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:9173 - slaframine
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
slaframine
ChEBI ID
CHEBI:9173
Definition
An indolizidine alkaloid that is octahydroindolizine substituted by an amino group at position 6 and an acetyloxy group at position 1.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Wikipedia
License
Read full article at Wikipedia
Formula
C10H18N2O2
Net Charge
0
Average Mass
198.26210
Monoisotopic Mass
198.13683
InChI
InChI=1S/C10H18N2O2/c1-7(13)14-10-4-5-12-6-8(11)2-3-9(10)12/h8-10H,2-6,11H2,1H3/t8-,9?,10-/m0/s1
InChIKey
YYIUHLPAZILPSG-SMILAEQMSA-N
SMILES
CC(=O)O[C@H]1CCN2C[C@@H](N)CCC12
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
)
mycotoxin
Poisonous substance produced by fungi.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
slaframine (
CHEBI:9173
)
has role
metabolite (
CHEBI:25212
)
slaframine (
CHEBI:9173
)
has role
mycotoxin (
CHEBI:25442
)
slaframine (
CHEBI:9173
)
is a
acetate ester (
CHEBI:47622
)
slaframine (
CHEBI:9173
)
is a
indolizidine alkaloid (
CHEBI:38511
)
IUPAC Name
(1
S
,6
S
)-6-aminooctahydroindolizin-1-yl acetate
Synonym
Source
(−)-Slaframine
KEGG COMPOUND
Manual Xrefs
Databases
C06185
KEGG COMPOUND
Slaframine
Wikipedia
View more database links
Registry Numbers
Types
Sources
20084-93-9
CAS Registry Number
ChemIDplus
4351925
Reaxys Registry Number
Reaxys
Citations
Types
Sources
3588504
PubMed citation
Europe PMC
3793651
PubMed citation
Europe PMC
7601787
PubMed citation
Europe PMC
8655443
PubMed citation
Europe PMC
Last Modified
28 July 2014