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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8O4S
Molecular Weight 188.201
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CRESOL SULFATE

SMILES

CC1=CC=C(OS(O)(=O)=O)C=C1

InChI

InChIKey=WGNAKZGUSRVWRH-UHFFFAOYSA-N
InChI=1S/C7H8O4S/c1-6-2-4-7(5-3-6)11-12(8,9)10/h2-5H,1H3,(H,8,9,10)

HIDE SMILES / InChI

Molecular Formula C7H8O4S
Molecular Weight 188.201
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Metabolome-wide association study identifies multiple biomarkers that discriminate north and south Chinese populations at differing risks of cardiovascular disease: INTERMAP study.
2010-12-03
Metabolomic search for uremic toxins as indicators of the effect of an oral sorbent AST-120 by liquid chromatography/tandem mass spectrometry.
2010-11-01
[Uremic toxins: the case of protein-bound compounds].
2010-10-06
Serum levels of total p-cresylsulphate are associated with angiographic coronary atherosclerosis severity in stable angina patients with early stage of renal failure.
2010-08
Prospective evaluation of the change of predialysis protein-bound uremic solute concentration with postdilution online hemodiafiltration.
2010-07
p-Cresol and cardiovascular risk in mild-to-moderate kidney disease.
2010-07
Metabolomic analysis of uremic toxins by liquid chromatography/electrospray ionization-tandem mass spectrometry.
2010-06-15
Free p-cresylsulphate is a predictor of mortality in patients at different stages of chronic kidney disease.
2010-04
Binding of p-cresylsulfate and p-cresol to human serum albumin studied by microcalorimetry.
2010-02-04
Protein-bound uraemic toxin removal in haemodialysis and post-dilution haemodiafiltration.
2010-01
p-Cresyl sulfate serum concentrations in haemodialysis patients are reduced by the prebiotic oligofructose-enriched inulin.
2010-01
Increased levels of total P-Cresylsulphate and indoxyl sulphate are associated with coronary artery disease in patients with diabetic nephropathy.
2010
p-Cresyl sulfate and indoxyl sulfate in hemodialysis patients.
2009-12
The uremic retention solute p-cresyl sulfate and markers of endothelial damage.
2009-11
Levels of circulating endothelial progenitor cells are related to uremic toxins and vascular injury in hemodialysis patients.
2009-09
Sodium octanoate to reverse indoxyl sulfate and p-cresyl sulfate albumin binding in uremic and normal serum during sample preparation followed by fluorescence liquid chromatography.
2009-05-29
Effective removal of protein-bound uraemic solutes by different convective strategies: a prospective trial.
2009-02
Temporal metabonomic modeling of l-arginine-induced exocrine pancreatitis.
2008-10
P-cresylsulphate, the main in vivo metabolite of p-cresol, activates leucocyte free radical production.
2007-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:50:29 GMT 2025
Edited
by admin
on Mon Mar 31 22:50:29 GMT 2025
Record UNII
56M34ZQY1S
Record Status Validated (UNII)
Record Version
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Name Type Language
CRESYL SULFATE, P-
Preferred Name English
P-CRESOL SULFATE
Common Name English
P-TOLYL SULFATE
Common Name English
(4-METHYLPHENYL) SULFATE
Systematic Name English
PARA-CRESOL SULFATE
Systematic Name English
(4-METHYLPHENYL)OXIDANESULFONIC ACID
Systematic Name English
P-CRESYL SULFATE
Common Name English
4-CRESOL SULFATE
Systematic Name English
4-CRESOL SULPHATE
Systematic Name English
P-TOLYL HYDROGEN SULFATE
Common Name English
SULFURIC ACID, MONO(4-METHYLPHENYL) ESTER
Systematic Name English
4-METHYLPHENYL HYDROGEN SULFATE
Systematic Name English
MONO(4-METHYLPHENYL) SULFATE
Systematic Name English
P-CRESYL SULPHATE
Common Name English
PARA-CRESOL SULPHATE
Systematic Name English
SULFURIC ACID, MONO(P-TOLYL) ESTER
Common Name English
Code System Code Type Description
CAS
3233-58-7
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY
CHEBI
133670
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY
CHEBI
82914
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY
PUBCHEM
4615423
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID80404921
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY
FDA UNII
56M34ZQY1S
Created by admin on Mon Mar 31 22:50:29 GMT 2025 , Edited by admin on Mon Mar 31 22:50:29 GMT 2025
PRIMARY