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:73025 -
O
-isovalerylcarnitine
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
O
-isovalerylcarnitine
ChEBI ID
CHEBI:73025
ChEBI ASCII Name
O-isovalerylcarnitine
Definition
A C
5
-acylcarnitine having isovaleryl as the acyl substituent.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
No supplier information found for this compound.
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C12H23NO4
Net Charge
0
Average Mass
245.31530
Monoisotopic Mass
245.16271
InChI
InChI=1S/C12H23NO4/c1-9(2)6-12(16)17-10(7-11(14)15)8-13(3,4)5/h9-10H,6-8H2,1-5H3
InChIKey
IGQBPDJNUXPEMT-UHFFFAOYSA-N
SMILES
CC(C)CC(=O)OC(CC([O-])=O)C[N+](C)(C)C
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
O
-isovalerylcarnitine (
CHEBI:73025
)
has functional parent
isovaleric acid (
CHEBI:28484
)
O
-isovalerylcarnitine (
CHEBI:73025
)
has role
human metabolite (
CHEBI:77746
)
O
-isovalerylcarnitine (
CHEBI:73025
)
is a
C
5
-acylcarnitine (
CHEBI:86492
)
Incoming
isovaleryl-
L
-carnitine (
CHEBI:70819
)
is a
O
-isovalerylcarnitine (
CHEBI:73025
)
IUPAC Name
3-[(3-methylbutanoyl)oxy]-4-(trimethylammonio)butanoate
Synonym
Source
3-methylbutyrylcarnitine
ChEBI
Manual Xref
Database
HMDB0000688
HMDB
View more database links
Registry Number
Type
Source
5814736
Reaxys Registry Number
Reaxys
Citations
Last Modified
23 October 2015