CHEBI:45086 - L-phenylalaninol

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ChEBI Name L-phenylalaninol
ChEBI ID CHEBI:45086
ChEBI ASCII Name L-phenylalaninol
Definition An amino alcohol resulting from the formal reduction of the carboxy group of L-phenylalanine to the corresponding alcohol.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C9H13NO
Net Charge 0
Average Mass 151.209
Monoisotopic Mass 151.09971
InChI InChI=1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m0/s1
InChIKey STVVMTBJNDTZBF-VIFPVBQESA-N
SMILES C([C@H](CC1=CC=CC=C1)N)O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): central nervous system stimulant
Any drug that enhances the activity of the central nervous system.
(via amphetamines )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-phenylalaninol (CHEBI:45086) is a amino alcohol (CHEBI:22478)
L-phenylalaninol (CHEBI:45086) is a amphetamines (CHEBI:35338)
L-phenylalaninol (CHEBI:45086) is a primary alcohol (CHEBI:15734)
L-phenylalaninol (CHEBI:45086) is a primary amino compound (CHEBI:50994)
Incoming N-benzoyl-L-phenylalaninol (CHEBI:145107) has functional parent L-phenylalaninol (CHEBI:45086)
IUPAC Name
(2S)-2-amino-3-phenylpropan-1-ol
Synonyms Sources
(−)-2-amino-3-phenyl-1-propanol ChEBI
(S)-(−)-2-amino-3-phenyl-1-propanol ChEBI
(S)-2-benzylethanolamine ChemIDplus
(S)-β-aminobenzenepropanol ChemIDplus
(S)-phenylalaninol ChemIDplus
L-2-amino-3-phenyl-1-propanol ChemIDplus
Manual Xrefs Databases
DB04484 DrugBank
LSM-19018 LINCS
PHL PDBeChem
View more database links
Registry Number Type Source
3182-95-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12840826 PubMed citation Europe PMC
27619990 PubMed citation Europe PMC
Last Modified
17 October 2019