CHEBI:28479 - D-tyrosine

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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 eMolecules:531518, ZINC000000002234
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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 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
Last Modified
02 June 2020