3-Iodotyrosine

3-Iodotyrosine

3-Iodo-L-tyrosine
Names
IUPAC name
(2S)-2-Amino-3-(4-hydroxy-3-iodophenyl)propanoic acid
Other names
Monoiodotyrosine; MIT[1]
Identifiers
CAS Number
  • 3078-39-5 (DL) checkY
  • 70-78-0 (L)
  • 25799-58-0 (D)
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL479789 checkY
ChemSpider
  • 388804 ☒N
DrugBank
  • DB01758 checkY
ECHA InfoCard 100.000.677 Edit this at Wikidata
IUPHAR/BPS
  • 5117
MeSH Monoiodotyrosine
PubChem CID
  • 6272 (DL)
  • 439744 (L)
UNII
  • FRQ98U4U27 checkY
CompTox Dashboard (EPA)
  • DTXSID1075353 Edit this at Wikidata
InChI
  • 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 ☒N
    Key: UQTZMGFTRHFAAM-ZETCQYMHSA-N ☒N
  • InChI=1/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
    Key: UQTZMGFTRHFAAM-ZETCQYMHBY
  • c1cc(c(cc1C[C@@H](C(=O)O)N)I)O
Properties
Chemical formula
C9H10INO3
Molar mass 307.087 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

3-Iodotyrosine is an intermediate in the synthesis of thyroid hormones which is derived from iodination of tyrosine at the meta-position of the benzene ring. One unit can combine with diiodotyrosine to form triiodothyronine, as occurs in the colloid of the thyroid follicle. Two units can combine to form 3,3'-diiodothyronine.

3-Iodotyrosine is a reversible inhibitor of the enzyme tyrosine hydroxylase.[2]

Relevance in dopamine studies

3-Iodotyrosine, a pathway inhibitor in the synthesis of the neurotransmitter dopamine, was used to determine the effects of decreased dopamine levels in social spacing of Drosophila melanogaster. 3-4 day old flies that were fed 3-iodotyrosine for 24 hours were shown to have altered dopamine levels.[3]

References

  1. ^ Tietze F, Kohn LD, Kohn AD, et al. (March 1989). "Carrier-mediated transport of monoiodotyrosine out of thyroid cell lysosomes". J. Biol. Chem. 264 (9): 4762–5. doi:10.1016/S0021-9258(18)83654-7. PMID 2925666.
  2. ^ Richelson E (November 1976). "Properties of tyrosine hydroxylation in living mouse neuroblastoma clone N1E-115". Journal of Neurochemistry. 27 (5): 1113–8. doi:10.1111/j.1471-4159.1976.tb00317.x. PMID 12170597. S2CID 24808699.
  3. ^ Fernandez, Robert W.; Akinleye, Adesanya A.; Nurilov, Marat; Feliciano, Omar; Lollar, Matthew; Aijuri, Rami R.; O'Donnell, Janis M.; Simon, Anne F. (2017-08-01). "Modulation of social space by dopamine in Drosophila melanogaster, but no effect on the avoidance of the Drosophila stress odorant". Biology Letters. 13 (8): 20170369. doi:10.1098/rsbl.2017.0369. ISSN 1744-9561. PMC 5582115. PMID 28794277.


  • v
  • t
  • e
Tyrosine / iodotyrosine
Thyronine / iodothyronine
Thyronamine / iodothyronamineIodothyroacetate / iodothyroacetic acid
  • v
  • t
  • e
Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine, epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
  • Substrates→Products: TyrosineL-DOPA (levodopa)
DBHTooltip Dopamine beta-monooxygenase
PNMTTooltip Phenylethanolamine N-methyltransferase
  • Inhibitors: CGS-19281A
  • SKF-64139
  • SKF-7698
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin, melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
  • Substrates→Products: L-Histidine→Histamine
HNMTTooltip Histamine N-methyltransferase
  • Substrates→Products: Histamine→N-Methylhistamine
DAOTooltip Diamine oxidase
  • Substrates→Products: Histamine→Imidazole acetic acid
See also: Receptor/signaling modulators • Adrenergics • Dopaminergics • Melatonergics • Serotonergics • Monoamine reuptake inhibitors • Monoamine releasing agents • Monoamine neurotoxins