U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Enantioselective molecular sensing of aromatic amines using tetra-(S)-di-2-naphthylprolinol calix[4]arene.
2001 Jul
Tuning and enhancing enantioselective quenching of calixarene hosts by chiral guest amines.
2002 Jan 1
Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol.
2003 Aug
Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.
2003 Nov 21
Identification of a novel system L amino acid transporter structurally distinct from heterodimeric amino acid transporters.
2003 Oct 31
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 Apr 7
Synthesis and activity of 2-oxoamides containing long chain beta-amino acids.
2005 Jul
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 Aug
Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.
2007 Jul 6
New route to enantiopure MalphaNP acid, a powerful resolution and chiral 1H NMR anisotropy reagent.
2007 May 15
Synthesis of enantiopure 2-aryl-2-methoxypropionic acids and determination of their absolute configurations by X-ray crystallography.
2008 Mar
Absolute configurations and CD spectra of axially chiral biphenyls prepared in a facile manner by crystallization-induced configuration transformation.
2010 Aug
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:29:32 GMT 2023
Edited
by admin
on Sat Dec 16 11:29:32 GMT 2023
Record UNII
9GE9QOP0ET
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
(S)-(-)-PHENYLALANINOL
Common Name English
L-PHENYLALANINOL
Systematic Name English
Code System Code Type Description
PUBCHEM
447213
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
CAS
3182-95-4
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
DRUG BANK
DB04484
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
221-674-4
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
FDA UNII
9GE9QOP0ET
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID001025528
Created by admin on Sat Dec 16 11:29:32 GMT 2023 , Edited by admin on Sat Dec 16 11:29:32 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER