CHEBI:27570 - histidine

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ChEBI Name histidine
Definition An α-amino acid that is propanoic acid bearing an amino substituent at position 2 and a 1H-imidazol-4-yl group at position 3.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:24598, CHEBI:43118, CHEBI:5733
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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)
SMILES NC(Cc1c[nH]cn1)C(O)=O
Metabolite of Species Details
Daphnia magna (NCBI:txid35525) See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyond Tine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De Coen Environment International 36 (2010) 254-268
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing histidine (CHEBI:27570) has part 1H-imidazol-4-ylmethyl group (CHEBI:50338)
histidine (CHEBI:27570) has role metabolite (CHEBI:25212)
histidine (CHEBI:27570) is a α-amino acid (CHEBI:33704)
histidine (CHEBI:27570) is a imidazoles (CHEBI:24780)
histidine (CHEBI:27570) is conjugate acid of histidinate(1−) (CHEBI:32529)
histidine (CHEBI:27570) is conjugate base of histidinium(1+) (CHEBI:32531)
Incoming α-methylhistidine (CHEBI:70960) has functional parent histidine (CHEBI:27570)
histidine derivative (CHEBI:24599) has functional parent histidine (CHEBI:27570)
D-histidine (CHEBI:27947) is a histidine (CHEBI:27570)
L-histidine (CHEBI:15971) is a histidine (CHEBI:27570)
histidinium(1+) (CHEBI:32531) is conjugate acid of histidine (CHEBI:27570)
histidinate(1−) (CHEBI:32529) is conjugate base of histidine (CHEBI:27570)
Nπ-histidino group (CHEBI:32533) is substituent group from histidine (CHEBI:27570)
Nτ-histidino group (CHEBI:32534) is substituent group from histidine (CHEBI:27570)
N2-histidino group (CHEBI:24601) is substituent group from histidine (CHEBI:27570)
histidine residue (CHEBI:32535) is substituent group from histidine (CHEBI:27570)
histidyl group (CHEBI:37906) is substituent group from histidine (CHEBI:27570)
2-amino-3-(1H-imidazol-4-yl)propanoic acid
Synonyms Sources
alpha-Amino-1H-imidazole-4-propionic acid KEGG COMPOUND
Histidin ChEBI
histidina ChEBI
Database Links Databases
C00001363 KNApSAcK
Histidine Wikipedia
View more database links
Registry Numbers Types Sources
3656 Gmelin Registry Number Gmelin
4998-57-6 CAS Registry Number ChemIDplus
84087 Reaxys Registry Number Reaxys
84087 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
17190852 PubMed citation Europe PMC
22264337 PubMed citation Europe PMC
22770225 PubMed citation Europe PMC
29286160 PubMed citation Europe PMC
Last Modified
09 February 2018