CHEBI:15768 - 3,5-diiodo-L-tyrosine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 3,5-diiodo-L-tyrosine
ChEBI ID CHEBI:15768
ChEBI ASCII Name 3,5-diiodo-L-tyrosine
Definition A diiodotyrosine that is L-tyrosine carrying iodo-substituents at positions C-3 and C-5 of the benzyl group. It is an intermediate in the thyroid hormone synthesis.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:11710, CHEBI:46196, CHEBI:1405, CHEBI:19909
Supplier Information
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Formula C9H9I2NO3
Net Charge 0
Average Mass 432.98164
Monoisotopic Mass 432.86718
InChI InChI=1S/C9H9I2NO3/c10-5-1-4(2-6(11)8(5)13)3-7(12)9(14)15/h1-2,7,13H,3,12H2,(H,14,15)/t7-/m0/s1
InChIKey NYPYHUZRZVSYKL-ZETCQYMHSA-N
SMILES N[C@@H](Cc1cc(I)c(O)c(I)c1)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
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): 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).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3,5-diiodo-L-tyrosine (CHEBI:15768) has role human metabolite (CHEBI:77746)
3,5-diiodo-L-tyrosine (CHEBI:15768) has role mouse metabolite (CHEBI:75771)
3,5-diiodo-L-tyrosine (CHEBI:15768) is a L-tyrosine derivative (CHEBI:27177)
3,5-diiodo-L-tyrosine (CHEBI:15768) is a diiodotyrosine (CHEBI:23796)
3,5-diiodo-L-tyrosine (CHEBI:15768) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
3,5-diiodo-L-tyrosine (CHEBI:15768) is conjugate acid of 3,5-diiodo-L-tyrosinate(1−) (CHEBI:57506)
Incoming N-acetyl-L-phenylalanyl-L-diiodotyrosine (CHEBI:28253) has functional parent 3,5-diiodo-L-tyrosine (CHEBI:15768)
3,5-diiodo-L-tyrosinate(1−) (CHEBI:57506) is conjugate base of 3,5-diiodo-L-tyrosine (CHEBI:15768)
3,5-diiodo-L-tyrosine residue (CHEBI:90871) is substituent group from 3,5-diiodo-L-tyrosine (CHEBI:15768)
IUPAC Name
3,5-diiodo-L-tyrosine
Synonyms Sources
(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid IUPAC
3,5-Diiodo-L-tyrosine KEGG COMPOUND
3,5-Diiodotyrosine KEGG COMPOUND
3,5-DIIODOTYROSINE PDBeChem
diiodotyrosine ChEBI
DiIY ChEBI
DIT ChemIDplus
L-3,5-diiodotyrosine ChemIDplus
L-Diiodotyrosine KEGG COMPOUND
Manual Xrefs Databases
3146 DrugCentral
C01060 KEGG COMPOUND
DB03374 DrugBank
HMDB0003474 HMDB
LSM-5697 LINCS
TYI PDBeChem
View more database links
Registry Numbers Types Sources
1128682 Gmelin Registry Number Gmelin
2218691 Beilstein Registry Number Beilstein
2218691 Reaxys Registry Number Reaxys
300-39-0 CAS Registry Number KEGG COMPOUND
300-39-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11344555 PubMed citation Europe PMC
15206581 PubMed citation Europe PMC
15589368 PubMed citation Europe PMC
Last Modified
30 January 2023