CHEBI:32524 - D-histidinate(2−)

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-histidinate(2−)
ChEBI ID CHEBI:32524
ChEBI ASCII Name D-histidinate(2-)
Definition The D-enantiomer of histidinate(2−).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H7N3O2
Net Charge -2
Average Mass 153.13880
Monoisotopic Mass 153.05492
InChI InChI=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
InChIKey TWRZMXZXJKNOLO-RXMQYKEDSA-L
SMILES N[C@H](Cc1c[n-]cn1)C([O-])=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 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 Sources
(2R)-2-amino-3-imidazol-1-id-4-ylpropanoate IUPAC
D-histidinate(2−) JCBN
D-histidine dianion JCBN
Last Modified
11 November 2014