Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:16765 - tryptamine
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
tryptamine
ChEBI ID
CHEBI:16765
Definition
An aminoalkylindole consisting of indole having a 2-aminoethyl group at the 3-position.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:9767, CHEBI:46157, CHEBI:15274, CHEBI:27161
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
more structures >>
Molfile
Molfile
expand
Wikipedia
License
Read full article at Wikipedia
Formulae
C10H12N2
C10H12N2
Net Charge
0
Average Mass
160.21570
Monoisotopic Mass
160.10005
InChI
InChI=1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2
InChIKey
APJYDQYYACXCRM-UHFFFAOYSA-N
SMILES
NCCc1c[nH]c2ccccc12
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
See:
PubMed
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
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
tryptamine (
CHEBI:16765
)
has role
human metabolite (
CHEBI:77746
)
tryptamine (
CHEBI:16765
)
has role
mouse metabolite (
CHEBI:75771
)
tryptamine (
CHEBI:16765
)
has role
plant metabolite (
CHEBI:76924
)
tryptamine (
CHEBI:16765
)
is a
aminoalkylindole (
CHEBI:38631
)
tryptamine (
CHEBI:16765
)
is a
aralkylamino compound (
CHEBI:64365
)
tryptamine (
CHEBI:16765
)
is a
indole alkaloid (
CHEBI:38958
)
tryptamine (
CHEBI:16765
)
is a
tryptamines (
CHEBI:27162
)
tryptamine (
CHEBI:16765
)
is conjugate base of
tryptaminium (
CHEBI:57887
)
Incoming
N
,
N
-dimethyltryptamine (
CHEBI:28969
)
has functional parent
tryptamine (
CHEBI:16765
)
N
-acetyltryptamine (
CHEBI:55515
)
has functional parent
tryptamine (
CHEBI:16765
)
N
-methyltryptamine (
CHEBI:28136
)
has functional parent
tryptamine (
CHEBI:16765
)
baeocystin (
CHEBI:139505
)
has functional parent
tryptamine (
CHEBI:16765
)
luzindole (
CHEBI:131788
)
has functional parent
tryptamine (
CHEBI:16765
)
melatonin (
CHEBI:16796
)
has functional parent
tryptamine (
CHEBI:16765
)
norbaeocystin (
CHEBI:139479
)
has functional parent
tryptamine (
CHEBI:16765
)
serotonin (
CHEBI:28790
)
has functional parent
tryptamine (
CHEBI:16765
)
tryptaminium (
CHEBI:57887
)
is conjugate acid of
tryptamine (
CHEBI:16765
)
IUPAC Name
2-(1
H
-indol-3-yl)ethanamine
Synonyms
Sources
1
H
-indole-3-ethanamine
NIST Chemistry WebBook
2-(1H-INDOL-3-YL)ETHANAMINE
PDBeChem
2-(3-indolyl)ethylamine
ChemIDplus
3-(2-Aminoethyl)indole
KEGG COMPOUND
Tryptamine
KEGG COMPOUND
Manual Xrefs
Databases
C00001434
KNApSAcK
C00398
KEGG COMPOUND
DB08653
DrugBank
HMDB0000303
HMDB
Tryptamine
Wikipedia
TRYPTAMINE
MetaCyc
TSS
PDBeChem
View more database links
Registry Numbers
Types
Sources
125513
Reaxys Registry Number
Reaxys
125513
Beilstein Registry Number
Beilstein
603448
Gmelin Registry Number
Gmelin
61-54-1
CAS Registry Number
NIST Chemistry WebBook
61-54-1
CAS Registry Number
ChemIDplus
Citations
Types
Sources
16126914
PubMed citation
Europe PMC
22770225
PubMed citation
Europe PMC
24345948
PubMed citation
Europe PMC
24558969
PubMed citation
Europe PMC
Last Modified
22 January 2018