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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H10INO3
Molecular Weight 307.0851
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-IODOTYROSINE

SMILES

N[C@@H](CC1=CC=C(O)C(I)=C1)C(O)=O

InChI

InChIKey=UQTZMGFTRHFAAM-ZETCQYMHSA-N
InChI=1S/C9H10INO3/c10-6-3-5(1-2-8(6)12)4-7(11)9(13)14/h1-3,7,12H,4,11H2,(H,13,14)/t7-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A variant of iodotyrosine-dehalogenase deficiency.
1977 Mar
Interference of iodine-125 ligands in radioimmunoassay: evidence implicating thyroxine-binding globulin.
1979 May
Prolactin-lowering and -releasing drugs. Mechanisms of action and therapeutic applications.
1983 Apr
Site-specific incorporation of an unnatural amino acid into proteins in mammalian cells.
2002 Nov 1
Use of a boroxazolidone complex of 3-iodo-L-tyrosine for palladium-catalyzed cross-coupling.
2003 Feb 21
Development of a validated HPLC method for the determination of iodotyrosines and iodothyronines in pharmaceuticals and biological samples using solid phase extraction.
2005 Jan 5
Bioinorganic chemistry in thyroid gland: effect of antithyroid drugs on peroxidase-catalyzed oxidation and iodination reactions.
2006
Nicotine promotes cell proliferation via alpha7-nicotinic acetylcholine receptor and catecholamine-synthesizing enzymes-mediated pathway in human colon adenocarcinoma HT-29 cells.
2007 Jun 15
Glucagon-like peptide 1 receptor stimulation reverses key deficits in distinct rodent models of Parkinson's disease.
2008 May 21
Requirement of a dopaminergic neuronal phenotype for toxicity of low concentrations of 1-methyl-4-phenylpyridinium to human cells.
2009 Nov 15
A mammalian reductive deiodinase has broad power to dehalogenate chlorinated and brominated substrates.
2009 Oct 14
Investigating bacterial sources of toxicity as an environmental contributor to dopaminergic neurodegeneration.
2009 Oct 6
Structural Aspects of Phenylalanylation and Quality Control in Three Major Forms of Phenylalanyl-tRNA Synthetase.
2010
A pair of dopamine neurons target the D1-like dopamine receptor DopR in the central complex to promote ethanol-stimulated locomotion in Drosophila.
2010 Apr 1
Dietary modulation of Drosophila sleep-wake behaviour.
2010 Aug 10
Early temporal effects of three thyroid hormone synthesis inhibitors in Xenopus laevis.
2010 Jun 1
Genetic encoding of non-natural amino acids in Drosophila melanogaster Schneider 2 cells.
2010 Mar
Patents
Name Type Language
3-IODOTYROSINE
MI  
Systematic Name English
MONOIODOTYROSINE
Systematic Name English
3-IODO-4-HYDROXYPHENYLALANINE
Systematic Name English
NSC-210787
Code English
TYROSINE, 3-IODO-, L-
Systematic Name English
L-TYROSINE, 3-IODO-
Systematic Name English
3-IODO-L-TYROSINE
Systematic Name English
3-IODOTYROSINE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C73539
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
Code System Code Type Description
WIKIPEDIA
3-IODOTYROSINE
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
NCI_THESAURUS
C595
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
CAS
70-78-0
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
FDA UNII
FRQ98U4U27
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
CHEBI
59898
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
NSC
210787
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
CHEBI
27847
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
MERCK INDEX
m6360
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY Merck Index
PUBCHEM
439744
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
EPA CompTox
DTXSID1075353
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
DRUG BANK
DB01758
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-744-8
Created by admin on Fri Dec 15 15:00:53 GMT 2023 , Edited by admin on Fri Dec 15 15:00:53 GMT 2023
PRIMARY