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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:28225 -
D
-leucine
Main
ChEBI Ontology
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Models
ChEBI Name
D
-leucine
ChEBI ID
CHEBI:28225
ChEBI ASCII Name
D-leucine
Definition
The
D
-enantiomer of leucine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:41908, CHEBI:4202, CHEBI:21045
Supplier Information
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Molfile
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Formula
C6H13NO2
Net Charge
0
Average Mass
131.17296
Monoisotopic Mass
131.09463
InChI
InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m1/s1
InChIKey
ROHFNLRQFUQHCH-RXMQYKEDSA-N
SMILES
CC(C)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
leucine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-leucine (
CHEBI:28225
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
D
-leucine (
CHEBI:28225
)
has role
bacterial metabolite (
CHEBI:76969
)
D
-leucine (
CHEBI:28225
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-leucine (
CHEBI:28225
)
is a
leucine (
CHEBI:25017
)
D
-leucine (
CHEBI:28225
)
is conjugate acid of
D
-leucinate (
CHEBI:32623
)
D
-leucine (
CHEBI:28225
)
is conjugate base of
D
-leucinium (
CHEBI:32624
)
D
-leucine (
CHEBI:28225
)
is enantiomer of
L
-leucine (
CHEBI:15603
)
D
-leucine (
CHEBI:28225
)
is tautomer of
D
-leucine zwitterion (
CHEBI:143079
)
Incoming
D
-leucine derivative (
CHEBI:84114
)
has functional parent
D
-leucine (
CHEBI:28225
)
D
-leucinium (
CHEBI:32624
)
is conjugate acid of
D
-leucine (
CHEBI:28225
)
D
-leucinate (
CHEBI:32623
)
is conjugate base of
D
-leucine (
CHEBI:28225
)
L
-leucine (
CHEBI:15603
)
is enantiomer of
D
-leucine (
CHEBI:28225
)
D
-leucine residue (
CHEBI:30005
)
is substituent group from
D
-leucine (
CHEBI:28225
)
D
-leucino group (
CHEBI:32626
)
is substituent group from
D
-leucine (
CHEBI:28225
)
D
-leucyl group (
CHEBI:32625
)
is substituent group from
D
-leucine (
CHEBI:28225
)
D
-leucine zwitterion (
CHEBI:143079
)
is tautomer of
D
-leucine (
CHEBI:28225
)
IUPAC Name
D
-leucine
Synonyms
Sources
(2
R
)-2-amino-4-methylpentanoic acid
IUPAC
(
R
)-(−)-leucine
NIST Chemistry WebBook
(
R
)-leucine
ChemIDplus
D-2-Amino-4-methylvaleric acid
KEGG COMPOUND
D
-Leucin
ChEBI
D-Leucine
KEGG COMPOUND
D-LEUCINE
PDBeChem
D
-Leuzin
ChEBI
DLE
PDBeChem
Manual Xrefs
Databases
C01570
KEGG COMPOUND
DB01746
DrugBank
DLE
PDBeChem
HMDB0013773
HMDB
YMDB00997
YMDB
View more database links
Registry Numbers
Types
Sources
1721721
Reaxys Registry Number
Reaxys
1721721
Beilstein Registry Number
Beilstein
328-38-1
CAS Registry Number
KEGG COMPOUND
328-38-1
CAS Registry Number
ChemIDplus
328-38-1
CAS Registry Number
NIST Chemistry WebBook
82675
Gmelin Registry Number
Gmelin
Citations
Types
Sources
15375647
PubMed citation
Europe PMC
21941889
PubMed citation
Europe PMC
24097941
PubMed citation
Europe PMC
Last Modified
14 September 2015