CHEBI:17847 - p-cresol

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ChEBI Name p-cresol
ChEBI ID CHEBI:17847
ChEBI ASCII Name p-cresol
Definition A cresol that consists of toluene substituted by a hydroxy group at position 4. It is a metabolite of aromatic amino acid metabolism produced by intestinal microflora in humans and animals.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:44726, CHEBI:1816, CHEBI:20352, CHEBI:11981
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Formula C7H8O
Net Charge 0
Average Mass 108.13782
Monoisotopic Mass 108.058
InChI InChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3
InChIKey IWDCLRJOBJJRNH-UHFFFAOYSA-N
SMILES Cc1ccc(O)cc1
Metabolite of Species Details
Escherichia coli (NCBI:562) See: PubMed
Roles Classification
Biological Role(s): uremic toxin
A toxin that accumulates in patients with chronic kidney disease.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
fungicide
A substance used to destroy fungal pests.
(via aromatic fungicide )
Application(s): fungicide
A substance used to destroy fungal pests.
(via aromatic fungicide )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing p-cresol (CHEBI:17847) has role Escherichia coli metabolite (CHEBI:76971)
p-cresol (CHEBI:17847) has role human metabolite (CHEBI:77746)
p-cresol (CHEBI:17847) has role uremic toxin (CHEBI:64584)
p-cresol (CHEBI:17847) is a cresol (CHEBI:25399)
Incoming 4-(trifluoromethyl)phenol (CHEBI:42578) has functional parent p-cresol (CHEBI:17847)
p-cresol sulfate (CHEBI:82914) has functional parent p-cresol (CHEBI:17847)
tolterodine (CHEBI:9622) has functional parent p-cresol (CHEBI:17847)
IUPAC Name
4-methylphenol
Synonyms Sources
1-hydroxy-4-methylbenzene NIST Chemistry WebBook
4-Cresol KEGG COMPOUND
4-Hydroxytoluene KEGG COMPOUND
4-methylphenol UniProt
4-Methylphenol KEGG COMPOUND
p-Cresol KEGG COMPOUND
P-CRESOL PDBeChem
p-Kresol NIST Chemistry WebBook
p-methylphenol NIST Chemistry WebBook
p-tolyl alcohol ChemIDplus
paracresol NIST Chemistry WebBook
Database Links Databases
C00002645 KNApSAcK
c0127 UM-BBD
C01468 KEGG COMPOUND
CPD-108 MetaCyc
DB01688 DrugBank
HMDB0001858 HMDB
P-cresol Wikipedia
PCR PDBeChem
View more database links
Registry Numbers Types Sources
106-44-5 CAS Registry Number ChemIDplus
106-44-5 CAS Registry Number NIST Chemistry WebBook
1305151 Reaxys Registry Number Reaxys
1305151 Beilstein Registry Number Beilstein
2779 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
12427124 PubMed citation Europe PMC
17660685 PubMed citation Europe PMC
Last Modified
07 October 2016