
Monoisotopic Mass154.06220
SMILESN[C@@H](Cc1cncn1)C(=O)[O-]
InChIInChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/p-1/t5-/m0/s1
InChIKeyHNDVDQJCIGZPNO-YFKPBYRVSA-M
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(1−) (CHEBI:32510) has role Escherichia coli metabolite (CHEBI:76971)
L-histidinate(1−) (CHEBI:32510) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-histidinate(1−) (CHEBI:32510) is a histidinate(1−) (CHEBI:32529)
L-histidinate(1−) (CHEBI:32510) is conjugate acid of L-histidinate(2−) (CHEBI:32511)
L-histidinate(1−) (CHEBI:32510) is conjugate base of L-histidine (CHEBI:15971)
L-histidinate(1−) (CHEBI:32510) is enantiomer of D-histidinate(1−) (CHEBI:32523)
Incoming Relation(s)
L-histidine (CHEBI:15971) is conjugate acid of L-histidinate(1−) (CHEBI:32510)
L-histidinate(2−) (CHEBI:32511) is conjugate base of L-histidinate(1−) (CHEBI:32510)
D-histidinate(1−) (CHEBI:32523) is enantiomer of L-histidinate(1−) (CHEBI:32510)
IUPAC Name 
hydrogen L-histidinate
Synonyms  Source
(2S)-2-amino-3-(1H-imidazol-4-yl)propanoateIUPAC
L-histidinate(1−)JCBN
L-histidine anionNIST Chemistry WebBook
L-histidine monoanionJCBN
Registry NumbersSources
Gmelin:328379Gmelin
Reaxys:5434027Reaxys