CHEBI:15760 - tyramine

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ChEBI Name tyramine
ChEBI ID CHEBI:15760
Definition A primary amino compound obtained by formal decarboxylation of the amino acid tyrosine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:9799, CHEBI:15276, CHEBI:27174
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Formula C8H11NO
Net Charge 0
Average Mass 137.17900
Monoisotopic Mass 137.08406
InChI InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2
InChIKey DZGWFCGJZKJUFP-UHFFFAOYSA-N
SMILES NCCc1ccc(O)cc1
Metabolite of Species Details
Solanum campaniforme (IPNI:818569-1) Found in leaf (BTO:0000713). Dried leaves were extracted with ethyl alcohol. See: PubMed
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:txid562) 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 )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
EC 3.1.1.8 (cholinesterase) inhibitor
An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of cholinesterase (EC 3.1.1.8).
neurotransmitter
An endogenous compound that is used to transmit information across the synapse between a neuron and another cell.
molecular messenger

(via monoamine molecular messenger )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing tyramine (CHEBI:15760) has role Escherichia coli metabolite (CHEBI:76971)
tyramine (CHEBI:15760) has role EC 3.1.1.8 (cholinesterase) inhibitor (CHEBI:37733)
tyramine (CHEBI:15760) has role human metabolite (CHEBI:77746)
tyramine (CHEBI:15760) has role mouse metabolite (CHEBI:75771)
tyramine (CHEBI:15760) has role neurotransmitter (CHEBI:25512)
tyramine (CHEBI:15760) is a monoamine molecular messenger (CHEBI:25375)
tyramine (CHEBI:15760) is a primary amino compound (CHEBI:50994)
tyramine (CHEBI:15760) is a tyramines (CHEBI:27175)
tyramine (CHEBI:15760) is conjugate base of tyraminium (CHEBI:327995)
Incoming γ-glutamyltyramine (CHEBI:84215) has functional parent tyramine (CHEBI:15760)
3-nitrotyramine (CHEBI:71233) has functional parent tyramine (CHEBI:15760)
N,O-dimethyltyramine (CHEBI:75143) has functional parent tyramine (CHEBI:15760)
N-trans-cinnamoyltyramine (CHEBI:177872) has functional parent tyramine (CHEBI:15760)
N-acetyltyramine (CHEBI:125610) has functional parent tyramine (CHEBI:15760)
N-butanoyltyramine (CHEBI:166900) has functional parent tyramine (CHEBI:15760)
N-hexanoyltyramine (CHEBI:166901) has functional parent tyramine (CHEBI:15760)
norbelladine (CHEBI:80666) has functional parent tyramine (CHEBI:15760)
tyramine phosphate (CHEBI:142808) has functional parent tyramine (CHEBI:15760)
tyramine sulfate (CHEBI:133530) has functional parent tyramine (CHEBI:15760)
tyraminium (CHEBI:327995) is conjugate acid of tyramine (CHEBI:15760)
IUPAC Name
4-(2-aminoethyl)phenol
Synonyms Sources
2-(p-Hydroxyphenyl)ethylamine KEGG COMPOUND
4-Hydroxy-beta-phenylethylamine HMDB
4-hydroxyphenethylamine ChEBI
4-Hydroxyphenylethylamine HMDB
beta-(4-Hydroxyphenyl)ethylamine HMDB
p-(2-Aminoethyl)phenol HMDB
p-(2-aminoethyl)phenol ChEBI
p-hydroxyphenethylamine HMDB
p-hydroxyphenylethylamine HMDB
p-tyramine HMDB
Tyramin ChemIDplus
Tyramine KEGG COMPOUND
Manual Xrefs Databases
2784 DrugCentral
AEF PDBeChem
C00001435 KNApSAcK
C00483 KEGG COMPOUND
HMDB0000306 HMDB
LSM-19016 LINCS
Tyramine Wikipedia
TYRAMINE MetaCyc
View more database links
Registry Numbers Types Sources
1099914 Beilstein Registry Number ChemIDplus
1099914 Reaxys Registry Number Reaxys
51-67-2 CAS Registry Number KEGG COMPOUND
51-67-2 CAS Registry Number ChemIDplus
51-67-2 CAS Registry Number NIST Chemistry WebBook
82946 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
11361052 PubMed citation Europe PMC
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Last Modified
30 May 2022