FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Chemical: L-leucine
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General Information
Name
L-leucine
FlyBase ID
FBch0000508
ChEBI Name
L-leucine
ChEBI ID
PubChem Name
L-Leucine
PubChem ID
Chemical Structure
Chemical structure of L-leucine
L-leucine
InChIKey

ROHFNLRQFUQHCH-YFKPBYRVSA-N

Definition (ChEBI)

ChEBI: L-leucine is the L-enantiomer of leucine. It has a role as a plant metabolite, an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite, a human metabolite, an algal metabolite and a mouse metabolite. It is a pyruvate family amino acid, a proteinogenic amino acid, a leucine and a L-alpha-amino acid. It is a conjugate base of a L-leucinium. It is a conjugate acid of a L-leucinate. It is an enantiomer of a D-leucine. It is a tautomer of a L-leucine zwitterion.NCI Thesaurus (NCIt): Leucine is one of nine essential amino acids in humans (provided by food), Leucine is important for protein synthesis and many metabolic functions. Leucine contributes to regulation of blood-sugar levels; growth and repair of muscle and bone tissue; growth hormone production; and wound healing. Leucine also prevents breakdown of muscle proteins after trauma or severe stress and may be beneficial for individuals with phenylketonuria. Leucine is available in many foods and deficiency is rare. (NCI04)

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (32)
Synonyms
(2S)-2-amino-4-methylpentanoic acid
(2S)-alpha-2-Amino-4-methylvaleric acid
(2S)-alpha-Leucine
(2s)-2-amino-4-methylpentanoic acid
(S)-(+)-Leucine
(S)-(+)-leucine
(S)-2-Amino-4-methylpentanoic acid
(S)-Leucine
(S)-leucine
(s)-(+)-leucine
(s)-2-amino-4-methylpentanoic acid
(s)-leucine
2-Amino-4-methylvaleric acid
H-Leu-OH
L-Leucin
L-Leucine
L-Leuzin
L-Norvaline, 4-methyl-
LEUCINE
PubChem:6106
h-leu-oh
l-leucine
l-norvaline, 4-methyl-
pubchem:6106
Secondary FlyBase IDs
    References (19)