CHEBI:32510 - L-histidinate(1−)

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ChEBI Name L-histidinate(1−)
ChEBI ID CHEBI:32510
ChEBI ASCII Name L-histidinate(1-)
Definition The L-enantiomer of histidinate(1−),
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H8N3O2
Net Charge -1
Average Mass 154.14660
Monoisotopic Mass 154.06220
InChI InChI=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
InChIKey HNDVDQJCIGZPNO-YFKPBYRVSA-M
SMILES N[C@@H](Cc1c[nH]cn1)C([O-])=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Biological Role(s): 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 ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 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 Sources
(2S)-2-amino-3-(1H-imidazol-4-yl)propanoate IUPAC
L-histidinate(1−) JCBN
L-histidine anion NIST Chemistry WebBook
L-histidine monoanion JCBN
Registry Numbers Types Sources
328379 Gmelin Registry Number Gmelin
5434027 Beilstein Registry Number Beilstein
5434027 Reaxys Registry Number Reaxys
Last Modified
11 November 2014