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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:24898 - isoleucine
Main
ChEBI Ontology
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ChEBI Name
isoleucine
ChEBI ID
CHEBI:24898
Definition
A 2-amino-3-methylpentanoic acid having either (2
R
,3
R
)- or (2
S
,3
S
)-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Formula
C6H13NO2
Net Charge
0
Average Mass
131.175
Monoisotopic Mass
131.09463
Metabolite of Species
Details
Daphnia magna
(NCBI:txid35525)
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
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
isoleucine (
CHEBI:24898
)
has part
sec
-butyl group (
CHEBI:45557
)
isoleucine (
CHEBI:24898
)
has role
Daphnia magna
metabolite (
CHEBI:83056
)
isoleucine (
CHEBI:24898
)
is a
2-amino-3-methylpentanoic acid (
CHEBI:38264
)
isoleucine (
CHEBI:24898
)
is conjugate acid of
isoleucinate (
CHEBI:32612
)
isoleucine (
CHEBI:24898
)
is conjugate base of
isoleucinium (
CHEBI:32613
)
Incoming
β-Asp-Ile (
CHEBI:68601
)
has functional parent
isoleucine (
CHEBI:24898
)
isoleucine derivative (
CHEBI:24899
)
has functional parent
isoleucine (
CHEBI:24898
)
D
-isoleucine (
CHEBI:27730
)
is a
isoleucine (
CHEBI:24898
)
L
-isoleucine (
CHEBI:17191
)
is a
isoleucine (
CHEBI:24898
)
isoleucinium (
CHEBI:32613
)
is conjugate acid of
isoleucine (
CHEBI:24898
)
isoleucinate (
CHEBI:32612
)
is conjugate base of
isoleucine (
CHEBI:24898
)
isoleucine residue (
CHEBI:32615
)
is substituent group from
isoleucine (
CHEBI:24898
)
isoleucino group (
CHEBI:32614
)
is substituent group from
isoleucine (
CHEBI:24898
)
isoleucyl group (
CHEBI:37905
)
is substituent group from
isoleucine (
CHEBI:24898
)
IUPAC Name
isoleucine
Synonyms
Sources
Hile
IUPAC
rel
-(2
R
,3
R
)-2-amino-3-methylpentanoic acid
IUPAC
Registry Numbers
Types
Sources
1721790
Reaxys Registry Number
Reaxys
443-79-8
CAS Registry Number
ChemIDplus
443-79-8
CAS Registry Number
NIST Chemistry WebBook
Citation
Type
Source
17190852
PubMed citation
Europe PMC
Last Modified
21 April 2021