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CHEBI:32524 - D-histidinate(2−)

ChEBI IDCHEBI:32524
ChEBI NameD-histidinate(2−)
Stars
ASCII NameD-histidinate(2-)
DefinitionThe D-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-/m1/s1
InChIKeyTWRZMXZXJKNOLO-RXMQYKEDSA-L
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(2−) (CHEBI:32524) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
D-histidinate(2−) (CHEBI:32524) is a histidinate(2−) (CHEBI:32530)
D-histidinate(2−) (CHEBI:32524) is conjugate base of D-histidinate(1−) (CHEBI:32523)
D-histidinate(2−) (CHEBI:32524) is enantiomer of L-histidinate(2−) (CHEBI:32511)
Incoming Relation(s)
D-histidinate(1−) (CHEBI:32523) is conjugate acid of D-histidinate(2−) (CHEBI:32524)
L-histidinate(2−) (CHEBI:32511) is enantiomer of D-histidinate(2−) (CHEBI:32524)
Synonyms  Source
D-histidinate(2−)JCBN
(2R)-2-amino-3-imidazol-1-id-4-ylpropanoateIUPAC
D-histidine dianionJCBN