78537-07-2

Upstream product

• 74825-83-5 Boc-(L)(α-Me)Tyr-OH 
• 67706-13-2 Boc-D-alanine-glycine-OMe 
• 71591-34-9 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 3978-80-1 Boc-Tyr-OH 
• 78551-49-2 H-ala-Gly-OMe*HCl 
• 74392-86-2 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester 

Downstream Products

• 78537-08-3 (R,S)-N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycine 1,3-dimethylbutyl amide 
• 64410-47-5 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycine 
• 90815-77-3 (S)-2-Amino-3-(4-hydroxy-phenyl)-N-((R)-1-{[(3-methyl-butylcarbamoyl)-methyl]-carbamoyl}-ethyl)-propionamide 
• 112550-36-4 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-N-methyl-L-leucylglycinol 
• 112550-37-5 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-N-methyl-L-leucylglycinol 
• 112550-35-3 (S)-2-[(2-{(R)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-propionylamino}-acetyl)-methyl-amino]-4-methyl-pentanoic acid benzyl ester 
• 113845-51-5 N-Boc-L-tyrosyl-D-alanyl-glycl-L-β-(adeninyl-N⁹)-α-alanine methyl ester 
• 113845-46-8 N-Boc-L-tyrosyl-D-alanyl-glycl-L-β-(adeninyl-N⁹)-α-alanyl-L-leucine amide 
• 113845-43-5 N-Boc-L-tyrosyl-D-alanyl-glycl-L-β-(adeninyl-N⁹)-α-alanyl-L-leucine methyl ester 
• 61090-95-7 (S)-2-[(S)-2-(2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-propionylamino}-acetylamino)-3-phenyl-propionylamino]-4-methylsulfanyl-butyramide 
• 65189-64-2 H-Tyr-D-Ala-Gly-Phe-Leu-NH₂ 
• 67581-53-7 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionine methyl ester 
• 67582-10-9 Boc Tyr D_.Ala Gly Phe OH 
• 74108-23-9 Tyr D_.Ala Gly (6H)Phe Pro NH₂ 

Relevant academic research and scientific papers

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