73793-91-6

Usage

InChI:InChI=1/C22H41NO5/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20(24)23-19(22(26)27)17-18-21(25)28-2/h19H,3-18H2,1-2H3,(H,23,24)(H,26,27)/t19-/m0/s1

Upstream product

• 73793-94-9 N^α-Hexadecanoyl-L-glutamic acid γ-benzyl ester α-methyl ester 
• 112-67-4 n-hexadecanoyl chloride 
• 6234-01-1 L-glutamic acid 5-tert-butyl 1-methyl ester hydrochloride 
• 57-10-3 1-hexadecylcarboxylic acid 
• 53838-27-0 H-Glu(tBu)-OMe 
• 2419-56-9 L-glutamic acid 5-tert-butyl ester 
• 73793-93-8 N^α-Hexadecanoyl-L-glutamic acid γ-benzyl ester 
• 1676-73-9 L-glutamic acid γ-benzyl ester 

Downstream Products

• 294855-90-6 5-(2,5-dioxopyrrolidin-1-yl)-1-methylpalmitoyl L-glutamate 

Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF PROTEIN OR PEPTIDE

The present application relates to a process for the preparation of peptides or proteins or derivatives thereof by expression of synthetic oligonucleotide encoding desired protein or peptide in prokaryotic cell as ubiquitin fusion construct.

IMMUNOSTIMULATING AGENT

The present invention aims to provide an immunostimulating agent superior in an immunostimulatory effect, particularly a compound useful as a vaccine adjuvant, a pharmaceutical composition containing the compound, a vaccine containing the compound and an

ACYLATION PROCESS FOR PREPARATION OF LIRAGLUTIDE

The present application relates to an acylation process for the preparation of Liraglutide.

Method of acylating peptides and novel acylating agents

Provided is a method for acylating one or more amino groups of a peptide or protein such as GLP-1. This method includes (a) reacting a peptide or protein having at least one free amino group with an acylating agent of formula I wherein n is 0-8; R1/

The Mitogenic Principle of Escherichia coli Lipoprotein: Synthesis, Spectroscopic Characterization, and Mitogenicity of N-Palmitoyl-S--(R)-cysteine Methyl Ester

The lipophilic N-terminal part of the lipoprotein from the outer membrane of Escherichia coli, N-palmitoyl-S--(R)-cysteine, was synthesized via diacylation of L-cystine dimethyl ester, reduction to N-palmitoyl-L-cysteine m