CHEBI:32623 - D-leucinate

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ChEBI Name D-leucinate
ChEBI ID CHEBI:32623
ChEBI ASCII Name D-leucinate
Definition The D-enantiomer of leucinate.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H12NO2
Net Charge -1
Average Mass 130.16502
Monoisotopic Mass 130.08735
InChI InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/p-1/t5-/m1/s1
InChIKey ROHFNLRQFUQHCH-RXMQYKEDSA-M
SMILES CC(C)C[C@@H](N)C([O-])=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
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ChEBI Ontology
Outgoing D-leucinate (CHEBI:32623) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
D-leucinate (CHEBI:32623) has role bacterial metabolite (CHEBI:76969)
D-leucinate (CHEBI:32623) is a leucinate (CHEBI:32627)
D-leucinate (CHEBI:32623) is conjugate base of D-leucine (CHEBI:28225)
D-leucinate (CHEBI:32623) is enantiomer of L-leucinate (CHEBI:32619)
Incoming D-leucine (CHEBI:28225) is conjugate acid of D-leucinate (CHEBI:32623)
L-leucinate (CHEBI:32619) is enantiomer of D-leucinate (CHEBI:32623)
IUPAC Name
D-leucinate
Synonyms Sources
(2R)-2-amino-4-methylpentanoate IUPAC
D-leucine anion JCBN
Registry Number Type Source
533394 Gmelin Registry Number Gmelin
Last Modified
11 November 2014