EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:17890 - tryptophol

ChEBI IDCHEBI:17890
ChEBI Nametryptophol
Stars
DefinitionAn indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2.
Secondary ChEBI IDsCHEBI:5910, CHEBI:14451, CHEBI:24811
Last Modified20 May 2020
DownloadsMolfile
FormulaC10H11NO
Net Charge0
Average Mass161.204
Monoisotopic Mass161.08406
SMILESOCCc1cnc2ccccc12
InChIInChI=1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2
InChIKeyMBBOMCVGYCRMEA-UHFFFAOYSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (24678285) Source: yeast.sf.net
Roles Classification
Biological Roles:
auxin  Any of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek αυξανω, "to grow").
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
tryptophol (CHEBI:17890) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
tryptophol (CHEBI:17890) has role auxin (CHEBI:22676)
tryptophol (CHEBI:17890) has role plant metabolite (CHEBI:76924)
tryptophol (CHEBI:17890) is a indolyl alcohol (CHEBI:38467)
Incoming Relation(s)
tryptophol-2-sulfonic acid (CHEBI:147413) has functional parent tryptophol (CHEBI:17890)
IUPAC Name 
2-(1H-indol-3-yl)ethanol
Synonyms  Source
Indole-3-ethanolKEGG COMPOUND
TryptopholKEGG COMPOUND
1H-indolyl-3-ethanolNIST Chemistry WebBook
3-(2-hydroxyethyl)indoleChemIDplus
1H-indole-3-ethanolNIST Chemistry WebBook
2-(indol-3-yl)ethanolChEBI
UniProt Name  Source
indole-3-ethanolUniProt
Manual XrefsDatabases
C00955KEGG COMPOUND
C00955KEGG COMPOUND
HMDB0003447HMDB
TryptopholWikipedia
CPD-341MetaCyc
C00000114KNApSAcK
Registry NumbersSources
Gmelin:142970Gmelin
Reaxys:125553Reaxys
CAS:526-55-6KEGG COMPOUND
CAS:526-55-6ChemIDplus
CAS:526-55-6NIST Chemistry WebBook
Citations