Page last updated: 2024-11-10

4-cresol sulfate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

p-cresol sulfate : An aryl sulfate that is p-cresol in which the phenolic hydrogen has been replaced by a sulfo group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID4615423
CHEMBL ID4551850
CHEBI ID82914
SCHEMBL ID195721
MeSH IDM0363499

Synonyms (41)

Synonym
p-cresol sulfate
p-cresylsulfate
(4-methylphenyl) hydrogen sulfate
4-METHYLPHENYL HYDROGEN SULFATE ,
p-tolyl hydrogen sulfate
p-cresyl sulfate
4-cresol sulphate
p-cresol sulphate
4-cresol sulfate
3233-58-7
sulfuric acid, mono(4-methylphenyl) ester
SCHEMBL195721
sulfuric acid mono-p-tolyl ester
CHEBI:82914
cresyl sulfate, p-
(4-methylphenyl)oxidanesulfonic acid
unii-56m34zqy1s
para-cresol sulfate
56m34zqy1s ,
para-cresol sulphate
p-cresyl sulphate
sulfuric acid, mono(p-tolyl) ester
mono(4-methylphenyl) sulfate
p-tolyl sulfate
DTXSID80404921
p-tolyl sulfate (6ci,7ci)
p-cresyl-sulfate
p-cresylsulphate
p-cresyl-sulphate
p-tolyl sulphate (6ci,7ci)
sulfuric acid mono(p-tolyl) ester (8ci)
EP-0022
Q27156456
6ei ,
FT-0778135
AKOS037652431
HY-111431
EN300-245883
CHEMBL4551850
CS-0040680
p-tolyl sulfate (potassium)

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" A quality score was developed, giving 1 point for each of the following criteria: six or more experiments, confirmation by more than one experimental approach, neutralization of the biologic effect by counteractive reagents or antibodies, use of a real-life model, and use of dose-response analyses in vitro and/or animal studies."( The uremic toxicity of indoxyl sulfate and p-cresyl sulfate: a systematic review.
Glorieux, G; Nagler, EV; Pletinck, A; Schepers, E; Vanholder, R, 2014
)
0.4
" The uptake of liposomes by direct incubation in vitro showed an obvious dose-response relationship for p-cresyl sulfate (PCS) and indoxyl sulfate (IS) but not for hippuric acid (HA)."( Increasing the removal of protein-bound uremic toxins by liposome-supported hemodialysis.
Ding, F; Li, Y; Liu, T; Ma, S; Shi, Y; Tian, H; Wang, W; Wang, Y; Zhu, Q, 2019
)
0.51
" In conclusion, the limited data reported in this present study indicates that monitoring IS in the blood is a very important determinant in the dosage plan for the administration of site II drugs such as ARP, if the efficacy of the drug in renal disease is to be considered."( The Binding of Aripiprazole to Plasma Proteins in Chronic Renal Failure Patients.
Chuang, VTG; Hirata, K; Ikeda, T; Maruyama, T; Nishi, K; Otagiri, M; Sakurama, K; Tanaka, M; Uchida, Y; Watanabe, H; Yamasaki, K, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
uremic toxinA toxin that accumulates in patients with chronic kidney disease.
gut flora metaboliteMetabolites produced by the gut microbiota or microorganisms (e.g. bacteria and fungi) that live in the digestive tracts of animals.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
aryl sulfate
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID1624947Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Kcat by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624946Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Vmax by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624942Stability of the compound in pH 7 ammonium acetate buffer by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624945Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Km by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624948Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring catalytic efficiency by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624944Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis using 1 U of enzyme measured after 24 hrs by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (224)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (0.89)18.7374
1990's0 (0.00)18.2507
2000's14 (6.25)29.6817
2010's160 (71.43)24.3611
2020's48 (21.43)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials24 (10.30%)5.53%
Reviews26 (11.16%)6.00%
Case Studies0 (0.00%)4.05%
Observational6 (2.58%)0.25%
Other177 (75.97%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]