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1 Relevance in dopamine studies  





2 References  














3-Iodotyrosine






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From Wikipedia, the free encyclopedia
 

(Redirected from Monoiodotyrosine)

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

  • 70-78-0 (L)
  • 25799-58-0 (D)
  • 3D model (JSmol)

    ChEMBL
    ChemSpider
    DrugBank
    ECHA InfoCard 100.000.677 Edit this at Wikidata

    IUPHAR/BPS

    MeSH Monoiodotyrosine

    PubChem CID

  • 439744 (L)
  • UNII

    CompTox Dashboard (EPA)

    • 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

    3-Iodotyrosine is an intermediate in the synthesis of thyroid hormones which is derived from iodinationoftyrosine 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

    [edit]

    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

    [edit]
    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.
  • ^ 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.
  • ^ 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.


  • Retrieved from "https://en.wikipedia.org/w/index.php?title=3-Iodotyrosine&oldid=1205360652"

    Categories: 
    Iodinated tyrosine derivatives
    Tyrosine hydroxylase inhibitors
    Hidden categories: 
    Chemical articles with multiple compound IDs
    Multiple chemicals in an infobox that need indexing
    Chemical articles with multiple CAS registry numbers
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    Articles without KEGG source
    Articles with changed ChemSpider identifier
    ECHA InfoCard ID from Wikidata
    Articles with changed InChI identifier
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    Articles with short description
    Short description matches Wikidata
     



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