74392-86-2

Upstream product

• 14316-06-4 D-alanine methyl ester hydrochloride 
• 74825-83-5 Boc-(L)(α-Me)Tyr-OH 
• 3978-80-1 Boc-Tyr-OH 

Downstream Products

• 153716-13-3 Ac-L-Tyr-D-Ala-OMe 
• 83049-21-2 (L,D)-Ac-Tyr(Ac)-D-Ala-OMe 
• 78537-11-8 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionyl-O-tert-butyl-L-threonine methyl ester 
• 78537-12-9 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionyl-O-tert-butyl-L-threonine 
• 78527-91-0 (R,S)-L-tyrosyl-D-alanylglycine 1,3-dimethylbutyl amide trifluoroacetate 
• 65059-13-4 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionine 
• 65229-99-4 L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionyl-L-threonine 
• 78537-08-3 (R,S)-N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycine 1,3-dimethylbutyl amide 
• 74392-87-3 Boc Tyr D_.Ala Gly Phe Leu OMe 
• 66960-03-0 Boc Tyr D_.Ala Gly Phe Met NH₂ 
• 74392-85-1 Boc Tyr D_.Ala Gly Phe Leu NH₂ 
• 66444-26-6 Methyl tert-butyloxycarbonyltyrosyl-(D)alanylglycylphenylalaninate 
• 66864-07-1 Tyr D_.Ala Gly Phe Pro NH₂ 
• 74108-23-9 Tyr D_.Ala Gly (6H)Phe Pro NH₂ 

Relevant academic research and scientific papers

5(4H)-oxazolones as intermediates in the carbodiimide- and cyanamide-promoted peptide activations in aqueous solution

The early days: Although considered a species to be avoided in peptide chemistry, the intermediacy of 5(4H)-oxazolones is demonstrated to be essential for the formation of peptides through cyanamide and carbodiimide activation in aqueous solution (see sch

Amphiphilic dendritic dipeptides and their self-assembly into helical pores

An amphiphilic dendritic dipeptide, comprises a dipeptide(s) comprising one or more of a naturally occurring or synthetic amino acids and a dendron. These are suitable for use in various formulations, films, coatings, membranes and sensors, among other ap

Evidence of the Preferential Involvement of μ Receptors in Analgesia Using Enkephalins Highly Selective for Peripheral μ or δ Receptors

In order to study the preferential involvement of μ or δ receptors in the analgesic effects of enkephalins, several peptides which selectively interact with these two kinds of receptors in peripheral organs were synthesized.The inhibitory potency on the e

Synthesis and pharmacological study of some enkephalin analogs in relation to the plurality of opiate receptors

We have synthesized a series of enkephalin analogs and measured their affinity for each type of 'opiate' receptor, the μ receptor and the δ receptor. Furthermore, we have determined their respective antinociceptive activity after intracerebroventricular i