U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Aromatic amino acids and their derivatives as ligands for the isolation of aspartic proteinases.
2002 Apr 25
The effects of dopamine synthesis inhibitors and dopamine antagonists on regeneration in the hydra Hydra attenuata.
2002 May-Jun
Bioinorganic chemistry in thyroid gland: effect of antithyroid drugs on peroxidase-catalyzed oxidation and iodination reactions.
2006
Chiral discrimination of D- and L-amino acids using iodinated tyrosines as chiral references: effect of iodine substituent.
2007 Aug
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
Interaction of dopamine, female pheromones, locomotion and sex behavior in Drosophila melanogaster.
2008 Oct-Nov
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
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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
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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
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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
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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
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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
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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
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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
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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