N-Acetyl-L-tryptophan

N-Acetyl-L-tryptophan Basic information
Product Name:N-Acetyl-L-tryptophan
Synonyms:ACETYL-L-TRYPTOPHANE;ACETYL-L-TRYPTOPHAN;AC-TRP-OH;AC-TRYPTOPHAN;L-N-ACETYL-2-AMINO-3-(3-INDOLYL)PROPIONIC ACID;(S)-2-acetaMido-3-(1H-indol-3-yl)propanoic acid;Tryptophan Related CoMpound B;N-Ac-Tryptohan
CAS:1218-34-4
MF:C13H14N2O3
MW:246.26
EINECS:214-935-9
Product Categories:Amino Acids Derivatives;Amino Acid Derivatives;amino;amino acid;A - H;Amino Acids;Modified Amino Acids;Tryptophan [Trp, W];Amino Acids and Derivatives;Ac-Amino Acids;Amino Acids (N-Protected);Biochemistry;Indoles;Tryptophans;N-Acetyl-Amino acid series;Amino Acids
Mol File:1218-34-4.mol
N-Acetyl-L-tryptophan Structure
N-Acetyl-L-tryptophan Chemical Properties
Melting point 186°C
Boiling point 389.26°C (rough estimate)
alpha +24.0~+30.0°(20℃/D)(c=1,C2H5OH)
density 1.1855 (rough estimate)
refractive index 1.6450 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka3.65±0.10(Predicted)
form Powder
color White to Off-white
Stability:Stable. Incompatible with strong oxidizing agents.
LogP0.702 (est)
CAS DataBase Reference1218-34-4(CAS DataBase Reference)
NIST Chemistry ReferenceL-tryptophan, n-acetyl-(1218-34-4)
EPA Substance Registry SystemL-Tryptophan, N-acetyl- (1218-34-4)
Safety Information
WGK Germany 2
RTECS YN6160000
TSCA Yes
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
N-Acetyl-L-tryptophan Usage And Synthesis
Chemical Propertiessolid
UsesN-Acetyl-L-Tryptophan, is a derivative of L-Tryptophan (T947210), that can be used as competitive inhibitor to identify and characterize tryptophanases. It can also be used as an NK1 tachykinin receptor antagonist, that may help to develop a novel therapeutic intervention for the treatment of reperfusion injury in acute ischemic stroke.
DefinitionChEBI: A N-acetyl-L-amino acid that is the N-acetyl derivative of L-tryptophan.
Safety ProfileModerately toxic by some routes. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOX,.
Acetyl-resveratrol 3-(2-FURYL)ACRYLOYL-L-TRYPTOPHAN METHYL ESTER H-VAL-TRP-OH 4-CHLOROBENZOYL-L-TRYPTOPHAN CALCIUM SALT H-HIS-TRP-OH AC-PHE-TRP-OH N-[(tert-Butoxy)carbonyl]-D-tryptophan H-BETA-ALA-TRP-OH H-LYS-TRP-OH L-ALANYL-L-TRYPTOPHAN H-PRO-TRP-OH H-GLU-TRP-OH Nα-Acetyl-L-tryptophan methyl ester,ACETYL-L-TRYPTOPHAN METHYL ESTER,N-ALPHA-ACETYL-L-TRYPTOPHAN METHYL ESTER Z-TRP-TRP-OH H-LEU-TRP-OH ACETYL-L-TRYPTOPHAN ETHYL ESTER,N-ACETYL-L-TRYPTOPHAN ETHYL ESTER 99%,N-ACETYL-L-TRYPTOPHAN ETHYL ESTER,N-ALPHA-ACETYL-L-TRYPTOPHAN ETHYL ESTER Z-HIS-PHE-TRP-OET BZ-TRP-OH

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.