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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:125610 -
N
-acetyltyramine
Main
ChEBI Ontology
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ChEBI Name
N
-acetyltyramine
ChEBI ID
CHEBI:125610
ChEBI ASCII Name
N-acetyltyramine
Definition
A member of the class of tyramines that is tyramine in which one of the hydrogens of the amino group is replaced by an acetyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula
C10H13NO2
Net Charge
0
Average Mass
179.219
Monoisotopic Mass
179.09463
InChI
InChI=1S/C10H13NO2/c1-8(12)11-7-6-9-2-4-10(13)5-3-9/h2-5,13H,6-7H2,1H3,(H,11,12)
InChIKey
ATDWJOOPFDQZNK-UHFFFAOYSA-N
SMILES
CC(=O)NCCC1=CC=C(O)C=C1
Metabolite of Species
Details
Armadillidium vulgare
(NCBI:txid13347)
See:
PubMed
Paramyrothecium roridum
(NCBI:txid1859971)
of strain IFB-E091 See:
PubMed
Actinokineospora
sp.
(NCBI:txid1872133)
of strain UTMC 968 See:
PubMed
Streptomyces acrimycini
(NCBI:txid1884)
See:
DOI
Streptomyces
sp.
(NCBI:txid1931)
of strain YIM 67086 See:
PubMed
Formica japonica
(NCBI:txid255794)
Found in brain
(BTO:0000142)
. See:
PubMed
Vibrio alginolyticus
(NCBI:txid663)
of strain M3-10 See:
PubMed
Tenebrio molitor
(NCBI:txid706)
See:
PubMed
Bombyx mori
(NCBI:txid7091)
See:
PubMed
Apis mellifera
(NCBI:txid7460)
Found in brain
(BTO:0000142)
. See:
PubMed
Aspergillus fumigatus
(NCBI:txid746128)
See:
DOI
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Aspergillus metabolite
Any fungal metabolite produced during a metabolic reaction in the mould,
Aspergillus
.
animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
quorum sensing inhibitor
Any compound that interferes with bacterial communication (quorum sensing, QS).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-acetyltyramine (
CHEBI:125610
)
has functional parent
tyramine (
CHEBI:15760
)
N
-acetyltyramine (
CHEBI:125610
)
has role
Aspergillus
metabolite (
CHEBI:76956
)
N
-acetyltyramine (
CHEBI:125610
)
has role
animal metabolite (
CHEBI:75767
)
N
-acetyltyramine (
CHEBI:125610
)
has role
bacterial metabolite (
CHEBI:76969
)
N
-acetyltyramine (
CHEBI:125610
)
has role
marine metabolite (
CHEBI:76507
)
N
-acetyltyramine (
CHEBI:125610
)
has role
quorum sensing inhibitor (
CHEBI:138977
)
N
-acetyltyramine (
CHEBI:125610
)
is a
acetamides (
CHEBI:22160
)
N
-acetyltyramine (
CHEBI:125610
)
is a
tyramines (
CHEBI:27175
)
IUPAC Name
N
-[2-(4-hydroxyphenyl)ethyl]acetamide
Synonyms
Sources
N
-(4-hydroxyphenethyl)acetamide
ChEBI
N
-(
p
-hydroxyphenethyl)acetamide
ChemIDplus
N
-acetyl tyramine
ChemIDplus
N
-acetyltyramine
UniProt
Manual Xrefs
Databases
108052
ChemSpider
C00043743
KNApSAcK
LSM-37158
LINCS
View more database links
Registry Numbers
Types
Sources
1202-66-0
CAS Registry Number
NIST Chemistry WebBook
1202-66-0
CAS Registry Number
ChemIDplus
2096467
Reaxys Registry Number
Reaxys
Citations
Types
Sources
12770030
PubMed citation
Europe PMC
13286844
PubMed citation
Europe PMC
13444076
PubMed citation
Europe PMC
13444078
PubMed citation
Europe PMC
13661993
PubMed citation
Europe PMC
19731603
PubMed citation
Europe PMC
20496234
PubMed citation
Europe PMC
23387977
PubMed citation
Europe PMC
25109748
PubMed citation
Europe PMC
25406072
PubMed citation
Europe PMC
26672331
PubMed citation
Europe PMC
26837178
PubMed citation
Europe PMC
28844963
PubMed citation
Europe PMC
29247559
PubMed citation
Europe PMC
30242664
PubMed citation
Europe PMC
31450549
PubMed citation
Europe PMC
3693136
PubMed citation
Europe PMC
Last Modified
27 November 2020