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Thyronine

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L-Thyronine
Skeletal formula of L-thyronine
Ball-and-stick model of the L-thyronine molecule as a zwitterion
Names
IUPAC name O-(4-Hydroxyphenyl)-L-tyrosine
Systematic IUPAC name (2S)-2-Amino-3-propanoic acid
Other names 4-(4-Hydroxyphenoxy)-L-phenylalanine
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.014.986 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C15H15NO4/c16-14(15(18)19)9-10-1-5-12(6-2-10)20-13-7-3-11(17)4-8-13/h1-8,14,17H,9,16H2,(H,18,19)/t14-/m0/s1Key: KKCIOUWDFWQUBT-AWEZNQCLSA-N
  • InChI=1/C15H15NO4/c16-14(15(18)19)9-10-1-5-12(6-2-10)20-13-7-3-11(17)4-8-13/h1-8,14,17H,9,16H2,(H,18,19)/t14-/m0/s1Key: KKCIOUWDFWQUBT-AWEZNQCLBR
SMILES
  • O=C(O)(N)Cc2ccc(Oc1ccc(O)cc1)cc2
Properties
Chemical formula C15H15NO4
Molar mass 273.28 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Thyronine is a metabolite derived from thyroxine and triiodothyronine via the peripheral enzymatic removal of iodines from the thyroxine nucleus. Thyronine is the thyroxine nucleus devoid of its four iodine atoms.

References

  1. Pubchem Compound summary, L-thyronine


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Thyroid hormone metabolic intermediates
Tyrosine / iodotyrosine
Thyronine / iodothyronine
Thyronamine / iodothyronamine
Iodothyroacetate / iodothyroacetic acid
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