309729-33-7

Upstream product

• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 309729-32-6 N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester 

Downstream Products

• 309729-38-2 N,N-dibenzyl-O-tert-butyl-L-tyrosylglycylglycyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester 
• 309729-39-3 N,N-dibenzyl-O-tert-butyl-L-tyrosylglycylglycyl-L-p-isothiocyanatophenylalanyl-L-leucine tert-butyl ester 
• 309729-40-6 N,N-dibenzyl-O-tert-butyl-L-tyrosylglycylglycyl-L-p-chloroacetamidophenylalanyl-L-leucine tert-butyl ester 
• 309729-41-7 N,N-dibenzyl-O-tert-butyl-L-tyrosylglycylglycyl-L-p-bromoacetamidophenylalanyl-L-leucine tert-butyl ester 
• 309729-36-0 N,N-dibenzyl-O-tert-butyl-L-tyrosylglycylglycyl-L-p-amino(9-fluorenylmethoxycarbonyl)phenylalanyl-L-leucine tert-butyl ester 

Relevant academic research and scientific papers

Synthesis and evaluation of n,n-dialkyl enkephalin-based affinity labels for δ opioid receptors

To develop affinity labels for δ opioid receptors based on peptide antagonists, the Phe4 residues of N,N-dibenzylleucine enkephalin and N,N-diallyl[Aib2,Aib3]leucine enkephalin (ICI-174,864) were substituted with either Ph