47689-13-4

Upstream product

• 10342-52-6 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester 
• 95930-15-7 3-(N^α-benzyloxycarbonyl-N^ε-t-butoxycarbonyl-lysyl)-1,3-thiazolidine-2-thione 
• 56-40-6 glycine 
• 2212-69-3 N₂-benzyloxycarbonyl-N₆-t-butoxycarbonyl-L-lysine 4-nitrophenyl ester 
• 2212-76-2 N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysine dicyclohexylamine salt 
• 2389-60-8 Z-Lys(Boc)-OH 
• 21869-27-2 N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine ethyl ester 

Downstream Products

• 87136-46-7 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Lithium Salt 
• 87136-45-6 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Methyl Ester 

Relevant academic research and scientific papers

Synthesis and angiotensin converting enzyme inhibitory activity of L-lysyl-N-substituted glycine derivatives

The synthesis and biological activity of novel L-lysyl-N-substituted glycine derivatives which exhibit in vitro and in vivo angiotensin converting enzyme (ACE) inhibition, are described. Particularly, N-[N(α)-(1-carboxy-3-phenylpropyl)-L-lysyl]-N-(4-pheny

Peptide-bond Formation, Chemoselective Acylation of Amino Acids, and Crosslinking Reaction between Amino Acids Utilizing a Functional Five-membered Heterocycle, 1,3-Thiazolidine-2-thione

The monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thiones has been extended to the peptide-bond formation, the chemoselective acylation of amino acids having multifunctional groups, and the crosslinking reaction between amino acids.

Synthetic Studies on Sequences of Vitamin K Dependent Proteins. Gla-Arg-Gla Sequences

The synthesis of peptides containing the Gla-Arg-Gla sequence is reported.Nuclear magnetic resonance studies suggest that intramolecular salt bridge interactions occur between the guanidino group of arginine and the γ-carboxyglutamic acid.