CHEBI:28225 - D-leucine

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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
Download Molfile XML SDF
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 (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted 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
(2R)-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 Waiting for Citations Types Sources
15375647 PubMed citation Europe PMC
21941889 PubMed citation Europe PMC
24097941 PubMed citation Europe PMC
Last Modified
14 September 2015