L-Thyronine
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| Names
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| IUPAC name
O-(4-Hydroxyphenyl)-L-tyrosine
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Systematic IUPAC name
(2S)-2-Amino-3-[4-(4-hydroxyphenoxy)phenyl]propanoic acid
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| Other names
4-(4-Hydroxyphenoxy)-L-phenylalanine
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| Identifiers
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CAS Number
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- 1596-67-4
Y
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3D model (JSmol)
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| ChEBI
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- CHEBI:30662
Y
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| ChemSpider
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- 4574450
Y
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| UNII
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- E4QN8G00CV
Y
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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/s1 YKey: KKCIOUWDFWQUBT-AWEZNQCLSA-N YInChI=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/s1 Key: KKCIOUWDFWQUBT-AWEZNQCLBR
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SMILES
O=C(O)[C@@H](N)Cc2ccc(Oc1ccc(O)cc1)cc2
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| Properties
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Chemical formula
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C15H15NO4
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| Molar mass
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273.28 g/mol
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N verify (what is Y N ?)
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| Infobox references
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Tracking categories (test):
A group of metabolites 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.[1]
References
- ↑ Pubchem Compound summary, L-thyronine
Thyroid hormone metabolic intermediates |
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| Tyrosine / iodotyrosine |
- 3-Iodotyrosine
- Diiodotyrosine
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| Thyronine / iodothyronine |
- 3'-Monoiodothyronine
- 3,3'-Diiodothyronine
- 3,5-Diiodothyronine
- 3,3',5-Triiodothyronine (T3)
- 3,3',5'-Triiodothyronine (Reverse T3)
- 3,5,3',5'-Tetraiodothyronine (Thyroxine, T4)
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| Thyronamine / iodothyronamine |
- 3-Iodothyronamine
- 3,3',5-Triiodothyronamine
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| Iodothyroacetate / iodothyroacetic acid |
- Triiodothyroacetate (TRIAC)
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 | Original source: https://en.wikipedia.org/wiki/Thyronine. Read more |