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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H15NO2
Molecular Weight 193.2423
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl L-phenylalaninate

SMILES

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

InChI

InChIKey=CJGXMNONHNZEQQ-JTQLQIEISA-N
InChI=1S/C11H15NO2/c1-2-14-11(13)10(12)8-9-6-4-3-5-7-9/h3-7,10H,2,8,12H2,1H3/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C11H15NO2
Molecular Weight 193.2423
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Influence of ion pairing on topical delivery of retinoic acid from microemulsions.
2003 Jan 17
Reaction of a peptide with polyvinylpyrrolidone in the solid state.
2003 Mar
In vitro enzymatic degradation of nanoparticles prepared from hydrophobically-modified poly(gamma-glutamic acid).
2005 Jul 14
Preparation and characterization of biodegradable nanoparticles based on poly(gamma-glutamic acid) with l-phenylalanine as a protein carrier.
2005 Nov 28
Hydrolytic and enzymatic degradation of nanoparticles based on amphiphilic poly(gamma-glutamic acid)-graft-L-phenylalanine copolymers.
2006 Jan
Microwave-Assisted Syntheses of Amino Acid Ester Substituted Benzoic Acid Amides: Potential Inhibitors of Human CD81-Receptor HCV-E2 Interaction.
2008 Apr 15
Selective adsorption of D- and L-phenylalanine on molecularly-imprinted polymerized organogels formed using polymerizable gelator N-octadecyl maleamic acid.
2008 Dec
Interaction between proteins and polyphosphazene derivatives having a galactose moiety.
2008 Feb
Polyphosphazene/nano-hydroxyapatite composite microsphere scaffolds for bone tissue engineering.
2008 Jul
[Efficacy and safety of poly (gamma-glutamic acid) based nanoparticles (gamma-PGA NPs) as vaccine carrier].
2008 Nov
Synthesis and characterization of new Pd(II) complexes of L-ethylphenylalanate.
2009 Sep
Amino Acid-based fluorescent chiral ionic liquid for enantiomeric recognition.
2010 Jun 15
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:50:15 GMT 2023
Edited
by admin
on Fri Dec 15 19:50:15 GMT 2023
Record UNII
26O5DCZ9XV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Ethyl L-phenylalaninate
Systematic Name English
L-Phenylalanine, ethyl ester
Systematic Name English
(S)-Phenylalanine ethyl este
Systematic Name English
Ethyl (S)-2-amino-3-phenyl-propanoate
Systematic Name English
O-Ethyl-L-phenylalanine
Systematic Name English
Ethyl (2S)-2-amino-3-phenylpropanoate
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
221-378-5
Created by admin on Fri Dec 15 19:50:15 GMT 2023 , Edited by admin on Fri Dec 15 19:50:15 GMT 2023
PRIMARY
FDA UNII
26O5DCZ9XV
Created by admin on Fri Dec 15 19:50:15 GMT 2023 , Edited by admin on Fri Dec 15 19:50:15 GMT 2023
PRIMARY
CAS
3081-24-1
Created by admin on Fri Dec 15 19:50:15 GMT 2023 , Edited by admin on Fri Dec 15 19:50:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID20184816
Created by admin on Fri Dec 15 19:50:15 GMT 2023 , Edited by admin on Fri Dec 15 19:50:15 GMT 2023
PRIMARY
PUBCHEM
76506
Created by admin on Fri Dec 15 19:50:15 GMT 2023 , Edited by admin on Fri Dec 15 19:50:15 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
SALT/SOLVATE -> PARENT