47689-13-4

Basic information

• Product Name: N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine
• Synonyms: N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine
• CAS NO: 47689-13-4
• Molecular Weight: 437.493
• Mol File: 47689-13-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine(47689-13-4)
• EPA Substance Registry System: N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine(47689-13-4)

Safety Data

• Hazardous Substances Data: 47689-13-4(Hazardous Substances Data)

Upstream product

• 10342-52-6 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycine Methyl Ester 
• 2212-76-2 N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysine dicyclohexylamine salt 
• 2212-69-3 N₂-benzyloxycarbonyl-N₆-t-butoxycarbonyl-L-lysine 4-nitrophenyl ester 
• 2389-60-8 Z-Lys(Boc)-OH 
• 95930-15-7 3-(N^α-benzyloxycarbonyl-N^ε-t-butoxycarbonyl-lysyl)-1,3-thiazolidine-2-thione 
• 56-40-6 glycine 
• 21869-27-2 N-(N^α-carbobenzoxy-N^ε-tert-butoxycarbonyl-L-lysyl)glycine ethyl ester 

Downstream Products

• 87136-46-7 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Lithium Salt 
• 87136-45-6 N^α-Benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-L-lysylglycyl-L-asparaginyl-L-leucine Methyl Ester 

Relevant articles and documents

Synthesis and angiotensin converting enzyme inhibitory activity of L-lysyl-N-substituted glycine derivatives

The synthesis and biological activity of novel L-lysyl-N-substituted glycine derivatives which exhibit in vitro and in vivo angiotensin converting enzyme (ACE) inhibition, are described. Particularly, N-[N(α)-(1-carboxy-3-phenylpropyl)-L-lysyl]-N-(4-pheny

Synthetic Studies on Sequences of Vitamin K Dependent Proteins. Gla-Arg-Gla Sequences

The synthesis of peptides containing the Gla-Arg-Gla sequence is reported.Nuclear magnetic resonance studies suggest that intramolecular salt bridge interactions occur between the guanidino group of arginine and the γ-carboxyglutamic acid.