CHEBI:21563 - N-acetyl-L-tyrosine

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ChEBI Name N-acetyl-L-tyrosine
ChEBI ID CHEBI:21563
ChEBI ASCII Name N-acetyl-L-tyrosine
Definition An N-acetyltyrosine in which the chiral centre has L configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C11H13NO4
Net Charge 0
Average Mass 223.226
Monoisotopic Mass 223.08446
InChI InChI=1S/C11H13NO4/c1-7(13)12-10(11(15)16)6-8-2-4-9(14)5-3-8/h2-5,10,14H,6H2,1H3,(H,12,13)(H,15,16)/t10-/m0/s1
InChIKey CAHKINHBCWCHCF-JTQLQIEISA-N
SMILES C([C@H](CC1=CC=C(C=C1)O)NC(C)=O)(=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): EC 2.1.1.4 (acetylserotonin O-methyltransferase) inhibitor
An EC 2.1.1.* (methyltransferases) inhibitor that interferes with the action of N-acetylserotonin methyltransferase (EC 2.1.1.4).
human urinary metabolite
Any metabolite (endogenous or exogenous) found in human urine samples.
(via N-acetyltyrosine )
Application(s): biomarker
A substance used as an indicator of a biological state.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-acetyl-L-tyrosine (CHEBI:21563) has role biomarker (CHEBI:59163)
N-acetyl-L-tyrosine (CHEBI:21563) has role EC 2.1.1.4 (acetylserotonin O-methyltransferase) inhibitor (CHEBI:71178)
N-acetyl-L-tyrosine (CHEBI:21563) has role human urinary metabolite (CHEBI:84087)
N-acetyl-L-tyrosine (CHEBI:21563) is a N-acetyltyrosine (CHEBI:68561)
N-acetyl-L-tyrosine (CHEBI:21563) is a N-acyl-L-tyrosine (CHEBI:90090)
N-acetyl-L-tyrosine (CHEBI:21563) is conjugate acid of N-acetyl-L-tyrosinate (CHEBI:133591)
Incoming N-acetyl-L-tyrosinate (CHEBI:133591) is conjugate base of N-acetyl-L-tyrosine (CHEBI:21563)
N-terminal N-acetyl-L-tyrosine residue (CHEBI:140860) is substituent group from N-acetyl-L-tyrosine (CHEBI:21563)
IUPAC Names
(2S)-2-(acetylamino)-3-(4-hydroxyphenyl)propanoic acid
N-acetyl-L-tyrosine
Synonyms Sources
N-Acetyl-4-hydroxyphenylalanine HMDB
N-Acetyltyrosine HMDB
Manual Xrefs Databases
3NF PDBeChem
4481 DrugCentral
HMDB0000866 HMDB
View more database links
Registry Numbers Types Sources
2697172 Reaxys Registry Number Reaxys
537-55-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11020336 PubMed citation Europe PMC
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Last Modified
22 February 2017