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:45525 - (
R
)-2-methylbutyric acid
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
(
R
)-2-methylbutyric acid
ChEBI ID
CHEBI:45525
ChEBI ASCII Name
(R)-2-methylbutyric acid
Definition
The (
R
)-enantiomer of 2-methylbutanoic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:38654, CHEBI:45523
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
C5H10O2
Net Charge
0
Average Mass
102.13170
Monoisotopic Mass
102.06808
InChI
InChI=1S/C5H10O2/c1-3-4(2)5(6)7/h4H,3H2,1-2H3,(H,6,7)/t4-/m1/s1
InChIKey
WLAMNBDJUVNPJU-SCSAIBSYSA-N
SMILES
CC[C@@H](C)C(O)=O
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):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via
2-methylbutyric acid
)
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
(via
2-methylbutyric acid
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
R
)-2-methylbutyric acid (
CHEBI:45525
)
is a
2-methylbutyric acid (
CHEBI:37070
)
(
R
)-2-methylbutyric acid (
CHEBI:45525
)
is enantiomer of
(
S
)-2-methylbutyric acid (
CHEBI:38655
)
Incoming
(
S
)-2-methylbutyric acid (
CHEBI:38655
)
is enantiomer of
(
R
)-2-methylbutyric acid (
CHEBI:45525
)
IUPAC Name
(2
R
)-2-methylbutanoic acid
Synonyms
Sources
(2
R
)-2-methylbutyric acid
ChEBI
2-METHYLBUTANOIC ACID
PDBeChem
Manual Xref
Database
SMB
PDBeChem
View more database links
Registry Numbers
Types
Sources
1041646
Gmelin Registry Number
Gmelin
1720484
Beilstein Registry Number
Beilstein
Citation
Type
Source
2026560
PubMed citation
Europe PMC
Last Modified
19 July 2010