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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:27730 -
D
-isoleucine
Main
ChEBI Ontology
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ChEBI Name
D
-isoleucine
ChEBI ID
CHEBI:27730
ChEBI ASCII Name
D-isoleucine
Definition
The
D
-enantiomer of isoleucine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:21044, CHEBI:42091, CHEBI:4201
Supplier Information
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Formula
C6H13NO2
Net Charge
0
Average Mass
131.17296
Monoisotopic Mass
131.09463
InChI
InChI=1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5-/m1/s1
InChIKey
AGPKZVBTJJNPAG-RFZPGFLSSA-N
SMILES
CC[C@@H](C)[C@@H](N)C(O)=O
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
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):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
(via
isoleucine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-isoleucine (
CHEBI:27730
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
D
-isoleucine (
CHEBI:27730
)
has role
bacterial metabolite (
CHEBI:76969
)
D
-isoleucine (
CHEBI:27730
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-isoleucine (
CHEBI:27730
)
is a
isoleucine (
CHEBI:24898
)
D
-isoleucine (
CHEBI:27730
)
is conjugate acid of
D
-isoleucinate (
CHEBI:32608
)
D
-isoleucine (
CHEBI:27730
)
is conjugate base of
D
-isoleucinium (
CHEBI:32609
)
D
-isoleucine (
CHEBI:27730
)
is enantiomer of
L
-isoleucine (
CHEBI:17191
)
D
-isoleucine (
CHEBI:27730
)
is tautomer of
D
-isoleucine zwitterion (
CHEBI:193151
)
Incoming
D
-isoleucine derivative (
CHEBI:84113
)
has functional parent
D
-isoleucine (
CHEBI:27730
)
D
-isoleucinium (
CHEBI:32609
)
is conjugate acid of
D
-isoleucine (
CHEBI:27730
)
D
-isoleucinate (
CHEBI:32608
)
is conjugate base of
D
-isoleucine (
CHEBI:27730
)
L
-isoleucine (
CHEBI:17191
)
is enantiomer of
D
-isoleucine (
CHEBI:27730
)
D
-isoleucine residue (
CHEBI:30010
)
is substituent group from
D
-isoleucine (
CHEBI:27730
)
D
-isoleucino group (
CHEBI:32611
)
is substituent group from
D
-isoleucine (
CHEBI:27730
)
D
-isoleucyl group (
CHEBI:32610
)
is substituent group from
D
-isoleucine (
CHEBI:27730
)
D
-isoleucine zwitterion (
CHEBI:193151
)
is tautomer of
D
-isoleucine (
CHEBI:27730
)
IUPAC Name
D
-isoleucine
Synonyms
Sources
(2
R
,3
R
)-2-amino-3-methylpentanoic acid
IUPAC
(2R,3R)-2-Amino-3-methylvaleric acid
KEGG COMPOUND
(R)-2-Amino-(S)-3-methylvaleric acid
KEGG COMPOUND
D-Isoleucine
KEGG COMPOUND
D-ISOLEUCINE
PDBeChem
DIL
PDBeChem
Manual Xrefs
Databases
C06418
KEGG COMPOUND
DIL
PDBeChem
US2011059503
Patent
US7741540
Patent
YMDB00853
YMDB
View more database links
Registry Numbers
Types
Sources
1721793
Beilstein Registry Number
Beilstein
1721793
Reaxys Registry Number
Reaxys
278733
Gmelin Registry Number
Gmelin
319-78-8
CAS Registry Number
ChemIDplus
Citations
Types
Sources
24312553
PubMed citation
Europe PMC
24966047
PubMed citation
Europe PMC
3289762
PubMed citation
Europe PMC
4150713
PubMed citation
Europe PMC
57739
PubMed citation
Europe PMC
Last Modified
14 September 2015