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:86366 -
N
-(2-methylbutanoyl)glycine
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
N
-(2-methylbutanoyl)glycine
ChEBI ID
CHEBI:86366
ChEBI ASCII Name
N-(2-methylbutanoyl)glycine
Definition
A
N
-acylglycine that is glycine substituted by a 2-methylbutanoyl group at the N atom.
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
Formula
C7H13NO3
Net Charge
0
Average Mass
159.18300
Monoisotopic Mass
159.08954
InChI
InChI=1S/C7H13NO3/c1-3-5(2)7(11)8-4-6(9)10/h5H,3-4H2,1-2H3,(H,8,11)(H,9,10)
InChIKey
HOACIBQKYRHBOW-UHFFFAOYSA-N
SMILES
CCC(C)C(=O)NCC(O)=O
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
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
N
-(2-methylbutanoyl)glycine (
CHEBI:86366
)
has functional parent
2-methylbutyric acid (
CHEBI:37070
)
N
-(2-methylbutanoyl)glycine (
CHEBI:86366
)
has role
human metabolite (
CHEBI:77746
)
N
-(2-methylbutanoyl)glycine (
CHEBI:86366
)
is a
N
-acylglycine (
CHEBI:16180
)
IUPAC Name
N
-(2-methylbutanoyl)glycine
Synonyms
Sources
2-Methylbutyrylglycine
HMDB
alpha-Methylbutyrylglycine
HMDB
Manual Xref
Database
HMDB0000339
HMDB
View more database links
Registry Numbers
Types
Sources
2206207
Reaxys Registry Number
Reaxys
52320-67-9
CAS Registry Number
ChemIDplus
Citation
Type
Source
24023812
PubMed citation
Europe PMC
Last Modified
12 March 2018