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
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Formula C11H12N2O3
Net Charge 0
Average Mass 220.22466
Monoisotopic Mass 220.085
InChI InChI=1S/C11H12N2O3/c12-9(11(15)16)3-6-5-13-10-2-1-7(14)4-8(6)10/h1-2,4-5,9,13-14H,3,12H2,(H,15,16)/t9-/m0/s1
InChIKey LDCYZAJDBXYCGN-VIFPVBQESA-N
SMILES N[C@@H](Cc1c[nH]c2ccc(O)cc12)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:9606) See: DOI
Roles Classification
Chemical Role(s): 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).
(via L-alpha-amino acid )
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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-hydroxy-L-tryptophan (CHEBI:17780) has role human metabolite (CHEBI:77746)
5-hydroxy-L-tryptophan (CHEBI:17780) has role mouse metabolite (CHEBI:75771)
5-hydroxy-L-tryptophan (CHEBI:17780) has role plant metabolite (CHEBI:76924)
5-hydroxy-L-tryptophan (CHEBI:17780) is a 5-hydroxytryptophan (CHEBI:28171)
5-hydroxy-L-tryptophan (CHEBI:17780) is a hydroxy-L-tryptophan (CHEBI:47995)
5-hydroxy-L-tryptophan (CHEBI:17780) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
5-hydroxy-L-tryptophan (CHEBI:17780) is enantiomer of 5-hydroxy-D-tryptophan (CHEBI:43186)
5-hydroxy-L-tryptophan (CHEBI:17780) is tautomer of 5-hydroxy-L-tryptophan zwitterion (CHEBI:58266)
Incoming 5-hydroxy-D-tryptophan (CHEBI:43186) is enantiomer of 5-hydroxy-L-tryptophan (CHEBI:17780)
5-hydroxy-L-tryptophan zwitterion (CHEBI:58266) is tautomer of 5-hydroxy-L-tryptophan (CHEBI:17780)
IUPAC Names
(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid
5-hydroxy-L-tryptophan
Synonyms Sources
5-hydroxy-L-tryptophan ChEBI
5-Hydroxy-L-tryptophan KEGG COMPOUND
5-hydroxytryptophan L-form ChemIDplus
Cincofarm ChemIDplus
L-5-hydroxytryptophan ChemIDplus
Levothym ChemIDplus
oxitriptan ChemIDplus
Oxitriptan KEGG COMPOUND
Tript-OH ChemIDplus
Database Links Databases
4006 DrugCentral
5-HYDROXY-TRYPTOPHAN MetaCyc
5-Hydroxytryptophan Wikipedia
C00001371 KNApSAcK
C00643 KEGG COMPOUND
D07339 KEGG DRUG
DB02959 DrugBank
HMDB0000472 HMDB
View more database links
Registry Numbers Types Sources
1862149 Gmelin Registry Number Gmelin
4350-09-8 CAS Registry Number ChemIDplus
88200 Reaxys Registry Number Reaxys
88200 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
22964922 PubMed citation Europe PMC
24321061 PubMed citation Europe PMC
24369991 PubMed citation Europe PMC
5297581 PubMed citation Europe PMC
9295177 PubMed citation Europe PMC
Last Modified
22 February 2017