Compound
4-nitrophenyl sulfate
An aryl sulfate oxoanion resulting from the deprotonation of the sulfooxy group of 4-nitrophenyl hydrogen sulfate. The major microspecies at pH 7.3.
Definition from ChEBI (CHEBI:140994), read 2026-09-23. CC BY 4.0.
Structure
Loading the model…
- Class
- Organic compound, anion
- Formula
- C6H4NO6S
- Mass
- 218.166 g/mol
- Charge
- -1
- InChIKey
- JBGHTSSFSSUKLR-UHFFFAOYSA-M
- SMILES
- O=[N+]([O-])c1ccc(OS(=O)(=O)[O-])cc1
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
3 entities
3 entities reached.
What the reference databases state
Statements
4 statements
4 statements · 2 reference databases · Subject: 4-nitrophenyl sulfate · Sources: Human-GEM, Rhea
- 4-nitrophenol is converted to 4-nitrophenyl sulfateCompoundHuman-GEM MAR07688Inferred only
- 4-nitrophenyl sulfate is metabolised by SULT1A1ProteinRhea RHEA:66548Inferred only
- 4-nitrophenyl sulfate is metabolised by SULT1A3ProteinRhea RHEA:66548Inferred only
- 4-nitrophenyl sulfate is metabolised by SULT1A4ProteinRhea RHEA:66548Inferred only
Reactions
4 reactions
3'-phospho-5'-adenylyl sulfate+4-nitrophenol4-nitrophenyl sulfate+proton+adenosine 3',5'-bismonophosphate
Catalysed by SULT1A1 or SULT1A2 or SULT1A4 or SULT1A3
Reaction pageLeft to rightBalancedEC 2.8.2.1GO:0005829
Human-GEM MAR07688CC BY 4.0Reference data
4-nitrophenyl sulfate4-nitrophenyl sulfate
Reaction pageReversibleBalancedGO:0005829, GO:0005615
Human-GEM MAR08101CC BY 4.0Reference data
Reaction pageReversibleBalance undeterminableGO:0005615
Human-GEM MAR09227CC BY 4.0Reference data
4-nitrophenol+3'-phosphoadenylyl sulfate4-nitrophenyl sulfate+adenosine 3',5'-bisphosphate
Catalysed by SULT1A3 or SULT1A4 or SULT1A1
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:66548CC BY 4.0Reference data
Other names
1 name
Resolves to: 4-nitrophenyl sulfate
- Systematic name
- p-nitrophenyl sulfate