CHEBI:28479 - D-tyrosine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-tyrosine
ChEBI ID CHEBI:28479
ChEBI ASCII Name D-tyrosine
Definition An optically active form of tyrosine having D-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:42299, CHEBI:4258, CHEBI:21111
Supplier Information
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Formula C9H11NO3
Net Charge 0
Average Mass 181.18858
Monoisotopic Mass 181.07389
InChI InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1
InChIKey OUYCCCASQSFEME-MRVPVSSYSA-N
SMILES N[C@H](Cc1ccc(O)cc1)C(O)=O
Metabolite of Species Details
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 )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Daphnia magna metabolite
A Daphnia metabolite produced by the species Daphnia magna.
(via tyrosine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-tyrosine (CHEBI:28479) has role Escherichia coli metabolite (CHEBI:76971)
D-tyrosine (CHEBI:28479) is a D-α-amino acid (CHEBI:16733)
D-tyrosine (CHEBI:28479) is a tyrosine (CHEBI:18186)
D-tyrosine (CHEBI:28479) is conjugate acid of D-tyrosinate(1−) (CHEBI:32773)
D-tyrosine (CHEBI:28479) is conjugate base of D-tyrosinium (CHEBI:32775)
D-tyrosine (CHEBI:28479) is enantiomer of L-tyrosine (CHEBI:17895)
D-tyrosine (CHEBI:28479) is tautomer of D-tyrosine zwitterion (CHEBI:58570)
Incoming D-tyrosine derivative (CHEBI:84124) has functional parent D-tyrosine (CHEBI:28479)
D-tyrosinyl radical (CHEBI:32777) has functional parent D-tyrosine (CHEBI:28479)
D-tyrosinyl radical cation (CHEBI:32776) has functional parent D-tyrosine (CHEBI:28479)
D-tyrosinium (CHEBI:32775) is conjugate acid of D-tyrosine (CHEBI:28479)
D-tyrosinate(1−) (CHEBI:32773) is conjugate base of D-tyrosine (CHEBI:28479)
L-tyrosine (CHEBI:17895) is enantiomer of D-tyrosine (CHEBI:28479)
D-tyrosin-O4-yl group (CHEBI:32780) is substituent group from D-tyrosine (CHEBI:28479)
D-tyrosine residue (CHEBI:29976) is substituent group from D-tyrosine (CHEBI:28479)
D-tyrosino group (CHEBI:32779) is substituent group from D-tyrosine (CHEBI:28479)
D-tyrosyl group (CHEBI:32778) is substituent group from D-tyrosine (CHEBI:28479)
D-tyrosine zwitterion (CHEBI:58570) is tautomer of D-tyrosine (CHEBI:28479)
IUPAC Name
D-tyrosine
Synonyms Sources
(2R)-2-amino-3-(4-hydroxyphenyl)propanoic acid IUPAC
(R)-2-Amino-3-(p-hydroxyphenyl)propionic acid KEGG COMPOUND
(R)-3-(p-Hydroxyphenyl)alanine KEGG COMPOUND
D-Tyr ChEBI
D-Tyrosin ChEBI
D-Tyrosine KEGG COMPOUND
D-TYROSINE PDBeChem
DTY PDBeChem
Manual Xrefs Databases
C06420 KEGG COMPOUND
D-TYROSINE MetaCyc
DB03839 DrugBank
DTY PDBeChem
ECMDB21520 ECMDB
YMDB00805 YMDB
View more database links
Registry Numbers Types Sources
2212157 Beilstein Registry Number Beilstein
2212157 Reaxys Registry Number Reaxys
556-02-5 CAS Registry Number KEGG COMPOUND
556-02-5 CAS Registry Number ChemIDplus
603524 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
15292242 PubMed citation Europe PMC
23381872 PubMed citation Europe PMC
24936396 PubMed citation Europe PMC
Last Modified
07 November 2018