146027-87-4

Upstream product

• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 146027-99-8 N-(dodecyloxycarbonyl)-(L-phenylalanyl)-L-histidyl-L-leucine methyl ester 
• 146027-74-9 N-(dodecyloxycarbonyl)-(L-phenylalanyl)-L-histidyl-L-leucine 
• 146028-13-9 N-(dodecyloxycarbonyl)-(L-phenylalanyl)-L-histidyl-L-leucyl-L-leucine methyl ester 

Downstream Products

• 146028-17-3 N-(dodecyloxycarbonyl)-(L-phenylalanyl)-L-histidyl-L-leucyl-L-leucyl-L-leucine methyl ester 

Relevant academic research and scientific papers

Mechanism of enantioselective ester cleavage by histidine-containing peptides at a micellar interface. 2. Effect of changing peptide chain length

Chiral p-nitrophenyl esters derived from the amino acid phenylalanine are cleaved by various histidine-containing tripeptides and higher oligopeptides as catalysts at a micellar interface.It is assumed that the oligopeptides adopt an internally hydrogen-b