Oxitriptan
(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid
Molecular Identity
Oxitriptan
(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid
PubChem CID: 439280
5-hydroxy-L-tryptophan is the L-enantiomer of 5-hydroxytryptophan. It has a role as a mouse metabolite, a plant metabolite and a human metabolite. It is a 5-hydroxytryptophan, a hydroxy-L-tryptophan and a non-proteinogenic L-alpha-amino acid. It is an enantiomer of a 5-hydroxy-D-tryptophan. It is a tautomer of a 5-hydroxy-L-tryptophan zwitterion.
2D Structure
Properties
C11H12N2O3
Molecular Formula
220.22
Molecular Weight
g/mol
220.0848
Exact Mass
Da
-1.2
XLogP
Drug-like (Lipinski: < 5)
99.3
TPSA
Good oral absorption (< 140 A²)
4
H-Bond Donors
4
H-Bond Acceptors
272
Complexity
SMILES
Canonical SMILES
SMILES: C1=CC2=C(C=C1O)C(=CN2)CC(C(=O)O)NIsomeric SMILES
SMILES: C1=CC2=C(C=C1O)C(=CN2)C[C@@H](C(=O)O)NSynonyms(20)
oxitriptanLevothymPretonineTripteneOxyfanQuietimLevotinineSerotonylTelesolOxitriptanoOxitriptanumTripten(S)-5-HydroxytryptophanC1LJO185Q9CCRIS 4418
Data from PubChem (NCBI)
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Drug Network
Trials and conditions connected to Oxitriptan
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