CHEBI:28136 - N-methyltryptamine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name N-methyltryptamine
ChEBI ID CHEBI:28136
ChEBI ASCII Name N-methyltryptamine
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7326, CHEBI:21774
Supplier Information
Download Molfile XML SDF
more structures >>
Formulae C11H14N2
C11H14N2
Net Charge 0
Average Mass 174.24230
Monoisotopic Mass 174.11570
InChI InChI=1S/C11H14N2/c1-12-7-6-9-8-13-11-5-3-2-4-10(9)11/h2-5,8,12-13H,6-7H2,1H3
InChIKey NCIKQJBVUNUXLW-UHFFFAOYSA-N
SMILES CNCCc1c[nH]c2ccccc12
Metabolite of Species Details
Paramuricea clavata (NCBI:txid317549) CH2Cl2:MeOH(1:1) extract of lyophilized material See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-methyltryptamine (CHEBI:28136) has functional parent tryptamine (CHEBI:16765)
N-methyltryptamine (CHEBI:28136) has role metabolite (CHEBI:25212)
N-methyltryptamine (CHEBI:28136) is a tryptamine alkaloid (CHEBI:48274)
N-methyltryptamine (CHEBI:28136) is a tryptamines (CHEBI:27162)
N-methyltryptamine (CHEBI:28136) is conjugate base of N-methyltryptaminium (CHEBI:193123)
Incoming N-methyltryptaminium (CHEBI:193123) is conjugate acid of N-methyltryptamine (CHEBI:28136)
IUPAC Name
2-(1H-indol-3-yl)-N-methylethanamine
Synonyms Sources
3-(2-methylaminoethyl)indole ChemIDplus
N-methyl-1H-indole-3-ethanamine ChemIDplus
N-Methyltryptamine KEGG COMPOUND
N-monomethyltryptamine ChemIDplus
Nω-methyltryptamine NIST Chemistry WebBook
Manual Xrefs Databases
C00026521 KNApSAcK
C06213 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
134134 Beilstein Registry Number Beilstein
61-49-4 CAS Registry Number ChemIDplus
61-49-4 CAS Registry Number NIST Chemistry WebBook
Last Modified
23 October 2015