2541-27-7

Basic information

• Product Name: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tyrosyl]-
• CAS NO: 2541-27-7
• Molecular Formula: C19H20N2O6
• Molecular Weight: 372.378
• Mol File: 2541-27-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tyrosyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tyrosyl]-(2541-27-7)
• EPA Substance Registry System: Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tyrosyl]-(2541-27-7)

Safety Data

• Hazardous Substances Data: 2541-27-7(Hazardous Substances Data)

Upstream product

• 1164-16-5 Z-L-Tyr-OH 
• 16679-94-0 N-[(phenylmethoxy)carbonyl]-L-tyrosine 
• 50715-59-8 Z-(S)-Tyr-Gly-O^tBu 
• 16677-09-1 Z-L-Tyr-Gly-OMe 
• 15373-56-5 glycyl-L-phenylalanyl-L-leucine 
• 41888-91-9 N-CBZ-L-tyrosylglycine ethyl ester 
• 13512-31-7 N-(benzyloxycarbonyl)-L-tyrosine methyl ester 

Downstream Products

• 18689-40-2 N-[N-(N-benzyloxycarbonyl-L-alanyl)-L-tyrosyl]-glycine 
• 100262-49-5 N-[N-(N-benzyloxycarbonyl-glycyl)-L-tyrosyl]-glycine 
• 6099-08-7 Gly-Tyr-Gly 
• 71667-73-7 L-alanyl=>L-tyrosyl=>glycine 
• 175659-67-3 (S)-2-[((3S,6S,8aS)-3-{2-[(S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetylamino}-4-oxo-hexahydro-pyrrolo[2,1-b][1,3]oxazine-6-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester 
• 175777-26-1 (S)-2-[((3S,6S,8aR)-3-{2-[(S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetylamino}-4-oxo-hexahydro-pyrrolo[2,1-b][1,3]oxazine-6-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester 
• 673-08-5 YG 

Relevant articles and documents

Synthesis of a precursor of bioactive pentapeptide OGP-(10-14) and the fragment of enkephalin catalyzed by MCM-22 immobilized or free proteases in organic solvents

Full enzymatic synthesis of a precursor of osteogenic growth peptide fragment (10-14), Z-Tyr-Gly-Phe-Gly-Gly-OEt, was accomplished using immobilized proteases on molecular sieve MCM-22 by adsorption as catalyst via 3+2 synthetic route for the first rime. The reuse time of immobilized enzyme was dependent on concrete reaction system. Compared with free enzyme, the reaction rate catalyzed by immobilized enzyme was remarkably enhanced and its synthetic yield was also increased in most cases. The effects of water content and the added amount of Et3N on synthesis of fragments of bioactive peptides including OGP-(10-14) and enkephalin by immobilized enzymes were different from free enzyme.

Synthesis and analysis of Leu-enkephalin analogues containing reverse turn peptidomimetics

The synthesis and 1H n.m.r. analysis of peptidomimetics of Leu-enkephalin containing bicyclic lactams is described.