N-Acetyl-L-tryptophan methyl ester

COC(=O)[C@H](CC1=CNC2=C1C=CC=C2)NC(C)=O

InChIKey=XZECNVJPYDPBAM-ZDUSSCGKSA-N

InChI=1S/C14H16N2O3/c1-9(17)16-13(14(18)19-2)7-10-8-15-12-6-4-3-5-11(10)12/h3-6,8,13,15H,7H2,1-2H3,(H,16,17)/t13-/m0/s1

PubMed

Title	Date	PubMed
Cellular effects of peptide and protein hydroperoxides.	2010-04-15	20109544
Oxidation and inactivation of SERCA by selective reaction of cysteine residues with amino acid peroxides.	2007-10	17892267
Enhanced ligand affinity for receptors in which components of the binding site are independently mobile.	2005-01	15664518
Infrared-induced conformational isomerization and vibrational relaxation dynamics in melatonin and 5-methoxy-N-acetyl tryptophan methyl amide.	2004-05-15	15267838
A mass spectrometric and molecular orbital study of H2O loss from protonated tryptophan and oxidized tryptophan derivatives.	2004	15116425

Patents

Name

Type

Language

Methyl L-N-acetyltryptophanate

Preferred Name

English

N-Acetyl-L-tryptophan methyl ester

Systematic Name

English

L-Tryptophan, N-acetyl-, methyl ester

Systematic Name

English

METHYL ACETYLTRYPTOPHANATE

Systematic Name

English

ACETYLTRYPTOPHAN METHYL ESTER

Systematic Name

English

Code System Code Type Description

FDA UNII

MUP4Y18ZQ5