CHEBI:28050 - homocarnosine

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ChEBI Name homocarnosine
ChEBI ID CHEBI:28050
Definition A histidine derivative that is histidine in which one of the hydrogens attached to the α-amino group has been replaced by a 4-aminobutanoyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:24607, CHEBI:5750
Supplier Information
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Formula C10H16N4O3
Net Charge 0
Average Mass 240.25900
Monoisotopic Mass 240.12224
InChI InChI=1S/C10H16N4O3/c11-3-1-2-9(15)14-8(10(16)17)4-7-5-12-6-13-7/h5-6,8H,1-4,11H2,(H,12,13)(H,14,15)(H,16,17)
InChIKey CCLQKVKJOGVQLU-UHFFFAOYSA-N
SMILES NCCCC(=O)NC(Cc1c[nH]cn1)C(O)=O
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.
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ChEBI Ontology
Outgoing homocarnosine (CHEBI:28050) has functional parent γ-aminobutyric acid (CHEBI:16865)
homocarnosine (CHEBI:28050) has role metabolite (CHEBI:25212)
homocarnosine (CHEBI:28050) is a N-acyl-amino acid (CHEBI:51569)
homocarnosine (CHEBI:28050) is a histidine derivative (CHEBI:24599)
homocarnosine (CHEBI:28050) is a imidazoles (CHEBI:24780)
Incoming L-homocarnosine (CHEBI:85981) is a homocarnosine (CHEBI:28050)
IUPAC Name
N-(4-aminobutanoyl)histidine
Synonyms Sources
gamma-Aminobutyryl histidine KEGG COMPOUND
N-(4-aminobutyryl)histidine ChEBI
Registry Number Type Source
11612459 Reaxys Registry Number Reaxys
Last Modified
10 June 2015