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Details

Stereochemistry RACEMIC
Molecular Formula C9H11NO2
Molecular Weight 165.1891
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLALANINE, DL-

SMILES

NC(CC1=CC=CC=C1)C(O)=O

InChI

InChIKey=COLNVLDHVKWLRT-UHFFFAOYSA-N
InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)

HIDE SMILES / InChI
Molecular Formula C9H11NO2
Molecular Weight 165.1891
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
N,N'-[(8-endo,11-endo-Dihy-droxy-penta-cyclo-[5.4.0.0.0.0]undecane-8,11-di-yl)bis-(methyl-enecarbon-yl)]di-l-phenyl-alanine.
2010-09-11
Complete genome sequence of Planctomyces limnophilus type strain (Mü 290).
2010-07-29
Mechanism of Inhibition of Novel Tryptophan Hydroxylase Inhibitors Revealed by Co-crystal Structures and Kinetic Analysis.
2010-04-14
Main-chain ionic chiral polymers: synthesis of optically active quaternary ammonium sulfonate polymers and their application in asymmetric catalysis.
2010-03-10
(S)-1-Carb-oxy-2-(4-nitro-phen-yl)ethanaminium bromide.
2009-09-09
[Chemical constituents from Centipeda minima].
2009-06
Standardized natural product cannabis in pain management and observations at a Canadian compassion society: a case report.
2009-05-18
Enantioselective lactate binding by chiral tripodal anion hosts derived from amino acids.
2009-04-21
Kinetic and thermodynamic control in the stereoselective formation of trans- and cis-2-ferrocenyl-3-pivaloyl-4-alkyl-1,3-oxazolidin-5-ones.
2009-02-07
Attention-deficit-hyperactivity disorder and reward deficiency syndrome.
2008-10
Enantioseparation of dopa and related compounds by cyclodextrin-modified microemulsion electrokinetic chromatography.
2008-09-19
1-Meth-oxycarbonyl-2-(4-nitro-phen-yl)ethanaminium nitrate.
2008-09-13
(S)-1-Methoxy-carbonyl-2-(4-nitro-phen-yl)ethanaminium chloride.
2008-07-12
2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.
2008-07-09
Oligopeptides and copeptides of homochiral sequence, via beta-sheets, from mixtures of racemic alpha-amino acids, in a one-pot reaction in water; relevance to biochirogenesis.
2008-07-09
(S)-2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.
2008-05-03
Diaqua-(nitrato-κO,O')bis-(l-phenyl-alaninato-κO,O')lead(II) nitrate.
2008-03-20
[In-vitro evaluation of cinnarizine as a competing agent to beta-cyclodextrin inclusion complexes: effect of cinnarizine on the membrane permeation rate of progesterone from its beta-cyclodextrin inclusion complex].
2008-01
Unusual mechanism for an aminomutase rearrangement: retention of configuration at the migration termini.
2007-08-28
Production and characterization of monoclonal antibodies against ochratoxin B.
2007-05
Raman spectroscopic investigation of solid samples using a low-repetition-rate pulsed Nd:YAG laser as the excitation source.
2007-01
Electron-transfer reactions through the associated interaction between cytochrome c and self-assembled monolayers of optically active cobalt(III) complexes: molecular recognition ability induced by the chirality of the cobalt(III) units.
2007
The glycolytic pathway of Trimastix pyriformis is an evolutionary mosaic.
2006-11-23
Spectral investigations of amino acid picrates.
2006-10
Performance of D-amino acid oxidase in presence of ionic liquids.
2006-06-25
Synthesis and thermal characterization of new ternary chelates of piroxicam and tenoxicam with glycine and DL-phenylalanine and some transition metals.
2006-05-01
Benzophenone-based farnesyltransferase inhibitors with high activity against Trypanosoma cruzi.
2005-11-17
Laser Raman and infrared spectral studies of dl-phenylalaninium nitrate.
2005-11
Synthesis of enantiomerically pure (purin-6-yl)phenylalanines and their nucleosides, a novel type of purine-amino acid conjugates.
2005-09-30
A novel HLA allele, DRB1*1609, identified in the Chinese Han population*.
2005-09
An investigation of enhanced secondary ion emission under Au(n)+ (n = 1-7) bombardment.
2005-05
Antiglucocorticoid RU38486 reduces net protein catabolism in experimental acute renal failure.
2005-02-17
Spirocyclic zwitterionic lambda5Si-silicates with two bidentate ligands derived from alpha-amino acids or alpha-hydroxycarboxylic acids: synthesis, structure, and stereodynamics.
2004-11-10
Synthesis, investigation and spectroscopic characterization of piroxicam ternary complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) with glycine and DL-phenylalanine.
2004-11
[Compared D-amino acid oxidase expression in different Pichia pastoris host strains].
2004-07
Electroreductive intramolecular coupling of chiral alpha-imino esters: stereoselective synthesis of mixed ketals of cis-2,4-disubstituted azetidine-3-ones.
2003-09-24
Chemometric modelling based on 2D-fluorescence spectra without a calibration measurement.
2003-01-22
Infrared and laser Raman studies of L-phenylalanine L-phenylalaninium perchlorate and bis(DL-phenylalaninium) sulphate monohydrate.
2002-07
Inspection of the reversal of enantiomer migration order in ligand exchange micellar electrokinetic capillary chromatography.
2001-05
Development of a thickness shear mode acoustic sensor based on an electrosynthesized molecularly imprinted polymer using an underivatized amino acid as the template.
2001-02
Patents

Patents

JP1063596A
1
JP1083017A
2
JP2000143693A
1
JP2000169391A
2
JP2001029077A
1
JP2001218579A
5
JP2002253171A
1
JP2002369690A
1
JP2002505281A
2
JP2002511777A
420
JP2003125732A
1
JP2003192633A
1
JP2003238507A
1
JP2004051507A
1
JP2004067575A
1
JP2004097058A
1
JP2004535461A
2
JP2005104874A
1
JP2005152428A
1
JP2005272473A
1
JP2005304363A
2
JP2005318892A
1
JP2005507376A
6
JP2006026156A
1
JP2006149377A
2
JP2006232860A
8
JP2007126358A
1
JP2007244379A
1
JP2007512228A
21
JP2007516939A
1
JP2007528194A
2
JP2008001713A
1
JP2008037872A
1
JP2009069085A
1
JP2009137992A
1
JP2009161485A
2
JP2009261249A
2
JP2009502145A
2
JP2010013418A
2
JP2010038796A
7
JP2010059120A
7
JP2010150272A
2
JP2010248153A
1
JP2010509982A
3
JP2010534856A
1
JP2011116724A
1
JP2011523937A
2
JP2011529084A
1
JP2012500803A
4
JP2013538564A
2
JP3926839B2
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:36:04 GMT 2025
Edited
by admin
on Mon Mar 31 17:36:04 GMT 2025
Record UNII
8P946UF12S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYLALANINE, DL-
Systematic Name English
DL-PHENYLALANINE
FCC   FHFI   WHO-DD  
Preferred Name English
PHENYLALANINE,DL-
Common Name English
2-AMINO-3-PHENYLPROPANOIC ACID
Systematic Name English
DL-PHENYLALANINE [FCC]
Common Name English
(±)-PHENYLALANINE
Systematic Name English
PHENYLALANINE DL
Common Name English
DL-2-AMINO-3-PHENYLPROPIONIC ACID
Common Name English
NSC-9959
Code English
PHENYLALANINE DL-FORM [MI]
Common Name English
DL-PHENYLALANINE [FHFI]
Common Name English
FEMA NO. 3726
Code English
PHENYLALANINE DL-FORM
MI  
Common Name English
DL-3-PHENYLALANINE
Common Name English
(±)-3-PHENYL-2-AMINOPROPANOIC ACID
Systematic Name English
Dl-phenylalanine [WHO-DD]
Common Name English
(±)-.BETA.-PHENYL-.ALPHA.-ALANINE
Common Name English
Classification Tree Code System Code
DSLD 2742 (Number of products:175)
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
NCI_THESAURUS C231
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
JECFA EVALUATION DL-PHENYLALANINE
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
CFR 21 CFR 862.1555
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
Code System Code Type Description
FDA UNII
8P946UF12S
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID9023463
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
SMS_ID
100000141659
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
CAS
150-30-1
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
PUBCHEM
994
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
CHEBI
28044
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
NSC
9959
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
NCI_THESAURUS
C61713
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-756-7
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
JECFA MONOGRAPH
1422
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
MERCK INDEX
m8652
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY Merck Index
EVMPD
SUB96039
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY
RXCUI
236948
Created by admin on Mon Mar 31 17:36:04 GMT 2025 , Edited by admin on Mon Mar 31 17:36:04 GMT 2025
PRIMARY RxNorm
Related Record Type Details
Structure of PHENYLALANINE, DL-
ACTIVE MOIETY
NIH
NCATS
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