Thyronamine

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Thyronamine
Thyronamine.svg
Thyronamine3d.png
Names
Preferred IUPAC name
4-[4-(2-Aminoethyl)phenoxy]phenol
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
MeSH thyronamine
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C14H15NO2/c15-10-9-11-1-5-13(6-2-11)17-14-7-3-12(16)4-8-14/h1-8,16H,9-10,15H2 checkY
    Key: OVUVNKDANCKDCK-UHFFFAOYSA-N checkY
  • InChI=1/C14H15NO2/c15-10-9-11-1-5-13(6-2-11)17-14-7-3-12(16)4-8-14/h1-8,16H,9-10,15H2
    Key: OVUVNKDANCKDCK-UHFFFAOYAP
  • O(c1ccc(cc1)CCN)c2ccc(O)cc2
Properties
Chemical formula
C14H15NO2
Molar mass 229.279 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

Thyronamine refers both to a molecule, and to derivatives of that molecule: a family of decarboxylated and deiodinated metabolites of the thyroid hormones thyroxine (T4) and 3,5,3'-triiodothyronine (T3).

Types[]

The group includes:

  • Thyronamine (T0AM)
  • 3-Iodothyronamine (T1AM), which is the most notable one as it is a trace amine found in the nervous system. It is a possible candidate for the natural ligand of the trace amine-associated receptor TAAR1 (TAR1), an intracellular G protein-coupled receptor[1]
  • 3,5-Diiodothyronamine (T2AM)
  • 3,5,3'-Triiodothyronamine (T3AM)

See also[]

  • Trace amines
  • Thyroid hormone

References[]

  1. ^ Piehl S, Hoefig CS, Scanlan TS, Köhrle J (2011). "Thyronamines - Past, Present, and Future". Endocrine Reviews. 32 (1): 64–80. doi:10.1210/er.2009-0040. PMID 20880963.
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