Record Information
Version1.0
Creation date2015-10-09 22:33:06 UTC
Update date2017-01-19 02:36:39 UTC
FoodComEx IDPC000853
FoodDB RecordFDB023181
Chemical Information
Name3,5-Diiodo-L-tyrosine
DescriptionA product from the iodination of monoiodotyrosine. In the biosynthesis of thyroid hormones, diiodotyrosine residues are coupled with other monoiodotyrosine or diiodotyrosine residues to form T4 or T3 thyroid hormones (thyroxine and triiodothyronine). [HMDB]
CAS Number300-39-0
Structure
Thumb
Synonyms
SynonymSource
(2S)-2-amino-3-(4-Hydroxy-3,5-diiodophenyl)propanoateGenerator
(2S)-2-amino-3-(4-Hydroxy-3,5-diiodophenyl)propanoic acidChEBI
3,5-Diiodotyrocinehmdb
3,5-DiiodotyrosineChEBI
3,5-Iodo-L-tyrosinehmdb
3,5-L-Diiodotyrosinehmdb
4-Hydroxy-3,5-diiodophenylalaninehmdb
DiiodotyrosineChEBI
DiIYChEBI
DITChEBI
L-3,5-DiioDOTyrosinehmdb
L-Diiodotyrosinehmdb
Chemical FormulaC9H9I2NO3
IUPAC name(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid
InChI IdentifierInChI=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
InChI KeyNYPYHUZRZVSYKL-ZETCQYMHSA-N
Isomeric SMILES[H][C@](N)(CC1=CC(I)=C(O)C(I)=C1)C(O)=O
Average Molecular Weight432.9816
Monoisotopic Molecular Weight432.867179999
Chemical Taxonomy
Description Belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentTyrosine and derivatives
Alternative Parents
Substituents
  • Tyrosine or derivatives
  • Phenylalanine or derivatives
  • 3-phenylpropanoic-acid
  • Amphetamine or derivatives
  • Alpha-amino acid
  • L-alpha-amino acid
  • 2-iodophenol
  • 2-halophenol
  • Aralkylamine
  • Halobenzene
  • Phenol
  • Iodobenzene
  • Aryl iodide
  • Monocyclic benzene moiety
  • Benzenoid
  • Aryl halide
  • Amino acid
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Amine
  • Primary aliphatic amine
  • Organonitrogen compound
  • Organooxygen compound
  • Primary amine
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organoiodide
  • Organohalogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointNot Available
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 2 g
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci 8172AF
AKSci F525
AKSci J10902
AKSci J40127
AKSci J93316
Toronto Research Chemicals D466055