CHEBI:3210 - bufotenin

ChEBI IDCHEBI:3210
ChEBI Namebufotenin
Stars
DefinitionA tertiary amine that consists of N,N-dimethyltryptamine bearing an additional hydroxy substituent at position 5.
Last Modified26 May 2015
DownloadsMolfile
FormulaC12H16N2O
Net Charge0
Average Mass204.273
Monoisotopic Mass204.12626
SMILESCN(C)CCc1cnc2ccc(O)cc12
InChIInChI=1S/C12H16N2O/c1-14(2)6-5-9-8-13-12-4-3-10(15)7-11(9)12/h3-4,7-8,13,15H,5-6H2,1-2H3
InChIKeyVTTONGPRPXSUTJ-UHFFFAOYSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Paramuricea clavata (ncbitaxon:317549) - PubMed (21939218) CH2Cl2:MeOH(1:1) extract of lyophilized material
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
coral metabolite  Any animal metabolite produced during a metabolic reaction in corals (marine invertebrates).
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application:
hallucinogen  Drugs capable of inducing illusions, hallucinations, delusions, paranoid ideations and other alterations of mood and thinking.
ChEBI Ontology
Outgoing Relation(s)
bufotenin (CHEBI:3210) has functional parent N,N-dimethyltryptamine (CHEBI:28969)
bufotenin (CHEBI:3210) has role coral metabolite (CHEBI:76498)
bufotenin (CHEBI:3210) has role hallucinogen (CHEBI:35499)
bufotenin (CHEBI:3210) is a tertiary amine (CHEBI:32876)
bufotenin (CHEBI:3210) is a tryptamine alkaloid (CHEBI:48274)
Incoming Relation(s)
5-methoxy-N,N-dimethyltryptamine (CHEBI:2086) has functional parent bufotenin (CHEBI:3210)
IUPAC Name 
3-[2-(dimethylamino)ethyl]-1H-indol-5-ol
Synonyms  Source
3-[2-(dimethylamino)ethyl]-5-indololNIST Chemistry WebBook
3-[2-(dimethylamino)ethyl]indol-5-olNIST Chemistry WebBook
3-[β-(dimethylamino)ethyl]-5-hydroxyindoleNIST Chemistry WebBook
5-hydroxy-N,N-dimethyltryptamineChemIDplus
BufoteninKEGG COMPOUND
BufotenineKEGG COMPOUND
Manual XrefsDatabases
BufoteninWikipedia
C00001402KNApSAcK
C08299KEGG COMPOUND
DB01445DrugBank
Registry NumbersSources
Reaxys:160628Reaxys
CAS:487-93-4KEGG COMPOUND
CAS:487-93-4NIST Chemistry WebBook
CAS:487-93-4ChemIDplus
Citations