CHEBI:17780 - 5-hydroxy-L-tryptophan

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ChEBI Name 5-hydroxy-L-tryptophan
ChEBI ID CHEBI:17780
ChEBI ASCII Name 5-hydroxy-L-tryptophan
Definition The L-enantiomer of 5-hydroxytryptophan.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12133, CHEBI:2064, CHEBI:20577
Supplier Information
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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): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via 5-hydroxytryptophan )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
neurotransmitter
An endogenous compound that is used to transmit information across the synapse between a neuron and another cell.
(via 5-hydroxytryptophan )
Related Structures
5-hydroxy-L-tryptophan is a Structural Derivative of
ammonia
Mass : 17.03056
Formula : H3N
16134 		tryptophan
Mass : 204.22526
Formula : C11H12N2O2
27897 		L-tryptophan
Mass : 204.22526
Formula : C11H12N2O2
16828 		proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
5-hydroxy-L-tryptophan is a Enantiomer of
5-hydroxy-D-tryptophan
Mass : 220.22466
Formula : C11H12N2O3
43186
5-hydroxy-L-tryptophan is a Tautomer of
5-hydroxy-L-tryptophan zwitterion
Mass : 220.22460
Formula : C11H12N2O3
58266
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