FB2026_02 , released June 18, 2026
Chemical: L-tryptophan
Open Close
General Information
Name
L-tryptophan
FlyBase ID
FBch0000510
ChEBI Name
L-tryptophan
ChEBI ID
PubChem Name
L-Tryptophan
PubChem ID
Chemical Structure
Chemical structure of L-tryptophan
L-tryptophan
InChIKey

QIVBCDIJIAJPQS-VIFPVBQESA-N

Definition (ChEBI)

ChEBI: L-tryptophan is the L-enantiomer of tryptophan. It has a role as an antidepressant, a nutraceutical, a micronutrient, a plant metabolite, a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an erythrose 4-phosphate/phosphoenolpyruvate family amino acid, a proteinogenic amino acid, a tryptophan and a L-alpha-amino acid. It is a conjugate base of a L-tryptophanium. It is a conjugate acid of a L-tryptophanate. It is an enantiomer of a D-tryptophan. It is a tautomer of a L-tryptophan zwitterion.NCI Thesaurus (NCIt): Tryptophan is the least plentiful of all 22 amino acids and an essential amino acid in humans (provided by food), Tryptophan is found in most proteins and a precursor of serotonin. Tryptophan is converted to 5-hydroxy-tryptophan (5-HTP), converted in turn to serotonin, a neurotransmitter essential in regulating appetite, sleep, mood, and pain. Tryptophan is a natural sedative and present in dairy products, meats, brown rice, fish, and soybeans. (NCI04)

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (29)
Synonyms
(2S)-2-amino-3-(1H-indol-3-yl)propanoic acid
(S)-Tryptophan
(S)-alpha-Amino-beta-(3-indolyl)-propionic acid
(S)-alpha-amino-1H-indole-3-propanoic acid
(S)-tryptophan
(s)-tryptophan
L-(-)-tryptophan
L-Tryptophan
L-Tryptophane
L-beta-3-indolylalanine
PubChem:6305
TRYPTOPHAN
Tryptophane
h-Trp-oh
h-trp-oh
l-tryptophan
l-tryptophane
pubchem:6305
tryptacin
tryptophane
Secondary FlyBase IDs
    References (11)