Structure
Loading the model…
- Class
- Organic compound, anion
- Formula
- C15H11I3NO7S
- Mass
- 730.032 g/mol
- Charge
- -1
- InChIKey
- BWRJFXXHPZMDPS-LBPRGKRZSA-M
- SMILES
- [NH3+][C@@H](Cc1ccc(Oc2cc(I)c(OS(=O)(=O)[O-])c(I)c2)c(I)c1)C(=O)[O-]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Chemical structure
- 3,3',5'-triiodo-L-thyronine sulfate has the functional parent 3,3',5'-triiodo-L-thyronineCompoundChEBI CHEBI:176513Inferred only
Statements
2 statements
2 statements · 1 reference database · Subject: 3,3',5'-triiodo-L-thyronine sulfate · Sources: Rhea
- 3,3',5'-triiodo-L-thyronine is converted to 3,3',5'-triiodo-L-thyronine sulfateCompoundRhea RHEA:67888Inferred only
- 3,3',5'-triiodo-L-thyronine sulfate is a substrate of DIO1ProteinRhea RHEA:83831Inferred only
Reactions
3 reactions
3,3',5'-triiodo-L-thyronine+3'-phosphoadenylyl sulfate3,3',5'-triiodo-L-thyronine sulfate+adenosine 3',5'-bisphosphate+hydron
Catalysed by SULT1B1 or SULT1A3 or SULT1A4 or SULT1A1
Reaction pageLeft to rightBalanced
Rhea RHEA:67888CC BY 4.0Reference data
3,3'-diiodo-L-thyronine sulfate+iodide+A+hydron3,3',5'-triiodo-L-thyronine sulfate+AH2
Catalysed by DIO1
Reaction pageRight to leftBalanced
Rhea RHEA:83831CC BY 4.0Reference data
3,3',5'-triiodo-L-thyronine sulfate+iodide+A+hydronL-thyroxine sulfate+AH2
Catalysed by DIO1
Reaction pageRight to leftBalanced
Rhea RHEA:83835CC BY 4.0Reference data