CHEBI:27947 - D-histidine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-histidine
ChEBI ID CHEBI:27947
ChEBI ASCII Name D-histidine
Definition An optically active form of histidine having D-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:42063, CHEBI:4197, CHEBI:21039
Supplier Information
Download Molfile XML SDF
Formula C6H9N3O2
Net Charge 0
Average Mass 155.15468
Monoisotopic Mass 155.069
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)/t5-/m1/s1
InChIKey HNDVDQJCIGZPNO-RXMQYKEDSA-N
SMILES N[C@H](Cc1c[nH]cn1)C(O)=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via histidine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-histidine (CHEBI:27947) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
D-histidine (CHEBI:27947) is a D-α-amino acid (CHEBI:16733)
D-histidine (CHEBI:27947) is a histidine (CHEBI:27570)
D-histidine (CHEBI:27947) is conjugate acid of D-histidinate(1−) (CHEBI:32523)
D-histidine (CHEBI:27947) is conjugate base of D-histidinium(1+) (CHEBI:32526)
D-histidine (CHEBI:27947) is enantiomer of L-histidine (CHEBI:15971)
Incoming D-histidine derivative (CHEBI:84077) has functional parent D-histidine (CHEBI:27947)
D-histidinium(1+) (CHEBI:32526) is conjugate acid of D-histidine (CHEBI:27947)
D-histidinate(1−) (CHEBI:32523) is conjugate base of D-histidine (CHEBI:27947)
L-histidine (CHEBI:15971) is enantiomer of D-histidine (CHEBI:27947)
Nπ-D-histidino group (CHEBI:32520) is substituent group from D-histidine (CHEBI:27947)
Nτ-D-histidino group (CHEBI:32521) is substituent group from D-histidine (CHEBI:27947)
N2-D-histidino group (CHEBI:32518) is substituent group from D-histidine (CHEBI:27947)
D-histidine residue (CHEBI:29980) is substituent group from D-histidine (CHEBI:27947)
D-histidyl group (CHEBI:32522) is substituent group from D-histidine (CHEBI:27947)
IUPAC Names
(2R)-2-amino-3-(1H-imidazol-4-yl)propanoic acid
D-histidine
Synonyms Sources
(R)-alpha-Amino-1H-imidazole-4-propionic acid KEGG COMPOUND
D-Histidin ChEBI
D-Histidine KEGG COMPOUND
D-HISTIDINE PDBeChem
DHI PDBeChem
Manual Xrefs Databases
C06419 KEGG COMPOUND
CPD-12151 MetaCyc
DHI PDBeChem
YMDB00794 YMDB
View more database links
Registry Numbers Types Sources
351-50-8 CAS Registry Number KEGG COMPOUND
351-50-8 CAS Registry Number ChemIDplus
83043 Gmelin Registry Number Gmelin
84089 Reaxys Registry Number Reaxys
84089 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
15744050 PubMed citation Europe PMC
24852066 PubMed citation Europe PMC
80988 PubMed citation Europe PMC
Last Modified
14 September 2015