《Post-synthetic functionalization of tryptophan protected peptide sequences through indole (C-2) photocatalytic alkylation》 was written by Lima, Rafaely N.; Delgado, Jose A. C.; Bernardi, Darlon I.; Berlinck, Roberto G. S.; Kaplaneris, Nikolaos; Ackermann, Lutz; Paixao, Marcio W.. HPLC of Formula: 7524-52-9This research focused ontryptophan photocatalytic alkylation bromo amino acid visible light; peptide photocatalytic alkylation bromo carbonyl functional group cyclic voltammetry. The article conveys some information:
We report a selective, mild, and efficient C-H functionalization of tryptophan and tryptophan-containing peptides with activated α-bromo-carbonyl compounds under visible-light irradiation The protocol efficiency is outlined by the wide substrate scope and excellent tolerance of sensitive functional groups present in the amino acid side chains. The method can be successfully extended to access pharmaco-peptide conjugate scaffolds. In the experimental materials used by the author, we found H-Trp-OMe.HCl(cas: 7524-52-9HPLC of Formula: 7524-52-9)
H-Trp-OMe.HCl(cas:7524-52-9) is one of amino acid derivatives. Amino acid derivatives represent an important category of skin penetration promoters. These compounds possess hydrophobic chains attached to an amino acid headgroup via a biodegradable ester bond. Due to the amphiphilic nature of these derivatives, it is possible for them to enter into the SC lipid barrier and significantly disorganize skin membrane lipids.HPLC of Formula: 7524-52-9
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics