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CHEBI:32523 - D-histidinate(1−)

ChEBI IDCHEBI:32523
ChEBI NameD-histidinate(1−)
Stars
ASCII NameD-histidinate(1-)
DefinitionThe D-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-/m1/s1
InChIKeyHNDVDQJCIGZPNO-RXMQYKEDSA-M
Species of MetaboliteComponentSourceComments
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (15744050)
Roles Classification
Biological Role:
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
ChEBI Ontology
Outgoing Relation(s)
D-histidinate(1−) (CHEBI:32523) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
D-histidinate(1−) (CHEBI:32523) is a histidinate(1−) (CHEBI:32529)
D-histidinate(1−) (CHEBI:32523) is conjugate acid of D-histidinate(2−) (CHEBI:32524)
D-histidinate(1−) (CHEBI:32523) is conjugate base of D-histidine (CHEBI:27947)
D-histidinate(1−) (CHEBI:32523) is enantiomer of L-histidinate(1−) (CHEBI:32510)
Incoming Relation(s)
D-histidine (CHEBI:27947) is conjugate acid of D-histidinate(1−) (CHEBI:32523)
D-histidinate(2−) (CHEBI:32524) is conjugate base of D-histidinate(1−) (CHEBI:32523)
L-histidinate(1−) (CHEBI:32510) is enantiomer of D-histidinate(1−) (CHEBI:32523)
IUPAC Name 
hydrogen D-histidinate
Synonyms  Source
D-histidinate(1−)JCBN
D-histidine monoanionJCBN
(2R)-2-amino-3-(1H-imidazol-4-yl)propanoateIUPAC
Registry NumbersSources
Beilstein:7251557Beilstein
Gmelin:774476Gmelin