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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H13NO
Molecular Weight 151.2056
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLALANINOL

SMILES

N[C@H](CO)CC1=CC=CC=C1

InChI

InChIKey=STVVMTBJNDTZBF-VIFPVBQESA-N
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

HIDE SMILES / InChI

Molecular Formula C9H13NO
Molecular Weight 151.2056
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: O75387
Gene ID: 8501.0
Gene Symbol: SLC43A1
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Absolute configurations and CD spectra of axially chiral biphenyls prepared in a facile manner by crystallization-induced configuration transformation.
2010-08
Synthesis of enantiopure 2-aryl-2-methoxypropionic acids and determination of their absolute configurations by X-ray crystallography.
2008-03
Direct high-performance liquid chromatographic separation of the enantiomers of an aromatic amine and four aminoalcohols using polysaccharide chiral stationary phases and acidic additive.
2007-08
Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.
2007-07-06
New route to enantiopure MalphaNP acid, a powerful resolution and chiral 1H NMR anisotropy reagent.
2007-05-15
Synthesis and activity of 2-oxoamides containing long chain beta-amino acids.
2005-07
Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars.
2005-04-07
Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.
2003-11-21
Identification of a novel system L amino acid transporter structurally distinct from heterodimeric amino acid transporters.
2003-10-31
Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol.
2003-08
Tuning and enhancing enantioselective quenching of calixarene hosts by chiral guest amines.
2002-01-01
Enantioselective molecular sensing of aromatic amines using tetra-(S)-di-2-naphthylprolinol calix[4]arene.
2001-07
Patents
Substance Class Chemical
Created
by admin
on Tue Apr 01 16:28:05 GMT 2025
Edited
by admin
on Tue Apr 01 16:28:05 GMT 2025
Record UNII
9GE9QOP0ET
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(S)-(-)-PHENYLALANINOL
Preferred Name English
PHENYLALANINOL
Common Name English
L-(-)-2-AMINO-3-PHENYL-1-PROPANOL
Systematic Name English
BENZENEPROPANOL, .BETA.-AMINO-, (.BETA.S)-
Systematic Name English
PHENYLALANINOL, (S)-
Common Name English
L-PHENYLALANINOL
Systematic Name English
Code System Code Type Description
PUBCHEM
447213
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
CAS
3182-95-4
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
DRUG BANK
DB04484
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
221-674-4
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
FDA UNII
9GE9QOP0ET
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID001025528
Created by admin on Tue Apr 01 16:28:05 GMT 2025 , Edited by admin on Tue Apr 01 16:28:05 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER