CHEBI:17847 - p-cresol

ChEBI IDCHEBI:17847
ChEBI Namep-cresol
Stars
ASCII Namep-cresol
DefinitionA 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.
Secondary ChEBI IDsCHEBI:1816, CHEBI:11981, CHEBI:20352, CHEBI:44726
Last Modified7 October 2016
DownloadsMolfile
FormulaC7H8O
Net Charge0
Average Mass108.140
Monoisotopic Mass108.05751
SMILESCc1ccc(O)cc1
InChIInChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3
InChIKeyIWDCLRJOBJJRNH-UHFFFAOYSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Escherichia coli (ncbitaxon:562) - PubMed (21988831)
Roles Classification
Biological Roles:
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.
Application:
fungicide  A substance used to destroy fungal pests.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
p-cresol sulfate (CHEBI:82914) has functional parent p-cresol (CHEBI:17847)
4-(trifluoromethyl)phenol (CHEBI:42578) has functional parent p-cresol (CHEBI:17847)
tolterodine (CHEBI:9622) has functional parent p-cresol (CHEBI:17847)
IUPAC Name 
4-methylphenol
Synonyms  Source
4-CresolKEGG COMPOUND
p-CresolKEGG COMPOUND
4-HydroxytolueneKEGG COMPOUND
p-tolyl alcoholChemIDplus
p-KresolNIST Chemistry WebBook
paracresolNIST Chemistry WebBook
UniProt Name  Source
4-methylphenolUniProt
Manual XrefsDatabases
C01468KEGG COMPOUND
c0127UM-BBD
PCRPDBeChem
DB01688DrugBank
CPD-108MetaCyc
P-cresolWikipedia
HMDB0001858HMDB
C00002645KNApSAcK
Registry NumbersSources
Gmelin:2779Gmelin
Reaxys:1305151Reaxys
CAS:106-44-5KEGG COMPOUND
CAS:106-44-5ChemIDplus
CAS:106-44-5NIST Chemistry WebBook
Citations